Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7508 |
| ensemblid | ENSG00000154767.15 |
| hgncid | 12816 |
| symbol | XPC |
| name | XPC complex subunit, DNA damage recognition and repair factor |
| refseq_nuc | NM_004628.5 |
| refseq_prot | NP_004619.3 |
| ensembl_nuc | ENST00000285021.12 |
| ensembl_prot | ENSP00000285021.8 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 14145147 |
| end | 14178601 |
| strand | - |
| ver | v1.2 |
| region | chr3:14145147-14178601 |
| region5000 | chr3:14140147-14183601 |
| regionname0 | XPC_chr3_14145147_14178601 |
| regionname5000 | XPC_chr3_14140147_14183601 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 940 | 116 | 58 | 24 | 8 | 4 | 21 | 7 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0002 | 1/0 | 940 | 99 | 15 | 21 | 50 | 4 | 8 | 40 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0003 | 0/0 | 940 | 91 | 12 | 14 | 56 | 5 | 4 | 44 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0004 | 0/0 | 940 | 44 | 0 | 10 | 34 | 0 | 0 | 29 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0005 | 0/0 | 940 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0006 | 0/0 | 940 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0007 | 0/0 | 940 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0008 | 0/0 | 940 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0009 | 0/0 | 940 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0010 | 0/0 | 940 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0011 | 0/0 | 940 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0012 | 0/0 | 940 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0013 | 0/0 | 940 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0014 | 0/0 | 940 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0015 | 0/0 | 940 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0016 | 0/0 | 940 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0017 | 0/0 | 940 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| a0018 | 0/0 | 940 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | MARKR others(935): Show |
chr3 | 14140147 | 14183601 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 2820 | 78 | 36 | 21 | 4 | 4 | 13 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0001c0005 | 0/0 | 2820 | 25 | 10 | 3 | 4 | 0 | 8 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0001c0006 | 0/0 | 2820 | 6 | 6 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0001c0007 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0001c0012 | 0/0 | 2820 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0001c0018 | 0/1 | 2820 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0002c0001 | 1/0 | 2820 | 97 | 14 | 21 | 49 | 4 | 8 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0002c0019 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0002c0022 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0003c0002 | 0/0 | 2820 | 91 | 12 | 14 | 56 | 5 | 4 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0004c0004 | 0/0 | 2820 | 44 | 0 | 10 | 34 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0005c0008 | 0/0 | 2820 | 4 | 0 | 3 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0005c0017 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0006c0009 | 0/0 | 2820 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0007c0013 | 0/0 | 2820 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0008c0011 | 0/0 | 2820 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0009c0014 | 0/0 | 2820 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0010c0010 | 0/0 | 2820 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0011c0021 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0012c0016 | 0/0 | 2820 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0013c0026 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0014c0015 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0015c0024 | 0/0 | 2820 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0016c0025 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0017c0023 | 0/0 | 2820 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 | ||
| a0018c0020 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ATGGC others(2815): Show |
chr3 | 14140147 | 14183601 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001 | 0/0 | 3650 | 5 | 5 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0003t0003 | 0/0 | 3650 | 67 | 25 | 21 | 4 | 4 | 13 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0003t0006 | 0/0 | 3650 | 5 | 5 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0003t0009 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0005t0001 | 0/0 | 3650 | 22 | 10 | 2 | 3 | 0 | 7 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0005t0002 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0005t0003 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0005t0010 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0006t0001 | 0/0 | 3650 | 6 | 6 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0007t0007 | 0/0 | 3650 | 4 | 4 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0012t0001 | 0/0 | 3650 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0001c0018t0003 | 0/1 | 3650 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0001t0001 | 0/0 | 3650 | 77 | 8 | 17 | 42 | 3 | 7 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0001t0002 | 0/0 | 3650 | 4 | 0 | 0 | 4 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0001t0005 | 1/0 | 3650 | 15 | 6 | 4 | 2 | 1 | 1 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0001t0011 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0019t0003 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0002c0022t0001 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0003c0002t0002 | 0/0 | 3650 | 73 | 11 | 4 | 56 | 0 | 2 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0003c0002t0004 | 0/0 | 3650 | 18 | 1 | 10 | 0 | 5 | 2 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0004c0004t0001 | 0/0 | 3650 | 43 | 0 | 10 | 33 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0004c0004t0002 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0005c0008t0004 | 0/0 | 3650 | 4 | 0 | 3 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0005c0017t0004 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0006c0009t0003 | 0/0 | 3650 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0007c0013t0012 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0007c0013t0013 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0008c0011t0008 | 0/0 | 3650 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0009c0014t0003 | 0/0 | 3650 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0010c0010t0001 | 0/0 | 3650 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0011c0021t0003 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0012c0016t0002 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0013c0026t0001 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0014c0015t0001 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0015c0024t0002 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0016c0025t0001 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0017c0023t0002 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| a0018c0020t0003 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | ACTCG others(3645): Show |
chr3 | 14140147 | 14183601 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0004 | 0/0 | 16 | 1 | 6 | 2 | 1 | 6 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0009 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0003t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0005t0010g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0006t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0006t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0006t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0007t0007g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0007t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0012t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0001c0018t0003g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0002 | 0/0 | 22 | 0 | 0 | 19 | 1 | 2 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0006 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0014 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0019t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0002c0022t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0001 | 0/0 | 32 | 5 | 3 | 23 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0005 | 0/0 | 12 | 1 | 4 | 0 | 5 | 2 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0003c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0003 | 0/0 | 17 | 0 | 5 | 12 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0007 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0004c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0005c0008t0004g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0005c0008t0004g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0005c0017t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0006c0009t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0006c0009t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0006c0009t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0007c0013t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0007c0013t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0008c0011t0008g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0009c0014t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0010c0010t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0011c0021t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0012c0016t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0013c0026t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0014c0015t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0015c0024t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0016c0025t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0017c0023t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| a0018c0020t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0004 | g0005 | EUR | GBR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0004 | EUR | GBR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00140 | hp1 | a0002 | c0001 | t0005 | g0014 | EUR | GBR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0048 | EUR | GBR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00280 | hp1 | a0011 | c0021 | t0003 | g0071 | EUR | FIN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00280 | hp2 | a0003 | c0002 | t0004 | g0005 | EUR | FIN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00423 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0145 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00438 | hp1 | a0004 | c0004 | t0001 | g0051 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00609 | hp1 | a0002 | c0001 | t0002 | g0045 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00609 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00621 | hp1 | a0003 | c0002 | t0002 | g0095 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00621 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | CHS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0025 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00642 | hp1 | a0005 | c0017 | t0004 | g0057 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00642 | hp2 | a0001 | c0005 | t0003 | g0063 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00735 | hp2 | a0003 | c0002 | t0004 | g0005 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00738 | hp1 | a0001 | c0003 | t0003 | g0078 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00738 | hp2 | a0003 | c0002 | t0004 | g0005 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00741 | hp1 | a0003 | c0002 | t0004 | g0005 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG00741 | hp2 | a0002 | c0001 | t0005 | g0014 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01069 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01070 | hp2 | a0003 | c0002 | t0004 | g0055 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0070 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01074 | hp2 | a0002 | c0001 | t0005 | g0137 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0046 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01081 | hp2 | a0003 | c0002 | t0002 | g0108 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0048 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01099 | hp2 | a0003 | c0002 | t0004 | g0056 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01106 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0154 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01109 | hp2 | a0005 | c0008 | t0004 | g0032 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01167 | hp1 | a0005 | c0008 | t0004 | g0031 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01167 | hp2 | a0003 | c0002 | t0004 | g0053 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01168 | hp1 | a0001 | c0003 | t0003 | g0036 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0047 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01169 | hp1 | a0005 | c0008 | t0004 | g0031 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01169 | hp2 | a0002 | c0001 | t0001 | g0146 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0036 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0080 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0087 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0030 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01243 | hp1 | a0003 | c0002 | t0004 | g0058 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01243 | hp2 | a0004 | c0004 | t0001 | g0165 | AMR | PUR | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0010 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0047 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01256 