| geneid | 7520 |
|---|---|
| ensemblid | ENSG00000079246.16 |
| hgncid | 12833 |
| symbol | XRCC5 |
| name | X-ray repair cross complementing 5 |
| refseq_nuc | NM_021141.4 |
| refseq_prot | NP_066964.1 |
| ensembl_nuc | ENST00000392132.7 |
| ensembl_prot | ENSP00000375977.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 216109348 |
| end | 216206293 |
| strand | + |
| ver | v1.2 |
| region | chr2:216109348-216206293 |
| region5000 | chr2:216104348-216211293 |
| regionname0 | XRCC5_chr2_216109348_216206293 |
| regionname5000 | XRCC5_chr2_216104348_216211293 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 732 | 349 | 95 | 66 | 130 | 14 | 42 | 96 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0002 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0003 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0004 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2199 | 305 | 85 | 58 | 115 | 14 | 32 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0002 | 1/0 | 2199 | 42 | 10 | 6 | 15 | 0 | 10 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0003 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0004 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0005 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0006 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| c0007 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1181 | 147 | 11 | 37 | 77 | 8 | 13 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0002 | 0/0 | 1181 | 69 | 38 | 8 | 13 | 0 | 10 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0003 | 1/0 | 1181 | 57 | 19 | 12 | 15 | 2 | 8 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0004 | 0/0 | 1181 | 53 | 14 | 3 | 24 | 3 | 9 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0005 | 0/0 | 1181 | 7 | 0 | 5 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0006 | 0/0 | 1181 | 7 | 7 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0007 | 0/0 | 1181 | 4 | 4 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0008 | 0/0 | 1181 | 3 | 0 | 0 | 0 | 1 | 2 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0009 | 0/0 | 1181 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0010 | 0/0 | 1181 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0011 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| t0012 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2199 | 305 | 85 | 58 | 115 | 14 | 32 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002 | 1/0 | 2199 | 42 | 10 | 6 | 15 | 0 | 10 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0005 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0006 | 0/0 | 2199 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0002c0007 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0003c0004 | 0/0 | 2199 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0004c0003 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3379 | 143 | 11 | 36 | 74 | 8 | 13 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0002 | 0/0 | 3379 | 37 | 34 | 2 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0003 | 0/0 | 3379 | 54 | 19 | 12 | 14 | 2 | 7 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0004 | 0/0 | 3379 | 51 | 12 | 3 | 24 | 3 | 9 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0005 | 0/0 | 3379 | 7 | 0 | 5 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0006 | 0/0 | 3379 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0007 | 0/0 | 3379 | 4 | 4 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0008 | 0/0 | 3379 | 3 | 0 | 0 | 0 | 1 | 2 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0009 | 0/0 | 3379 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0011 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0001t0012 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0001 | 0/0 | 3379 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0002 | 0/0 | 3379 | 31 | 4 | 5 | 13 | 0 | 9 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0003 | 1/0 | 3379 | 2 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0004 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0006 | 0/0 | 3379 | 5 | 5 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0002t0010 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0005t0001 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0001c0006t0002 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0002c0007t0003 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0003c0004t0001 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| a0004c0003t0004 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | copy fasta | chr2 | 216104348 | 216211293 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0003g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0010g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0006t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0002c0007t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0003c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0004c0003t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0248 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0204 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | FIN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0056 | EUR | FIN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0317 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0338 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0303 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0337 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01175 | hp1 | a0001 | c0006 | t0002 | g0284 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0256 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0335 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0293 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01433 | hp1 | a0001 | c0005 | t0001 | g0045 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0334 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0288 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0318 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0287 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02293 | hp2 | a0001 | c0002 | t0010 | g0296 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0349 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0300 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0271 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0188 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0331 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0327 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0326 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02965 | hp2 | a0004 | c0003 | t0004 | g0129 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0329 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0270 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0003 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0330 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0295 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0313 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0301 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0249 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0325 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0003 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0291 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0292 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0184 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0216 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0217 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0259 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0213 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0312 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0273 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18959 | hp1 | a0003 | c0004 | t0001 | g0102 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19002 | hp2 | a0002 | c0007 | t0003 | g0082 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | LWK | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | LWK | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0063 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ASW | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0316 | AFR | ASW | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0053 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0258 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0214 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | GIH | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | GIH | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0328 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0182 | REF | REF | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0272 | REF | REF | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216122110
|
T | A | 1 | a0004 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.540T>A | p.Asp180Glu | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/21 | 629/3379 | 540/2199 | 180/732 | chr2 | 216122110 | ||
| chr2:216125952
|
T | C | 1 | a0003 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.719T>C | p.Ile240Thr | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/21 | 808/3379 | 719/2199 | 240/732 | chr2 | 216125952 | ||
| chr2:216148212
|
C | G | 1 | a0002 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1606C>G | p.Leu536Val | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/21 | 1695/3379 | 1606/2199 | 536/732 | chr2 | 216148212 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216137159
|
T | C | 1 | a0001c0005 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1185T>C | p.Tyr395Tyr | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/21 | 1274/3379 | 1185/2199 | 395/732 | chr2 | 216137159 | ||
| chr2:216148178
|
A | G | 6 | a0001c0001a0001c0005a0001c0006others(3): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
synonymous_variant | LOW | c.1572A>G | p.Thr524Thr | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/21 | 1661/3379 | 1572/2199 | 524/732 | chr2 | 216148178 | ||
| chr2:216204378
|
T | C | 1 | a0001c0006 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.2166T>C | p.Gly722Gly | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/21 | 2255/3379 | 2166/2199 | 722/732 | chr2 | 216204378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216109433
|
C | G | 1 | a0001c0001t0012 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/21 | 4 | chr2 | 216109433 | |||||
| chr2:216205334
|
G | A | 2 | a0001c0001t0005a0001c0002t0010 | 8 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*132G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 132 | chr2 | 216205334 | |||||
| chr2:216205503
|
A | G | 1 | a0001c0001t0007 | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*301A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 301 | chr2 | 216205503 | |||||
| chr2:216205525
|
T | C | 4 | a0001c0001t0004a0001c0001t0008a0001c0002t0004others(1): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*323T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 323 | chr2 | 216205525 | |||||
| chr2:216205653
|
A | G | 5 | a0001c0001t0002a0001c0001t0012a0001c0002t0002others(2): Show | 71 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*451A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 451 | chr2 | 216205653 | |||||
| chr2:216205845
|
T | A | 2 | a0001c0001t0006a0001c0002t0006 | 7 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*643T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 643 | chr2 | 216205845 | |||||
| chr2:216205929
|
C | A | 4 | a0001c0001t0004a0001c0001t0008a0001c0002t0004others(1): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*727C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 727 | chr2 | 216205929 | |||||
| chr2:216206013
|
G | A | 1 | a0001c0001t0008 | 3 | HG00140.hp2 HG03492.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*811G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 811 | chr2 | 216206013 | |||||
| chr2:216206043
|
G | A | 6 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(3): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 841 | chr2 | 216206043 | |||||
| chr2:216206098
|
A | G | 1 | a0001c0001t0011 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*896A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 896 | chr2 | 216206098 | |||||
| chr2:216206254
|
A | G | 1 | a0001c0001t0012 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 1052 | chr2 | 216206254 | |||||
| chr2:216206270
|
A | G | 1 | a0001c0001t0009 | 2 | HG02886.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1068A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 21/21 | 1068 | chr2 | 216206270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216109481
|
G | C | 1 | a0001c0001t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.21+24G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109481 | ||||||
| chr2:216109496
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0006g0007a0001c0001t0012g0005 | 3 | HG02109.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.21+39G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109496 | ||||||
| chr2:216109545
|
A | T | 3 | a0001c0001t0002g0347a0001c0001t0002g0348a0001c0001t0003g0349 | 3 | HG02145.hp2 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.21+88A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109545 | ||||||
| chr2:216109566
|
G | A | 33 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.21+109G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109566 | ||||||
| chr2:216109567
|
A | G | 4 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345others(1): Show | 4 | NA18952.hp1 NA18964.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+110A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109567 | ||||||
| chr2:216109587
|
A | C | 5 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.21+130A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109587 | ||||||
| chr2:216109671
|
C | T | 4 | a0001c0001t0001g0339a0001c0001t0004g0340a0001c0001t0004g0341others(1): Show | 4 | NA18942.hp2 NA18963.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+214C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109671 | ||||||
| chr2:216109770
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.21+313T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109770 | ||||||
| chr2:216109808
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+351C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109808 | ||||||
| chr2:216109833
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21+376T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216109833 | ||||||
| chr2:216110013
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.21+556A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110013 | ||||||
| chr2:216110071
|
C | T | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.21+614C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110071 | ||||||
| chr2:216110247
|
AT | A | 183 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(180): Show | 183 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.21+801delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 216110247 | |||||
| chr2:216110420
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.21+963T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110420 | ||||||
| chr2:216110490
|
G | A | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.21+1033G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110490 | ||||||
| chr2:216110582
|
G | A | 125 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0196others(122): Show | 126 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.21+1125G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110582 | ||||||
| chr2:216110583
|
G | A | 33 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.21+1126G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110583 | ||||||
| chr2:216110865
|
A | G | 144 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(141): Show | 144 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.21+1408A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110865 | ||||||
| chr2:216110890
|
G | GT | 37 | a0001c0001t0001g0183a0001c0001t0002g0009a0001c0001t0002g0010others(34): Show | 37 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.21+1443dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 216110890 | |||||
| chr2:216111174
|
T | C | 1 | a0001c0005t0001g0045 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.21+1717T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111174 | ||||||
| chr2:216111321
|
A | C | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-1695A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111321 | ||||||
| chr2:216111411
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.22-1605C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111411 | ||||||
| chr2:216111857
|
A | C | 16 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(13): Show | 16 | HG01884.hp2 HG01975.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.22-1159A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111857 | ||||||
| chr2:216111908
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.22-1108C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111908 | ||||||
| chr2:216111908
|
C | T | 1 | a0001c0001t0001g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.22-1108C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111908 | ||||||
| chr2:216111995
|
C | T | 4 | a0001c0001t0004g0330a0001c0001t0004g0331a0001c0001t0004g0332others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-1021C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111995 | ||||||
| chr2:216112049
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.22-967G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112049 | ||||||
| chr2:216112077
|
G | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.22-939G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112077 | ||||||
| chr2:216112164
|
T | A | 2 | a0001c0001t0002g0347a0001c0001t0002g0348 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.22-852T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112164 | ||||||
| chr2:216112230
|
T | A | 1 | a0001c0001t0003g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22-786T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112230 | ||||||
| chr2:216112305
|
A | G | 125 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0196others(122): Show | 126 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.22-711A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112305 | ||||||
| chr2:216112335
|
T | TCACCGCT others(13): Show |
5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-676_22-657dupGC others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 216112335 | |||||
| chr2:216112451
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22-565G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112451 | ||||||
| chr2:216112487
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.22-529T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112487 | ||||||
| chr2:216112532
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18961.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.22-484C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112532 | ||||||
| chr2:216112600
|
G | A | 83 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0196others(80): Show | 84 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.22-416G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112600 | ||||||
| chr2:216112859
|
T | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG00438.hp1 NA18966.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-157T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112859 | ||||||
| chr2:216112907
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00438.hp2 NA18949.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.22-109C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112907 | ||||||
| chr2:216112961
|
A | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.22-55A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112961 | ||||||
| chr2:216112978
|
C | G | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.22-38C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112978 | ||||||
| chr2:216112978
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.22-38C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216112978 | ||||||
| chr2:216113006
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.22-10T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216113006 | ||||||
| chr2:216113221
|
G | A | 1 | a0001c0001t0004g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135+92G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113221 | ||||||
| chr2:216113354
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.135+225C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113354 | ||||||
| chr2:216113369
|
G | A | 1 | a0001c0001t0004g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.135+240G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113369 | ||||||
| chr2:216113452
|
C | A | 2 | a0001c0001t0009g0188a0001c0001t0009g0189 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.135+323C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113452 | ||||||
| chr2:216113735
|
G | T | 12 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(9): Show | 12 | HG00673.hp2 HG02015.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.135+606G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113735 | ||||||
| chr2:216113776
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.135+647G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113776 | ||||||
| chr2:216113795
|
A | T | 74 | a0001c0001t0001g0185a0001c0001t0001g0196a0001c0001t0001g0198others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.135+666A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113795 | ||||||
| chr2:216113799
|
T | C | 125 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0196others(122): Show | 126 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.135+670T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113799 | ||||||
| chr2:216113801
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+672C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216113801 | ||||||
| chr2:216114121
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(4): Show | 7 | HG00438.hp1 NA18966.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+992A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114121 | ||||||
| chr2:216114136
|
G | A | 2 | a0001c0001t0004g0053a0001c0001t0004g0054 | 2 | HG03486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.135+1007G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114136 | ||||||
| chr2:216114382
|
C | T | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1253C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114382 | ||||||
| chr2:216114445
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+1316A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114445 | ||||||
| chr2:216114732
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+1603A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114732 | ||||||
| chr2:216114748
|
T | G | 2 | a0001c0001t0004g0053a0001c0001t0004g0054 | 2 | HG03486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.135+1619T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114748 | ||||||
| chr2:216114756
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0004g0055 | 2 | HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.135+1627G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114756 | ||||||
| chr2:216114773
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp2 HG03453.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+1644T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114773 | ||||||
| chr2:216114904
|
A | G | 1 | a0001c0001t0003g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.136-1755A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114904 | ||||||
| chr2:216114907
|
A | C | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0008others(35): Show | 38 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-1752A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114907 | ||||||
| chr2:216114934
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01884.hp1 HG01952.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1725A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114934 | ||||||
| chr2:216114956
|
A | C | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-1703A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114956 | ||||||
| chr2:216114957
|
G | C | 23 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0013others(20): Show | 23 | HG01884.hp2 HG01975.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.136-1702G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216114957 | ||||||
| chr2:216115030
|
CAAAG | C | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0008others(35): Show | 38 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-1626_136-1623d others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115030 | |||||
| chr2:216115131
|
A | G | 23 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0013others(20): Show | 23 | HG01884.hp2 HG01975.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.136-1528A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115131 | ||||||
| chr2:216115175
|
TTG | T | 129 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0185others(126): Show | 130 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.136-1482_136-1481d others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115175 | |||||
| chr2:216115185
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-1474C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115185 | ||||||
| chr2:216115205
|
A | T | 9 | a0001c0001t0001g0336a0001c0001t0003g0006a0001c0001t0003g0041others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1454A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115205 | ||||||
| chr2:216115305
|
T | C | 1 | a0001c0001t0006g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.136-1354T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115305 | ||||||
| chr2:216115437
|
G | A | 137 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(134): Show | 137 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.136-1222G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115437 | ||||||
| chr2:216115535
|
ATTG | A | 74 | a0001c0001t0001g0185a0001c0001t0001g0198a0001c0001t0001g0242others(71): Show | 75 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.136-1119_136-1117d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115535 | |||||
| chr2:216115659
|
TAGAC | T | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0008others(35): Show | 38 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-997_136-994del others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115659 | |||||
| chr2:216115754
|
G | C | 1 | a0001c0001t0001g0264 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.136-905G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115754 | ||||||
| chr2:216115799
|
A | G | 1 | a0001c0001t0007g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136-860A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216115799 | ||||||
| chr2:216115810
|
A | AT | 77 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0242others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.136-839dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115810 | |||||
| chr2:216115945
|
ATACT | A | 6 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0004g0259others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-711_136-708del others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 216115945 | |||||
| chr2:216116053
|
C | A | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-606C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116053 | ||||||
| chr2:216116079
|
A | T | 1 | a0001c0001t0003g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136-580A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116079 | ||||||
| chr2:216116110
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.136-549T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116110 | ||||||
| chr2:216116239
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02145.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.136-420C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116239 | ||||||
| chr2:216116345
|
C | G | 2 | a0001c0002t0002g0323a0001c0002t0002g0324 | 2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.136-314C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116345 | ||||||
| chr2:216116361
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.136-298C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116361 | ||||||
| chr2:216116463
|
G | A | 132 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.136-196G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 2/20 | chr2 | 216116463 | ||||||
| chr2:216116922
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.319+80C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216116922 | ||||||
| chr2:216116943
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319+101A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216116943 | ||||||
| chr2:216117208
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.319+366C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117208 | ||||||
| chr2:216117382
|
G | T | 2 | a0001c0001t0005g0337a0001c0001t0005g0338 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.320-364G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117382 | ||||||
| chr2:216117394
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0006g0007a0001c0001t0012g0005 | 3 | HG02109.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.320-352G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117394 | ||||||
| chr2:216117412
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA18964.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.320-334A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117412 | ||||||
| chr2:216117455
|
G | A | 132 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.320-291G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117455 | ||||||
| chr2:216117582
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.320-164G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117582 | ||||||
| chr2:216117631
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.320-115A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117631 | ||||||
| chr2:216117647
|
C | G | 71 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(68): Show | 71 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.320-99C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117647 | ||||||
| chr2:216117729
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-17A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 3/20 | chr2 | 216117729 | ||||||
| chr2:216117968
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.368+174T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216117968 | ||||||
| chr2:216118056
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.368+262A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118056 | ||||||
| chr2:216118135
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+341C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118135 | ||||||
