Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MVRSG others(727): Show |
chr2 | 216104348 | 216211293 |
| a0002 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | MVRSG others(727): Show |
chr2 | 216104348 | 216211293 |
| a0003 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | MVRSG others(727): Show |
chr2 | 216104348 | 216211293 |
| a0004 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | MVRSG others(727): Show |
chr2 | 216104348 | 216211293 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2196 | 305 | 85 | 58 | 115 | 14 | 32 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0001c0002 | 1/0 | 2196 | 42 | 10 | 6 | 15 | 0 | 10 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0001c0005 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0001c0006 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0002c0003 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0003c0004 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
chr2 | 216104348 | 216211293 | ||
| a0004c0007 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | ATGGT others(2191): Show |
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 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0002 | 0/0 | 3379 | 37 | 34 | 2 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0003 | 0/0 | 3379 | 54 | 19 | 12 | 14 | 2 | 7 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0004 | 0/0 | 3379 | 51 | 12 | 3 | 24 | 3 | 9 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0005 | 0/0 | 3379 | 7 | 0 | 5 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0006 | 0/0 | 3379 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0007 | 0/0 | 3379 | 4 | 4 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0008 | 0/0 | 3379 | 3 | 0 | 0 | 0 | 1 | 2 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0009 | 0/0 | 3379 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0011 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0001t0012 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0001 | 0/0 | 3379 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0002 | 0/0 | 3379 | 31 | 4 | 5 | 13 | 0 | 9 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0003 | 1/0 | 3379 | 2 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0004 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0006 | 0/0 | 3379 | 5 | 5 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0002t0010 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0005t0001 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0001c0006t0002 | 0/0 | 3379 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0002c0003t0004 | 0/0 | 3379 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0003c0004t0001 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| a0004c0007t0003 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | GCTAT others(3374): Show |
chr2 | 216104348 | 216211293 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0063 | 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 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0115 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0145 | 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 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0001g0342 | 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 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 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 | 1 | 0 | 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 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0025 | 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 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0009 | 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 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0157 | 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 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0004g0204 | 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 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0329 | 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 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0005g0334 | 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 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0007g0191 | 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 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0003g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0002t0010g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0005t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0001c0006t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0002c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0003c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| a0004c0007t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0278 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0203 | EUR | GBR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | FIN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0314 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0335 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0334 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01175 | hp1 | a0001 | c0006 | t0002 | g0283 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0255 | 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 | g0262 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0132 | 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 | g0332 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01433 | hp1 | a0001 | c0005 | t0001 | g0046 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0331 | AMR | CLM | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0250 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0285 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0138 | 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 | g0315 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0286 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0193 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02293 | hp2 | a0001 | c0002 | t0010 | g0295 | AMR | PEL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0301 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0270 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0328 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0324 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0323 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0188 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0128 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0326 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0269 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0191 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0327 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0294 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0299 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0303 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0248 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0322 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ESN | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0072 | 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 | g0239 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0290 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0183 | SAS | PJL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0215 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0209 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0300 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0272 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | STU | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18959 | hp1 | a0003 | c0004 | t0001 | g0101 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19002 | hp2 | a0004 | c0007 | t0003 | g0083 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | LWK | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ASW | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0313 | AFR | ASW | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0054 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0257 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0210 | EUR | TSI | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | GIH | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | GIH | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0325 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0330 | AFR | ACB | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0329 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | USA | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0181 | REF | REF | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0271 | REF | REF | XRCC5_chr2_216104348_216211293 | XRCC5 | chr2 | 216104348 | 216211293 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216122110 | T | A | 1 | a0002 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001 a0001c0005 a0001c0006 others(3): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0005 a0001c0002t0010 |
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 | a0001c0001t0004 a0001c0001t0008 a0001c0002t0004 others(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 | a0001c0001t0002 a0001c0001t0012 a0001c0002t0002 others(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 | a0001c0001t0006 a0001c0002t0006 |
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 | a0001c0001t0004 a0001c0001t0008 a0001c0002t0004 others(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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(3): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216109481 | G | C | 1 | a0001c0001t0004g0007 | 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 | a0001c0001t0003g0009 a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | a0001c0001t0002g0344 a0001c0001t0002g0345 a0001c0001t0003g0346 |
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 | 32 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(29): 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 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(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 | 4 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): 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 | a0001c0001t0001g0336 a0001c0001t0004g0337 a0001c0001t0004g0338 others(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 | a0001c0001t0003g0042 | 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0002g0011 | 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 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | 180 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(177): Show |