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01261 | hp1 | a0003 | c0002 | t0004 | g0054 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01261 | hp2 | a0003 | c0002 | t0004 | g0059 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0010 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0069 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0171 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01361 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01361 | hp2 | a0002 | c0001 | t0005 | g0135 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0044 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0099 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01515 | hp1 | a0001 | c0003 | t0003 | g0009 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01515 | hp2 | a0003 | c0002 | t0004 | g0005 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0066 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01516 | hp2 | a0003 | c0002 | t0004 | g0005 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01517 | hp1 | a0003 | c0002 | t0004 | g0005 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01517 | hp2 | a0001 | c0003 | t0003 | g0009 | EUR | IBS | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01884 | hp2 | a0001 | c0003 | t0006 | g0034 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01891 | hp1 | a0001 | c0003 | t0006 | g0033 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01891 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01943 | hp2 | a0002 | c0001 | t0001 | g0046 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0067 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01975 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01978 | hp2 | a0003 | c0002 | t0004 | g0005 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0007 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0035 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0007 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0062 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02015 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02040 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02055 | hp1 | a0003 | c0002 | t0002 | g0011 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02056 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0068 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02071 | hp2 | a0003 | c0002 | t0002 | g0115 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02074 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02074 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02135 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02135 | hp2 | a0003 | c0002 | t0002 | g0111 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02145 | hp2 | a0003 | c0002 | t0002 | g0011 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02155 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | CDX | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | CDX | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02165 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | CDX | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | CDX | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02257 | hp1 | a0003 | c0002 | t0004 | g0005 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02257 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02258 | hp1 | a0007 | c0013 | t0013 | g0158 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0082 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02273 | hp2 | a0012 | c0016 | t0002 | g0106 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0153 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02293 | hp2 | a0004 | c0004 | t0001 | g0007 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02300 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | PEL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0064 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0004 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02523 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02572 | hp1 | a0001 | c0007 | t0007 | g0019 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0084 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02602 | hp1 | a0005 | c0008 | t0004 | g0032 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02602 | hp2 | a0013 | c0026 | t0001 | g0170 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02615 | hp1 | a0006 | c0009 | t0003 | g0089 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02615 | hp2 | a0007 | c0013 | t0012 | g0157 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02622 | hp1 | a0001 | c0003 | t0006 | g0034 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0144 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02647 | hp1 | a0008 | c0011 | t0008 | g0042 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02647 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0142 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0027 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02717 | hp2 | a0003 | c0002 | t0002 | g0011 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02723 | hp2 | a0001 | c0007 | t0007 | g0019 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0098 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0079 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02738 | hp2 | a0003 | c0002 | t0002 | g0112 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02809 | hp1 | a0003 | c0002 | t0002 | g0107 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0104 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02818 | hp1 | a0008 | c0011 | t0008 | g0042 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0136 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0049 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02896 | hp2 | a0001 | c0003 | t0006 | g0033 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0049 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02922 | hp1 | a0001 | c0003 | t0009 | g0086 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0030 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02965 | hp2 | a0014 | c0015 | t0001 | g0096 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02970 | hp1 | a0003 | c0002 | t0002 | g0011 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02970 | hp2 | a0009 | c0014 | t0003 | g0037 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02976 | hp1 | a0006 | c0009 | t0003 | g0090 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02976 | hp2 | a0002 | c0001 | t0005 | g0128 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03017 | hp1 | a0001 | c0003 | t0003 | g0083 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03017 | hp2 | a0001 | c0005 | t0001 | g0022 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0161 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03041 | hp2 | a0001 | c0007 | t0007 | g0019 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03098 | hp1 | a0003 | c0002 | t0002 | g0011 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03098 | hp2 | a0001 | c0003 | t0006 | g0074 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0015 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03130 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03139 | hp1 | a0002 | c0001 | t0005 | g0129 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0029 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03195 | hp2 | a0002 | c0019 | t0003 | g0085 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0035 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03209 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0124 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03225 | hp2 | a0002 | c0001 | t0005 | g0130 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03453 | hp1 | a0001 | c0012 | t0001 | g0126 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0029 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0159 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03486 | hp2 | a0002 | c0001 | t0005 | g0026 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03490 | hp1 | a0001 | c0005 | t0001 | g0022 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03490 | hp2 | a0003 | c0002 | t0004 | g0005 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03492 | hp1 | a0002 | c0001 | t0005 | g0014 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03492 | hp2 | a0003 | c0002 | t0004 | g0005 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ESN | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03540 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | GWD | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0061 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0025 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0148 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03831 | hp1 | a0001 | c0003 | t0003 | g0004 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03831 | hp2 | a0001 | c0003 | t0003 | g0077 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03834 | hp1 | a0001 | c0005 | t0001 | g0021 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03834 | hp2 | a0001 | c0003 | t0003 | g0060 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03927 | hp1 | a0015 | c0024 | t0002 | g0121 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0081 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0021 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04115 | hp1 | a0001 | c0005 | t0001 | g0021 | SAS | STU | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04115 | hp2 | a0001 | c0003 | t0003 | g0004 | SAS | STU | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0149 | SAS | BEB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04204 | hp1 | a0001 | c0005 | t0010 | g0156 | SAS | STU | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0022 | SAS | STU | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0093 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18522 | hp2 | a0002 | c0001 | t0005 | g0026 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18747 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | CHB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18906 | hp2 | a0009 | c0014 | t0003 | g0037 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18939 | hp1 | a0010 | c0010 | t0001 | g0043 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18939 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18940 | hp1 | a0001 | c0005 | t0001 | g0103 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18940 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18942 | hp1 | a0003 | c0002 | t0002 | g0023 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0147 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18943 | hp2 | a0004 | c0004 | t0001 | g0174 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18944 | hp1 | a0003 | c0002 | t0002 | g0040 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18944 | hp2 | a0003 | c0002 | t0002 | g0105 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18945 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18946 | hp2 | a0003 | c0002 | t0002 | g0012 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18948 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18950 | hp1 | a0003 | c0002 | t0002 | g0012 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18951 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18951 | hp2 | a0003 | c0002 | t0002 | g0012 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18952 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18953 | hp1 | a0016 | c0025 | t0001 | g0164 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18954 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18960 | hp1 | a0003 | c0002 | t0002 | g0012 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18961 | hp1 | a0004 | c0004 | t0001 | g0050 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18961 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18962 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18962 | hp2 | a0001 | c0005 | t0002 | g0150 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18963 | hp1 | a0004 | c0004 | t0001 | g0050 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18963 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18964 | hp1 | a0003 | c0002 | t0002 | g0016 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18965 | hp1 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18965 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18967 | hp1 | a0004 | c0004 | t0001 | g0166 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18968 | hp1 | a0003 | c0002 | t0002 | g0117 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18969 | hp1 | a0003 | c0002 | t0002 | g0012 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18970 | hp1 | a0010 | c0010 | t0001 | g0043 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18970 | hp2 | a0004 | c0004 | t0001 | g0176 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18971 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18974 | hp1 | a0003 | c0002 | t0002 | g0122 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18975 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18977 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18977 | hp2 | a0003 | c0002 | t0002 | g0016 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18981 | hp1 | a0004 | c0004 | t0001 | g0163 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18981 | hp2 | a0003 | c0002 | t0002 | g0118 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18982 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18983 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18983 | hp2 | a0017 | c0023 | t0002 | g0120 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18984 | hp2 | a0003 | c0002 | t0002 | g0109 