| chr2:216118174
|
T | C | 4 | a0001c0001t0003g0191a0001c0001t0006g0190a0001c0001t0009g0188others(1): Show | 4 | HG02280.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+380T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118174 | ||||||
| chr2:216118176
|
G | GT | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG01884.hp1 HG01943.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.368+395dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr2 | 216118176 | |||||
| chr2:216118179
|
T | G | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.368+385T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118179 | ||||||
| chr2:216118222
|
A | T | 78 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.368+428A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118222 | ||||||
| chr2:216118277
|
A | G | 92 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.368+483A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118277 | ||||||
| chr2:216118442
|
G | A | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.369-601G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118442 | ||||||
| chr2:216118451
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.369-592A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118451 | ||||||
| chr2:216118592
|
C | A | 1 | a0001c0002t0002g0265 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.369-451C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118592 | ||||||
| chr2:216118606
|
T | A | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.369-437T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118606 | ||||||
| chr2:216118697
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.369-346G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118697 | ||||||
| chr2:216118725
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.369-318T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118725 | ||||||
| chr2:216118850
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.369-193A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118850 | ||||||
| chr2:216118911
|
A | G | 4 | a0001c0001t0003g0191a0001c0001t0006g0190a0001c0001t0009g0188others(1): Show | 4 | HG02280.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-132A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 4/20 | chr2 | 216118911 | ||||||
| chr2:216119407
|
A | T | 1 | a0001c0001t0003g0257 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.491+242A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216119407 | ||||||
| chr2:216119454
|
A | C | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491+289A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216119454 | ||||||
| chr2:216119538
|
T | C | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.491+373T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216119538 | ||||||
| chr2:216119692
|
G | T | 1 | a0001c0001t0004g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.491+527G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216119692 | ||||||
| chr2:216119773
|
C | T | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.491+608C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216119773 | ||||||
| chr2:216120021
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.491+856T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120021 | ||||||
| chr2:216120092
|
C | CGACA | 57 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(54): Show | 57 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.491+928_491+931dup others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 216120092 | |||||
| chr2:216120340
|
T | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.491+1175T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120340 | ||||||
| chr2:216120535
|
AT | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00438.hp2 NA18949.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.491+1371delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120535 | ||||||
| chr2:216120538
|
C | G | 1 | a0001c0001t0003g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.491+1373C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120538 | ||||||
| chr2:216120738
|
G | A | 1 | a0001c0001t0003g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.492-1324G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120738 | ||||||
| chr2:216120741
|
G | GTTGT | 132 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.492-1314_492-1311d others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 216120741 | |||||
| chr2:216120767
|
G | A | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.492-1295G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120767 | ||||||
| chr2:216120857
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.492-1205T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120857 | ||||||
| chr2:216120892
|
C | T | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.492-1170C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120892 | ||||||
| chr2:216120942
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.492-1120G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120942 | ||||||
| chr2:216120963
|
G | T | 1 | a0001c0001t0003g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.492-1099G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216120963 | ||||||
| chr2:216121007
|
A | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.492-1055A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121007 | ||||||
| chr2:216121015
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG00544.hp2 HG01070.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.492-1047C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121015 | ||||||
| chr2:216121016
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.492-1046G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121016 | ||||||
| chr2:216121046
|
T | C | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.492-1016T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121046 | ||||||
| chr2:216121618
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.492-444C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121618 | ||||||
| chr2:216121768
|
G | C | 1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.492-294G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121768 | ||||||
| chr2:216121972
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0006g0007a0001c0001t0012g0005 | 3 | HG02109.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.492-90A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216121972 | ||||||
| chr2:216122016
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.492-46C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 5/20 | chr2 | 216122016 | ||||||
| chr2:216122273
|
A | T | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.683+20A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122273 | ||||||
| chr2:216122403
|
C | A | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.683+150C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122403 | ||||||
| chr2:216122445
|
A | G | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.683+192A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122445 | ||||||
| chr2:216122666
|
T | C | 1 | a0001c0001t0004g0101 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.683+413T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122666 | ||||||
| chr2:216122720
|
T | A | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.683+467T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122720 | ||||||
| chr2:216122741
|
G | A | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.683+488G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122741 | ||||||
| chr2:216122753
|
G | GA | 6 | a0001c0001t0001g0339a0001c0001t0001g0343a0001c0001t0002g0014others(3): Show | 6 | HG00140.hp2 HG00597.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.683+513dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr2 | 216122753 | |||||
| chr2:216122753
|
GA | G | 9 | a0001c0001t0001g0058a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG00438.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.683+513delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr2 | 216122753 | |||||
| chr2:216122766
|
A | C | 1 | a0001c0001t0004g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.683+513A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122766 | ||||||
| chr2:216122958
|
A | G | 1 | a0001c0001t0004g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.683+705A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216122958 | ||||||
| chr2:216123186
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.683+933A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123186 | ||||||
| chr2:216123238
|
A | C | 132 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.683+985A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123238 | ||||||
| chr2:216123241
|
C | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(9): Show | 12 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.683+988C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123241 | ||||||
| chr2:216123486
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.683+1233G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123486 | ||||||
| chr2:216123511
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.683+1258C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123511 | ||||||
| chr2:216123748
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683+1495A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123748 | ||||||
| chr2:216123801
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0174 | 3 | HG00639.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.683+1548G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123801 | ||||||
| chr2:216123894
|
A | G | 1 | a0001c0002t0002g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.683+1641A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123894 | ||||||
| chr2:216123922
|
T | G | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+1669T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123922 | ||||||
| chr2:216123949
|
A | G | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+1696A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216123949 | ||||||
| chr2:216124015
|
C | G | 14 | a0001c0001t0001g0186a0001c0001t0001g0336a0001c0001t0003g0006others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.683+1762C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124015 | ||||||
| chr2:216124112
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.684-1805T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124112 | ||||||
| chr2:216124186
|
T | A | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.684-1731T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124186 | ||||||
| chr2:216124208
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684-1709A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124208 | ||||||
| chr2:216124268
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.684-1649A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124268 | ||||||
| chr2:216124403
|
T | C | 92 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.684-1514T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124403 | ||||||
| chr2:216124831
|
C | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02293.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.684-1086C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216124831 | ||||||
| chr2:216125095
|
A | C | 9 | a0001c0001t0001g0336a0001c0001t0003g0006a0001c0001t0003g0041others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-822A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216125095 | ||||||
| chr2:216125202
|
CT | C | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.684-703delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr2 | 216125202 | |||||
| chr2:216125344
|
T | C | 1 | a0001c0001t0003g0254 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.684-573T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216125344 | ||||||
| chr2:216125424
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.684-493C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216125424 | ||||||
| chr2:216125445
|
C | T | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.684-472C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216125445 | ||||||
| chr2:216125805
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.684-112C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 6/20 | chr2 | 216125805 | ||||||
| chr2:216126049
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0004g0199a0001c0001t0004g0200others(5): Show | 8 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+18A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126049 | ||||||
| chr2:216126097
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+66A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126097 | ||||||
| chr2:216126203
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.798+172G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126203 | ||||||
| chr2:216126231
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+200A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126231 | ||||||
| chr2:216126248
|
C | T | 92 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.798+217C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126248 | ||||||
| chr2:216126316
|
A | T | 1 | a0001c0001t0004g0145 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.798+285A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126316 | ||||||
| chr2:216126381
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.798+350G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126381 | ||||||
| chr2:216126409
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.798+378T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126409 | ||||||
| chr2:216126504
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0322 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.798+473T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126504 | ||||||
| chr2:216126606
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.798+575A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126606 | ||||||
| chr2:216126770
|
G | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+739G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126770 | ||||||
| chr2:216126845
|
C | T | 14 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0133others(11): Show | 14 | HG01258.hp1 HG01496.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-691C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126845 | ||||||
| chr2:216126870
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.799-666A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126870 | ||||||
| chr2:216126906
|
T | G | 32 | a0001c0001t0001g0185a0001c0001t0001g0251a0001c0001t0001g0252others(29): Show | 33 | HG00597.hp2 HG01099.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.799-630T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216126906 | ||||||
| chr2:216127035
|
T | G | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.799-501T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127035 | ||||||
| chr2:216127139
|
C | G | 5 | a0001c0001t0001g0186a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-397C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127139 | ||||||
| chr2:216127212
|
C | A | 150 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(147): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.799-324C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127212 | ||||||
| chr2:216127273
|
C | T | 4 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0247others(1): Show | 4 | HG00099.hp2 HG01243.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-263C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127273 | ||||||
| chr2:216127370
|
T | C | 150 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(147): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.799-166T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127370 | ||||||
| chr2:216127388
|
T | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.799-148T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 7/20 | chr2 | 216127388 | ||||||
| chr2:216128197
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.937+523C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128197 | ||||||
| chr2:216128235
|
T | C | 14 | a0001c0001t0001g0186a0001c0001t0001g0336a0001c0001t0003g0006others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.937+561T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128235 | ||||||
| chr2:216128442
|
A | AGGT | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+778_937+780dup others(3): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr2 | 216128442 | |||||
| chr2:216128467
|
C | T | 1 | a0001c0001t0004g0221 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.937+793C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128467 | ||||||
| chr2:216128648
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.937+974G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128648 | ||||||
| chr2:216128755
|
A | G | 132 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.937+1081A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128755 | ||||||
| chr2:216128797
|
G | A | 14 | a0001c0001t0001g0186a0001c0001t0001g0336a0001c0001t0003g0006others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.937+1123G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128797 | ||||||
| chr2:216128819
|
T | G | 78 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.937+1145T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128819 | ||||||
| chr2:216128888
|
C | A | 282 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(279): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.937+1214C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128888 | ||||||
| chr2:216129029
|
G | A | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.937+1355G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129029 | ||||||
| chr2:216129182
|
C | T | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG00741.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.937+1508C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129182 | ||||||
| chr2:216129332
|
T | C | 18 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.938-1543T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129332 | ||||||
| chr2:216129371
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0322 | 2 | HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.938-1504C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129371 | ||||||
| chr2:216129423
|
T | C | 14 | a0001c0001t0001g0186a0001c0001t0001g0336a0001c0001t0003g0006others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.938-1452T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129423 | ||||||
| chr2:216129639
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.938-1236T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129639 | ||||||
| chr2:216129667
|
G | A | 5 | a0001c0001t0001g0186a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-1208G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129667 | ||||||
| chr2:216129674
|
A | C | 38 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0242others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.938-1201A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129674 | ||||||
| chr2:216129846
|
T | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.938-1029T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129846 | ||||||
| chr2:216129901
|
C | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG01891.hp2 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.938-974C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129901 | ||||||
| chr2:216129927
|
C | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-948C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216129927 | ||||||
| chr2:216130021
|
A | G | 18 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.938-854A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130021 | ||||||
| chr2:216130061
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0006g0007a0001c0001t0012g0005 | 3 | HG02109.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.938-814G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130061 | ||||||
| chr2:216130236
|
C | CT | 149 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(146): Show | 149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.938-622dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr2 | 216130236 | |||||
| chr2:216130236
|
CT | C | 21 | a0001c0001t0001g0058a0001c0001t0001g0251a0001c0001t0002g0008others(18): Show | 21 | HG01515.hp1 HG01515.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.938-622delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr2 | 216130236 | |||||
| chr2:216130315
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.938-560A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130315 | ||||||
| chr2:216130359
|
C | G | 3 | a0001c0001t0003g0006a0001c0001t0006g0007a0001c0001t0012g0005 | 3 | HG02109.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.938-516C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130359 | ||||||
| chr2:216130427
|
C | A | 1 | a0001c0001t0003g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.938-448C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130427 | ||||||
| chr2:216130868
|
T | C | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.938-7T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216130868 | ||||||
| chr2:216131120
|
A | T | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+133A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216131120 | ||||||
| chr2:216131237
|
C | T | 1 | a0001c0002t0006g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1050+250C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216131237 | ||||||
| chr2:216131455
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1050+468T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216131455 | ||||||
| chr2:216131864
|
T | C | 78 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1051-461T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216131864 | ||||||
| chr2:216131920
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1051-405A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216131920 | ||||||
| chr2:216132130
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1051-195A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 9/20 | chr2 | 216132130 | ||||||
| chr2:216132443
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1113+56G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216132443 | ||||||
| chr2:216132636
|
G | A | 2 | a0001c0001t0006g0007a0001c0001t0012g0005 | 2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1113+249G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216132636 | ||||||
| chr2:216132759
|
T | C | 18 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(15): Show | 18 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+372T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216132759 | ||||||
| chr2:216132827
|
C | A | 1 | a0001c0001t0003g0257 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1113+440C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216132827 | ||||||
| chr2:216132897
|
G | C | 1 | a0001c0001t0004g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1113+510G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216132897 | ||||||
| chr2:216133127
|
AG | A | 5 | a0001c0001t0001g0336a0001c0001t0003g0334a0001c0001t0005g0335others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+741delG | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133127 | ||||||
| chr2:216133227
|
A | T | 1 | a0001c0002t0002g0315 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1113+840A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133227 | ||||||
| chr2:216133363
|
G | A | 33 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1113+976G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133363 | ||||||
| chr2:216133387
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1113+1000G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133387 | ||||||
| chr2:216133458
|
G | A | 1 | a0001c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1113+1071G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133458 | ||||||
| chr2:216133496
|
C | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+1109C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133496 | ||||||
| chr2:216133496
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1113+1109C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133496 | ||||||
| chr2:216133590
|
A | G | 346 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(343): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1113+1203A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133590 | ||||||
| chr2:216133636
|
A | G | 6 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0085others(3): Show | 6 | HG02004.hp1 HG02027.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+1249A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133636 | ||||||
| chr2:216133735
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1113+1348A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133735 | ||||||
| chr2:216133741
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1113+1354A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133741 | ||||||
| chr2:216133938
|
A | G | 79 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0185others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1113+1551A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133938 | ||||||
| chr2:216133966
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1113+1579A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216133966 | ||||||
| chr2:216134056
|
T | A | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+1669T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134056 | ||||||
| chr2:216134170
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1113+1783A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134170 | ||||||
| chr2:216134245
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1113+1858A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134245 | ||||||
| chr2:216134281
|
T | G | 5 | a0001c0001t0001g0186a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+1894T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134281 | ||||||
| chr2:216134292
|
A | T | 5 | a0001c0001t0002g0157a0001c0001t0003g0156a0001c0001t0003g0158others(2): Show | 5 | HG03130.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+1905A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134292 | ||||||
| chr2:216134417
|
T | C | 1 | a0001c0001t0002g0348 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1113+2030T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134417 | ||||||
| chr2:216134419
|
G | GT | 12 | a0001c0001t0001g0186a0001c0001t0003g0041a0001c0001t0003g0191others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+2043dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216134419 | |||||
| chr2:216134432
|
T | G | 1 | a0001c0001t0003g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1113+2045T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134432 | ||||||
| chr2:216134588
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1113+2201C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134588 | ||||||
| chr2:216134616
|
A | T | 282 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(279): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+2229A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134616 | ||||||
| chr2:216134672
|
A | AC | 19 | a0001c0001t0001g0198a0001c0001t0003g0006a0001c0001t0003g0245others(16): Show | 19 | HG00140.hp2 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+2295dupC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216134672 | |||||
| chr2:216134672
|
AC | A | 170 | a0001c0001t0001g0042a0001c0001t0001g0059a0001c0001t0001g0060others(167): Show | 170 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.1113+2295delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216134672 | |||||
| chr2:216134675
|
C | G | 1 | a0001c0002t0006g0003 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1113+2288C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134675 | ||||||
| chr2:216134676
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1113+2289C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134676 | ||||||
| chr2:216134678
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1113+2291C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134678 | ||||||
| chr2:216134681
|
C | G | 1 | a0001c0001t0003g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113+2294C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134681 | ||||||
| chr2:216134682
|
C | G | 2 | a0001c0002t0002g0312a0001c0002t0002g0313 | 2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1113+2295C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134682 | ||||||
| chr2:216134682
|
CT | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0205a0001c0001t0004g0206others(1): Show | 5 | NA18943.hp2 NA18969.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+2296delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134682 | ||||||
| chr2:216134706
|
G | A | 36 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1113+2319G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216134706 | ||||||
| chr2:216135092
|
T | G | 282 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(279): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1114-1996T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135092 | ||||||
| chr2:216135095
|
TTTTG | T | 279 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1114-1973_1114-197 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216135095 | |||||
| chr2:216135111
|
GTTTGT | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0174 | 3 | HG00639.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1114-1968_1114-196 others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216135111 | |||||
| chr2:216135120
|
G | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0174 | 3 | HG00639.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1114-1968G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135120 | ||||||
| chr2:216135345
|
T | TGGTATGA others(10): Show |
1 | a0001c0001t0003g0239 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114-1742_1114-172 others(21): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216135345 | |||||
| chr2:216135364
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114-1724G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135364 | ||||||
| chr2:216135601
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1114-1487C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135601 | ||||||
| chr2:216135677
|
T | C | 1 | a0001c0001t0011g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1114-1411T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135677 | ||||||
| chr2:216135798
|
CA | C | 149 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(146): Show | 149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1114-1278delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216135798 | |||||