182 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(179): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(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 | 124 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0195 others(121): 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 | 32 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(29): 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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(139): Show |
143 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.21+1408A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216110865 | |||||||
| chr2:216110890 | G | GT | 36 | a0001c0001t0001g0182 a0001c0001t0002g0001 a0001c0001t0002g0012 others(33): 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 | a0001c0005t0001g0046 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0002g0034 | 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 | 15 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(12): 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 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.22-1108C>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 1/20 | chr2 | 216111908 | |||||||
| chr2:216111995 | C | T | 4 | a0001c0001t0004g0327 a0001c0001t0004g0328 a0001c0001t0004g0329 others(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 | a0001c0001t0008g0183 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0344 a0001c0001t0002g0345 |
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 | a0001c0001t0003g0009 | 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 | 124 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0195 others(121): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0004g0054 | 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 | a0001c0001t0008g0183 | 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 | a0001c0001t0004g0186 | 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 | a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0195 a0001c0001t0001g0197 others(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 | 124 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0195 others(121): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
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 | a0001c0001t0001g0195 a0001c0001t0004g0056 |
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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0040 |
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 | a0001c0001t0003g0259 | 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 | 37 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0001 others(34): 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 | a0001c0001t0001g0173 a0001c0001t0002g0017 a0001c0001t0002g0018 others(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 | a0001c0001t0003g0042 | 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 | 22 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0001 others(19): 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 | 37 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0001 others(34): 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 | 22 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0001 others(19): 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 | 128 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0184 others(125): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0009 a0001c0001t0003g0042 others(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 | a0001c0001t0006g0010 | 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 | 135 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(132): Show |
136 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(133): 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 | a0001c0001t0001g0184 a0001c0001t0001g0197 a0001c0001t0001g0241 others(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 | 37 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0002g0001 others(34): 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0007g0194 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0241 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0004g0258 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0257 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0002t0002g0320 a0001c0002t0002g0321 |
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 | a0001c0001t0001g0148 | 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 | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(128): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0005g0334 a0001c0001t0005g0335 |
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 | a0001c0001t0003g0009 a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(128): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0319 | 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 | 70 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(67): Show |
70 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(67): 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0003g0200 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0190 a0001c0001t0006g0189 a0001c0001t0009g0187 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0001g0110 | 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 | a0001c0002t0002g0264 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0003g0190 a0001c0001t0006g0189 a0001c0001t0009g0187 others(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 | a0001c0001t0003g0256 | 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 | a0001c0001t0004g0055 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0004g0255 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0319 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
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 | a0001c0001t0003g0254 | 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 | a0001c0001t0003g0346 | 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 | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(128): 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0266 | 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 | 39 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0003g0109 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0002g0039 | 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 | a0001c0001t0003g0009 a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | a0001c0001t0001g0333 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0004g0100 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0001g0336 a0001c0001t0001g0340 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0174 a0001c0001t0001g0175 others(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 | a0001c0001t0004g0252 | 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 | a0001c0001t0004g0252 | 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(128): 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 | 11 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(8): 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0173 |
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 | a0001c0002t0002g0314 | 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 | 39 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): 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 | 39 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): 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 | a0001c0001t0001g0185 a0001c0001t0001g0333 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0333 a0001c0001t0003g0009 a0001c0001t0003g0042 others(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 | 39 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): 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 | a0001c0001t0003g0253 | 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 | a0001c0001t0001g0195 | 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0197 a0001c0001t0004g0198 a0001c0001t0004g0199 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0001t0004g0144 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0268 a0001c0001t0001g0319 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0001t0004g0258 | 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 | a0001c0001t0001g0185 a0001c0001t0007g0191 a0001c0001t0007g0192 others(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 | 148 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(145): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0003g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 others(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 | 148 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(145): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0333 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0220 | 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 | a0001c0001t0001g0062 | 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 | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(128): 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 | a0001c0001t0001g0185 a0001c0001t0001g0333 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | 279 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(276): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.937+1214C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 8/20 | chr2 | 216128888 | |||||||
| chr2:216129029 | G | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): 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 | a0001c0001t0003g0242 a0001c0001t0003g0243 |
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 | 17 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0015 others(14): 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 | a0001c0001t0001g0268 a0001c0001t0001g0319 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0333 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0018 | 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 | a0001c0001t0001g0185 a0001c0001t0007g0191 a0001c0001t0007g0192 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0241 others(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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0033 a0001c0001t0002g0034 |