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18985 | hp1 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18985 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18991 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18991 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18995 | hp1 | a0001 | c0005 | t0001 | g0101 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18995 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18998 | hp2 | a0004 | c0004 | t0001 | g0168 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18999 | hp1 | a0003 | c0002 | t0002 | g0116 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18999 | hp2 | a0004 | c0004 | t0001 | g0173 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19000 | hp1 | a0003 | c0002 | t0002 | g0016 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19003 | hp1 | a0003 | c0002 | t0002 | g0119 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19004 | hp1 | a0004 | c0004 | t0001 | g0175 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19004 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19007 | hp1 | a0002 | c0001 | t0005 | g0014 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19007 | hp2 | a0003 | c0002 | t0002 | g0016 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19009 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19009 | hp2 | a0004 | c0004 | t0001 | g0172 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19012 | hp1 | a0003 | c0002 | t0002 | g0040 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19012 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0075 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0020 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19043 | hp1 | a0018 | c0020 | t0003 | g0076 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0094 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19056 | hp2 | a0003 | c0002 | t0002 | g0110 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19057 | hp1 | a0003 | c0002 | t0002 | g0114 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19060 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19062 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19062 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19063 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19064 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19066 | hp1 | a0001 | c0005 | t0001 | g0102 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19066 | hp2 | a0003 | c0002 | t0002 | g0023 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19070 | hp1 | a0003 | c0002 | t0002 | g0023 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0045 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19074 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19075 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19075 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19077 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19080 | hp1 | a0003 | c0002 | t0002 | g0113 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19080 | hp2 | a0002 | c0001 | t0011 | g0151 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19082 | hp2 | a0004 | c0004 | t0001 | g0162 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19083 | hp1 | a0003 | c0002 | t0002 | g0125 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19084 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19085 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19085 | hp2 | a0002 | c0022 | t0001 | g0141 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19086 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19088 | hp2 | a0002 | c0001 | t0005 | g0014 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19089 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19089 | hp2 | a0004 | c0004 | t0002 | g0167 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA19240 | hp2 | a0001 | c0007 | t0007 | g0052 | AFR | YRI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0002 | EUR | TSI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0025 | EUR | TSI | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0073 | SAS | GIH | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20905 | hp2 | a0003 | c0002 | t0002 | g0001 | SAS | GIH | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01123 | hp1 | a0002 | c0001 | t0005 | g0139 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | CLM | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0015 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02109 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG02559 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ACB | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03471 | hp1 | a0006 | c0009 | t0003 | g0088 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0152 | AFR | MSL | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0123 | AFR | USA | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| HG06807 | hp2 | a0001 | c0003 | t0003 | g0092 | AFR | USA | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18955 | hp1 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20300 | hp1 | a0001 | c0012 | t0001 | g0100 | AFR | USA | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA20300 | hp2 | a0002 | c0001 | t0005 | g0026 | AFR | USA | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0091 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | LWK | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| homoSapiens | chm13v2 | a0001 | c0018 | t0003 | g0065 | REF | REF | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0005 | g0097 | REF | REF | XPC_chr3_14140147_14183601 | XPC | chr3 | 14140147 | 14183601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14145949 | G | T | 16 | a0001 a0003 a0004 others(13): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
missense_variant | MODERATE | c.2815C>A | p.Gln939Lys | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 2848/3650 | 2815/2823 | 939/940 | chr3 | 14145949 | |||
| chr3:14152384 | G | A | 1 | a0009 | 2 | HG02970.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2066C>T | p.Thr689Met | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/16 | 2099/3650 | 2066/2823 | 689/940 | chr3 | 14152384 | |||
| chr3:14158042 | A | G | 1 | a0007 | 2 | HG02258.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1841T>C | p.Phe614Ser | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1874/3650 | 1841/2823 | 614/940 | chr3 | 14158042 | |||
| chr3:14158103 | G | A | 1 | a0018 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1780C>T | p.Arg594Cys | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1813/3650 | 1780/2823 | 594/940 | chr3 | 14158103 | |||
| chr3:14158387 | G | A | 5 | a0003 a0005 a0012 others(2): Show |
99 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(96): Show |
missense_variant | MODERATE | c.1496C>T | p.Ala499Val | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1529/3650 | 1496/2823 | 499/940 | chr3 | 14158387 | |||
| chr3:14158408 | C | T | 1 | a0005 | 5 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(2): Show |
missense_variant | MODERATE | c.1475G>A | p.Arg492His | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1508/3650 | 1475/2823 | 492/940 | chr3 | 14158408 | |||
| chr3:14158440 | C | A | 1 | a0011 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1443G>T | p.Lys481Asn | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1476/3650 | 1443/2823 | 481/940 | chr3 | 14158440 | |||
| chr3:14158568 | C | G | 1 | a0016 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.1315G>C | p.Ala439Pro | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1348/3650 | 1315/2823 | 439/940 | chr3 | 14158568 | |||
| chr3:14158633 | G | A | 1 | a0014 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1250C>T | p.Pro417Leu | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1283/3650 | 1250/2823 | 417/940 | chr3 | 14158633 | |||
| chr3:14158882 | G | T | 1 | a0008 | 2 | HG02647.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1001C>A | p.Pro334His | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1034/3650 | 1001/2823 | 334/940 | chr3 | 14158882 | |||
| chr3:14158883 | G | A | 1 | a0013 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1000C>T | p.Pro334Ser | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1033/3650 | 1000/2823 | 334/940 | chr3 | 14158883 | |||
| chr3:14164835 | C | T | 1 | a0012 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.878G>A | p.Arg293Gln | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/16 | 911/3650 | 878/2823 | 293/940 | chr3 | 14164835 | |||
| chr3:14164853 | A | C | 1 | a0006 | 3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.860T>G | p.Phe287Cys | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/16 | 893/3650 | 860/2823 | 287/940 | chr3 | 14164853 | |||
| chr3:14172879 | C | T | 1 | a0014 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.287G>A | p.Gly96Glu | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/16 | 320/3650 | 287/2823 | 96/940 | chr3 | 14172879 | |||
| chr3:14172963 | T | A | 1 | a0017 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.203A>T | p.Asp68Val | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/16 | 236/3650 | 203/2823 | 68/940 | chr3 | 14172963 | |||
| chr3:14173024 | G | A | 1 | a0015 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.142C>T | p.Leu48Phe | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/16 | 175/3650 | 142/2823 | 48/940 | chr3 | 14173024 | |||
| chr3:14173061 | A | T | 1 | a0010 | 2 | NA18939.hp1 NA18970.hp1 |
missense_variant&splice_region_variant | MODERATE | c.105T>A | p.Asp35Glu | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/16 | 138/3650 | 105/2823 | 35/940 | chr3 | 14173061 | |||
| chr3:14178523 | G | C | 3 | a0004 a0013 a0016 |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
missense_variant | MODERATE | c.46C>G | p.Leu16Val | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/16 | 79/3650 | 46/2823 | 16/940 | chr3 | 14178523 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14152362 | C | T | 1 | a0018c0020 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2088G>A | p.Val696Val | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/16 | 2121/3650 | 2088/2823 | 696/940 | chr3 | 14152362 | |||
| chr3:14152389 | C | T | 5 | a0001c0003 a0002c0019 a0009c0014 others(2): Show |
83 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(80): Show |
synonymous_variant | LOW | c.2061G>A | p.Arg687Arg | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/16 | 2094/3650 | 2061/2823 | 687/940 | chr3 | 14152389 | |||
| chr3:14156340 | G | A | 1 | a0008c0011 | 2 | HG02647.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.2028C>T | p.Tyr676Tyr | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/16 | 2061/3650 | 2028/2823 | 676/940 | chr3 | 14156340 | |||
| chr3:14156346 | C | T | 1 | a0005c0017 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.2022G>A | p.Ala674Ala | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/16 | 2055/3650 | 2022/2823 | 674/940 | chr3 | 14156346 | |||
| chr3:14158149 | G | T | 1 | a0001c0012 | 2 | HG03453.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1734C>A | p.Val578Val | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1767/3650 | 1734/2823 | 578/940 | chr3 | 14158149 | |||
| chr3:14158521 | A | G | 1 | a0001c0007 | 4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.1362T>C | p.Asp454Asp | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1395/3650 | 1362/2823 | 454/940 | chr3 | 14158521 | |||
| chr3:14158842 | T | A | 1 | a0002c0022 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1041A>T | p.Ser347Ser | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/16 | 1074/3650 | 1041/2823 | 347/940 | chr3 | 14158842 | |||
| chr3:14170550 | C | T | 1 | a0001c0006 | 6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.300G>A | p.Arg100Arg | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/16 | 333/3650 | 300/2823 | 100/940 | chr3 | 14170550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14145257 | C | A | 1 | a0007c0013t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 684 | chr3 | 14145257 | ||||||
| chr3:14145257 | C | G | 35 | a0001c0003t0001 a0001c0003t0003 a0001c0003t0006 others(32): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 684 | chr3 | 14145257 | ||||||
| chr3:14145323 | T | C | 6 | a0001c0003t0009 a0003c0002t0004 a0005c0008t0004 others(3): Show |
26 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*618A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 618 | chr3 | 14145323 | ||||||
| chr3:14145330 | A | G | 1 | a0008c0011t0008 | 2 | HG02647.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*611T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 611 | chr3 | 14145330 | ||||||
| chr3:14145330 | A | T | 6 | a0001c0003t0009 a0003c0002t0004 a0005c0008t0004 others(3): Show |
26 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*611T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 611 | chr3 | 14145330 | ||||||
| chr3:14145543 | C | T | 1 | a0002c0001t0001 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 398 | chr3 | 14145543 | ||||||
| chr3:14145698 | G | A | 1 | a0002c0001t0011 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*243C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 243 | chr3 | 14145698 | ||||||
| chr3:14145749 | A | G | 1 | a0001c0003t0006 | 5 | HG01884.hp2 HG01891.hp1 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 192 | chr3 | 14145749 | ||||||
| chr3:14145808 | C | T | 1 | a0001c0005t0010 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 133 | chr3 | 14145808 | ||||||
| chr3:14145845 | G | C | 12 | a0001c0005t0002 a0002c0001t0002 a0003c0002t0002 others(9): Show |
107 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 16/16 | 96 | chr3 | 14145845 | ||||||