| chr2:216135832
|
G | A | 1 | a0001c0001t0005g0275 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1114-1256G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135832 | ||||||
| chr2:216136217
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1114-871G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136217 | ||||||
| chr2:216136356
|
C | CA | 22 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(19): Show | 23 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.1114-717dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216136356 | |||||
| chr2:216136367
|
A | AAAAAAAG | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG01346.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-717_1114-716i others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216136367 | |||||
| chr2:216136367
|
A | AAAAAAG | 264 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(261): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1114-717_1114-716i others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216136367 | |||||
| chr2:216136367
|
A | AAAAAG | 9 | a0001c0001t0001g0062a0001c0001t0001g0336a0001c0001t0003g0334others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-717_1114-713d others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr2 | 216136367 | |||||
| chr2:216136617
|
A | G | 2 | a0001c0002t0002g0323a0001c0002t0002g0324 | 2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1114-471A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136617 | ||||||
| chr2:216136753
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1114-335A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136753 | ||||||
| chr2:216136824
|
C | T | 151 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(148): Show | 151 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1114-264C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136824 | ||||||
| chr2:216136869
|
G | A | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-219G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136869 | ||||||
| chr2:216136955
|
C | T | 1 | a0001c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1114-133C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136955 | ||||||
| chr2:216136983
|
A | C | 1 | a0001c0001t0004g0145 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1114-105A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136983 | ||||||
| chr2:216136989
|
A | G | 1 | a0001c0001t0003g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1114-99A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216136989 | ||||||
| chr2:216137272
|
T | G | 29 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.1251+47T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216137272 | ||||||
| chr2:216137355
|
C | G | 4 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0247others(1): Show | 4 | HG00099.hp2 HG01243.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251+130C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216137355 | ||||||
| chr2:216137480
|
T | C | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1251+255T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216137480 | ||||||
| chr2:216137483
|
CATA | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251+260_1251+262d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 216137483 | |||||
| chr2:216137816
|
T | C | 347 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(344): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1252-273T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216137816 | ||||||
| chr2:216137860
|
C | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1252-229C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216137860 | ||||||
| chr2:216138081
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG01070.hp2 | splice_region_variant&intron_variant | LOW | c.1252-8C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 11/20 | chr2 | 216138081 | ||||||
| chr2:216138214
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1342+35A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138214 | ||||||
| chr2:216138228
|
T | C | 2 | a0001c0001t0004g0250a0001c0001t0004g0263 | 2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1342+49T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138228 | ||||||
| chr2:216138429
|
T | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1342+250T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138429 | ||||||
| chr2:216138702
|
G | A | 28 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0339others(25): Show | 28 | HG01099.hp1 HG01515.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.1342+523G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138702 | ||||||
| chr2:216138823
|
AC | A | 8 | a0001c0001t0003g0334a0001c0001t0005g0275a0001c0001t0005g0286others(5): Show | 8 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1342+645delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138823 | ||||||
| chr2:216138952
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1342+773G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138952 | ||||||
| chr2:216139205
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0174 | 3 | HG00639.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1342+1026G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139205 | ||||||
| chr2:216139233
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1342+1054A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139233 | ||||||
| chr2:216139235
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1342+1056C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139235 | ||||||
| chr2:216139289
|
G | A | 7 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1342+1110G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139289 | ||||||
| chr2:216139315
|
TAC | T | 102 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(99): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1342+1138_1342+113 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 216139315 | |||||
| chr2:216139376
|
G | C | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1342+1197G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139376 | ||||||
| chr2:216139485
|
C | T | 1 | a0001c0001t0004g0207 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1342+1306C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139485 | ||||||
| chr2:216139519
|
C | T | 23 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(20): Show | 23 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1342+1340C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139519 | ||||||
| chr2:216139678
|
T | C | 2 | a0001c0001t0003g0231a0001c0001t0003g0255 | 2 | HG00597.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1342+1499T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139678 | ||||||
| chr2:216139752
|
C | T | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1343-1434C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139752 | ||||||
| chr2:216139931
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0030others(1): Show | 4 | HG01891.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343-1255C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139931 | ||||||
| chr2:216139965
|
A | G | 10 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0014others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1343-1221A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216139965 | ||||||
| chr2:216140065
|
G | A | 1 | a0001c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1343-1121G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216140065 | ||||||
| chr2:216140577
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1343-609G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216140577 | ||||||
| chr2:216140954
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18961.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1343-232G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216140954 | ||||||
| chr2:216141098
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1343-88A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216141098 | ||||||
| chr2:216141496
|
A | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0030others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+177A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141496 | ||||||
| chr2:216141502
|
T | TAAAAAGA | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | NA18962.hp2 NA18964.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1476+188_1476+194d others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141502 | |||||
| chr2:216141540
|
C | CTTTTT | 59 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0046others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1476+243_1476+247d others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141540 | |||||
| chr2:216141540
|
C | CTTTTTT | 49 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0057others(46): Show | 49 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1476+242_1476+247d others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141540 | |||||
| chr2:216141540
|
C | CTTTTTTT | 18 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0058others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1476+241_1476+247d others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141540 | |||||
| chr2:216141543
|
T | TTC | 19 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(16): Show | 19 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1476+225_1476+226i others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141543 | |||||
| chr2:216141544
|
T | TC | 6 | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0031others(3): Show | 6 | HG01891.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1476+225_1476+226i others(3): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141544 | ||||||
| chr2:216141545
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1476+226T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141545 | ||||||
| chr2:216141553
|
TTTTTTTT others(7): Show |
T | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(9): Show | 12 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1476+235_1476+248d others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141553 | ||||||
| chr2:216141554
|
TTTTTTTT others(6): Show |
T | 95 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(92): Show | 96 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1476+236_1476+248d others(15): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141554 | ||||||
| chr2:216141555
|
TTTTTTTT others(5): Show |
T | 3 | a0001c0001t0001g0116a0001c0001t0003g0191a0001c0005t0001g0045 | 3 | HG01433.hp1 HG02040.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1476+237_1476+248d others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141555 | ||||||
| chr2:216141556
|
TTTTTTTT others(4): Show |
T | 3 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0148 | 3 | HG02132.hp2 NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1476+238_1476+248d others(13): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141556 | ||||||
| chr2:216141557
|
TTTTTTTT others(3): Show |
T | 2 | a0001c0001t0001g0133a0001c0001t0006g0007 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1476+239_1476+248d others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141557 | ||||||
| chr2:216141560
|
TTTTTTTC | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | NA18953.hp1 NA18962.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.1476+242_1476+248d others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141560 | ||||||
| chr2:216141566
|
TC | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290 | 3 | HG02559.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1476+249delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216141566 | |||||
| chr2:216141567
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(171): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1476+248C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141567 | ||||||
| chr2:216141616
|
T | C | 37 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0009others(34): Show | 37 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(34): Show |
intron_variant | MODIFIER | c.1476+297T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141616 | ||||||
| chr2:216141675
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1476+356G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141675 | ||||||
| chr2:216141777
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02145.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1476+458G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141777 | ||||||
| chr2:216141781
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1476+462G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141781 | ||||||
| chr2:216141955
|
G | A | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+636G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141955 | ||||||
| chr2:216141991
|
G | T | 145 | a0001c0001t0001g0150a0001c0001t0001g0251a0001c0001t0001g0252others(142): Show | 146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1476+672G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141991 | ||||||
| chr2:216142105
|
C | G | 1 | a0001c0002t0002g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1476+786C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142105 | ||||||
| chr2:216142218
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1476+899T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142218 | ||||||
| chr2:216142249
|
A | T | 1 | a0001c0001t0003g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1476+930A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142249 | ||||||
| chr2:216142389
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1476+1070C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142389 | ||||||
| chr2:216142496
|
A | G | 7 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0004g0219others(4): Show | 7 | HG00597.hp2 NA18942.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1476+1177A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142496 | ||||||
| chr2:216142605
|
A | T | 3 | a0001c0001t0006g0190a0001c0001t0009g0188a0001c0001t0009g0189 | 3 | HG02280.hp1 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1476+1286A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142605 | ||||||
| chr2:216142611
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+1292T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142611 | ||||||
| chr2:216142824
|
A | G | 8 | a0001c0001t0003g0334a0001c0001t0005g0275a0001c0001t0005g0286others(5): Show | 8 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1476+1505A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142824 | ||||||
| chr2:216142825
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0165 | 2 | HG02155.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1476+1506T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216142825 | ||||||
| chr2:216143055
|
G | A | 2 | a0001c0001t0006g0007a0001c0001t0012g0005 | 2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1476+1736G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143055 | ||||||
| chr2:216143069
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1476+1750A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143069 | ||||||
| chr2:216143132
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+1813T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143132 | ||||||
| chr2:216143175
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+1856G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143175 | ||||||
| chr2:216143181
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1476+1862C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143181 | ||||||
| chr2:216143252
|
A | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1476+1933A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143252 | ||||||
| chr2:216143450
|
G | T | 5 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0030others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+2131G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143450 | ||||||
| chr2:216143503
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1476+2184G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143503 | ||||||
| chr2:216143534
|
G | A | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1476+2215G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143534 | ||||||
| chr2:216143544
|
G | A | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1476+2225G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143544 | ||||||
| chr2:216143548
|
G | A | 1 | a0001c0001t0006g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1476+2229G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143548 | ||||||
| chr2:216143551
|
C | T | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1476+2232C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143551 | ||||||
| chr2:216143576
|
T | A | 5 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1476+2257T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143576 | ||||||
| chr2:216143628
|
G | C | 1 | a0001c0001t0009g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1476+2309G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143628 | ||||||
| chr2:216143682
|
C | T | 3 | a0001c0001t0006g0190a0001c0001t0009g0188a0001c0001t0009g0189 | 3 | HG02280.hp1 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1476+2363C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143682 | ||||||
| chr2:216143701
|
C | CT | 11 | a0001c0001t0001g0086a0001c0001t0003g0024a0001c0001t0003g0025others(8): Show | 11 | HG01884.hp2 HG02148.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1476+2395dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216143701 | |||||
| chr2:216143709
|
T | A | 1 | a0001c0001t0003g0240 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1476+2390T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143709 | ||||||
| chr2:216143714
|
T | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0030others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+2395T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143714 | ||||||
| chr2:216143781
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+2462C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143781 | ||||||
| chr2:216143800
|
T | TG | 34 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0009others(31): Show | 34 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.1476+2483dupG | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216143800 | |||||
| chr2:216143849
|
G | T | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+2530G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143849 | ||||||
| chr2:216143853
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1476+2534C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143853 | ||||||
| chr2:216143858
|
C | A | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1476+2539C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143858 | ||||||
| chr2:216143873
|
A | AT | 19 | a0001c0001t0001g0080a0001c0001t0002g0009a0001c0001t0002g0012others(16): Show | 19 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1476+2568dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216143873 | |||||
| chr2:216143873
|
AT | A | 114 | a0001c0001t0001g0150a0001c0001t0001g0251a0001c0001t0001g0252others(111): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1476+2568delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216143873 | |||||
| chr2:216143887
|
T | G | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1476+2568T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143887 | ||||||
| chr2:216143929
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1476+2610T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143929 | ||||||
| chr2:216143958
|
C | T | 1 | a0001c0001t0004g0132 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1476+2639C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216143958 | ||||||
| chr2:216144182
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1476+2863G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144182 | ||||||
| chr2:216144210
|
G | T | 10 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0014others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1476+2891G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144210 | ||||||
| chr2:216144246
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1476+2927G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144246 | ||||||
| chr2:216144251
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1476+2932G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144251 | ||||||
| chr2:216144288
|
G | A | 2 | a0001c0001t0004g0053a0001c0001t0004g0054 | 2 | HG03486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1476+2969G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144288 | ||||||
| chr2:216144374
|
C | G | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+3055C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144374 | ||||||
| chr2:216144757
|
C | T | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1477-3326C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144757 | ||||||
| chr2:216144772
|
C | T | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477-3311C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144772 | ||||||
| chr2:216144806
|
A | T | 3 | a0001c0001t0001g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02145.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1477-3277A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144806 | ||||||
| chr2:216144884
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1477-3199A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144884 | ||||||
| chr2:216144940
|
T | C | 34 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0009others(31): Show | 34 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.1477-3143T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216144940 | ||||||
| chr2:216145161
|
A | G | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1477-2922A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145161 | ||||||
| chr2:216145363
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-2720T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145363 | ||||||
| chr2:216145454
|
G | A | 1 | a0001c0001t0001g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1477-2629G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145454 | ||||||
| chr2:216145469
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1477-2614A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145469 | ||||||
| chr2:216145620
|
G | T | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-2463G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145620 | ||||||
| chr2:216145631
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00673.hp2 HG02523.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-2452G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145631 | ||||||
| chr2:216145690
|
C | T | 30 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.1477-2393C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145690 | ||||||
| chr2:216145719
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1477-2364A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145719 | ||||||
| chr2:216145795
|
A | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1477-2288A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145795 | ||||||
| chr2:216145826
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-2257T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145826 | ||||||
| chr2:216145835
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1477-2248T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216145835 | ||||||
| chr2:216146045
|
C | A | 1 | a0001c0001t0001g0345 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1477-2038C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146045 | ||||||
| chr2:216146098
|
C | A | 50 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0113others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1477-1985C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146098 | ||||||
| chr2:216146114
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477-1969C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146114 | ||||||
| chr2:216146400
|
G | GTCCAGGG others(45): Show |
7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1477-1681_1477-163 others(56): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 216146400 | |||||
| chr2:216146575
|
G | A | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-1508G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146575 | ||||||
| chr2:216146749
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1477-1334G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146749 | ||||||
| chr2:216146752
|
G | C | 1 | a0001c0001t0001g0339 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1477-1331G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146752 | ||||||
| chr2:216146889
|
G | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1477-1194G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146889 | ||||||
| chr2:216146919
|
T | C | 8 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0014others(5): Show | 8 | HG01884.hp1 HG01952.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1477-1164T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146919 | ||||||
| chr2:216146951
|
G | C | 1 | a0001c0001t0001g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1477-1132G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146951 | ||||||
| chr2:216147036
|
C | G | 30 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.1477-1047C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147036 | ||||||
| chr2:216147090
|
T | TA | 308 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1477-993_1477-992i others(3): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147090 | ||||||
| chr2:216147103
|
CTACTTCA others(1): Show |
C | 9 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(6): Show | 9 | HG01975.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1477-979_1477-972d others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147103 | ||||||
| chr2:216147135
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-948C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147135 | ||||||
| chr2:216147148
|
A | G | 8 | a0001c0001t0003g0334a0001c0001t0005g0275a0001c0001t0005g0286others(5): Show | 8 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1477-935A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147148 | ||||||
| chr2:216147175
|
A | T | 6 | a0001c0001t0001g0147a0001c0001t0001g0344a0001c0001t0007g0192others(3): Show | 6 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-908A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147175 | ||||||
| chr2:216147276
|
G | T | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1477-807G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147276 | ||||||
| chr2:216147302
|
A | G | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1477-781A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147302 | ||||||
| chr2:216147366
|
A | G | 35 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(32): Show | 36 | HG00280.hp2 HG00597.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1477-717A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147366 | ||||||
| chr2:216147369
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(149): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1477-714A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147369 | ||||||
| chr2:216147370
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-713T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147370 | ||||||
| chr2:216147389
|
G | A | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1477-694G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147389 | ||||||
| chr2:216147489
|
T | C | 10 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0014others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477-594T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147489 | ||||||
| chr2:216147659
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1477-424A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216147659 | ||||||
| chr2:216148016
|
A | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(9): Show | 12 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477-67A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216148016 | ||||||
| chr2:216148040
|
T | C | 3 | a0001c0002t0002g0273a0001c0002t0002g0291a0001c0002t0002g0292 | 3 | HG03669.hp1 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1477-43T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216148040 | ||||||
| chr2:216148335
|
A | G | 10 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0014others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1670+59A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216148335 | ||||||
| chr2:216148387
|
GGAA | G | 10 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1670+116_1670+118d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216148387 | |||||
| chr2:216148446
|
G | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1670+170G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216148446 | ||||||
| chr2:216148783
|
G | T | 4 | a0001c0001t0003g0041a0001c0001t0003g0156a0001c0001t0003g0158others(1): Show | 4 | HG03130.hp2 HG03540.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+507G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216148783 | ||||||
| chr2:216148904
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1670+628A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216148904 | ||||||
| chr2:216148917
|
CAAG | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1670+647_1670+649d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216148917 | |||||
| chr2:216148932
|
G | T | 1 | a0001c0001t0009g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1670+656G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216148932 | ||||||
| chr2:216149114
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290 | 3 | HG02559.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1670+838A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149114 | ||||||
| chr2:216149179
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+903G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149179 | ||||||
| chr2:216149268
|
A | AATT | 7 | a0001c0002t0002g0304a0001c0002t0002g0305a0001c0002t0002g0306others(4): Show | 7 | NA18960.hp2 NA18961.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1670+993_1670+994i others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216149268 | |||||
| chr2:216149323
|
C | T | 1 | a0001c0005t0001g0045 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1670+1047C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149323 | ||||||
| chr2:216149361
|
C | A | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1670+1085C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149361 | ||||||
| chr2:216149544
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1670+1268G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149544 | ||||||
| chr2:216149577
|