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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 17 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0015 others(14): 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 | a0001c0001t0003g0009 a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | 148 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(145): 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 | a0001c0001t0001g0059 a0001c0001t0001g0250 a0001c0001t0002g0011 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0003g0009 a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | a0001c0001t0003g0009 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0002t0006g0313 | 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 | a0001c0001t0002g0017 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0002t0002g0114 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | 17 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0015 others(14): 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 | a0001c0001t0003g0256 | 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0332 others(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 | a0001c0002t0002g0312 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0002g0344 | 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 | a0001c0002t0002g0270 | 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0001g0089 | 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 | 342 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(339): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0311 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0185 a0001c0001t0007g0191 a0001c0001t0007g0192 others(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 | a0001c0001t0002g0156 a0001c0001t0003g0155 a0001c0001t0003g0157 others(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 | a0001c0001t0002g0345 | 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 | a0001c0001t0001g0185 a0001c0001t0003g0042 a0001c0001t0003g0190 others(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 | a0001c0001t0003g0109 | 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 | a0001c0001t0001g0153 | 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 | 279 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(276): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): 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 | a0001c0001t0001g0197 a0001c0001t0003g0009 a0001c0001t0003g0244 others(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 | 167 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0060 others(164): Show |
169 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(166): 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 | a0001c0002t0006g0006 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0003g0346 | 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 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0211 a0001c0001t0004g0212 others(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 | 35 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(32): 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 | 279 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(276): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1114-1996T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 10/20 | chr2 | 216135092 | |||||||
| chr2:216135095 | TTTTG | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(273): Show |
279 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(276): 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0173 |
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 | a0001c0001t0003g0238 | 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 | a0001c0001t0003g0238 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0011g0064 | 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 | 147 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(144): Show |
148 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(145): 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 | a0001c0001t0005g0274 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 261 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(258): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): 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 | a0001c0001t0001g0063 a0001c0001t0001g0333 a0001c0001t0003g0331 others(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 | a0001c0002t0002g0320 a0001c0002t0002g0321 |
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 | a0001c0001t0003g0237 | 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 | 149 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(146): Show |
150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0002t0002g0270 | 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 | a0001c0001t0004g0144 | 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 | a0001c0001t0003g0346 | 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 | 28 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(25): 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 | a0001c0001t0003g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 others(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 | a0001c0001t0003g0190 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | 343 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(340): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0249 a0001c0001t0004g0262 |
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 | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1342+250T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 12/20 | chr2 | 216138429 | |||||||
| chr2:216138702 | G | A | 27 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0336 others(24): 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 | a0001c0001t0003g0331 a0001c0001t0005g0274 a0001c0001t0005g0285 others(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 | a0001c0001t0003g0227 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0173 |
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 | a0001c0001t0002g0014 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 others(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 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0004g0218 | 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 | 22 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): 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 | a0001c0001t0003g0230 a0001c0001t0003g0254 |
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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0033 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0017 others(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 | a0001c0002t0002g0270 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0033 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(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 | 58 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0047 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): 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 | 48 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0052 others(45): 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 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0059 others(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 | 18 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0015 others(15): 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 | a0001c0001t0002g0013 a0001c0001t0002g0033 a0001c0001t0002g0034 others(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 | a0001c0001t0002g0014 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(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 | a0001c0001t0001g0115 a0001c0001t0003g0190 a0001c0005t0001g0046 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0132 a0001c0001t0006g0010 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 |
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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(168): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1476+248C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216141567 | |||||||
| chr2:216141616 | T | C | 36 | a0001c0001t0001g0149 a0001c0001t0002g0001 a0001c0001t0002g0011 others(33): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 144 | a0001c0001t0001g0149 a0001c0001t0001g0250 a0001c0001t0001g0251 others(141): 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 | a0001c0002t0002g0308 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0003g0254 | 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 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0217 others(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 | a0001c0001t0006g0189 a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0331 a0001c0001t0005g0274 a0001c0001t0005g0285 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
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 | a0001c0001t0006g0010 a0001c0001t0012g0008 |
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 | a0001c0001t0001g0087 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0033 others(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 | a0001c0001t0001g0125 | 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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0006g0010 | 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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(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 | a0001c0001t0009g0188 | 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 | a0001c0001t0006g0189 a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0001g0087 a0001c0001t0003g0027 a0001c0001t0003g0028 others(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 | a0001c0001t0003g0239 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0033 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 33 | a0001c0001t0001g0149 a0001c0001t0002g0001 a0001c0001t0002g0011 others(30): 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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | a0001c0001t0003g0224 | 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 | a0001c0001t0003g0190 | 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 | 18 | a0001c0001t0001g0081 a0001c0001t0002g0001 a0001c0001t0002g0012 others(15): 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 | a0001c0001t0001g0149 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0004 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(148): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): 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 | a0001c0001t0004g0131 | 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 | a0001c0001t0003g0208 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0017 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0003g0190 | 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 others(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 | 33 | a0001c0001t0001g0149 a0001c0001t0002g0001 a0001c0001t0002g0011 others(30): 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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | |||||||