| chr3:14178590 | C | T | 1 | a0001c0007t0007 | 4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/16 | 22 | chr3 | 14178590 | ||||||
| chr3:14178595 | C | G | 13 | a0001c0003t0003 a0001c0003t0006 a0001c0003t0009 others(10): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/16 | 27 | chr3 | 14178595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14146199 | T | C | 133 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(130): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2605-40A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146199 | |||||||
| chr3:14146210 | T | C | 45 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(42): Show |
87 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2605-51A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146210 | |||||||
| chr3:14146215 | G | A | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2605-56C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146215 | |||||||
| chr3:14146373 | C | T | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2605-214G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146373 | |||||||
| chr3:14146538 | C | T | 21 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(18): Show |
51 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2605-379G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146538 | |||||||
| chr3:14146541 | C | T | 2 | a0001c0003t0003g0020 a0002c0019t0003g0085 |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2605-382G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146541 | |||||||
| chr3:14146600 | G | A | 1 | a0003c0002t0002g0115 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2605-441C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146600 | |||||||
| chr3:14146669 | C | A | 1 | a0001c0003t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2605-510G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146669 | |||||||
| chr3:14146676 | G | A | 1 | a0002c0001t0001g0131 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2605-517C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146676 | |||||||
| chr3:14146678 | G | A | 1 | a0016c0025t0001g0164 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2605-519C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146678 | |||||||
| chr3:14146790 | C | A | 3 | a0001c0005t0001g0030 a0001c0005t0001g0124 a0001c0005t0001g0161 |
5 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2604+500G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146790 | |||||||
| chr3:14146798 | T | G | 1 | a0018c0020t0003g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2604+492A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146798 | |||||||
| chr3:14146977 | A | G | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2604+313T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14146977 | |||||||
| chr3:14147143 | C | T | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2604+147G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14147143 | |||||||
| chr3:14147200 | C | A | 53 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(50): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2604+90G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14147200 | |||||||
| chr3:14147262 | G | C | 53 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(50): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2604+28C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 15/15 | chr3 | 14147262 | |||||||
| chr3:14147388 | AAAAATGA others(8): Show |
A | 2 | a0003c0002t0002g0110 a0003c0002t0002g0117 |
2 | NA18968.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2515-24_2515-10del others(15): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 14/15 | chr3 | 14147388 | |||||||
| chr3:14147569 | C | T | 1 | a0006c0009t0003g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2515-190G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 14/15 | chr3 | 14147569 | |||||||
| chr3:14147577 | G | C | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2515-198C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 14/15 | chr3 | 14147577 | |||||||
| chr3:14147647 | A | G | 130 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(127): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2514+261T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 14/15 | chr3 | 14147647 | |||||||
| chr3:14147840 | A | G | 62 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(59): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2514+68T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 14/15 | chr3 | 14147840 | |||||||
| chr3:14148012 | A | G | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2421-11T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 13/15 | chr3 | 14148012 | |||||||
| chr3:14148077 | A | G | 6 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0006c0009t0003g0088 others(3): Show |
9 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2421-76T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 13/15 | chr3 | 14148077 | |||||||
| chr3:14148174 | T | C | 5 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0006c0009t0003g0088 others(2): Show |
7 | HG02572.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2421-173A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 13/15 | chr3 | 14148174 | |||||||
| chr3:14148250 | G | A | 2 | a0002c0001t0001g0018 a0002c0001t0001g0144 |
5 | HG02630.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2421-249C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 13/15 | chr3 | 14148250 | |||||||
| chr3:14148414 | C | T | 1 | a0004c0004t0001g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2420+148G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 13/15 | chr3 | 14148414 | |||||||
| chr3:14148737 | T | G | 128 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(125): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
splice_region_variant&intron_variant | LOW | c.2251-6A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 12/15 | chr3 | 14148737 | |||||||
| chr3:14148768 | G | C | 53 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(50): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2251-37C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 12/15 | chr3 | 14148768 | |||||||
| chr3:14148990 | C | T | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2116-42G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14148990 | |||||||
| chr3:14149143 | G | A | 3 | a0003c0002t0002g0011 a0003c0002t0002g0107 a0003c0002t0002g0108 |
7 | HG01081.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-195C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149143 | |||||||
| chr3:14149147 | A | G | 3 | a0003c0002t0002g0012 a0003c0002t0002g0110 a0003c0002t0002g0117 |
7 | NA18946.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-199T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149147 | |||||||
| chr3:14149159 | C | A | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2116-211G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149159 | |||||||
| chr3:14149250 | A | C | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2116-302T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149250 | |||||||
| chr3:14149271 | A | G | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2116-323T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149271 | |||||||
| chr3:14149272 | C | G | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2116-324G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149272 | |||||||
| chr3:14149273 | G | A | 3 | a0001c0005t0001g0030 a0001c0005t0001g0124 a0001c0005t0001g0161 |
5 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-325C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149273 | |||||||
| chr3:14149386 | C | G | 1 | a0001c0005t0003g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2116-438G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149386 | |||||||
| chr3:14149386 | C | T | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2116-438G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149386 | |||||||
| chr3:14149448 | A | G | 2 | a0004c0004t0001g0169 a0016c0025t0001g0164 |
2 | NA18953.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2116-500T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149448 | |||||||
| chr3:14149555 | G | A | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2116-607C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149555 | |||||||
| chr3:14149737 | G | A | 53 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(50): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2116-789C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149737 | |||||||
| chr3:14149738 | G | C | 1 | a0001c0003t0003g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2116-790C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149738 | |||||||
| chr3:14149759 | C | T | 1 | a0002c0001t0005g0137 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2116-811G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149759 | |||||||
| chr3:14149818 | C | A | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2116-870G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14149818 | |||||||
| chr3:14150149 | G | A | 27 | a0003c0002t0002g0001 a0003c0002t0002g0011 a0003c0002t0002g0012 others(24): Show |
76 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2116-1201C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150149 | |||||||
| chr3:14150213 | C | T | 1 | a0001c0003t0003g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2116-1265G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150213 | |||||||
| chr3:14150246 | G | A | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2116-1298C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150246 | |||||||
| chr3:14150453 | C | T | 5 | a0003c0002t0002g0119 a0006c0009t0003g0088 a0006c0009t0003g0089 others(2): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2116-1505G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150453 | |||||||
| chr3:14150514 | T | C | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2116-1566A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150514 | |||||||
| chr3:14150609 | C | T | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2116-1661G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150609 | |||||||
| chr3:14150674 | C | T | 2 | a0001c0005t0001g0101 a0001c0005t0001g0102 |
2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2115+1661G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150674 | |||||||
| chr3:14150682 | G | C | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2115+1653C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150682 | |||||||
| chr3:14150779 | A | C | 8 | a0001c0005t0002g0150 a0002c0001t0001g0006 a0002c0001t0001g0027 others(5): Show |
23 | HG01934.hp1 HG01975.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.2115+1556T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150779 | |||||||
| chr3:14150865 | T | G | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2115+1470A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150865 | |||||||
| chr3:14150907 | C | T | 1 | a0001c0005t0003g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2115+1428G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150907 | |||||||
| chr3:14150941 | A | G | 1 | a0002c0001t0005g0135 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2115+1394T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14150941 | |||||||
| chr3:14151004 | A | G | 129 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(126): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2115+1331T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151004 | |||||||
| chr3:14151066 | C | T | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2115+1269G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151066 | |||||||
| chr3:14151114 | T | C | 1 | a0002c0001t0001g0138 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2115+1221A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151114 | |||||||
| chr3:14151184 | C | G | 1 | a0004c0004t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2115+1151G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151184 | |||||||
| chr3:14151433 | A | G | 129 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(126): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2115+902T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151433 | |||||||
| chr3:14151536 | C | T | 1 | a0004c0004t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2115+799G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151536 | |||||||
| chr3:14151553 | A | C | 1 | a0001c0003t0003g0036 | 2 | HG01168.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2115+782T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151553 | |||||||
| chr3:14151668 | C | T | 83 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(80): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2115+667G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151668 | |||||||
| chr3:14151757 | G | A | 1 | a0003c0002t0002g0040 | 2 | NA18944.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2115+578C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14151757 | |||||||
| chr3:14152107 | T | C | 1 | a0006c0009t0003g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2115+228A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14152107 | |||||||
| chr3:14152161 | A | G | 1 | a0003c0002t0002g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2115+174T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14152161 | |||||||
| chr3:14152199 | C | T | 1 | a0001c0005t0001g0038 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2115+136G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 11/15 | chr3 | 14152199 | |||||||