G | C | 30 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.1670+1301G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149577 | ||||||
| chr2:216149603
|
T | TTC | 3 | a0001c0001t0005g0286a0001c0001t0005g0287a0001c0001t0005g0288 | 3 | HG01928.hp1 HG01981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1670+1335_1670+133 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216149603 | |||||
| chr2:216149611
|
C | CTG | 97 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(94): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1670+1341_1670+134 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216149611 | |||||
| chr2:216149658
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1670+1382G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149658 | ||||||
| chr2:216149778
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1670+1502A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149778 | ||||||
| chr2:216149962
|
G | A | 1 | a0001c0001t0008g0249 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1670+1686G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149962 | ||||||
| chr2:216149976
|
T | C | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1670+1700T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149976 | ||||||
| chr2:216149988
|
A | C | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1670+1712A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216149988 | ||||||
| chr2:216150028
|
GGTTCAGT others(3): Show |
G | 1 | a0001c0001t0001g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1670+1753_1670+176 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150028 | ||||||
| chr2:216150395
|
A | T | 24 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(21): Show | 24 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1670+2119A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150395 | ||||||
| chr2:216150503
|
A | G | 1 | a0001c0001t0004g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1670+2227A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150503 | ||||||
| chr2:216150561
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1670+2285T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150561 | ||||||
| chr2:216150735
|
A | G | 110 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(107): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1670+2459A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150735 | ||||||
| chr2:216150743
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1670+2467A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150743 | ||||||
| chr2:216150762
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0002g0151a0001c0001t0002g0152 | 3 | HG02145.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1670+2486G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150762 | ||||||
| chr2:216150916
|
G | A | 1 | a0001c0001t0004g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1670+2640G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216150916 | ||||||
| chr2:216151093
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0002g0008a0001c0001t0002g0151others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+2817A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151093 | ||||||
| chr2:216151180
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1670+2904G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151180 | ||||||
| chr2:216151201
|
A | G | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1670+2925A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151201 | ||||||
| chr2:216151224
|
A | T | 133 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0261others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1670+2948A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151224 | ||||||
| chr2:216151340
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1670+3064C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151340 | ||||||
| chr2:216151452
|
T | C | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1670+3176T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151452 | ||||||
| chr2:216151995
|
A | G | 2 | a0001c0001t0004g0101a0001c0001t0004g0203 | 2 | HG00597.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1670+3719A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216151995 | ||||||
| chr2:216152244
|
C | A | 1 | a0001c0001t0002g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1670+3968C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152244 | ||||||
| chr2:216152302
|
G | A | 60 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(57): Show | 60 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1670+4026G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152302 | ||||||
| chr2:216152332
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1670+4056C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152332 | ||||||
| chr2:216152438
|
TAAAAAA | T | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1670+4167_1670+417 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216152438 | |||||
| chr2:216152487
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0085others(1): Show | 4 | HG02027.hp2 HG02132.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+4211G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152487 | ||||||
| chr2:216152505
|
G | A | 1 | a0001c0001t0011g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1670+4229G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152505 | ||||||
| chr2:216152526
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1670+4250T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152526 | ||||||
| chr2:216152649
|
GT | G | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1670+4386delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216152649 | |||||
| chr2:216152692
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1670+4416C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152692 | ||||||
| chr2:216152772
|
T | C | 8 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(5): Show | 8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1670+4496T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152772 | ||||||
| chr2:216152804
|
A | T | 2 | a0001c0001t0004g0131a0001c0001t0004g0216 | 2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1670+4528A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152804 | ||||||
| chr2:216152807
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00438.hp2 NA18949.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1670+4531C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152807 | ||||||
| chr2:216152822
|
A | G | 2 | a0001c0001t0003g0197a0001c0001t0003g0266 | 2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1670+4546A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216152822 | ||||||
| chr2:216153231
|
A | G | 1 | a0001c0001t0003g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1670+4955A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153231 | ||||||
| chr2:216153316
|
A | G | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+5040A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153316 | ||||||
| chr2:216153386
|
A | G | 348 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1670+5110A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153386 | ||||||
| chr2:216153533
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(123): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1670+5257T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153533 | ||||||
| chr2:216153699
|
G | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(284): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1670+5423G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153699 | ||||||
| chr2:216153911
|
A | G | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1670+5635A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153911 | ||||||
| chr2:216154155
|
C | T | 11 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1670+5879C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216154155 | ||||||
| chr2:216154437
|
C | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1671-5631C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216154437 | ||||||
| chr2:216154602
|
C | A | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-5466C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216154602 | ||||||
| chr2:216154775
|
T | G | 4 | a0001c0001t0004g0103a0001c0001t0004g0187a0001c0001t0004g0218others(1): Show | 4 | NA18971.hp2 NA18986.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-5293T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216154775 | ||||||
| chr2:216155236
|
C | CA | 8 | a0001c0001t0001g0067a0001c0001t0001g0076a0001c0001t0001g0164others(5): Show | 8 | HG01167.hp2 HG01361.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1671-4813dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216155236 | |||||
| chr2:216155236
|
C | CAA | 148 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0013others(145): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1671-4814_1671-481 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216155236 | |||||
| chr2:216155236
|
C | CAAA | 20 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0002g0032others(17): Show | 20 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1671-4815_1671-481 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216155236 | |||||
| chr2:216155236
|
CA | C | 9 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0268others(6): Show | 9 | HG01167.hp1 HG02015.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1671-4813delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216155236 | |||||
| chr2:216155403
|
A | G | 8 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(5): Show | 8 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1671-4665A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216155403 | ||||||
| chr2:216155794
|
A | C | 1 | a0001c0001t0008g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1671-4274A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216155794 | ||||||
| chr2:216155970
|
T | G | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-4098T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216155970 | ||||||
| chr2:216156005
|
G | A | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-4063G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156005 | ||||||
| chr2:216156082
|
C | T | 2 | a0001c0001t0009g0188a0001c0001t0009g0189 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1671-3986C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156082 | ||||||
| chr2:216156332
|
A | G | 8 | a0001c0001t0004g0101a0001c0001t0004g0103a0001c0001t0004g0187others(5): Show | 8 | HG00597.hp2 NA18971.hp2 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.1671-3736A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156332 | ||||||
| chr2:216156356
|
C | T | 12 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(9): Show | 12 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1671-3712C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156356 | ||||||
| chr2:216156385
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1671-3683A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156385 | ||||||
| chr2:216156398
|
G | A | 11 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(8): Show | 11 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1671-3670G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156398 | ||||||
| chr2:216156421
|
T | G | 1 | a0001c0002t0002g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1671-3647T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156421 | ||||||
| chr2:216156444
|
CTA | C | 17 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1671-3622_1671-362 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216156444 | |||||
| chr2:216156658
|
G | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-3410G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156658 | ||||||
| chr2:216156771
|
A | G | 17 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1671-3297A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156771 | ||||||
| chr2:216156777
|
A | G | 13 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(10): Show | 13 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1671-3291A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156777 | ||||||
| chr2:216156879
|
C | A | 110 | a0001c0001t0001g0261a0001c0001t0001g0320a0001c0001t0001g0321others(107): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1671-3189C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156879 | ||||||
| chr2:216156920
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1671-3148C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216156920 | ||||||
| chr2:216157144
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-2924T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157144 | ||||||
| chr2:216157192
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1671-2876T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157192 | ||||||
| chr2:216157227
|
T | C | 58 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(55): Show | 58 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1671-2841T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157227 | ||||||
| chr2:216157228
|
GT | G | 122 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(119): Show | 123 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.1671-2830delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216157228 | |||||
| chr2:216157229
|
T | G | 1 | a0001c0001t0009g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1671-2839T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157229 | ||||||
| chr2:216157235
|
TTTTG | T | 34 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1671-2830_1671-282 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216157235 | |||||
| chr2:216157335
|
G | A | 1 | a0001c0001t0004g0311 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1671-2733G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157335 | ||||||
| chr2:216157358
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1671-2710C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157358 | ||||||
| chr2:216157434
|
C | T | 3 | a0001c0001t0007g0192a0001c0001t0007g0194a0001c0001t0007g0195 | 3 | HG02055.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1671-2634C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157434 | ||||||
| chr2:216157492
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1671-2576C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157492 | ||||||
| chr2:216157566
|
G | GGCT | 181 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(178): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1671-2500_1671-249 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216157566 | |||||
| chr2:216157596
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0177 | 2 | NA18949.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1671-2472T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157596 | ||||||
| chr2:216157795
|
A | G | 9 | a0001c0001t0003g0246a0001c0001t0003g0247a0001c0001t0004g0199others(6): Show | 9 | HG00140.hp2 HG01175.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1671-2273A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157795 | ||||||
| chr2:216157871
|
C | G | 1 | a0001c0001t0004g0215 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1671-2197C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157871 | ||||||
| chr2:216157876
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-2192C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157876 | ||||||
| chr2:216157877
|
G | A | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-2191G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216157877 | ||||||
| chr2:216158090
|
C | T | 50 | a0001c0001t0001g0092a0001c0001t0002g0013a0001c0001t0002g0019others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1671-1978C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158090 | ||||||
| chr2:216158147
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0177 | 2 | NA18949.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1671-1921A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158147 | ||||||
| chr2:216158152
|
C | G | 1 | a0001c0001t0003g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1671-1916C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158152 | ||||||
| chr2:216158173
|
T | C | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1671-1895T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158173 | ||||||
| chr2:216158302
|
G | A | 1 | a0001c0002t0002g0305 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1671-1766G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158302 | ||||||
| chr2:216158314
|
C | CT | 6 | a0001c0002t0002g0115a0001c0002t0002g0273a0001c0002t0002g0291others(3): Show | 6 | HG02683.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-1753dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216158314 | |||||
| chr2:216158398
|
G | A | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-1670G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158398 | ||||||
| chr2:216158428
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1671-1640C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158428 | ||||||
| chr2:216158591
|
C | T | 1 | a0001c0001t0009g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1671-1477C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158591 | ||||||
| chr2:216158769
|
G | A | 24 | a0001c0001t0004g0001a0001c0001t0004g0101a0001c0001t0004g0103others(21): Show | 25 | HG00597.hp2 HG01255.hp2 HG03654.hp1 others(22): Show |
intron_variant | MODIFIER | c.1671-1299G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158769 | ||||||
| chr2:216158772
|
T | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-1296T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158772 | ||||||
| chr2:216158962
|
A | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0322 | 2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1671-1106A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216158962 | ||||||
| chr2:216159001
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(6): Show | 9 | HG01975.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671-1067A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159001 | ||||||
| chr2:216159152
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1671-916A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159152 | ||||||
| chr2:216159357
|
CTGT | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-709_1671-707d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216159357 | |||||
| chr2:216159384
|
C | A | 36 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1671-684C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159384 | ||||||
| chr2:216159472
|
C | A | 35 | a0001c0001t0001g0261a0001c0001t0003g0212a0001c0001t0004g0001others(32): Show | 36 | HG00280.hp2 HG00597.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1671-596C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159472 | ||||||
| chr2:216159619
|
G | A | 5 | a0001c0001t0001g0147a0001c0001t0001g0343a0001c0001t0001g0344others(2): Show | 5 | NA18952.hp1 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-449G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159619 | ||||||
| chr2:216159879
|
A | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1671-189A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216159879 | ||||||
| chr2:216159955
|
TTTC | T | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-101_1671-99de others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216159955 | |||||
| chr2:216159974
|
CT | C | 186 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(183): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1671-82delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 216159974 | |||||
| chr2:216160032
|
G | T | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-36G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216160032 | ||||||
| chr2:216160318
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1764+157T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160318 | ||||||
| chr2:216160443
|
T | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+282T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160443 | ||||||
| chr2:216160542
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1764+381C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160542 | ||||||
| chr2:216160600
|
T | C | 181 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(178): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1764+439T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160600 | ||||||
| chr2:216160663
|
C | CTTAA | 91 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(88): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1764+529_1764+532d others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr2 | 216160663 | |||||
| chr2:216160663
|
C | CTTAATTA others(1): Show |
7 | a0001c0001t0001g0112a0001c0001t0001g0174a0001c0001t0001g0180others(4): Show | 7 | HG00423.hp1 HG01952.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1764+525_1764+532d others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr2 | 216160663 | |||||
| chr2:216160678
|
A | T | 2 | a0001c0001t0003g0254a0001c0002t0002g0293 | 2 | HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1764+517A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160678 | ||||||
| chr2:216160682
|
A | T | 88 | a0001c0001t0001g0092a0001c0001t0001g0282a0001c0001t0001g0283others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1764+521A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160682 | ||||||
| chr2:216160686
|
A | T | 180 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(177): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1764+525A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160686 | ||||||
| chr2:216160690
|
A | T | 197 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(194): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1764+529A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160690 | ||||||
| chr2:216160866
|
C | T | 161 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(158): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1764+705C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160866 | ||||||
| chr2:216160951
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1764+790C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216160951 | ||||||
| chr2:216161025
|
T | C | 1 | a0001c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1764+864T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216161025 | ||||||
| chr2:216161052
|
G | A | 36 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1764+891G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216161052 | ||||||
| chr2:216161057
|
C | G | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+896C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216161057 | ||||||
| chr2:216161706
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1765-273G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216161706 | ||||||
| chr2:216161737
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1765-242G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 15/20 | chr2 | 216161737 | ||||||
| chr2:216162360
|
A | G | 8 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0156others(5): Show | 8 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+312A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162360 | ||||||
| chr2:216162407
|
C | CT | 63 | a0001c0001t0001g0261a0001c0001t0001g0320a0001c0001t0001g0321others(60): Show | 65 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1834+370dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216162407 | |||||
| chr2:216162407
|
CT | C | 36 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1834+370delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216162407 | |||||
| chr2:216162504
|
C | G | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+456C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162504 | ||||||
| chr2:216162662
|
G | A | 1 | a0001c0001t0004g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1834+614G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162662 | ||||||
| chr2:216162742
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1834+694T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162742 | ||||||
| chr2:216162837
|
G | A | 181 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(178): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1834+789G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162837 | ||||||
| chr2:216162882
|
C | T | 160 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(157): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1834+834C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216162882 | ||||||
| chr2:216163062
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+1014C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163062 | ||||||
| chr2:216163080
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+1032T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163080 | ||||||
| chr2:216163114
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1834+1066C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163114 | ||||||
| chr2:216163125
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1834+1077G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163125 | ||||||
| chr2:216163139
|
CT | C | 160 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(157): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1834+1103delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216163139 | |||||
| chr2:216163161
|
G | T | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834+1113G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163161 | ||||||
| chr2:216163241
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1834+1193C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163241 | ||||||
| chr2:216163451
|
G | A | 50 | a0001c0001t0001g0092a0001c0001t0002g0013a0001c0001t0002g0019others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1834+1403G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163451 | ||||||
| chr2:216163479
|
G | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1834+1431G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163479 | ||||||
| chr2:216163487
|
G | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+1439G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163487 | ||||||
| chr2:216163495
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+1447G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163495 | ||||||
| chr2:216163509
|
T | C | 195 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(192): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1834+1461T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163509 | ||||||
| chr2:216163559
|
G | T | 5 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327others(2): Show | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834+1511G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163559 | ||||||
| chr2:216163566
|
T | C | 162 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(159): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1834+1518T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163566 | ||||||
| chr2:216163567
|
G | GTGAGCCA others(8): Show |
41 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(38): Show | 42 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1834+1528_1834+154 others(19): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216163567 | |||||
| chr2:216163633
|
A | G | 3 | a0001c0001t0006g0007a0001c0002t0006g0003a0001c0002t0006g0316 | 4 | HG02109.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+1585A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163633 | ||||||
| chr2:216163638
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1834+1590C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163638 | ||||||
| chr2:216163708
|
C | T | 160 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(157): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1834+1660C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163708 | ||||||
| chr2:216163867
|
G | A | 7 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0250others(4): Show | 7 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+1819G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163867 | ||||||
| chr2:216163904
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1834+1856T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163904 | ||||||
| chr2:216163923
|
G | T | 50 | a0001c0001t0001g0092a0001c0001t0002g0013a0001c0001t0002g0019others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1834+1875G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216163923 | ||||||
| chr2:216164147
|
G | A | 195 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(192): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1834+2099G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164147 | ||||||
| chr2:216164239
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1834+2191A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164239 | ||||||
| chr2:216164325
|
T | C | 8 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0156others(5): Show | 8 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+2277T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164325 | ||||||
| chr2:216164396
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1834+2348G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164396 | ||||||
| chr2:216164609
|
G | A | 1 | a0001c0001t0003g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1834+2561G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164609 | ||||||
| chr2:216164724
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1834+2676G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164724 | ||||||
| chr2:216164732
|
A | G | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+2684A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164732 | ||||||
| chr2:216164821
|
GGCAGTTT | G | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1834+2775_1834+278 others(11): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216164821 | |||||
| chr2:216164841
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+2793T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216164841 | ||||||
| chr2:216165083
|
T | A | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+3035T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165083 | ||||||
| chr2:216165125
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+3077C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165125 | ||||||
| chr2:216165126
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+3078A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165126 | ||||||
| chr2:216165127
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+3079C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165127 | ||||||
| chr2:216165129
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+3081T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165129 | ||||||
| chr2:216165138
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1834+3090C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165138 | ||||||
| chr2:216165277
|