| chr2:216145469 | A | G | 1 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0168 others(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 | 29 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(26): 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 | a0001c0001t0004g0255 | 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 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0342 | 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 | 49 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0112 others(46): Show |
49 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1477-1985C>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 13/20 | chr2 | 216146098 | |||||||
| chr2:216146114 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0002g0095 others(1): 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0336 | 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 | 292 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): 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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0002g0017 others(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 | |||||||
| chr2:216147036 | C | G | 29 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(26): 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(5): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0331 a0001c0001t0005g0274 a0001c0001t0005g0285 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0341 a0001c0001t0007g0191 others(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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(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 | 150 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(147): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0017 others(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 | a0001c0001t0002g0011 | 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 | 11 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(8): 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 | a0001c0002t0002g0272 a0001c0002t0002g0290 a0001c0002t0002g0291 |
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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0017 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0042 a0001c0001t0003g0155 a0001c0001t0003g0157 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 others(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 | a0001c0001t0009g0187 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 |
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 | 4 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0002g0095 others(1): 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 | 6 | a0001c0002t0002g0005 a0001c0002t0002g0305 a0001c0002t0002g0306 others(3): 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 | a0001c0005t0001g0046 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0001g0317 | 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 | 29 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(26): 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 | a0001c0001t0005g0285 a0001c0001t0005g0286 a0001c0001t0005g0287 |
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 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0008g0248 | 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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | a0001c0001t0001g0266 | 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 | 23 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(20): 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 | a0001c0001t0004g0215 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(148): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(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 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
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 | a0001c0001t0001g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0004g0221 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0011 a0001c0001t0002g0150 others(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 | a0001c0001t0001g0105 | 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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | 132 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0260 others(129): 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 | a0001c0001t0004g0255 | 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 | a0001c0001t0004g0258 | 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 | a0001c0001t0004g0100 a0001c0001t0004g0202 |
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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0268 | 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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0086 others(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 | a0001c0001t0011g0064 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(151): 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0004g0130 a0001c0001t0004g0214 |
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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
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 | a0001c0001t0003g0196 a0001c0001t0003g0265 |
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 | a0001c0001t0003g0265 | 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | |||||||
| chr2:216153533 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0044 others(121): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1670+5257T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 14/20 | chr2 | 216153533 | |||||||
| chr2:216153699 | G | A | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0186 a0001c0001t0004g0216 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0163 others(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 | 146 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0001 others(143): 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 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0001t0001g0267 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0008g0183 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0004g0186 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(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 | a0001c0001t0002g0021 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0002t0002g0296 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 120 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(117): 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 | a0001c0001t0009g0187 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0004g0310 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0007g0191 a0001c0001t0007g0193 a0001c0001t0007g0194 |
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 | a0001c0001t0001g0116 | 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 | 179 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(176): 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
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 | a0001c0001t0003g0246 a0001c0001t0003g0247 a0001c0001t0004g0198 others(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 | a0001c0001t0004g0213 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | 48 | a0001c0001t0001g0093 a0001c0001t0002g0001 a0001c0001t0002g0016 others(45): 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
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 | a0001c0001t0003g0109 | 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 | a0001c0001t0004g0258 | 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 | a0001c0002t0002g0306 | 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 | a0001c0002t0002g0114 a0001c0002t0002g0272 a0001c0002t0002g0290 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0009g0187 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0100 a0001c0001t0004g0102 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0279 a0001c0001t0001g0319 |
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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(5): 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 | a0001c0002t0002g0114 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0260 a0001c0001t0003g0208 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0340 a0001c0001t0001g0341 others(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 | a0001c0001t0012g0008 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 184 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(181): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0088 | 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 | 179 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(176): 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(87): 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 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0179 others(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 | a0001c0001t0003g0253 a0001c0002t0002g0292 |
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 | 86 | a0001c0001t0001g0093 a0001c0001t0001g0281 a0001c0001t0001g0282 others(83): 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 | 178 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(175): 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 | 195 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(192): 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 | 159 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(156): 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 | 200 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(197): 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 | a0001c0002t0002g0270 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0003g0096 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0155 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0002g0011 | 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 | a0001c0001t0004g0102 | 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 | a0001c0001t0001g0267 | 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 | 179 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(176): 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 | 158 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(155): 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0145 | 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 | 158 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(155): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | a0001c0001t0001g0176 | 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 | 48 | a0001c0001t0001g0093 a0001c0001t0002g0001 a0001c0001t0002g0016 others(45): 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | 193 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(190): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 others(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 | 160 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(157): 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0006g0010 a0001c0002t0006g0006 a0001c0002t0006g0313 |