| chr3:14152523 | C | T | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2034-107G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152523 | |||||||
| chr3:14152594 | T | G | 34 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(31): Show |
68 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.2034-178A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152594 | |||||||
| chr3:14152687 | C | T | 1 | a0001c0003t0003g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2034-271G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152687 | |||||||
| chr3:14152689 | C | T | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2034-273G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152689 | |||||||
| chr3:14152690 | C | T | 1 | a0003c0002t0002g0016 | 4 | NA18964.hp1 NA18977.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034-274G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152690 | |||||||
| chr3:14152763 | A | C | 43 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(40): Show |
83 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.2034-347T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152763 | |||||||
| chr3:14152853 | G | C | 1 | a0002c0001t0005g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2034-437C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152853 | |||||||
| chr3:14152877 | T | C | 1 | a0002c0001t0001g0046 | 2 | HG01081.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.2034-461A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152877 | |||||||
| chr3:14152930 | T | G | 11 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(8): Show |
16 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.2034-514A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152930 | |||||||
| chr3:14152958 | C | T | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2034-542G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14152958 | |||||||
| chr3:14153014 | G | A | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2034-598C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153014 | |||||||
| chr3:14153286 | A | T | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2034-870T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153286 | |||||||
| chr3:14153389 | A | G | 1 | a0001c0003t0003g0067 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2034-973T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153389 | |||||||
| chr3:14153650 | C | T | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2034-1234G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153650 | |||||||
| chr3:14153753 | A | G | 1 | a0002c0001t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2034-1337T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153753 | |||||||
| chr3:14153781 | C | T | 10 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0098 others(7): Show |
14 | HG00642.hp2 HG01433.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2034-1365G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153781 | |||||||
| chr3:14153804 | T | C | 1 | a0001c0003t0001g0041 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2034-1388A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153804 | |||||||
| chr3:14153941 | A | G | 4 | a0002c0001t0001g0017 a0002c0001t0001g0132 a0002c0001t0001g0142 others(1): Show |
7 | HG02015.hp1 HG02155.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2034-1525T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14153941 | |||||||
| chr3:14154105 | G | A | 9 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0061 others(6): Show |
15 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2034-1689C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154105 | |||||||
| chr3:14154135 | G | A | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2034-1719C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154135 | |||||||
| chr3:14154182 | T | G | 4 | a0001c0003t0003g0009 a0001c0003t0003g0064 a0001c0003t0003g0066 others(1): Show |
8 | HG00735.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2034-1766A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154182 | |||||||
| chr3:14154186 | G | A | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2034-1770C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154186 | |||||||
| chr3:14154257 | C | T | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2034-1841G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154257 | |||||||
| chr3:14154262 | T | C | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2034-1846A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154262 | |||||||
| chr3:14154276 | T | C | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2034-1860A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154276 | |||||||
| chr3:14154365 | A | AT | 1 | a0001c0005t0001g0021 | 3 | HG03834.hp1 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2034-1950dupA | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154365 | |||||||
| chr3:14154420 | G | C | 1 | a0003c0002t0002g0122 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2033+1915C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154420 | |||||||
| chr3:14154426 | A | C | 1 | a0003c0002t0002g0122 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2033+1909T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154426 | |||||||
| chr3:14154439 | C | A | 2 | a0002c0001t0001g0018 a0002c0001t0001g0144 |
5 | HG02630.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033+1896G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154439 | |||||||
| chr3:14154514 | G | GC | 128 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(125): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2033+1820dupG | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154514 | |||||||
| chr3:14154572 | A | C | 1 | a0001c0005t0001g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2033+1763T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154572 | |||||||
| chr3:14154628 | G | T | 1 | a0002c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2033+1707C>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154628 | |||||||
| chr3:14154636 | G | A | 1 | a0004c0004t0001g0166 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2033+1699C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154636 | |||||||
| chr3:14154666 | G | A | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1669C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154666 | |||||||
| chr3:14154667 | A | C | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1668T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154667 | |||||||
| chr3:14154795 | TAATATTT others(70): Show |
T | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1463_2033+153 others(81): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154795 | |||||||
| chr3:14154795 | TAATATTT others(71): Show |
T | 126 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(123): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2033+1462_2033+153 others(82): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154795 | |||||||
| chr3:14154873 | A | G | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1462T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154873 | |||||||
| chr3:14154874 | T | G | 126 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(123): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2033+1461A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154874 | |||||||
| chr3:14154876 | T | A | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1459A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154876 | |||||||
| chr3:14154877 | A | C | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1458T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154877 | |||||||
| chr3:14154878 | T | A | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2033+1457A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154878 | |||||||
| chr3:14154878 | T | C | 126 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(123): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2033+1457A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154878 | |||||||
| chr3:14154941 | A | G | 1 | a0018c0020t0003g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2033+1394T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154941 | |||||||
| chr3:14154996 | C | A | 1 | a0003c0002t0002g0108 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2033+1339G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14154996 | |||||||
| chr3:14155270 | T | C | 6 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0006c0009t0003g0088 others(3): Show |
9 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2033+1065A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155270 | |||||||
| chr3:14155418 | T | A | 1 | a0002c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2033+917A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155418 | |||||||
| chr3:14155440 | C | T | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2033+895G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155440 | |||||||
| chr3:14155443 | T | G | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2033+892A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155443 | |||||||
| chr3:14155575 | TGATACGG others(6): Show |
T | 1 | a0006c0009t0003g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2033+747_2033+759d others(15): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155575 | |||||||
| chr3:14155607 | G | C | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2033+728C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155607 | |||||||
| chr3:14155621 | G | A | 1 | a0001c0003t0003g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2033+714C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155621 | |||||||
| chr3:14155668 | C | T | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2033+667G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155668 | |||||||
| chr3:14155757 | A | C | 1 | a0002c0001t0005g0135 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2033+578T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155757 | |||||||
| chr3:14155853 | C | T | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2033+482G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155853 | |||||||
| chr3:14155876 | G | A | 4 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 others(1): Show |
5 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033+459C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14155876 | |||||||
| chr3:14156046 | A | G | 3 | a0005c0008t0004g0031 a0005c0008t0004g0032 a0005c0017t0004g0057 |
5 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033+289T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14156046 | |||||||
| chr3:14156150 | CCT | C | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2033+183_2033+184d others(4): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14156150 | |||||||
| chr3:14156278 | G | A | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2033+57C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 10/15 | chr3 | 14156278 | |||||||
| chr3:14156748 | G | A | 1 | a0001c0003t0003g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1873-253C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156748 | |||||||
| chr3:14156775 | G | A | 3 | a0003c0002t0004g0056 a0003c0002t0004g0058 a0003c0002t0004g0059 |
3 | HG01099.hp2 HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1873-280C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156775 | |||||||
| chr3:14156810 | A | G | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1873-315T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156810 | |||||||
| chr3:14156888 | G | A | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1873-393C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156888 | |||||||
| chr3:14156920 | C | G | 1 | a0001c0006t0001g0049 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1873-425G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156920 | |||||||
| chr3:14156945 | T | C | 1 | a0002c0001t0001g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1873-450A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156945 | |||||||
| chr3:14156947 | T | A | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873-452A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14156947 | |||||||
| chr3:14157083 | A | G | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1873-588T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157083 | |||||||
| chr3:14157134 | C | A | 1 | a0001c0003t0003g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1873-639G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157134 | |||||||
| chr3:14157134 | C | T | 3 | a0002c0001t0001g0025 a0002c0001t0001g0044 a0002c0001t0001g0133 |
6 | HG00639.hp1 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1873-639G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157134 | |||||||
| chr3:14157307 | T | C | 1 | a0002c0001t0005g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1872+704A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157307 | |||||||
| chr3:14157616 | G | A | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1872+395C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157616 | |||||||
| chr3:14157625 | C | T | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1872+386G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157625 | |||||||
| chr3:14157753 | C | T | 1 | a0002c0001t0001g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1872+258G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157753 | |||||||
| chr3:14157839 | T | A | 1 | a0004c0004t0002g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1872+172A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 9/15 | chr3 | 14157839 | |||||||