G | A | 38 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0032others(35): Show | 38 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1834+3229G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165277 | ||||||
| chr2:216165419
|
G | A | 15 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0004g0004others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1834+3371G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165419 | ||||||
| chr2:216165423
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1834+3375A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165423 | ||||||
| chr2:216165524
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1834+3476C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165524 | ||||||
| chr2:216165561
|
A | G | 53 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(50): Show | 53 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1834+3513A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165561 | ||||||
| chr2:216165580
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+3532G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165580 | ||||||
| chr2:216165677
|
G | C | 1 | a0001c0001t0004g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1834+3629G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165677 | ||||||
| chr2:216165743
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA18979.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1834+3695G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165743 | ||||||
| chr2:216165749
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+3701C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165749 | ||||||
| chr2:216165893
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1834+3845C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165893 | ||||||
| chr2:216165965
|
A | G | 2 | a0001c0002t0002g0298a0001c0002t0002g0299 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1834+3917A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216165965 | ||||||
| chr2:216166176
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | NA18990.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1834+4128A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166176 | ||||||
| chr2:216166318
|
C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0274 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1834+4270C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166318 | ||||||
| chr2:216166322
|
A | G | 2 | a0001c0002t0002g0298a0001c0002t0002g0299 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1834+4274A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166322 | ||||||
| chr2:216166358
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1834+4310G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166358 | ||||||
| chr2:216166411
|
C | T | 1 | a0001c0001t0001g0345 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1834+4363C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166411 | ||||||
| chr2:216166492
|
T | C | 2 | a0001c0001t0009g0188a0001c0001t0009g0189 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1834+4444T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166492 | ||||||
| chr2:216166493
|
A | G | 4 | a0001c0001t0004g0001a0001c0001t0004g0205a0001c0001t0004g0206others(1): Show | 5 | NA18943.hp2 NA18969.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834+4445A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166493 | ||||||
| chr2:216166553
|
G | A | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1834+4505G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166553 | ||||||
| chr2:216166605
|
T | C | 124 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(121): Show | 125 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.1834+4557T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166605 | ||||||
| chr2:216166633
|
T | C | 1 | a0001c0001t0004g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1834+4585T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166633 | ||||||
| chr2:216166786
|
C | T | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+4738C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166786 | ||||||
| chr2:216166904
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1834+4856A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166904 | ||||||
| chr2:216166955
|
C | T | 146 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(143): Show | 148 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1834+4907C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216166955 | ||||||
| chr2:216167237
|
C | T | 22 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(19): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1834+5189C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167237 | ||||||
| chr2:216167446
|
A | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0289others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+5398A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167446 | ||||||
| chr2:216167471
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+5423A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167471 | ||||||
| chr2:216167523
|
C | T | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+5475C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167523 | ||||||
| chr2:216167545
|
A | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(3): Show | 6 | HG01891.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+5497A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167545 | ||||||
| chr2:216167553
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+5505C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167553 | ||||||
| chr2:216167553
|
CGTGTGTG others(29): Show |
C | 1 | a0001c0001t0006g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1834+5519_1834+555 others(40): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167553 | |||||
| chr2:216167569
|
TTTGTGTG others(8): Show |
T | 1 | a0001c0002t0002g0274 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1834+5523_1834+553 others(19): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167569 | |||||
| chr2:216167570
|
T | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG02523.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1834+5522T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167570 | ||||||
| chr2:216167570
|
T | TG | 5 | a0001c0001t0001g0107a0001c0001t0001g0173a0001c0001t0001g0262others(2): Show | 5 | HG00544.hp2 HG02615.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834+5522_1834+552 others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167570 | ||||||
| chr2:216167570
|
T | TTG | 36 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0062others(33): Show | 36 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1834+5565_1834+556 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
T | TTGTG | 36 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0051others(33): Show | 36 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1834+5563_1834+556 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
T | TTGTGTG | 17 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0059others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1834+5561_1834+556 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0001g0174 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1834+5555_1834+556 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTG | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0065others(42): Show | 45 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1834+5565_1834+556 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTG | T | 10 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0118others(7): Show | 10 | HG00140.hp1 HG00673.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1834+5563_1834+556 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTG | T | 11 | a0001c0001t0001g0077a0001c0001t0001g0168a0001c0001t0001g0169others(8): Show | 11 | HG01071.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1834+5561_1834+556 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTGT others(1): Show |
T | 6 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(3): Show | 7 | HG00423.hp1 HG03130.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+5559_1834+556 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+5555_1834+556 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTGT others(7): Show |
T | 11 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(8): Show | 11 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1834+5553_1834+556 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTGT others(9): Show |
T | 96 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(93): Show | 97 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(94): Show |
intron_variant | MODIFIER | c.1834+5551_1834+556 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167570
|
TTGTGTGT others(19): Show |
T | 14 | a0001c0001t0004g0101a0001c0001t0004g0103a0001c0001t0004g0187others(11): Show | 14 | HG00597.hp2 NA18942.hp1 NA18963.hp1 others(11): Show |
intron_variant | MODIFIER | c.1834+5541_1834+556 others(30): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216167570 | |||||
| chr2:216167598
|
GTGTGTGT others(8): Show |
G | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+5551_1834+556 others(19): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167598 | ||||||
| chr2:216167614
|
G | A | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+5566G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167614 | ||||||
| chr2:216167615
|
A | T | 5 | a0001c0001t0002g0125a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834+5567A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167615 | ||||||
| chr2:216167625
|
A | C | 40 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(37): Show | 40 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1834+5577A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167625 | ||||||
| chr2:216167626
|
T | A | 40 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(37): Show | 40 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1834+5578T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167626 | ||||||
| chr2:216167661
|
T | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1834+5613T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167661 | ||||||
| chr2:216167674
|
A | T | 1 | a0001c0002t0006g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1834+5626A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167674 | ||||||
| chr2:216167724
|
C | T | 10 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1834+5676C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167724 | ||||||
| chr2:216167770
|
T | G | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1834+5722T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167770 | ||||||
| chr2:216167798
|
C | G | 53 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(50): Show | 53 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1834+5750C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167798 | ||||||
| chr2:216167818
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0149others(1): Show | 4 | HG02155.hp2 NA18960.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+5770A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167818 | ||||||
| chr2:216167907
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1834+5859T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167907 | ||||||
| chr2:216167948
|
T | G | 57 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0004g0001others(54): Show | 58 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1834+5900T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216167948 | ||||||
| chr2:216168083
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+6035A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168083 | ||||||
| chr2:216168133
|
T | C | 126 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1834+6085T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168133 | ||||||
| chr2:216168216
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+6168A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168216 | ||||||
| chr2:216168571
|
G | A | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+6523G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168571 | ||||||
| chr2:216168657
|
A | C | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+6609A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168657 | ||||||
| chr2:216168741
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1834+6693A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168741 | ||||||
| chr2:216168822
|
TATTATTA others(5): Show |
T | 3 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0001t0003g0225 | 3 | NA18982.hp2 NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1834+6778_1834+678 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216168822 | |||||
| chr2:216168823
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+6775A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168823 | ||||||
| chr2:216168871
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+6823C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168871 | ||||||
| chr2:216168894
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1834+6846G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168894 | ||||||
| chr2:216168986
|
T | A | 1 | a0001c0002t0002g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1834+6938T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216168986 | ||||||
| chr2:216169037
|
A | G | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+6989A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169037 | ||||||
| chr2:216169252
|
C | T | 126 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1834+7204C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169252 | ||||||
| chr2:216169260
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1834+7212G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169260 | ||||||
| chr2:216169271
|
G | A | 15 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1834+7223G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169271 | ||||||
| chr2:216169281
|
C | T | 2 | a0001c0001t0004g0250a0001c0001t0004g0263 | 2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1834+7233C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169281 | ||||||
| chr2:216169425
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1834+7377C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169425 | ||||||
| chr2:216169499
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+7451G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169499 | ||||||
| chr2:216169618
|
A | G | 197 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(194): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1834+7570A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169618 | ||||||
| chr2:216169710
|
T | C | 53 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(50): Show | 53 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1834+7662T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169710 | ||||||
| chr2:216169736
|
AAAAGGAG others(19): Show |
A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+7689_1834+771 others(30): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169736 | ||||||
| chr2:216169768
|
G | A | 3 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0001t0003g0225 | 3 | NA18982.hp2 NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1834+7720G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169768 | ||||||
| chr2:216169870
|
T | TA | 151 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0282others(148): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1834+7836dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216169870 | |||||
| chr2:216169870
|
T | TAA | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(3): Show | 6 | HG01891.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+7835_1834+783 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216169870 | |||||
| chr2:216169916
|
G | A | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+7868G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216169916 | ||||||
| chr2:216170037
|
C | CA | 29 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0069others(26): Show | 29 | HG00544.hp1 HG01169.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1834+8022dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
C | CAA | 19 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0076others(16): Show | 19 | HG00280.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1834+8021_1834+802 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
C | CAAA | 10 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0093others(7): Show | 10 | HG00099.hp1 HG00423.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1834+8020_1834+802 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CA | C | 43 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(40): Show | 43 | HG01258.hp1 HG01433.hp1 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.1834+8022delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAA | C | 11 | a0001c0001t0002g0032a0001c0001t0003g0266a0001c0001t0004g0155others(8): Show | 11 | HG01106.hp1 HG02027.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1834+8019_1834+802 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAA | C | 55 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0019others(52): Show | 55 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1834+8018_1834+802 others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAA | C | 72 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0020others(69): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1834+8017_1834+802 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0005g0286 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1834+8009_1834+802 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAAA others(9): Show |
C | 12 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(9): Show | 12 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1834+8007_1834+802 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0002t0006g0316 | 3 | HG02145.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1834+8006_1834+802 others(21): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAAA others(11): Show |
C | 9 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0289others(6): Show | 10 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1834+8005_1834+802 others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170037
|
CAAAAAAA others(12): Show |
C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+8004_1834+802 others(23): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170037 | |||||
| chr2:216170130
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+8082C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170130 | ||||||
| chr2:216170195
|
G | A | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+8147G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170195 | ||||||
| chr2:216170213
|
T | G | 1 | a0001c0001t0001g0346 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1834+8165T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170213 | ||||||
| chr2:216170295
|
A | C | 1 | a0001c0001t0004g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1834+8247A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170295 | ||||||
| chr2:216170322
|
C | A | 1 | a0001c0001t0004g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1834+8274C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170322 | ||||||
| chr2:216170392
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1834+8344A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170392 | ||||||
| chr2:216170477
|
G | A | 195 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(192): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1834+8429G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170477 | ||||||
| chr2:216170489
|
GGA | G | 185 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(182): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1834+8460_1834+846 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216170489 | |||||
| chr2:216170550
|
A | G | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+8502A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170550 | ||||||
| chr2:216170711
|
A | G | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+8663A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170711 | ||||||
| chr2:216170720
|
G | A | 11 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0133others(8): Show | 11 | HG01258.hp1 HG01496.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1834+8672G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170720 | ||||||
| chr2:216170973
|
C | T | 1 | a0001c0001t0008g0249 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1834+8925C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170973 | ||||||
| chr2:216170987
|
C | G | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+8939C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216170987 | ||||||
| chr2:216171013
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1834+8965G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171013 | ||||||
| chr2:216171111
|
A | T | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1834+9063A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171111 | ||||||
| chr2:216171265
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1834+9217G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171265 | ||||||
| chr2:216171310
|
C | T | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1834+9262C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171310 | ||||||
| chr2:216171563
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1834+9515A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171563 | ||||||
| chr2:216171586
|
T | G | 1 | a0001c0001t0003g0349 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1834+9538T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171586 | ||||||
| chr2:216171610
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1834+9562A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171610 | ||||||
| chr2:216171706
|
T | G | 5 | a0001c0001t0006g0007a0001c0002t0006g0003a0001c0002t0006g0316others(2): Show | 6 | HG02109.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834+9658T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171706 | ||||||
| chr2:216171718
|
A | G | 195 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(192): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1834+9670A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171718 | ||||||
| chr2:216171829
|
C | G | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+9781C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171829 | ||||||
| chr2:216171949
|
G | A | 195 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(192): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1834+9901G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216171949 | ||||||
| chr2:216172356
|
G | A | 7 | a0001c0001t0002g0094a0001c0001t0006g0007a0001c0001t0006g0190others(4): Show | 8 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+10308G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172356 | ||||||
| chr2:216172389
|
C | T | 73 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0003g0024others(70): Show | 74 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1834+10341C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172389 | ||||||
| chr2:216172464
|
C | CTTTCCTT others(4): Show |
1 | a0001c0002t0004g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1834+10419_1834+10 others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172464 | |||||
| chr2:216172469
|
C | CTTT | 17 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1834+10436_1834+10 others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTT | 8 | a0001c0001t0003g0006a0001c0001t0003g0156a0001c0001t0003g0158others(5): Show | 8 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+10435_1834+10 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTT | 11 | a0001c0001t0002g0008a0001c0001t0002g0014a0001c0001t0002g0015others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1834+10434_1834+10 others(11): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT | 75 | a0001c0001t0001g0092a0001c0001t0002g0013a0001c0001t0002g0020others(72): Show | 75 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1834+10432_1834+10 others(13): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0261a0001c0001t0002g0019a0001c0001t0002g0039others(7): Show | 10 | HG01109.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1834+10431_1834+10 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0006g0003 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1834+10429_1834+10 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0002g0094a0001c0001t0006g0007a0001c0001t0006g0190others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+10428_1834+10 others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(5): Show |
14 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0004g0023others(11): Show | 14 | HG02040.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1834+10427_1834+10 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(6): Show |
24 | a0001c0001t0004g0001a0001c0001t0004g0101a0001c0001t0004g0131others(21): Show | 25 | HG00140.hp2 HG01175.hp2 HG03492.hp2 others(22): Show |
intron_variant | MODIFIER | c.1834+10426_1834+10 others(19): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(7): Show |
14 | a0001c0001t0004g0004a0001c0001t0004g0056a0001c0001t0004g0130others(11): Show | 14 | HG00280.hp2 HG00597.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1834+10425_1834+10 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0004g0055a0001c0001t0004g0103a0001c0001t0004g0145others(2): Show | 5 | HG01255.hp2 HG02698.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834+10424_1834+10 others(21): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0007g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1834+10438_1834+10 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0007g0193a0001c0001t0007g0194a0001c0001t0007g0195 | 3 | HG02055.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1834+10438_1834+10 others(27): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216172469 | |||||
| chr2:216172469
|
C | T | 1 | a0001c0002t0004g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1834+10421C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172469 | ||||||
| chr2:216172550
|
C | T | 54 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0013others(51): Show | 54 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1834+10502C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172550 | ||||||
| chr2:216172559
|
C | G | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+10511C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172559 | ||||||
| chr2:216172626
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+10578G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172626 | ||||||
| chr2:216172631
|
G | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0134others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+10583G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172631 | ||||||
| chr2:216172746
|
C | G | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+10698C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172746 | ||||||
| chr2:216172887
|
A | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1834+10839A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216172887 | ||||||
| chr2:216173000
|
T | A | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(3): Show | 6 | HG01884.hp2 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+10952T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173000 | ||||||
| chr2:216173176
|
A | C | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1834+11128A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173176 | ||||||
| chr2:216173196
|
A | G | 80 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1834+11148A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173196 | ||||||
| chr2:216173299
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834+11251T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173299 | ||||||
| chr2:216173433
|
G | A | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+11385G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173433 | ||||||
| chr2:216173465
|
A | G | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1834+11417A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173465 | ||||||
| chr2:216173558
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+11510G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173558 | ||||||
| chr2:216173602
|
T | G | 88 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0013others(85): Show | 88 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1834+11554T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173602 | ||||||
| chr2:216173604
|
C | T | 2 | a0001c0001t0003g0239a0001c0001t0003g0334 | 2 | HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1834+11556C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173604 | ||||||
| chr2:216173665
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1834+11617G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173665 | ||||||
| chr2:216173672
|
G | T | 16 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(13): Show | 17 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1834+11624G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173672 | ||||||
| chr2:216173745
|
T | C | 190 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(187): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1834+11697T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173745 | ||||||
| chr2:216173761
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+11713A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173761 | ||||||
| chr2:216173775
|
C | T | 1 | a0001c0002t0003g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1834+11727C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216173775 | ||||||
| chr2:216174151
|
T | TTTTG | 51 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0013others(48): Show | 51 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1834+12107_1834+12 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216174151 | |||||
| chr2:216174214
|
T | C | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+12166T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174214 | ||||||
| chr2:216174341
|
G | T | 67 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0002g0009others(64): Show | 68 | HG01081.hp1 HG01106.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.1834+12293G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174341 | ||||||
| chr2:216174380
|
T | C | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+12332T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174380 | ||||||
| chr2:216174390
|
T | A | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1834+12342T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174390 | ||||||
| chr2:216174424
|
T | C | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+12376T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174424 | ||||||
| chr2:216174451