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 | a0001c0001t0012g0008 | 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 | 158 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(155): 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 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0249 others(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 | a0001c0001t0003g0234 | 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 | 48 | a0001c0001t0001g0093 a0001c0001t0002g0001 a0001c0001t0002g0016 others(45): 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 | 193 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(190): 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0155 others(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 | a0001c0001t0003g0122 | 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 | a0001c0001t0003g0346 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0011 | 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0003g0208 | 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 | 37 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0035 others(34): 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 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0004g0007 others(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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0343 | 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 | 51 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(48): 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0004g0056 | 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 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0278 | 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 | a0001c0002t0002g0297 a0001c0002t0002g0298 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 |
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 | a0001c0002t0002g0264 a0001c0002t0002g0273 |
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 | a0001c0002t0002g0297 a0001c0002t0002g0298 |
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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0342 | 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 | a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0211 a0001c0001t0004g0212 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 122 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(119): 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 | a0001c0001t0004g0130 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0162 | 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 | 144 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(141): 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0288 others(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 | a0001c0001t0002g0011 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0011 | 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 | a0001c0001t0006g0010 | 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 | a0001c0002t0002g0273 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0341 |
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 | a0001c0001t0001g0106 a0001c0001t0001g0172 a0001c0001t0001g0261 others(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 | 35 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0051 others(32): Show |
35 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(32): 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 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0167 a0001c0001t0001g0168 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | 94 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(91): 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 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0004g0186 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0002g0124 a0001c0001t0007g0191 a0001c0001t0007g0192 others(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 | 39 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(36): 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 | 39 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(36): 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0002t0006g0313 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 51 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(48): 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 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0071 | 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 | 124 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(121): 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0224 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0182 | 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 | a0001c0002t0002g0308 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | 124 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(121): 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 | a0001c0001t0003g0205 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0004g0249 a0001c0001t0004g0262 |
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 | a0001c0001t0001g0071 | 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 | 195 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(192): 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 | 51 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(48): 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0224 |
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 | 149 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0281 others(146): 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0062 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0094 others(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 | 42 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(39): Show |
42 | HG01258.hp1 HG01433.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0002g0035 a0001c0001t0003g0265 a0001c0001t0004g0154 others(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 | 54 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0022 others(51): 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 | 71 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0016 others(68): 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 | a0001c0001t0005g0287 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0002t0006g0313 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0288 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0001g0343 | 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 | a0001c0001t0004g0330 | 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 | a0001c0001t0004g0154 | 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 | a0001c0001t0001g0260 | 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 | 193 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(190): 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 | 183 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(180): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0112 a0001c0001t0001g0132 others(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 | a0001c0001t0008g0248 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0311 | 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 | a0001c0001t0003g0346 | 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 | a0001c0001t0004g0210 | 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 | a0001c0001t0006g0010 a0001c0002t0006g0006 a0001c0002t0006g0313 others(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 | 193 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(190): 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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | 193 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(190): 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 | a0001c0001t0002g0095 a0001c0001t0006g0010 a0001c0001t0006g0189 others(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 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0003g0027 others(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 | a0001c0002t0004g0294 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0155 a0001c0001t0003g0157 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0017 a0001c0001t0002g0018 others(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 | 73 | a0001c0001t0001g0093 a0001c0001t0002g0001 a0001c0001t0002g0016 others(70): 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 | a0001c0001t0001g0260 a0001c0001t0002g0022 a0001c0001t0002g0040 others(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 | a0001c0002t0006g0006 | 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 | a0001c0001t0002g0095 a0001c0001t0006g0010 a0001c0001t0006g0189 others(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 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0004g0026 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0100 a0001c0001t0004g0130 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0057 a0001c0001t0004g0129 others(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 | a0001c0001t0004g0056 a0001c0001t0004g0102 a0001c0001t0004g0144 others(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 | a0001c0001t0007g0191 | 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 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 |
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 | a0001c0002t0004g0294 | 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 | 52 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0001 others(49): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 others(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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0011 | 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 | 86 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0001 others(83): 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 | a0001c0001t0003g0238 a0001c0001t0003g0331 |