| chr3:14158924 | T | C | 1 | a0002c0001t0001g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.991-32A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14158924 | |||||||
| chr3:14158973 | G | A | 1 | a0001c0005t0001g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.991-81C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14158973 | |||||||
| chr3:14159266 | A | G | 1 | a0003c0002t0002g0114 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.991-374T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14159266 | |||||||
| chr3:14159292 | T | C | 1 | a0001c0003t0003g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.991-400A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14159292 | |||||||
| chr3:14159430 | C | T | 1 | a0003c0002t0002g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.990+311G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14159430 | |||||||
| chr3:14159695 | T | C | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.990+46A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 8/15 | chr3 | 14159695 | |||||||
| chr3:14159852 | T | C | 12 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(9): Show |
17 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.901-22A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14159852 | |||||||
| chr3:14159900 | T | G | 25 | a0001c0003t0003g0004 a0001c0003t0003g0009 a0001c0003t0003g0010 others(22): Show |
51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.901-70A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14159900 | |||||||
| chr3:14159921 | C | T | 1 | a0001c0003t0003g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.901-91G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14159921 | |||||||
| chr3:14159956 | G | C | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.901-126C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14159956 | |||||||
| chr3:14160027 | C | A | 1 | a0002c0001t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.901-197G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160027 | |||||||
| chr3:14160057 | A | C | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.901-227T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160057 | |||||||
| chr3:14160110 | T | C | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.901-280A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160110 | |||||||
| chr3:14160199 | C | T | 4 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 others(1): Show |
5 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-369G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160199 | |||||||
| chr3:14160231 | C | T | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-401G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160231 | |||||||
| chr3:14160296 | C | T | 1 | a0003c0002t0002g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.901-466G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160296 | |||||||
| chr3:14160463 | G | A | 1 | a0001c0005t0001g0038 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.901-633C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160463 | |||||||
| chr3:14160479 | A | C | 1 | a0003c0002t0002g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.901-649T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160479 | |||||||
| chr3:14160554 | T | C | 2 | a0001c0005t0001g0030 a0001c0005t0001g0161 |
4 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-724A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160554 | |||||||
| chr3:14160578 | G | A | 1 | a0001c0005t0001g0038 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.901-748C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160578 | |||||||
| chr3:14160595 | G | A | 1 | a0001c0003t0003g0080 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.901-765C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160595 | |||||||
| chr3:14160712 | G | A | 1 | a0006c0009t0003g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901-882C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160712 | |||||||
| chr3:14160720 | G | A | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.901-890C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160720 | |||||||
| chr3:14160757 | G | A | 1 | a0001c0003t0003g0036 | 2 | HG01168.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.901-927C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160757 | |||||||
| chr3:14160904 | G | A | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-1074C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160904 | |||||||
| chr3:14160974 | G | C | 1 | a0009c0014t0003g0037 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.901-1144C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14160974 | |||||||
| chr3:14161219 | T | C | 1 | a0001c0012t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901-1389A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161219 | |||||||
| chr3:14161255 | T | C | 1 | a0001c0003t0003g0008 | 5 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-1425A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161255 | |||||||
| chr3:14161284 | C | T | 3 | a0002c0001t0001g0152 a0002c0001t0001g0153 a0002c0001t0001g0154 |
3 | HG01109.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.901-1454G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161284 | |||||||
| chr3:14161299 | A | G | 1 | a0001c0005t0001g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.901-1469T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161299 | |||||||
| chr3:14161325 | C | T | 1 | a0001c0003t0003g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.901-1495G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161325 | |||||||
| chr3:14161501 | GGATGGTT others(38): Show |
G | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.901-1716_901-1672d others(47): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161501 | |||||||
| chr3:14161513 | A | T | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-1683T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161513 | |||||||
| chr3:14161629 | TA | T | 28 | a0001c0003t0003g0060 a0001c0003t0003g0066 a0001c0005t0001g0098 others(25): Show |
56 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.901-1800delT | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161629 | |||||||
| chr3:14161637 | A | C | 3 | a0002c0001t0001g0152 a0002c0001t0001g0153 a0002c0001t0001g0154 |
3 | HG01109.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.901-1807T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161637 | |||||||
| chr3:14161676 | G | C | 1 | a0001c0005t0001g0103 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.901-1846C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161676 | |||||||
| chr3:14161678 | G | C | 1 | a0018c0020t0003g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.901-1848C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161678 | |||||||
| chr3:14161836 | A | G | 43 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(40): Show |
83 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.901-2006T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161836 | |||||||
| chr3:14161876 | G | A | 1 | a0013c0026t0001g0170 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.901-2046C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161876 | |||||||
| chr3:14161940 | A | G | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.901-2110T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14161940 | |||||||
| chr3:14162126 | A | T | 1 | a0001c0005t0001g0038 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.901-2296T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162126 | |||||||
| chr3:14162210 | G | C | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.901-2380C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162210 | |||||||
| chr3:14162224 | C | T | 1 | a0001c0003t0003g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.901-2394G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162224 | |||||||
| chr3:14162530 | T | C | 1 | a0004c0004t0001g0171 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.900+2283A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162530 | |||||||
| chr3:14162539 | T | C | 2 | a0001c0005t0001g0030 a0001c0005t0001g0161 |
4 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+2274A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162539 | |||||||
| chr3:14162712 | T | C | 1 | a0003c0002t0002g0116 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.900+2101A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14162712 | |||||||
| chr3:14163140 | G | A | 1 | a0003c0002t0002g0117 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.900+1673C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163140 | |||||||
| chr3:14163186 | C | A | 4 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 others(1): Show |
5 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+1627G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163186 | |||||||
| chr3:14163262 | A | G | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.900+1551T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163262 | |||||||
| chr3:14163296 | A | G | 1 | a0004c0004t0001g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.900+1517T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163296 | |||||||
| chr3:14163364 | A | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+1449T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163364 | |||||||
| chr3:14163494 | C | T | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.900+1319G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163494 | |||||||
| chr3:14163595 | CA | C | 3 | a0003c0002t0002g0011 a0003c0002t0002g0107 a0003c0002t0002g0108 |
7 | HG01081.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.900+1217delT | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163595 | |||||||
| chr3:14163645 | G | A | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.900+1168C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163645 | |||||||
| chr3:14163691 | T | C | 1 | a0002c0001t0001g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.900+1122A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163691 | |||||||
| chr3:14163758 | TAAACAAA others(6): Show |
T | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.900+1042_900+1054d others(15): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163758 | |||||||
| chr3:14163766 | TAAAC | T | 6 | a0004c0004t0001g0003 a0004c0004t0001g0050 a0004c0004t0001g0163 others(3): Show |
8 | NA18943.hp2 NA18963.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+1043_900+1046d others(6): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163766 | |||||||
| chr3:14163774 | A | C | 1 | a0004c0004t0001g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.900+1039T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163774 | |||||||
| chr3:14163775 | C | A | 1 | a0004c0004t0001g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.900+1038G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163775 | |||||||
| chr3:14163818 | G | A | 1 | a0002c0001t0002g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.900+995C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163818 | |||||||
| chr3:14163899 | A | G | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.900+914T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163899 | |||||||
| chr3:14163968 | G | C | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.900+845C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163968 | |||||||
| chr3:14163971 | C | T | 1 | a0004c0004t0001g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.900+842G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14163971 | |||||||
| chr3:14164105 | G | T | 2 | a0001c0003t0003g0064 a0001c0003t0003g0087 |
2 | HG01192.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.900+708C>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164105 | |||||||
| chr3:14164155 | T | C | 3 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0061 |
7 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.900+658A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164155 | |||||||
| chr3:14164181 | A | G | 1 | a0001c0005t0001g0038 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.900+632T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164181 | |||||||
| chr3:14164233 | G | A | 1 | a0003c0002t0002g0118 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.900+580C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164233 | |||||||
| chr3:14164421 | A | G | 1 | a0002c0001t0005g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.900+392T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164421 | |||||||
| chr3:14164449 | C | T | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.900+364G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164449 | |||||||
| chr3:14164617 | C | T | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+196G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164617 | |||||||
| chr3:14164719 | C | T | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.900+94G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 7/15 | chr3 | 14164719 | |||||||
| chr3:14164948 | G | A | 1 | a0001c0003t0003g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.780-15C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 6/15 | chr3 | 14164948 | |||||||
| chr3:14165033 | C | T | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.780-100G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 6/15 | chr3 | 14165033 | |||||||
| chr3:14165072 | A | G | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.780-139T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 6/15 | chr3 | 14165072 | |||||||
| chr3:14165122 | C | G | 18 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(15): Show |