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18953.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1834+12403G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174451 | ||||||
| chr2:216174455
|
A | T | 6 | a0001c0001t0006g0007a0001c0001t0006g0190a0001c0002t0006g0003others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1834+12407A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174455 | ||||||
| chr2:216174555
|
C | T | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+12507C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174555 | ||||||
| chr2:216174565
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+12517A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174565 | ||||||
| chr2:216174577
|
A | G | 1 | a0001c0002t0002g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1834+12529A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174577 | ||||||
| chr2:216174638
|
T | C | 136 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(133): Show | 137 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1834+12590T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174638 | ||||||
| chr2:216174642
|
C | G | 1 | a0001c0001t0004g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1834+12594C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174642 | ||||||
| chr2:216174652
|
A | T | 65 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1834+12604A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174652 | ||||||
| chr2:216174881
|
C | G | 7 | a0001c0001t0004g0101a0001c0001t0004g0103a0001c0001t0004g0187others(4): Show | 7 | NA18971.hp2 NA18986.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1834+12833C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174881 | ||||||
| chr2:216174923
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0182 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1834+12875G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174923 | ||||||
| chr2:216174930
|
G | A | 38 | a0001c0001t0001g0267a0001c0001t0003g0041a0001c0001t0003g0110others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1834+12882G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174930 | ||||||
| chr2:216174972
|
T | G | 124 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0267others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.1834+12924T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216174972 | ||||||
| chr2:216175081
|
A | G | 35 | a0001c0001t0003g0123a0001c0001t0003g0197a0001c0001t0003g0201others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1834+13033A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175081 | ||||||
| chr2:216175164
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00733.hp2 HG01081.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1834+13116A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175164 | ||||||
| chr2:216175260
|
A | AACCACCT others(8): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0134others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834+13222_1834+13 others(21): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216175260 | |||||
| chr2:216175310
|
C | T | 35 | a0001c0001t0003g0123a0001c0001t0003g0197a0001c0001t0003g0201others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1834+13262C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175310 | ||||||
| chr2:216175370
|
C | G | 3 | a0001c0002t0002g0325a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1834+13322C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175370 | ||||||
| chr2:216175420
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1834+13372G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175420 | ||||||
| chr2:216175448
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1834+13400C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175448 | ||||||
| chr2:216175756
|
T | C | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1834+13708T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175756 | ||||||
| chr2:216175831
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+13783C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175831 | ||||||
| chr2:216175863
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+13815A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175863 | ||||||
| chr2:216175933
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+13885T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175933 | ||||||
| chr2:216175935
|
G | A | 1 | a0001c0001t0004g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1834+13887G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175935 | ||||||
| chr2:216175953
|
C | A | 1 | a0001c0001t0004g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1834+13905C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216175953 | ||||||
| chr2:216176096
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1834+14048G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176096 | ||||||
| chr2:216176150
|
ACT | A | 38 | a0001c0001t0001g0261a0001c0001t0002g0032a0001c0001t0002g0033others(35): Show | 38 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1835-14072_1835-14 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216176150 | |||||
| chr2:216176184
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1835-14041T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176184 | ||||||
| chr2:216176264
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1835-13961G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176264 | ||||||
| chr2:216176268
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1835-13957G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176268 | ||||||
| chr2:216176381
|
A | G | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1835-13844A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176381 | ||||||
| chr2:216176399
|
G | A | 63 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(60): Show | 64 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1835-13826G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176399 | ||||||
| chr2:216176464
|
G | A | 51 | a0001c0001t0001g0261a0001c0001t0002g0013a0001c0001t0002g0019others(48): Show | 51 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1835-13761G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176464 | ||||||
| chr2:216176618
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(11): Show | 14 | HG00423.hp2 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1835-13607T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176618 | ||||||
| chr2:216176735
|
CCTT | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-13483_1835-13 others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216176735 | |||||
| chr2:216176944
|
T | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1835-13281T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176944 | ||||||
| chr2:216176983
|
A | G | 1 | a0001c0001t0004g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1835-13242A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216176983 | ||||||
| chr2:216177075
|
G | A | 13 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1835-13150G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177075 | ||||||
| chr2:216177158
|
A | G | 203 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(200): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1835-13067A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177158 | ||||||
| chr2:216177237
|
T | C | 55 | a0001c0001t0001g0042a0001c0001t0001g0059a0001c0001t0001g0060others(52): Show | 55 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1835-12988T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177237 | ||||||
| chr2:216177260
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-12965C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177260 | ||||||
| chr2:216177269
|
T | C | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-12956T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177269 | ||||||
| chr2:216177477
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1835-12748C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177477 | ||||||
| chr2:216177479
|
A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG01071.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1835-12746A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177479 | ||||||
| chr2:216177586
|
G | C | 3 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0001t0003g0225 | 3 | NA18982.hp2 NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1835-12639G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177586 | ||||||
| chr2:216177676
|
TC | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-12548delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177676 | ||||||
| chr2:216177730
|
C | G | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-12495C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177730 | ||||||
| chr2:216177775
|
A | C | 122 | a0001c0001t0001g0261a0001c0001t0002g0008a0001c0001t0002g0009others(119): Show | 123 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1835-12450A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177775 | ||||||
| chr2:216177830
|
A | C | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-12395A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177830 | ||||||
| chr2:216177834
|
T | G | 1 | a0001c0002t0004g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1835-12391T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177834 | ||||||
| chr2:216177946
|
A | G | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-12279A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216177946 | ||||||
| chr2:216178018
|
C | T | 122 | a0001c0001t0001g0261a0001c0001t0002g0008a0001c0001t0002g0009others(119): Show | 123 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1835-12207C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178018 | ||||||
| chr2:216178072
|
T | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0289others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-12153T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178072 | ||||||
| chr2:216178269
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-11956T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178269 | ||||||
| chr2:216178453
|
G | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-11772G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178453 | ||||||
| chr2:216178501
|
AC | A | 37 | a0001c0001t0003g0041a0001c0001t0003g0110a0001c0001t0003g0123others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1835-11721delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216178501 | |||||
| chr2:216178738
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1835-11487A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178738 | ||||||
| chr2:216178865
|
C | A | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-11360C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178865 | ||||||
| chr2:216178909
|
A | G | 1 | a0001c0002t0006g0003 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1835-11316A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216178909 | ||||||
| chr2:216179107
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1835-11118C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179107 | ||||||
| chr2:216179114
|
C | G | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1835-11111C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179114 | ||||||
| chr2:216179219
|
A | G | 340 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(337): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1835-11006A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179219 | ||||||
| chr2:216179242
|
C | G | 196 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0320others(193): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1835-10983C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179242 | ||||||
| chr2:216179254
|
A | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-10971A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179254 | ||||||
| chr2:216179460
|
G | A | 1 | a0001c0002t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1835-10765G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179460 | ||||||
| chr2:216179662
|
C | G | 122 | a0001c0001t0001g0261a0001c0001t0002g0008a0001c0001t0002g0009others(119): Show | 123 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1835-10563C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179662 | ||||||
| chr2:216179807
|
G | A | 3 | a0001c0001t0001g0267a0001c0001t0001g0278a0001c0001t0001g0314 | 3 | HG00140.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1835-10418G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179807 | ||||||
| chr2:216179865
|
G | C | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1835-10360G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179865 | ||||||
| chr2:216179889
|
G | C | 51 | a0001c0001t0001g0261a0001c0001t0002g0013a0001c0001t0002g0019others(48): Show | 51 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1835-10336G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179889 | ||||||
| chr2:216179952
|
C | A | 74 | a0001c0001t0001g0092a0001c0001t0001g0320a0001c0001t0001g0321others(71): Show | 75 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1835-10273C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179952 | ||||||
| chr2:216180000
|
A | G | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1835-10225A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180000 | ||||||
| chr2:216180162
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1835-10063G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180162 | ||||||
| chr2:216180270
|
G | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1835-9955G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180270 | ||||||
| chr2:216180331
|
T | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1835-9894T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180331 | ||||||
| chr2:216180336
|
C | T | 58 | a0001c0001t0001g0092a0001c0001t0001g0320a0001c0001t0001g0321others(55): Show | 59 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1835-9889C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180336 | ||||||
| chr2:216180344
|
G | A | 1 | a0001c0001t0011g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1835-9881G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180344 | ||||||
| chr2:216180469
|
T | C | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1835-9756T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180469 | ||||||
| chr2:216180488
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1835-9737T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180488 | ||||||
| chr2:216180503
|
G | T | 58 | a0001c0001t0001g0092a0001c0001t0001g0320a0001c0001t0001g0321others(55): Show | 59 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1835-9722G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180503 | ||||||
| chr2:216180603
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-9622G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180603 | ||||||
| chr2:216180675
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1835-9550A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180675 | ||||||
| chr2:216180698
|
G | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG00423.hp2 HG02015.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1835-9527G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180698 | ||||||
| chr2:216180720
|
A | T | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1835-9505A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180720 | ||||||
| chr2:216180722
|
C | A | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1835-9503C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180722 | ||||||
| chr2:216180723
|
A | T | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1835-9502A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180723 | ||||||
| chr2:216180724
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1835-9501C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180724 | ||||||
| chr2:216180736
|
C | G | 3 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159 | 3 | HG03130.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1835-9489C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180736 | ||||||
| chr2:216180812
|
CT | C | 13 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1835-9398delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216180812 | |||||
| chr2:216180917
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1835-9308A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216180917 | ||||||
| chr2:216181058
|
C | T | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1835-9167C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181058 | ||||||
| chr2:216181104
|
C | T | 1 | a0001c0001t0004g0311 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1835-9121C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181104 | ||||||
| chr2:216181195
|
G | A | 2 | a0001c0001t0004g0055a0001c0001t0004g0217 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1835-9030G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181195 | ||||||
| chr2:216181213
|
A | G | 16 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1835-9012A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181213 | ||||||
| chr2:216181216
|
T | C | 123 | a0001c0001t0001g0107a0001c0001t0001g0261a0001c0001t0002g0008others(120): Show | 124 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.1835-9009T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181216 | ||||||
| chr2:216181339
|
T | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1835-8886T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181339 | ||||||
| chr2:216181475
|
C | T | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1835-8750C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181475 | ||||||
| chr2:216181570
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0322 | 2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1835-8655C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181570 | ||||||
| chr2:216181596
|
T | A | 55 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(52): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1835-8629T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181596 | ||||||
| chr2:216181627
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1835-8598C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181627 | ||||||
| chr2:216181628
|
G | A | 1 | a0001c0002t0004g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1835-8597G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181628 | ||||||
| chr2:216181720
|
T | C | 122 | a0001c0001t0001g0261a0001c0001t0002g0008a0001c0001t0002g0009others(119): Show | 123 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1835-8505T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216181720 | ||||||
| chr2:216182148
|
A | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1835-8077A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182148 | ||||||
| chr2:216182174
|
G | T | 11 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(8): Show | 11 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1835-8051G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182174 | ||||||
| chr2:216182417
|
A | G | 3 | a0001c0001t0004g0131a0001c0001t0004g0216a0001c0001t0004g0253 | 3 | HG02698.hp2 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1835-7808A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182417 | ||||||
| chr2:216182591
|
C | G | 1 | a0001c0001t0004g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1835-7634C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182591 | ||||||
| chr2:216182737
|
G | T | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.1835-7488G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182737 | ||||||
| chr2:216182917
|
A | G | 41 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(38): Show | 41 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1835-7308A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182917 | ||||||
| chr2:216182944
|
T | A | 3 | a0001c0002t0006g0316a0001c0002t0006g0328a0001c0002t0006g0329 | 3 | HG02486.hp1 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1835-7281T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182944 | ||||||
| chr2:216183124
|
A | G | 1 | a0001c0002t0001g0294 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1835-7101A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183124 | ||||||
| chr2:216183160
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-7065C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183160 | ||||||
| chr2:216183253
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1835-6972G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183253 | ||||||
| chr2:216183271
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-6954A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183271 | ||||||
| chr2:216183509
|
A | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835-6716A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183509 | ||||||
| chr2:216183513
|
T | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-6712T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183513 | ||||||
| chr2:216183570
|
C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-6655C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183570 | ||||||
| chr2:216183610
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-6615A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183610 | ||||||
| chr2:216183842
|
A | G | 50 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1835-6383A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183842 | ||||||
| chr2:216183994
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1835-6231G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216183994 | ||||||
| chr2:216184032
|
C | CTG | 50 | a0001c0001t0002g0008a0001c0001t0002g0021a0001c0001t0002g0347others(47): Show | 51 | HG00597.hp2 HG00741.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.1835-6152_1835-615 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTG | 17 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0036others(14): Show | 18 | HG00140.hp2 HG02257.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1835-6154_1835-615 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTG | 6 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0004g0023others(3): Show | 6 | HG00280.hp2 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-6156_1835-615 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTGT others(1): Show |
14 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0020others(11): Show | 14 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1835-6158_1835-615 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTGT others(3): Show |
13 | a0001c0001t0002g0015a0001c0001t0004g0054a0001c0002t0002g0265others(10): Show | 13 | HG01109.hp2 HG01167.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1835-6160_1835-615 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTGT others(5): Show |
18 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(15): Show | 18 | HG01106.hp1 HG01358.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1835-6162_1835-615 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTGT others(7): Show |
5 | a0001c0001t0002g0096a0001c0001t0004g0132a0001c0002t0002g0309others(2): Show | 5 | HG01175.hp1 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1835-6164_1835-615 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0002g0277 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1835-6166_1835-615 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTG | C | 35 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(32): Show | 35 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1835-6152_1835-615 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTG | C | 5 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0209others(2): Show | 5 | HG01175.hp2 HG02602.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-6154_1835-615 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTG | C | 4 | a0001c0001t0003g0210a0001c0001t0003g0239a0001c0001t0003g0255others(1): Show | 4 | HG00597.hp1 HG01099.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-6156_1835-615 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0081a0001c0001t0001g0283a0001c0001t0007g0192others(3): Show | 6 | HG00280.hp1 HG02055.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-6158_1835-615 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTGT others(3): Show |
C | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0086others(5): Show | 8 | HG00423.hp1 HG00639.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1835-6160_1835-615 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTGT others(5): Show |
C | 142 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1835-6162_1835-615 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1835-6164_1835-615 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184032
|
CTGTGTGT others(15): Show |
C | 2 | a0001c0001t0001g0071a0001c0001t0001g0089 | 2 | HG01496.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1835-6172_1835-615 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216184032 | |||||
| chr2:216184067
|
TGTGTGTG others(1): Show |
T | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1835-6157_1835-615 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184067 | ||||||
| chr2:216184074
|
G | GTGTGTGT others(6): Show |
1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1835-6151_1835-615 others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184074 | ||||||
| chr2:216184075
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1835-6150A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184075 | ||||||
| chr2:216184075
|
A | T | 57 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0019others(54): Show | 57 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.1835-6150A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184075 | ||||||
| chr2:216184109
|
T | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0289others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-6116T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184109 | ||||||
| chr2:216184248
|
A | G | 4 | a0001c0001t0004g0103a0001c0001t0004g0187a0001c0001t0004g0218others(1): Show | 4 | NA18971.hp2 NA18986.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-5977A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184248 | ||||||
| chr2:216184455
|
C | T | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1835-5770C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184455 | ||||||
| chr2:216184750
|
T | G | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1835-5475T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184750 | ||||||
| chr2:216184754
|
T | G | 48 | a0001c0001t0001g0075a0001c0001t0001g0105a0001c0001t0001g0111others(45): Show | 48 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1835-5471T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184754 | ||||||
| chr2:216184761
|
T | A | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1835-5464T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184761 | ||||||
| chr2:216184812
|
C | T | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.1835-5413C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184812 | ||||||
| chr2:216184874
|
T | C | 37 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(34): Show | 37 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1835-5351T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184874 | ||||||
| chr2:216185018
|
G | A | 37 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(34): Show | 37 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1835-5207G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185018 | ||||||
| chr2:216185027
|
G | A | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.1835-5198G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185027 | ||||||
| chr2:216185167
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1835-5058G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185167 | ||||||
| chr2:216185294
|
T | A | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1835-4931T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185294 | ||||||
| chr2:216185331
|
G | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-4894G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185331 | ||||||
| chr2:216185382
|
C | T | 57 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 57 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.1835-4843C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185382 | ||||||
| chr2:216185646
|
T | C | 4 | a0001c0001t0007g0192a0001c0001t0007g0193a0001c0001t0007g0194others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-4579T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185646 | ||||||
| chr2:216185681
|
C | CT | 85 | a0001c0001t0001g0105a0001c0001t0002g0008a0001c0001t0002g0009others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1835-4532dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216185681 | |||||
| chr2:216185744
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-4481C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185744 | ||||||
| chr2:216185745
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1835-4480G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185745 | ||||||
| chr2:216185887
|
G | A | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.1835-4338G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216185887 | ||||||
| chr2:216186059
|
G | T | 1 | a0001c0002t0010g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1835-4166G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186059 | ||||||
| chr2:216186082
|
A | C | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-4143A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186082 | ||||||
| chr2:216186465
|
T | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1835-3760T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186465 | ||||||
| chr2:216186668
|
A | G | 2 | a0001c0001t0002g0347a0001c0001t0002g0348 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1835-3557A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186668 | ||||||
| chr2:216186734
|
G | A | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835-3491G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186734 | ||||||
| chr2:216186885
|
A | AT | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1835-3334dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216186885 | |||||
| chr2:216186956
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1835-3269G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186956 | ||||||
| chr2:216186997
|
A | G | 2 | a0001c0001t0004g0131a0001c0001t0004g0216 | 2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1835-3228A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216186997 | ||||||
| chr2:216187049
|
T | C | 2 | a0001c0002t0002g0326a0001c0002t0002g0327 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1835-3176T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187049 | ||||||
| chr2:216187146
|