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 | a0001c0001t0002g0095 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 188 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(185): 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 | a0001c0001t0002g0011 | 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 | a0001c0002t0003g0269 | 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 | 49 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0001 others(46): 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 65 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0002g0001 others(62): 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0002g0011 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0189 a0001c0002t0006g0006 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0001g0071 | 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 | a0001c0002t0002g0296 | 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 | 134 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(131): 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 | a0001c0001t0004g0240 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0004g0186 others(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 | 1 | a0001c0001t0001g0126 | 1 | NA20752.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 | a0001c0001t0001g0266 a0001c0001t0003g0042 a0001c0001t0003g0109 others(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 | 122 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0266 others(119): 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 | a0001c0001t0003g0122 a0001c0001t0003g0196 a0001c0001t0003g0200 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 others(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 | a0001c0001t0003g0122 a0001c0001t0003g0196 a0001c0001t0003g0200 others(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 | a0001c0002t0002g0322 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0001g0165 | 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0004g0207 | 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 | a0001c0001t0004g0249 | 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 | a0001c0001t0001g0071 | 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 | 37 | a0001c0001t0001g0260 a0001c0001t0002g0035 a0001c0001t0002g0036 others(34): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | 49 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0016 others(46): 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 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0001t0004g0215 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 201 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(198): 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 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0061 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0012g0008 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 |
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 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0224 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 120 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0011 others(117): 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 | a0001c0001t0012g0008 | 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 | a0001c0002t0004g0294 | 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 120 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0011 others(117): 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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0288 others(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 | a0001c0001t0002g0095 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0003g0042 a0001c0001t0003g0109 a0001c0001t0003g0122 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0002t0006g0006 | 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 336 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1835-11006A>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216179219 | |||||||
| chr2:216179242 | C | G | 194 | a0001c0001t0001g0093 a0001c0001t0001g0260 a0001c0001t0001g0317 others(191): 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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0149 |
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 | a0001c0002t0002g0301 | 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 | 120 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0011 others(117): 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 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0311 |
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 | a0001c0001t0003g0190 | 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 | 49 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0016 others(46): 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 | a0001c0001t0001g0093 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0006g0189 | 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 | a0001c0001t0001g0340 | 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(290): 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 | a0001c0001t0001g0093 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0011g0064 | 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0093 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0002g0095 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0003g0122 | 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 | a0001c0001t0003g0122 | 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 | a0001c0001t0003g0122 | 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 | a0001c0001t0003g0122 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0003g0109 | 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0004g0310 | 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 | a0001c0001t0004g0056 a0001c0001t0004g0215 |
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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 121 | a0001c0001t0001g0106 a0001c0001t0001g0260 a0001c0001t0002g0001 others(118): 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0001t0003g0190 | 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 | a0001c0001t0001g0279 a0001c0001t0001g0319 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
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 | a0001c0002t0004g0294 | 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 | 120 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0011 others(117): 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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | 10 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(7): 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 | a0001c0001t0004g0130 a0001c0001t0004g0214 a0001c0001t0004g0252 |
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 | a0001c0001t0004g0215 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1835-7488G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216182737 | |||||||
| chr2:216182917 | A | G | 40 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(37): 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 | a0001c0002t0006g0313 a0001c0002t0006g0325 a0001c0002t0006g0326 |
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 | a0001c0002t0001g0293 | 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 | a0001c0001t0012g0008 | 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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | a0001c0001t0002g0095 | 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 | 48 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(45): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0344 others(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 | 16 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(13): 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 | a0001c0001t0002g0021 a0001c0001t0002g0025 a0001c0001t0004g0026 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0024 others(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 | a0001c0001t0002g0018 a0001c0001t0004g0055 a0001c0002t0002g0264 others(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 |
17 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(14): 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 | a0001c0001t0002g0097 a0001c0001t0004g0131 a0001c0002t0002g0300 others(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 | a0001c0001t0002g0276 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0205 others(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 | a0001c0001t0003g0206 a0001c0001t0003g0238 a0001c0001t0003g0254 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0282 a0001c0001t0007g0191 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(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 | 140 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(138): 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0090 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | a0001c0001t0002g0038 | 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 | a0001c0001t0002g0038 | 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 | 55 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0016 others(52): 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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0288 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0186 a0001c0001t0004g0216 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 83 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): 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 | 47 | a0001c0001t0001g0073 a0001c0001t0001g0104 a0001c0001t0001g0110 others(44): Show |
47 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1835-5471T>G | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184754 | |||||||
| chr2:216184761 | T | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1835-5413C>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 16/20 | chr2 | 216184812 | |||||||
| chr2:216184874 | T | C | 36 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(33): 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 | 36 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(33): 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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0001g0071 | 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 | 83 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): 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 | a0001c0001t0012g0008 | 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 | 55 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(52): 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 83 | a0001c0001t0001g0104 a0001c0001t0002g0001 a0001c0001t0002g0011 others(80): 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0001g0058 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0002t0010g0295 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0001t0002g0344 a0001c0001t0002g0345 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0004g0130 a0001c0001t0004g0214 |