45 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.780-189G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 6/15 | chr3 | 14165122 | |||||||
| chr3:14165601 | G | C | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.622-16C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14165601 | |||||||
| chr3:14165702 | A | T | 1 | a0006c0009t0003g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.622-117T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14165702 | |||||||
| chr3:14165713 | T | C | 1 | a0001c0006t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622-128A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14165713 | |||||||
| chr3:14165828 | CTTTGTTT others(15): Show |
C | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.622-265_622-244del others(22): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14165828 | |||||||
| chr3:14166208 | C | A | 37 | a0003c0002t0002g0001 a0003c0002t0002g0011 a0003c0002t0002g0012 others(34): Show |
99 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.622-623G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166208 | |||||||
| chr3:14166209 | C | A | 4 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 others(1): Show |
5 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-624G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166209 | |||||||
| chr3:14166240 | G | A | 2 | a0002c0001t0001g0047 a0002c0001t0001g0146 |
3 | HG01168.hp2 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.622-655C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166240 | |||||||
| chr3:14166306 | G | A | 25 | a0001c0003t0003g0004 a0001c0003t0003g0009 a0001c0003t0003g0010 others(22): Show |
51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.622-721C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166306 | |||||||
| chr3:14166332 | C | T | 1 | a0001c0005t0003g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.622-747G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166332 | |||||||
| chr3:14166483 | T | C | 43 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(40): Show |
83 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.621+686A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166483 | |||||||
| chr3:14166496 | A | G | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.621+673T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166496 | |||||||
| chr3:14166539 | C | T | 11 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(8): Show |
16 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.621+630G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166539 | |||||||
| chr3:14166548 | C | T | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.621+621G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166548 | |||||||
| chr3:14166873 | G | A | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.621+296C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166873 | |||||||
| chr3:14166897 | G | A | 3 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0061 |
7 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+272C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166897 | |||||||
| chr3:14166963 | G | C | 1 | a0001c0003t0003g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.621+206C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14166963 | |||||||
| chr3:14167117 | A | G | 1 | a0001c0003t0006g0033 | 2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.621+52T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14167117 | |||||||
| chr3:14167125 | G | C | 73 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(70): Show |
146 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.621+44C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14167125 | |||||||
| chr3:14167130 | G | A | 26 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(23): Show |
58 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.621+39C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14167130 | |||||||
| chr3:14167144 | CT | C | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.621+24delA | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 5/15 | chr3 | 14167144 | |||||||
| chr3:14167474 | A | C | 1 | a0002c0001t0001g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.537-221T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167474 | |||||||
| chr3:14167605 | T | A | 2 | a0003c0002t0002g0023 a0003c0002t0002g0119 |
4 | NA18942.hp1 NA19003.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.537-352A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167605 | |||||||
| chr3:14167738 | C | T | 2 | a0001c0003t0003g0060 a0001c0003t0003g0061 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.537-485G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167738 | |||||||
| chr3:14167750 | C | A | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.537-497G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167750 | |||||||
| chr3:14167915 | C | T | 1 | a0001c0003t0003g0008 | 5 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.536+342G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167915 | |||||||
| chr3:14167958 | G | A | 2 | a0001c0003t0003g0081 a0008c0011t0008g0042 |
3 | HG02647.hp1 HG02818.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.536+299C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14167958 | |||||||
| chr3:14168016 | C | T | 1 | a0001c0003t0003g0004 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.536+241G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14168016 | |||||||
| chr3:14168144 | G | C | 1 | a0002c0001t0002g0147 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.536+113C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14168144 | |||||||
| chr3:14168246 | C | A | 1 | a0004c0004t0001g0174 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.536+11G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 4/15 | chr3 | 14168246 | |||||||
| chr3:14168388 | C | G | 1 | a0003c0002t0002g0095 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.413-8G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168388 | |||||||
| chr3:14168539 | A | G | 12 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(9): Show |
17 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-159T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168539 | |||||||
| chr3:14168748 | C | T | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.413-368G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168748 | |||||||
| chr3:14168783 | T | A | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.413-403A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168783 | |||||||
| chr3:14168946 | T | A | 1 | a0001c0003t0003g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413-566A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168946 | |||||||
| chr3:14168977 | G | A | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413-597C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14168977 | |||||||
| chr3:14169030 | G | A | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.413-650C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169030 | |||||||
| chr3:14169162 | C | T | 12 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(9): Show |
17 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-782G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169162 | |||||||
| chr3:14169319 | A | AAAT | 6 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0006c0009t0003g0088 others(3): Show |
9 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-940_413-939ins others(3): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169319 | |||||||
| chr3:14169489 | G | A | 3 | a0002c0001t0001g0148 a0002c0001t0001g0149 a0005c0008t0004g0031 |
4 | HG01167.hp1 HG01169.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+949C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169489 | |||||||
| chr3:14169601 | A | G | 48 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(45): Show |
114 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.412+837T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169601 | |||||||
| chr3:14169995 | C | T | 1 | a0001c0003t0003g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.412+443G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14169995 | |||||||
| chr3:14170048 | C | T | 3 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0061 |
7 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.412+390G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170048 | |||||||
| chr3:14170140 | T | C | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+298A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170140 | |||||||
| chr3:14170168 | C | T | 1 | a0003c0002t0002g0105 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.412+270G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170168 | |||||||
| chr3:14170319 | T | C | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.412+119A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170319 | |||||||
| chr3:14170365 | C | A | 35 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(32): Show |
69 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.412+73G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170365 | |||||||
| chr3:14170404 | C | T | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.412+34G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 3/15 | chr3 | 14170404 | |||||||
| chr3:14170645 | T | C | 1 | a0002c0001t0005g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300-95A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14170645 | |||||||
| chr3:14170656 | T | C | 1 | a0004c0004t0001g0175 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.300-106A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14170656 | |||||||
| chr3:14170658 | G | C | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.300-108C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14170658 | |||||||
| chr3:14170740 | T | C | 1 | a0002c0001t0001g0048 | 2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.300-190A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14170740 | |||||||
| chr3:14170758 | C | A | 31 | a0001c0005t0010g0156 a0001c0006t0001g0029 a0001c0006t0001g0049 others(28): Show |
64 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.300-208G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14170758 | |||||||
| chr3:14171073 | C | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-523G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171073 | |||||||
| chr3:14171229 | T | G | 1 | a0015c0024t0002g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.300-679A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171229 | |||||||
| chr3:14171531 | T | A | 3 | a0001c0003t0003g0092 a0001c0003t0003g0093 a0001c0003t0003g0094 |
3 | HG06807.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300-981A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171531 | |||||||
| chr3:14171591 | G | A | 1 | a0001c0005t0001g0039 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.300-1041C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171591 | |||||||
| chr3:14171723 | C | A | 1 | a0001c0003t0003g0015 | 4 | HG02109.hp1 HG02280.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+1144G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171723 | |||||||
| chr3:14171847 | A | G | 4 | a0001c0005t0001g0030 a0001c0005t0001g0123 a0001c0005t0001g0124 others(1): Show |
6 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+1020T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171847 | |||||||
| chr3:14171858 | C | T | 1 | a0014c0015t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299+1009G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14171858 | |||||||
| chr3:14172061 | C | G | 2 | a0001c0007t0007g0019 a0001c0007t0007g0052 |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.299+806G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172061 | |||||||
| chr3:14172138 | T | C | 1 | a0002c0001t0001g0131 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299+729A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172138 | |||||||
| chr3:14172218 | G | T | 3 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0008c0011t0008g0042 |
6 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+649C>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172218 | |||||||
| chr3:14172256 | G | T | 14 | a0001c0003t0003g0004 a0001c0003t0003g0009 a0001c0003t0003g0062 others(11): Show |
33 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.299+611C>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172256 | |||||||
| chr3:14172407 | G | A | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299+460C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172407 | |||||||
| chr3:14172531 | A | C | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.299+336T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172531 | |||||||
| chr3:14172533 | T | C | 52 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(49): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.299+334A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172533 | |||||||
| chr3:14172559 | A | G | 1 | a0003c0002t0004g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.299+308T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172559 | |||||||
| chr3:14172589 | G | A | 1 | a0001c0003t0003g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.299+278C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172589 | |||||||
| chr3:14172600 | A | G | 12 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0039 others(9): Show |
17 | HG00642.hp2 HG01433.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.299+267T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172600 | |||||||
| chr3:14172615 | G | A | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299+252C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172615 | |||||||