A | G | 1 | a0001c0005t0001g0045 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1835-3079A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187146 | ||||||
| chr2:216187300
|
A | AT | 32 | a0001c0001t0001g0126a0001c0001t0002g0009a0001c0001t0002g0010others(29): Show | 33 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1835-2914dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187300 | |||||
| chr2:216187300
|
A | ATT | 43 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(40): Show | 43 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1835-2915_1835-291 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187300 | |||||
| chr2:216187322
|
T | C | 50 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1835-2903T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187322 | ||||||
| chr2:216187332
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-2893G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187332 | ||||||
| chr2:216187459
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1835-2766A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187459 | ||||||
| chr2:216187466
|
C | CTG | 47 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0064others(44): Show | 47 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.1835-2705_1835-270 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
C | CTGTG | 31 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(28): Show | 32 | HG00438.hp2 HG00609.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.1835-2707_1835-270 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
C | CTGTGTG | 26 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0059others(23): Show | 26 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1835-2709_1835-270 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0072a0001c0001t0001g0081a0001c0001t0001g0142others(8): Show | 11 | HG00673.hp2 HG01106.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1835-2711_1835-270 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0004g0256a0001c0001t0004g0340 | 2 | HG01255.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1835-2713_1835-270 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0004g0213a0001c0001t0004g0219 | 2 | HG03942.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1835-2717_1835-270 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTG | C | 48 | a0001c0001t0001g0066a0001c0001t0001g0093a0001c0001t0001g0098others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1835-2705_1835-270 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTG | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(29): Show | 33 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1835-2707_1835-270 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTG | C | 10 | a0001c0001t0001g0127a0001c0001t0002g0016a0001c0001t0003g0026others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1835-2709_1835-270 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(1): Show |
C | 12 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0126others(9): Show | 12 | HG00741.hp1 HG01243.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1835-2711_1835-270 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0001g0058a0001c0001t0002g0015a0001c0001t0002g0017others(3): Show | 6 | HG01346.hp2 HG01515.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-2713_1835-270 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(5): Show |
C | 3 | a0001c0001t0003g0110a0001c0002t0002g0326a0001c0002t0002g0327 | 3 | HG02572.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1835-2715_1835-270 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0002g0014a0001c0001t0002g0094 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1835-2717_1835-270 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(9): Show |
C | 2 | a0001c0001t0003g0095a0001c0001t0009g0189 | 2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1835-2719_1835-270 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(11): Show |
C | 2 | a0001c0001t0001g0285a0001c0005t0001g0045 | 2 | HG01433.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1835-2721_1835-270 others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(15): Show |
C | 3 | a0001c0001t0003g0006a0001c0001t0003g0289a0001c0001t0003g0290 | 3 | HG02559.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1835-2725_1835-270 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(19): Show |
C | 1 | a0001c0002t0002g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1835-2729_1835-270 others(30): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(21): Show |
C | 1 | a0001c0001t0002g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1835-2731_1835-270 others(32): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187466
|
CTGTGTGT others(23): Show |
C | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 55 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1835-2733_1835-270 others(34): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187466 | |||||
| chr2:216187520
|
G | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-2705G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187520 | ||||||
| chr2:216187522
|
T | A | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1835-2703T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187522 | ||||||
| chr2:216187529
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0002t0002g0325 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1835-2696T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187529 | ||||||
| chr2:216187589
|
T | G | 1 | a0001c0002t0004g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1835-2636T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187589 | ||||||
| chr2:216187592
|
C | T | 1 | a0001c0001t0004g0214 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1835-2633C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187592 | ||||||
| chr2:216187711
|
G | A | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.1835-2514G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187711 | ||||||
| chr2:216187776
|
A | G | 1 | a0001c0001t0004g0263 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1835-2449A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187776 | ||||||
| chr2:216187786
|
G | GAC | 7 | a0001c0001t0003g0123a0001c0001t0003g0212a0001c0001t0004g0053others(4): Show | 7 | HG01361.hp2 HG02055.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1835-2404_1835-240 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACAC | 4 | a0001c0001t0006g0007a0001c0002t0002g0313a0001c0002t0006g0003others(1): Show | 5 | HG02109.hp1 HG03195.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-2408_1835-240 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(1): Show |
4 | a0001c0002t0002g0273a0001c0002t0002g0297a0001c0002t0002g0312others(1): Show | 4 | HG01109.hp2 HG02293.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2410_1835-240 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(3): Show |
5 | a0001c0002t0002g0271a0001c0002t0002g0292a0001c0002t0002g0301others(2): Show | 5 | HG02738.hp1 HG02976.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1835-2412_1835-240 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(5): Show |
6 | a0001c0001t0002g0035a0001c0002t0002g0265a0001c0002t0002g0274others(3): Show | 6 | HG01167.hp2 HG02895.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1835-2414_1835-240 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(7): Show |
4 | a0001c0001t0002g0019a0001c0001t0002g0096a0001c0002t0002g0299others(1): Show | 4 | HG01175.hp1 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2416_1835-240 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(9): Show |
1 | a0001c0001t0002g0034 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1835-2418_1835-240 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(11): Show |
1 | a0001c0001t0002g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1835-2420_1835-240 others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACA others(15): Show |
1 | a0001c0001t0003g0289 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1835-2424_1835-240 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
G | GACACACG others(5): Show |
1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1835-2433_1835-243 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
GAC | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | HG02258.hp2 NA18949.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-2404_1835-240 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
GACAC | G | 10 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0104others(7): Show | 10 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.1835-2406_1835-240 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
GACACAC | G | 19 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0046others(16): Show | 19 | HG01099.hp2 HG01258.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1835-2408_1835-240 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187786
|
GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0001g0285 | 3 | HG01070.hp2 HG01975.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1835-2410_1835-240 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187786 | |||||
| chr2:216187811
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0061 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1835-2412_1835-240 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187811 | |||||
| chr2:216187811
|
ACACACAC others(9): Show |
A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1835-2412_1835-239 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187811 | |||||
| chr2:216187813
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1835-2412A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187813 | ||||||
| chr2:216187813
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0011g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1835-2410_1835-240 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187813 | |||||
| chr2:216187815
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1835-2410A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187815 | ||||||
| chr2:216187815
|
ACACACAC others(1): Show |
A | 77 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0047others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1835-2408_1835-240 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187815 | |||||
| chr2:216187815
|
ACACACAC others(3): Show |
A | 6 | a0001c0001t0001g0073a0001c0001t0001g0097a0001c0001t0001g0148others(3): Show | 6 | HG01243.hp2 HG01433.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1835-2408_1835-239 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187815 | |||||
| chr2:216187815
|
ACACACAC others(5): Show |
A | 11 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0069others(8): Show | 11 | HG00544.hp1 HG00733.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1835-2408_1835-239 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187815 | |||||
| chr2:216187817
|
A | ACTCTCTC others(3): Show |
1 | a0001c0001t0003g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1835-2407_1835-240 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187817
|
A | T | 2 | a0001c0001t0001g0111a0001c0001t0005g0275 | 2 | HG00423.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1835-2408A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187817 | ||||||
| chr2:216187817
|
ACACACT | A | 9 | a0001c0001t0001g0138a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG00673.hp2 HG02155.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1835-2406_1835-240 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187817
|
ACACACTC others(1): Show |
A | 4 | a0001c0001t0001g0149a0001c0001t0001g0169a0001c0001t0001g0178others(1): Show | 4 | HG00639.hp1 NA18960.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2406_1835-239 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187817
|
ACACACTC others(3): Show |
A | 1 | a0001c0001t0001g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1835-2406_1835-239 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187817
|
ACACACTC others(5): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1835-2406_1835-239 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187817
|
ACACACTC others(7): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1835-2406_1835-239 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187817 | |||||
| chr2:216187819
|
A | T | 16 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0150others(13): Show | 16 | HG00423.hp1 HG00423.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1835-2406A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187819 | ||||||
| chr2:216187819
|
ACACTCT | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0118a0001c0001t0002g0094others(1): Show | 4 | HG02071.hp1 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1835-2404_1835-239 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187819 | |||||
| chr2:216187821
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0003g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(34): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(28): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0003g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(30): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(33): Show |
1 | a0001c0002t0002g0325 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(44): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(34): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(29): Show |
1 | a0001c0001t0002g0152 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(40): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0002g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(24): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0002g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0002g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(36): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(13): Show |
2 | a0001c0001t0002g0020a0001c0001t0002g0039 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1835-2403_1835-240 others(24): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0002g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(7): Show |
2 | a0001c0001t0002g0032a0001c0001t0002g0037 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1835-2403_1835-240 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(15): Show |
2 | a0001c0001t0002g0038a0001c0002t0002g0300 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1835-2403_1835-240 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0002g0348 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(30): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0002g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(32): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0002g0013 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(36): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(5): Show |
3 | a0001c0001t0002g0277a0001c0002t0002g0315a0001c0002t0006g0328 | 3 | HG01081.hp1 HG02486.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1835-2403_1835-240 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0002g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0002g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(3): Show |
1 | a0001c0002t0002g0318 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(5): Show |
1 | a0001c0002t0002g0293 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0002g0319 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1835-2403_1835-240 others(28): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACACACTC others(5): Show |
3 | a0001c0001t0002g0010a0001c0001t0009g0188a0001c0001t0009g0189 | 3 | HG02886.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1835-2403_1835-240 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACT | 6 | a0001c0001t0003g0231a0001c0001t0003g0235a0001c0001t0003g0239others(3): Show | 6 | HG00099.hp2 HG01106.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1835-2364_1835-236 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACTCTCTC others(7): Show |
4 | a0001c0001t0002g0014a0001c0001t0002g0016a0001c0001t0002g0018others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2376_1835-236 others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | ACTCTCTC others(9): Show |
1 | a0001c0001t0002g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1835-2378_1835-236 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
A | T | 27 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0104others(24): Show | 27 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.1835-2404A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187821 | ||||||
| chr2:216187821
|
ACT | A | 5 | a0001c0001t0003g0025a0001c0001t0003g0229a0001c0001t0003g0244others(2): Show | 5 | HG00741.hp2 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-2364_1835-236 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
ACTCT | A | 22 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0197others(19): Show | 22 | HG00609.hp1 HG00673.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1835-2366_1835-236 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
ACTCTCT | A | 11 | a0001c0001t0003g0349a0001c0001t0004g0055a0001c0001t0004g0103others(8): Show | 11 | HG01256.hp2 HG02451.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.1835-2368_1835-236 others(10): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
ACTCTCTC others(1): Show |
A | 26 | a0001c0001t0003g0201a0001c0001t0004g0001a0001c0001t0004g0101others(23): Show | 27 | HG00140.hp2 HG00597.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1835-2370_1835-236 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
ACTCTCTC others(3): Show |
A | 3 | a0001c0001t0003g0024a0001c0001t0004g0250a0001c0001t0004g0256 | 3 | HG01175.hp2 HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1835-2372_1835-236 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187821
|
ACTCTCTC others(5): Show |
A | 4 | a0001c0001t0004g0131a0001c0001t0004g0205a0001c0001t0004g0211others(1): Show | 4 | HG03654.hp1 HG03831.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2374_1835-236 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187821 | |||||
| chr2:216187823
|
T | A | 25 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0012others(22): Show | 25 | HG00280.hp2 HG01106.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1835-2402T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187823 | ||||||
| chr2:216187825
|
T | A | 20 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0244others(17): Show | 20 | HG00280.hp2 HG00741.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1835-2400T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187825 | ||||||
| chr2:216187827
|
T | A | 25 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029others(22): Show | 26 | HG01106.hp1 HG01358.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1835-2398T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187827 | ||||||
| chr2:216187829
|
T | A | 30 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(27): Show | 30 | HG01106.hp1 HG01256.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1835-2396T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187829 | ||||||
| chr2:216187831
|
T | A | 44 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(41): Show | 45 | HG00597.hp2 HG01256.hp2 HG02040.hp1 others(42): Show |
intron_variant | MODIFIER | c.1835-2394T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187831 | ||||||
| chr2:216187833
|
T | A | 34 | a0001c0001t0003g0024a0001c0001t0004g0001a0001c0001t0004g0004others(31): Show | 35 | HG01175.hp2 HG01255.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1835-2392T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187833 | ||||||
| chr2:216187835
|
T | A | 4 | a0001c0001t0004g0131a0001c0001t0004g0205a0001c0001t0004g0216others(1): Show | 4 | HG03209.hp1 HG03654.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1835-2390T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187835 | ||||||
| chr2:216187837
|
T | A | 1 | a0001c0001t0004g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1835-2388T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187837 | ||||||
| chr2:216187857
|
T | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0095 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1835-2368T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187857 | ||||||
| chr2:216187857
|
T | TCTCTCTC others(3): Show |
2 | a0001c0001t0005g0286a0001c0001t0005g0287 | 2 | HG01981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1835-2363_1835-236 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187857 | |||||
| chr2:216187857
|
T | TCTCTCTC others(5): Show |
1 | a0001c0001t0005g0335 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1835-2363_1835-236 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187857 | |||||
| chr2:216187859
|
T | C | 13 | a0001c0001t0002g0348a0001c0001t0003g0006a0001c0001t0003g0095others(10): Show | 14 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1835-2366T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187859 | ||||||
| chr2:216187859
|
T | TC | 14 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0096others(11): Show | 14 | HG01167.hp2 HG02622.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1835-2365dupC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187859 | |||||
| chr2:216187861
|
T | C | 35 | a0001c0001t0001g0127a0001c0001t0001g0182a0001c0001t0001g0281others(32): Show | 36 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1835-2364T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187861 | ||||||
| chr2:216187861
|
T | TCCC | 12 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0032others(9): Show | 12 | HG01175.hp1 HG01358.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.1835-2362_1835-236 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187861 | |||||
| chr2:216187861
|
T | TCTCCC | 8 | a0001c0001t0002g0033a0001c0002t0002g0304a0001c0002t0002g0305others(5): Show | 8 | HG01106.hp1 HG02723.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1835-2363_1835-236 others(9): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187861 | |||||
| chr2:216187861
|
T | TCTCTCTC others(6): Show |
1 | a0001c0001t0002g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1835-2363_1835-236 others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 216187861 | |||||
| chr2:216187977
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1835-2248A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216187977 | ||||||
| chr2:216188092
|
C | G | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1835-2133C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188092 | ||||||
| chr2:216188151
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1835-2074A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188151 | ||||||
| chr2:216188389
|
T | C | 1 | a0001c0001t0008g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1835-1836T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188389 | ||||||
| chr2:216188496
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1835-1729A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188496 | ||||||
| chr2:216188541
|
T | A | 61 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1835-1684T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188541 | ||||||
| chr2:216188572
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1835-1653G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188572 | ||||||
| chr2:216188599
|
T | C | 1 | a0001c0002t0002g0303 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1835-1626T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188599 | ||||||
| chr2:216188877
|
G | T | 7 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0196others(4): Show | 7 | HG01169.hp1 HG01433.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1835-1348G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188877 | ||||||
| chr2:216188941
|
C | T | 9 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(6): Show | 10 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1835-1284C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188941 | ||||||
| chr2:216188991
|
A | G | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1835-1234A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216188991 | ||||||
| chr2:216189048
|
G | C | 2 | a0001c0001t0009g0188a0001c0001t0009g0189 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1835-1177G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189048 | ||||||
| chr2:216189228
|
C | T | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1835-997C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189228 | ||||||
| chr2:216189369
|
T | C | 1 | a0001c0001t0004g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1835-856T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189369 | ||||||
| chr2:216189457
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1835-768C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189457 | ||||||
| chr2:216189503
|
T | C | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1835-722T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189503 | ||||||
| chr2:216189790
|
C | G | 55 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(52): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1835-435C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189790 | ||||||
| chr2:216189811
|
T | G | 75 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(72): Show | 75 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.1835-414T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216189811 | ||||||
| chr2:216190211
|
G | T | 1 | a0001c0002t0002g0313 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1835-14G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216190211 | ||||||
| chr2:216190366
|
A | G | 1 | a0001c0002t0002g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1944+32A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190366 | ||||||
| chr2:216190377
|
G | A | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | HG01099.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1944+43G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190377 | ||||||
| chr2:216190428
|
T | C | 75 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(72): Show | 75 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.1944+94T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190428 | ||||||
| chr2:216190435
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1944+101T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190435 | ||||||
| chr2:216190448
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.1944+114A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190448 | ||||||
| chr2:216190939
|
T | C | 7 | a0001c0001t0005g0275a0001c0001t0005g0286a0001c0001t0005g0287others(4): Show | 7 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1944+605T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216190939 | ||||||
| chr2:216191192
|
A | G | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1944+858A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191192 | ||||||
| chr2:216191288
|
T | C | 14 | a0001c0001t0004g0004a0001c0001t0004g0023a0001c0001t0004g0053others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1944+954T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191288 | ||||||
| chr2:216191303
|
T | C | 85 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(82): Show | 86 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.1944+969T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191303 | ||||||
| chr2:216191703
|
G | T | 1 | a0001c0001t0004g0208 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1945-936G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191703 | ||||||
| chr2:216191706
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(146): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1945-933C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191706 | ||||||
| chr2:216191764
|
A | G | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-875A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191764 | ||||||
| chr2:216191821
|
G | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0095a0001c0001t0003g0289others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945-818G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191821 | ||||||
| chr2:216191866
|
A | G | 1 | a0001c0002t0002g0325 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1945-773A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216191866 | ||||||
| chr2:216192078
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1945-561A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192078 | ||||||
| chr2:216192307
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0012 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1945-332A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192307 | ||||||
| chr2:216192313
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1945-326G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192313 | ||||||
| chr2:216192453
|
A | G | 4 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(1): Show | 4 | HG03130.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945-186A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192453 | ||||||
| chr2:216192520
|
C | T | 1 | a0001c0001t0004g0213 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1945-119C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192520 | ||||||
| chr2:216192612
|
C | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1945-27C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 17/20 | chr2 | 216192612 | ||||||
| chr2:216192761
|
T | A | 71 | a0001c0001t0001g0087a0001c0001t0002g0008a0001c0001t0002g0009others(68): Show | 71 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.2041+26T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216192761 | ||||||
| chr2:216192996
|
A | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2041+261A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216192996 | ||||||
| chr2:216193082
|
A | G | 6 | a0001c0001t0006g0007a0001c0001t0006g0190a0001c0002t0006g0003others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041+347A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193082 | ||||||
| chr2:216193085
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2041+350C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193085 | ||||||
| chr2:216193123
|
G | A | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2041+388G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193123 | ||||||
| chr2:216193170
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2041+435G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193170 | ||||||
| chr2:216193186
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2041+451A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193186 | ||||||
| chr2:216193214
|
T | C | 83 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(80): Show | 84 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(81): Show |
intron_variant | MODIFIER | c.2041+479T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193214 | ||||||
| chr2:216193358
|
G | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041+623G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193358 | ||||||
| chr2:216193435