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 | a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0005t0001g0046 | 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 | 31 | a0001c0001t0001g0125 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): 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 | 42 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(39): 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 | 48 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(45): 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0197 | 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 | 46 | a0001c0001t0001g0051 a0001c0001t0001g0062 a0001c0001t0001g0065 others(43): Show |
46 | HG00438.hp1 HG00544.hp1 HG01070.hp2 others(43): 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0141 others(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 | a0001c0001t0004g0255 a0001c0001t0004g0337 |
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 | a0001c0001t0004g0209 a0001c0001t0004g0217 |
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 | 47 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0094 others(44): 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 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0126 a0001c0001t0002g0019 a0001c0001t0003g0029 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0123 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0059 a0001c0001t0002g0018 a0001c0001t0002g0020 others(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 | a0001c0001t0003g0109 a0001c0002t0002g0323 a0001c0002t0002g0324 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0095 |
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 | a0001c0001t0003g0096 a0001c0001t0009g0188 |
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 | a0001c0001t0001g0284 a0001c0005t0001g0046 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0288 a0001c0001t0003g0289 |
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 | a0001c0002t0002g0296 | 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 | a0001c0001t0002g0022 | 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 | 53 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(50): 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0002t0002g0322 |
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 | a0001c0002t0004g0294 | 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 | a0001c0001t0004g0210 | 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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0004g0262 | 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 | a0001c0001t0003g0122 a0001c0001t0003g0208 a0001c0001t0004g0054 others(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 | a0001c0001t0006g0010 a0001c0002t0002g0299 a0001c0002t0006g0006 others(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 | a0001c0002t0002g0272 a0001c0002t0002g0296 a0001c0002t0002g0300 others(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 | a0001c0002t0002g0270 a0001c0002t0002g0290 a0001c0002t0002g0302 others(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 | a0001c0001t0002g0038 a0001c0002t0002g0264 a0001c0002t0002g0273 others(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 | a0001c0001t0002g0022 a0001c0001t0002g0097 a0001c0002t0002g0298 others(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 | a0001c0001t0002g0037 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0003g0288 | 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 | a0001c0001t0002g0036 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0284 |
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 | a0001c0001t0001g0062 | 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 | a0001c0001t0003g0030 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0011g0064 | 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 | a0001c0001t0001g0110 | 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 | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0045 others(72): Show |
77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): 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 | a0001c0001t0001g0075 a0001c0001t0001g0098 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0070 others(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 | a0001c0001t0003g0109 | 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 | a0001c0001t0001g0110 a0001c0001t0005g0274 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0161 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0168 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0095 others(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 | a0001c0001t0003g0096 | 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 | a0001c0001t0003g0289 | 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 | a0001c0001t0003g0009 | 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 | a0001c0002t0002g0322 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0002g0151 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0002g0023 | 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 | a0001c0001t0002g0150 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0040 |
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 | a0001c0001t0002g0039 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0035 |
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 | a0001c0001t0002g0001 a0001c0002t0002g0301 |
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 | a0001c0001t0002g0345 | 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 | a0001c0001t0002g0344 | 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 | a0001c0001t0002g0016 | 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 | a0001c0001t0002g0276 a0001c0002t0002g0312 a0001c0002t0006g0325 |
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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0025 | 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 | a0001c0002t0002g0315 | 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 | a0001c0002t0002g0292 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0002g0013 a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0003g0230 a0001c0001t0003g0234 a0001c0001t0003g0238 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0019 a0001c0001t0002g0021 others(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 | a0001c0001t0002g0020 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0103 others(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 | a0001c0001t0003g0028 a0001c0001t0003g0228 a0001c0001t0003g0243 others(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 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0196 others(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 | a0001c0001t0003g0346 a0001c0001t0004g0056 a0001c0001t0004g0102 others(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 | a0001c0001t0003g0200 a0001c0001t0004g0003 a0001c0001t0004g0100 others(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 | a0001c0001t0003g0027 a0001c0001t0004g0249 a0001c0001t0004g0255 |
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 | a0001c0001t0004g0130 a0001c0001t0004g0207 a0001c0001t0004g0211 others(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 | 24 | a0001c0001t0002g0012 a0001c0001t0002g0014 a0001c0001t0002g0015 others(21): 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 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0243 others(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 | a0001c0001t0003g0029 a0001c0001t0003g0031 a0001c0001t0003g0032 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | a0001c0001t0003g0027 a0001c0001t0004g0003 a0001c0001t0004g0007 others(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 | a0001c0001t0004g0130 a0001c0001t0004g0211 a0001c0001t0004g0214 others(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 | a0001c0001t0004g0211 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0096 |
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 | a0001c0001t0005g0286 a0001c0001t0005g0287 |
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 | a0001c0001t0005g0332 | 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 | a0001c0001t0002g0345 a0001c0001t0003g0009 a0001c0001t0003g0096 others(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 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0097 others(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 | 34 | a0001c0001t0001g0126 a0001c0001t0001g0280 a0001c0001t0002g0037 others(31): Show |
35 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(32): 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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0035 others(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 | 7 | a0001c0001t0002g0036 a0001c0002t0002g0005 a0001c0002t0002g0305 others(4): 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 | a0001c0001t0002g0014 | 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 | a0001c0001t0003g0236 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0249 | 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 | a0001c0001t0008g0183 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0095 | 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 | a0001c0002t0002g0304 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0195 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 83 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): 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 | a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0339 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0004g0258 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | 73 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(70): 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 | a0001c0002t0002g0299 | 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 | a0001c0002t0002g0308 | 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 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
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 | 73 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(70): 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 | a0001c0001t0001g0143 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0005g0274 a0001c0001t0005g0285 a0001c0001t0005g0286 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0007 a0001c0001t0004g0026 a0001c0001t0004g0054 others(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 | 83 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): 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 | a0001c0001t0004g0204 | 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 | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(144): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0096 a0001c0001t0003g0288 others(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 | a0001c0002t0002g0322 | 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0015 |