| chr3:14172729 | T | A | 1 | a0001c0003t0003g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299+138A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 2/15 | chr3 | 14172729 | |||||||
| chr3:14173138 | A | G | 1 | a0002c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.104-76T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173138 | |||||||
| chr3:14173141 | A | G | 1 | a0002c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.104-79T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173141 | |||||||
| chr3:14173150 | T | C | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.104-88A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173150 | |||||||
| chr3:14173515 | C | T | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-453G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173515 | |||||||
| chr3:14173593 | C | G | 1 | a0002c0001t0001g0131 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.104-531G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173593 | |||||||
| chr3:14173657 | G | A | 81 | a0001c0003t0003g0004 a0001c0003t0003g0008 a0001c0003t0003g0009 others(78): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.104-595C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173657 | |||||||
| chr3:14173984 | A | T | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-922T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14173984 | |||||||
| chr3:14174022 | T | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-960A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174022 | |||||||
| chr3:14174146 | T | A | 1 | a0001c0005t0010g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.104-1084A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174146 | |||||||
| chr3:14174149 | C | T | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.104-1087G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174149 | |||||||
| chr3:14174308 | T | C | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1246A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174308 | |||||||
| chr3:14174320 | T | TAAGATTT others(1247): Show |
1 | a0001c0003t0003g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.104-1259_104-1258i others(1256): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174320 | |||||||
| chr3:14174320 | T | TAAGATTT others(1246): Show |
1 | a0001c0003t0003g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.104-1259_104-1258i others(1255): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174320 | |||||||
| chr3:14174424 | T | A | 1 | a0002c0001t0001g0155 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.104-1362A>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174424 | |||||||
| chr3:14174447 | C | A | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.104-1385G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174447 | |||||||
| chr3:14174550 | G | C | 1 | a0001c0003t0003g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.104-1488C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174550 | |||||||
| chr3:14174747 | A | G | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.104-1685T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174747 | |||||||
| chr3:14174789 | GGA | G | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.104-1729_104-1728d others(4): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174789 | |||||||
| chr3:14174792 | A | T | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.104-1730T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14174792 | |||||||
| chr3:14175008 | A | T | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.104-1946T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175008 | |||||||
| chr3:14175069 | C | A | 1 | a0001c0003t0003g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104-2007G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175069 | |||||||
| chr3:14175117 | T | C | 2 | a0001c0003t0003g0020 a0002c0019t0003g0085 |
4 | HG02559.hp1 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-2055A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175117 | |||||||
| chr3:14175208 | T | C | 1 | a0001c0003t0009g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.104-2146A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175208 | |||||||
| chr3:14175348 | C | T | 1 | a0004c0004t0001g0162 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.104-2286G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175348 | |||||||
| chr3:14175442 | T | C | 1 | a0001c0003t0003g0008 | 5 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-2380A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175442 | |||||||
| chr3:14175445 | G | A | 2 | a0003c0002t0002g0122 a0008c0011t0008g0042 |
3 | HG02647.hp1 HG02818.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.104-2383C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175445 | |||||||
| chr3:14175457 | CTTG | C | 2 | a0004c0004t0001g0051 a0004c0004t0001g0175 |
3 | HG00438.hp1 NA18955.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.104-2398_104-2396d others(5): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175457 | |||||||
| chr3:14175504 | A | T | 4 | a0002c0001t0005g0026 a0002c0001t0005g0128 a0002c0001t0005g0129 others(1): Show |
6 | HG02976.hp2 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2442T>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175504 | |||||||
| chr3:14175526 | T | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2464A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175526 | |||||||
| chr3:14175606 | A | G | 1 | a0002c0001t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.104-2544T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175606 | |||||||
| chr3:14175627 | G | A | 1 | a0008c0011t0008g0042 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.104-2565C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175627 | |||||||
| chr3:14175729 | C | T | 1 | a0001c0003t0003g0062 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.104-2667G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175729 | |||||||
| chr3:14175777 | T | G | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.103+2689A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175777 | |||||||
| chr3:14175789 | C | A | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.103+2677G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175789 | |||||||
| chr3:14175924 | C | G | 3 | a0006c0009t0003g0088 a0006c0009t0003g0089 a0006c0009t0003g0090 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.103+2542G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175924 | |||||||
| chr3:14175974 | T | C | 1 | a0003c0002t0002g0013 | 5 | NA18939.hp2 NA18963.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+2492A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175974 | |||||||
| chr3:14175975 | A | G | 1 | a0001c0012t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.103+2491T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14175975 | |||||||
| chr3:14176076 | G | A | 51 | a0001c0003t0003g0004 a0001c0003t0003g0008 a0001c0003t0003g0009 others(48): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.103+2390C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176076 | |||||||
| chr3:14176078 | A | G | 1 | a0002c0001t0001g0025 | 3 | HG00639.hp1 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.103+2388T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176078 | |||||||
| chr3:14176088 | T | C | 3 | a0001c0005t0002g0150 a0002c0001t0001g0028 a0002c0001t0011g0151 |
5 | NA18962.hp2 NA18968.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+2378A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176088 | |||||||
| chr3:14176147 | A | C | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.103+2319T>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176147 | |||||||
| chr3:14176189 | G | C | 1 | a0001c0003t0003g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103+2277C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176189 | |||||||
| chr3:14176372 | C | T | 22 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 others(19): Show |
52 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.103+2094G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176372 | |||||||
| chr3:14176420 | T | C | 1 | a0001c0005t0001g0123 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.103+2046A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176420 | |||||||
| chr3:14176537 | A | G | 1 | a0002c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.103+1929T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176537 | |||||||
| chr3:14176606 | C | T | 1 | a0003c0002t0004g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.103+1860G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176606 | |||||||
| chr3:14176661 | C | T | 12 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0061 others(9): Show |
28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.103+1805G>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176661 | |||||||
| chr3:14176678 | T | C | 1 | a0001c0007t0007g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103+1788A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176678 | |||||||
| chr3:14176695 | G | A | 3 | a0001c0003t0003g0092 a0001c0003t0003g0093 a0001c0003t0003g0094 |
3 | HG06807.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.103+1771C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176695 | |||||||
| chr3:14176746 | C | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0049 a0001c0006t0001g0159 |
6 | HG02895.hp1 HG02897.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+1720G>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176746 | |||||||
| chr3:14176823 | G | A | 57 | a0001c0003t0003g0004 a0001c0003t0003g0008 a0001c0003t0003g0009 others(54): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.103+1643C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176823 | |||||||
| chr3:14176892 | G | A | 1 | a0001c0005t0001g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.103+1574C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176892 | |||||||
| chr3:14176935 | T | C | 1 | a0003c0002t0002g0125 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.103+1531A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14176935 | |||||||
| chr3:14177033 | G | C | 1 | a0001c0012t0001g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.103+1433C>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177033 | |||||||
| chr3:14177099 | TAAATA | T | 56 | a0001c0003t0003g0004 a0001c0003t0003g0008 a0001c0003t0003g0009 others(53): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.103+1362_103+1366d others(7): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177099 | |||||||
| chr3:14177261 | T | C | 2 | a0007c0013t0012g0157 a0007c0013t0013g0158 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.103+1205A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177261 | |||||||
| chr3:14177393 | T | C | 19 | a0004c0004t0001g0003 a0004c0004t0001g0007 a0004c0004t0001g0050 others(16): Show |
46 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+1073A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177393 | |||||||
| chr3:14177502 | A | G | 128 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(125): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.103+964T>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177502 | |||||||
| chr3:14177705 | AT | A | 145 | a0001c0003t0001g0024 a0001c0003t0001g0041 a0001c0003t0003g0004 others(142): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.103+760delA | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177705 | |||||||
| chr3:14177705 | ATT | A | 26 | a0001c0003t0003g0091 a0001c0006t0001g0029 a0001c0006t0001g0049 others(23): Show |
55 | HG00423.hp1 HG00438.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.103+759_103+760del others(2): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177705 | |||||||
| chr3:14177713 | T | C | 5 | a0001c0007t0007g0019 a0001c0007t0007g0052 a0006c0009t0003g0088 others(2): Show |
7 | HG02572.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+753A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177713 | |||||||
| chr3:14177786 | T | C | 1 | a0001c0003t0003g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103+680A>G | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177786 | |||||||
| chr3:14177810 | G | T | 1 | a0003c0002t0002g0095 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.103+656C>A | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177810 | |||||||
| chr3:14177814 | C | A | 1 | a0004c0004t0001g0176 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.103+652G>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177814 | |||||||
| chr3:14177860 | CT | C | 81 | a0001c0003t0003g0004 a0001c0003t0003g0008 a0001c0003t0003g0009 others(78): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.103+605delA | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177860 | |||||||
| chr3:14177908 | T | G | 2 | a0002c0001t0001g0006 a0002c0001t0001g0160 |
12 | HG01934.hp1 HG01975.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.103+558A>C | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14177908 | |||||||
| chr3:14178091 | GAAGTT | G | 2 | a0001c0005t0001g0030 a0001c0005t0001g0161 |
4 | HG01192.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+370_103+374del others(5): Show |
XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14178091 | |||||||
| chr3:14178224 | G | A | 3 | a0001c0003t0003g0092 a0001c0003t0003g0093 a0001c0003t0003g0094 |
3 | HG06807.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.103+242C>T | XPC | ENSG00000154767.15 | transcript | ENST00000285021.12 | protein_coding | 1/15 | chr3 | 14178224 |