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2041+700A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193435 | ||||||
| chr2:216193467
|
T | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2041+732T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193467 | ||||||
| chr2:216193627
|
T | G | 73 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(70): Show | 73 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.2041+892T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193627 | ||||||
| chr2:216193737
|
T | G | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2041+1002T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193737 | ||||||
| chr2:216194280
|
T | G | 37 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(34): Show | 37 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2042-639T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194280 | ||||||
| chr2:216194348
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2042-571G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194348 | ||||||
| chr2:216194364
|
T | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2042-555T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194364 | ||||||
| chr2:216194371
|
T | G | 83 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(80): Show | 84 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(81): Show |
intron_variant | MODIFIER | c.2042-548T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194371 | ||||||
| chr2:216194531
|
G | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-388G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194531 | ||||||
| chr2:216194665
|
A | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042-254A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194665 | ||||||
| chr2:216194705
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2042-214G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194705 | ||||||
| chr2:216194853
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2042-66G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216194853 | ||||||
| chr2:216195025
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2109+39A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195025 | ||||||
| chr2:216195086
|
G | A | 55 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(52): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2109+100G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195086 | ||||||
| chr2:216195241
|
C | T | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2109+255C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195241 | ||||||
| chr2:216195327
|
G | A | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2109+341G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195327 | ||||||
| chr2:216195341
|
C | CTTGTTTT others(13): Show |
1 | a0001c0001t0001g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2109+357_2109+358i others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195341 | |||||
| chr2:216195341
|
C | CTTGTTTT others(18): Show |
1 | a0001c0001t0001g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2109+357_2109+358i others(27): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195341 | |||||
| chr2:216195341
|
C | CTTGTTTT others(28): Show |
1 | a0001c0001t0001g0119 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2109+357_2109+358i others(37): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195341 | |||||
| chr2:216195341
|
C | CTTGTTTT others(33): Show |
1 | a0001c0001t0001g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2109+357_2109+358i others(42): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195341 | |||||
| chr2:216195345
|
T | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00733.hp2 HG01081.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+359T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195345 | ||||||
| chr2:216195345
|
T | TCTTTTCT others(9): Show |
1 | a0001c0001t0001g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2109+359_2109+360i others(18): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195345 | ||||||
| chr2:216195345
|
T | TTCTTTTC others(15): Show |
1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2109+360_2109+361i others(24): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTCTTT others(22): Show |
1 | a0001c0001t0001g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2109+362_2109+363i others(31): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTC | 18 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0242others(15): Show | 18 | HG00597.hp1 HG01099.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.2109+401_2109+405d others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(3): Show |
8 | a0001c0001t0001g0160a0001c0001t0001g0269a0001c0001t0001g0322others(5): Show | 8 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.2109+396_2109+405d others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(8): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 29 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.2109+391_2109+405d others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(13): Show |
41 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0051others(38): Show | 41 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2109+386_2109+405d others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(18): Show |
32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0070others(29): Show | 32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.2109+381_2109+405d others(27): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(23): Show |
33 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0068others(30): Show | 33 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2109+376_2109+405d others(32): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTCTT others(28): Show |
17 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0086others(14): Show | 17 | HG01070.hp2 HG01109.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2109+371_2109+405d others(37): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
T | TTTTTTTC others(15): Show |
1 | a0001c0001t0011g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2109+363_2109+364i others(24): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
TTTTTC | T | 9 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0012others(6): Show | 9 | HG01106.hp2 HG01891.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2109+401_2109+405d others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
TTTTTCTT others(3): Show |
T | 59 | a0001c0001t0002g0011a0001c0001t0003g0006a0001c0001t0003g0095others(56): Show | 60 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2109+396_2109+405d others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
TTTTTCTT others(8): Show |
T | 13 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(10): Show | 13 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2109+391_2109+405d others(17): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
TTTTTCTT others(13): Show |
T | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109+386_2109+405d others(22): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195345
|
TTTTTCTT others(18): Show |
T | 37 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(34): Show | 37 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2109+381_2109+405d others(27): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195345 | |||||
| chr2:216195411
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2109+425C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195411 | ||||||
| chr2:216195605
|
T | TA | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109+623dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216195605 | |||||
| chr2:216195767
|
T | G | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2109+781T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216195767 | ||||||
| chr2:216196044
|
G | A | 14 | a0001c0001t0004g0004a0001c0001t0004g0023a0001c0001t0004g0053others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2109+1058G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196044 | ||||||
| chr2:216196193
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2109+1207A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196193 | ||||||
| chr2:216196197
|
T | G | 2 | a0001c0001t0002g0277a0001c0006t0002g0284 | 2 | HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2109+1211T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196197 | ||||||
| chr2:216196218
|
T | TA | 16 | a0001c0001t0001g0090a0001c0001t0001g0343a0001c0001t0001g0345others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.2109+1248dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216196218 | |||||
| chr2:216196218
|
T | TTA | 5 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0009g0188others(2): Show | 5 | HG02145.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109+1232_2109+123 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196218 | ||||||
| chr2:216196218
|
TA | T | 65 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0178others(62): Show | 67 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2109+1248delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216196218 | |||||
| chr2:216196218
|
TAA | T | 8 | a0001c0001t0004g0103a0001c0001t0004g0199a0001c0001t0004g0200others(5): Show | 8 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2109+1247_2109+124 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216196218 | |||||
| chr2:216196228
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2109+1242A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196228 | ||||||
| chr2:216196229
|
A | C | 1 | a0001c0001t0003g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2109+1243A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196229 | ||||||
| chr2:216196234
|
A | C | 2 | a0001c0002t0001g0084a0001c0002t0001g0294 | 2 | NA18962.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.2109+1248A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196234 | ||||||
| chr2:216196362
|
A | G | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109+1376A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196362 | ||||||
| chr2:216196366
|
G | C | 6 | a0001c0001t0004g0023a0001c0001t0004g0054a0001c0001t0004g0128others(3): Show | 6 | HG02280.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109+1380G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196366 | ||||||
| chr2:216196377
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2109+1391C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196377 | ||||||
| chr2:216196403
|
G | A | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2109+1417G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196403 | ||||||
| chr2:216196453
|
A | G | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2109+1467A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196453 | ||||||
| chr2:216196529
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2109+1543C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196529 | ||||||
| chr2:216196531
|
T | TAC | 4 | a0001c0001t0002g0008a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2109+1555_2109+155 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216196531 | |||||
| chr2:216196551
|
G | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2109+1565G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196551 | ||||||
| chr2:216196997
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2109+2011A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196997 | ||||||
| chr2:216197008
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2109+2022A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197008 | ||||||
| chr2:216197106
|
A | G | 1 | a0001c0001t0005g0275 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2109+2120A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197106 | ||||||
| chr2:216197322
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2109+2336G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197322 | ||||||
| chr2:216197370
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0022a0001c0001t0002g0347others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+2384G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197370 | ||||||
| chr2:216197432
|
C | T | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2109+2446C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197432 | ||||||
| chr2:216197448
|
G | GA | 209 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(206): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2109+2482dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216197448 | |||||
| chr2:216197448
|
G | GAA | 11 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0111others(8): Show | 11 | HG01433.hp1 HG02135.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109+2481_2109+248 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216197448 | |||||
| chr2:216197448
|
GA | G | 16 | a0001c0001t0002g0008a0001c0001t0002g0151a0001c0001t0002g0152others(13): Show | 16 | HG02004.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2109+2482delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216197448 | |||||
| chr2:216197569
|
C | G | 1 | a0001c0001t0002g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2109+2583C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197569 | ||||||
| chr2:216197688
|
C | T | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2109+2702C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197688 | ||||||
| chr2:216197735
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2109+2749A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197735 | ||||||
| chr2:216197818
|
C | CT | 55 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(52): Show | 56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2109+2839dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216197818 | |||||
| chr2:216197930
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2109+2944A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197930 | ||||||
| chr2:216197995
|
A | T | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2109+3009A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216197995 | ||||||
| chr2:216198039
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2109+3053A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216198039 | ||||||
| chr2:216198289
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0086others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+3303G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216198289 | ||||||
| chr2:216198322
|
G | GA | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2109+3338dupA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198322 | |||||
| chr2:216198533
|
T | TTTTA | 43 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0112others(40): Show | 44 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2109+3584_2109+358 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198533 | |||||
| chr2:216198533
|
TTTTA | T | 65 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(62): Show | 65 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2109+3584_2109+358 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198533 | |||||
| chr2:216198533
|
TTTTATTT others(1): Show |
T | 27 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(24): Show | 27 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.2109+3580_2109+358 others(12): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198533 | |||||
| chr2:216198533
|
TTTTATTT others(5): Show |
T | 2 | a0001c0001t0001g0097a0001c0001t0002g0152 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2109+3576_2109+358 others(16): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198533 | |||||
| chr2:216198533
|
TTTTATTT others(9): Show |
T | 38 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(35): Show | 38 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2109+3572_2109+358 others(20): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216198533 | |||||
| chr2:216198844
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2109+3858G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216198844 | ||||||
| chr2:216198924
|
A | G | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2109+3938A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216198924 | ||||||
| chr2:216198944
|
CA | C | 9 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(6): Show | 9 | HG01975.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2109+3959delA | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216198944 | ||||||
| chr2:216199017
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2109+4031C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199017 | ||||||
| chr2:216199336
|
T | C | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2109+4350T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199336 | ||||||
| chr2:216199470
|
C | G | 1 | a0001c0002t0002g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2109+4484C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199470 | ||||||
| chr2:216199586
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2109+4600A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199586 | ||||||
| chr2:216199641
|
G | A | 309 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(306): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2109+4655G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199641 | ||||||
| chr2:216199738
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2110-4584C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199738 | ||||||
| chr2:216199808
|
A | AT | 7 | a0001c0001t0001g0064a0001c0001t0001g0085a0001c0001t0001g0127others(4): Show | 7 | HG00140.hp1 HG01433.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2110-4513dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199808 | |||||
| chr2:216199808
|
A | ATT | 118 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0044others(115): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.2110-4513_2110-451 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199808 | |||||
| chr2:216199808
|
A | ATTT | 25 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0059others(22): Show | 25 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.2110-4513_2110-451 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199808 | |||||
| chr2:216199808
|
A | ATTTT | 4 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0176others(1): Show | 4 | HG00438.hp2 HG02129.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110-4513_2110-451 others(8): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199808 | |||||
| chr2:216199810
|
C | CT | 11 | a0001c0001t0003g0026a0001c0001t0003g0156a0001c0001t0003g0158others(8): Show | 12 | HG00280.hp2 HG01175.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2110-4488dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199810 | |||||
| chr2:216199810
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2110-4512C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199810 | ||||||
| chr2:216199810
|
CT | C | 15 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(12): Show | 15 | HG01109.hp2 HG01258.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2110-4488delT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199810 | |||||
| chr2:216199810
|
CTT | C | 44 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(41): Show | 44 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.2110-4489_2110-448 others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199810 | |||||
| chr2:216199810
|
CTTT | C | 7 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0022others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2110-4490_2110-448 others(7): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199810 | |||||
| chr2:216199810
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(6): Show | 9 | HG01975.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110-4497_2110-448 others(14): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216199810 | |||||
| chr2:216199870
|
T | A | 7 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0250others(4): Show | 7 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2110-4452T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216199870 | ||||||
| chr2:216200009
|
ATTGGCCA others(15): Show |
A | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2110-4296_2110-427 others(26): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216200009 | |||||
| chr2:216200024
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG01891.hp2 HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2110-4298A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200024 | ||||||
| chr2:216200145
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2110-4177C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200145 | ||||||
| chr2:216200179
|
C | T | 54 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0023others(51): Show | 55 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2110-4143C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200179 | ||||||
| chr2:216200199
|
G | A | 1 | a0001c0002t0002g0324 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2110-4123G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200199 | ||||||
| chr2:216200253
|
A | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2110-4069A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200253 | ||||||
| chr2:216200371
|
A | C | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2110-3951A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200371 | ||||||
| chr2:216200375
|
G | A | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2110-3947G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200375 | ||||||
| chr2:216200582
|
A | G | 1 | a0001c0001t0009g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2110-3740A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200582 | ||||||
| chr2:216200790
|
A | G | 1 | a0001c0001t0004g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2110-3532A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200790 | ||||||
| chr2:216200943
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2110-3379A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216200943 | ||||||
| chr2:216201067
|
A | G | 1 | a0001c0001t0003g0191 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2110-3255A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201067 | ||||||
| chr2:216201093
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2110-3229T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201093 | ||||||
| chr2:216201463
|
G | A | 71 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(68): Show | 71 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.2110-2859G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201463 | ||||||
| chr2:216201914
|
G | A | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2110-2408G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201914 | ||||||
| chr2:216201979
|
C | T | 1 | a0001c0001t0004g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2110-2343C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201979 | ||||||
| chr2:216201980
|
G | A | 61 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(58): Show | 61 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.2110-2342G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216201980 | ||||||
| chr2:216202114
|
C | T | 2 | a0001c0001t0009g0188a0001c0001t0009g0189 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2110-2208C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202114 | ||||||
| chr2:216202367
|
A | C | 1 | a0001c0001t0004g0227 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2110-1955A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202367 | ||||||
| chr2:216202444
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2110-1878T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202444 | ||||||
| chr2:216202446
|
A | G | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2110-1876A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202446 | ||||||
| chr2:216202474
|
T | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(152): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2110-1848T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202474 | ||||||
| chr2:216202492
|
G | T | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2110-1830G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202492 | ||||||
| chr2:216202521
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2110-1801C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202521 | ||||||
| chr2:216202624
|
G | T | 10 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2110-1698G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202624 | ||||||
| chr2:216202662
|
A | T | 1 | a0001c0001t0004g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2110-1660A>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202662 | ||||||
| chr2:216202702
|
C | T | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2110-1620C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202702 | ||||||
| chr2:216202708
|
C | T | 1 | a0001c0001t0005g0275 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2110-1614C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202708 | ||||||
| chr2:216202713
|
AG | A | 9 | a0001c0002t0002g0115a0001c0002t0002g0273a0001c0002t0002g0291others(6): Show | 9 | HG01167.hp2 HG02683.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.2110-1608delG | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202713 | ||||||
| chr2:216202744
|
G | A | 1 | a0001c0002t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2110-1578G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202744 | ||||||
| chr2:216203013
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0002t0002g0325 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2110-1309G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203013 | ||||||
| chr2:216203158
|
A | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2110-1164A>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203158 | ||||||
| chr2:216203178
|
T | G | 81 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(78): Show | 82 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.2110-1144T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203178 | ||||||
| chr2:216203268
|
T | C | 9 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2110-1054T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203268 | ||||||
| chr2:216203285
|
G | A | 1 | a0001c0002t0006g0329 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2110-1037G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203285 | ||||||
| chr2:216203369
|
A | G | 10 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2110-953A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203369 | ||||||
| chr2:216203454
|
G | A | 1 | a0001c0001t0002g0348 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2110-868G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203454 | ||||||
| chr2:216203495
|
AC | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0118 | 3 | HG00558.hp1 NA18988.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2110-826delC | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203495 | ||||||
| chr2:216203498
|
G | C | 57 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(54): Show | 57 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.2110-824G>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203498 | ||||||
| chr2:216203666
|
TTTTCTCA others(4): Show |
T | 1 | a0001c0001t0005g0286 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2110-646_2110-636d others(13): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216203666 | |||||
| chr2:216203811
|
T | C | 1 | a0001c0001t0012g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2110-511T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203811 | ||||||
| chr2:216203848
|
C | CT | 19 | a0001c0001t0004g0004a0001c0001t0004g0023a0001c0001t0004g0053others(16): Show | 19 | HG02055.hp2 HG02280.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.2110-457dupT | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216203848 | |||||
| chr2:216203848
|
C | CTT | 64 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0135others(61): Show | 65 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2110-458_2110-457d others(4): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216203848 | |||||
| chr2:216203848
|
C | CTTT | 214 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(211): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.2110-459_2110-457d others(5): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216203848 | |||||
| chr2:216203848
|
C | CTTTT | 6 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0108others(3): Show | 6 | HG00423.hp2 HG01978.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.2110-460_2110-457d others(6): Show |
XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr2 | 216203848 | |||||
| chr2:216203970
|
C | A | 1 | a0001c0001t0003g0226 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2110-352C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216203970 | ||||||
| chr2:216204023
|
C | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0349 | 3 | HG02451.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2110-299C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216204023 | ||||||
| chr2:216204143
|
C | G | 1 | a0001c0002t0010g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2110-179C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216204143 | ||||||
| chr2:216204425
|
T | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184+29T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204425 | ||||||
| chr2:216204428
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2184+32A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204428 | ||||||
| chr2:216204586
|
T | A | 1 | a0001c0001t0006g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2184+190T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204586 | ||||||
| chr2:216204605
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2184+209C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204605 | ||||||
| chr2:216204632
|
C | T | 1 | a0001c0002t0001g0294 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2184+236C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204632 | ||||||
| chr2:216204903
|
G | T | 7 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0250others(4): Show | 7 | HG00140.hp2 HG01175.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2185-285G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204903 | ||||||
| chr2:216204997
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0086others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2185-191G>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216204997 | ||||||
| chr2:216205148
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18953.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2185-40T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216205148 | ||||||
| chr2:216205153
|
T | G | 50 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0020others(47): Show | 50 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.2185-35T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 20/20 | chr2 | 216205153 |