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 | a0001c0001t0002g0095 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0209 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(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 | 69 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0011 others(66): 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0001t0006g0010 a0001c0001t0006g0189 a0001c0002t0006g0006 others(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 | a0001c0001t0001g0268 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0003g0122 | 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 | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(78): 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 | a0001c0001t0002g0011 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0278 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.2041+732T>C | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 18/20 | chr2 | 216193467 | |||||||
| chr2:216193627 | T | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 36 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(33): 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 | a0001c0001t0004g0127 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(78): 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0241 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0001g0319 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 |
40 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0052 others(37): Show |
40 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(37): 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 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0071 others(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 |
32 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0068 others(29): 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 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0087 others(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 | a0001c0001t0011g0064 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(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 | a0001c0001t0002g0014 a0001c0001t0003g0009 a0001c0001t0003g0096 others(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 | 12 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(9): 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 36 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(33): 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0012g0008 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0026 a0001c0001t0004g0054 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0002g0276 a0001c0006t0002g0283 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0340 a0001c0001t0001g0342 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0009g0187 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0116 a0001c0001t0001g0177 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0198 a0001c0001t0004g0199 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0003g0245 | 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 | a0001c0002t0001g0085 a0001c0002t0001g0293 |
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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0026 a0001c0001t0004g0055 a0001c0001t0004g0127 others(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 | a0001c0001t0002g0095 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0001t0004g0056 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0044 others(203): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2109+1565G>T | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216196551 | |||||||
| chr2:216196997 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0005g0274 | 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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0002g0016 a0001c0001t0002g0025 a0001c0001t0002g0344 others(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 | a0001c0001t0003g0190 | 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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(202): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): 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 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0110 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | a0001c0001t0002g0344 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0258 | 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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | a0001c0001t0002g0095 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 26 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(23): 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 | a0001c0001t0001g0098 a0001c0001t0002g0151 |
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 | 37 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(34): 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 | a0001c0002t0002g0296 | 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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(5): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0002t0002g0308 | 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 | a0001c0001t0001g0103 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(302): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0086 a0001c0001t0001g0126 others(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 | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(113): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(115): 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 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0175 others(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 | a0001c0001t0003g0029 a0001c0001t0003g0155 a0001c0001t0003g0157 others(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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 43 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(40): 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 | a0001c0001t0002g0011 a0001c0001t0002g0016 a0001c0001t0002g0025 others(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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0023 others(5): 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 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0249 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0033 a0001c0001t0002g0034 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
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 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0026 others(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 | a0001c0002t0002g0321 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0009g0187 | 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 | a0001c0001t0004g0215 | 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 | a0001c0001t0004g0258 | 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 | a0001c0001t0003g0190 | 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 | a0001c0001t0001g0163 | 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 | 69 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(66): 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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0004g0054 | 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 | 59 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): 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 | a0001c0001t0009g0187 a0001c0001t0009g0188 |
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 | a0001c0001t0004g0226 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(150): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2110-1848T>A | XRCC5 | ENSG00000079246.16 | transcript | ENST00000392132.7 | protein_coding | 19/20 | chr2 | 216202474 | |||||||
| chr2:216202492 | G | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0004g0329 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0158 others(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 | a0001c0001t0004g0252 | 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0005g0274 | 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 | a0001c0002t0002g0114 a0001c0002t0002g0272 a0001c0002t0002g0290 others(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 | a0001c0002t0002g0301 | 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 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0002t0002g0322 |
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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | 79 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(76): 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0002t0006g0326 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0345 | 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 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0001g0117 |
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 | 55 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(52): 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 | a0001c0001t0005g0287 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0004g0007 a0001c0001t0004g0026 a0001c0001t0004g0054 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0134 others(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 | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(207): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): 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 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(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 | a0001c0001t0003g0225 | 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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0003g0346 |
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 | a0001c0002t0010g0295 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(149): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0001g0075 | 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 | a0001c0002t0001g0293 | 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 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0249 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | 48 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0022 others(45): 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 |