Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2072 |
| ensemblid | ENSG00000175595.16 |
| hgncid | 3436 |
| symbol | ERCC4 |
| name | ERCC excision repair 4, endonuclease catalytic subunit |
| refseq_nuc | NM_005236.3 |
| refseq_prot | NP_005227.1 |
| ensembl_nuc | ENST00000311895.8 |
| ensembl_prot | ENSP00000310520.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 13920154 |
| end | 13952348 |
| strand | + |
| ver | v1.2 |
| region | chr16:13920154-13952348 |
| region5000 | chr16:13915154-13957348 |
| regionname0 | ERCC4_chr16_13920154_13952348 |
| regionname5000 | ERCC4_chr16_13915154_13957348 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 916 | 303 | 65 | 54 | 143 | 10 | 30 | 109 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0002 | 0/0 | 916 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0003 | 0/0 | 916 | 6 | 0 | 2 | 0 | 3 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0004 | 0/0 | 916 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0005 | 0/0 | 916 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0006 | 0/0 | 916 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0007 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0008 | 0/0 | 916 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0009 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| a0010 | 0/1 | 916 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | MESGQ others(911): Show |
chr16 | 13915154 | 13957348 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2748 | 198 | 36 | 41 | 90 | 10 | 20 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0002 | 0/0 | 2748 | 93 | 20 | 10 | 53 | 0 | 10 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0005 | 0/0 | 2748 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0009 | 0/0 | 2748 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0011 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0014 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0016 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0001c0017 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0002c0003 | 0/0 | 2748 | 19 | 17 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0003c0004 | 0/0 | 2748 | 6 | 0 | 2 | 0 | 3 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0004c0007 | 0/0 | 2748 | 3 | 0 | 1 | 0 | 1 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0005c0006 | 0/0 | 2748 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0006c0008 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0007c0010 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0008c0012 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0009c0015 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 | ||
| a0010c0013 | 0/1 | 2748 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | ATGGA others(2743): Show |
chr16 | 13915154 | 13957348 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6764 | 150 | 7 | 29 | 88 | 7 | 18 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0003 | 0/0 | 6763 | 11 | 0 | 8 | 0 | 3 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0004 | 0/0 | 6764 | 10 | 9 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0005 | 0/0 | 6764 | 9 | 9 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0008 | 0/0 | 6764 | 5 | 3 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0012 | 0/0 | 6763 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0013 | 0/0 | 6764 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0016 | 0/0 | 6764 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0017 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0018 | 0/0 | 6764 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0019 | 0/0 | 6764 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0020 | 0/0 | 6764 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0025 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0001t0028 | 0/0 | 6764 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0002 | 0/0 | 6762 | 71 | 13 | 3 | 46 | 0 | 9 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0007 | 0/0 | 6764 | 7 | 0 | 7 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0009 | 0/0 | 6762 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0010 | 0/0 | 6762 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0011 | 0/0 | 6764 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0014 | 0/0 | 6762 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0021 | 0/0 | 6762 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0023 | 0/0 | 6764 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0002t0027 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0001c0005t0001 | 0/0 | 6764 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0009t0015 | 0/0 | 6763 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0001c0011t0022 | 0/0 | 6764 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0014t0024 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0001c0016t0029 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0001c0017t0001 | 0/0 | 6764 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0002c0003t0001 | 0/0 | 6764 | 12 | 10 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0002c0003t0006 | 0/0 | 6764 | 7 | 7 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0003c0004t0002 | 0/0 | 6762 | 6 | 0 | 2 | 0 | 3 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0004c0007t0002 | 0/0 | 6762 | 3 | 0 | 1 | 0 | 1 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6757): Show |
chr16 | 13915154 | 13957348 |
| a0005c0006t0001 | 0/0 | 6764 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0006c0008t0001 | 0/0 | 6764 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0007c0010t0005 | 0/0 | 6764 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0008c0012t0001 | 0/0 | 6764 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| a0009c0015t0026 | 0/0 | 6763 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6758): Show |
chr16 | 13915154 | 13957348 |
| a0010c0013t0001 | 0/1 | 6764 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | GGAAG others(6759): Show |
chr16 | 13915154 | 13957348 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 27 | 0 | 5 | 17 | 2 | 3 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0004 | 0/0 | 17 | 0 | 3 | 11 | 0 | 3 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0011 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0020 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0004g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0005g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0008g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0012g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0013g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0016g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0018g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0019g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0025g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0001t0028g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0002 | 0/0 | 25 | 0 | 0 | 24 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0003 | 0/0 | 14 | 0 | 0 | 9 | 0 | 5 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0007g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0010g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0011g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0014g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0021g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0023g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0002t0027g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0005t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0009t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0009t0015g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0011t0022g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0014t0024g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0016t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0001c0017t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0001g0007 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0002c0003t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0003c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0003c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0003c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0003c0004t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0004c0007t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0004c0007t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0005c0006t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0006c0008t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0006c0008t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0007c0010t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0008c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0009c0015t0026g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| a0010c0013t0001g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00140 | hp2 | a0003 | c0004 | t0002 | g0066 | EUR | GBR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00280 | hp1 | a0004 | c0007 | t0002 | g0003 | EUR | FIN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | FIN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0160 | EUR | FIN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00438 | hp2 | a0001 | c0002 | t0014 | g0050 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0009 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0141 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0071 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01069 | hp1 | a0001 | c0017 | t0001 | g0001 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01069 | hp2 | a0005 | c0006 | t0001 | g0017 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01071 | hp2 | a0005 | c0006 | t0001 | g0017 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01099 | hp1 | a0001 | c0011 | t0022 | g0009 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01109 | hp1 | a0001 | c0002 | t0007 | g0009 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0104 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01167 | hp1 | a0001 | c0009 | t0015 | g0167 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01175 | hp2 | a0005 | c0006 | t0001 | g0017 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0150 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01257 | hp1 | a0001 | c0002 | t0007 | g0101 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01258 | hp1 | a0001 | c0002 | t0007 | g0009 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01358 | hp2 | a0003 | c0004 | t0002 | g0069 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01496 | hp1 | a0004 | c0007 | t0002 | g0003 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01515 | hp1 | a0003 | c0004 | t0002 | g0025 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01516 | hp1 | a0003 | c0004 | t0002 | g0025 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0118 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0038 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01934 | hp2 | a0001 | c0002 | t0007 | g0098 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01952 | hp1 | a0001 | c0002 | t0007 | g0099 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01975 | hp1 | a0001 | c0002 | t0007 | g0009 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01978 | hp1 | a0001 | c0001 | t0020 | g0122 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02056 | hp2 | a0001 | c0002 | t0027 | g0165 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02155 | hp1 | a0001 | c0001 | t0019 | g0044 | EAS | CDX | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02257 | hp1 | a0001 | c0002 | t0010 | g0023 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02257 | hp2 | a0006 | c0008 | t0001 | g0107 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02572 | hp2 | a0001 | c0002 | t0009 | g0051 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02698 | hp2 | a0001 | c0001 | t0016 | g0081 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02717 | hp1 | a0002 | c0003 | t0006 | g0145 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0143 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02738 | hp1 | a0001 | c0002 | t0023 | g0100 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0149 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0022 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0148 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02965 | hp1 | a0002 | c0003 | t0006 | g0111 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02970 | hp2 | a0002 | c0003 | t0006 | g0016 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0038 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03041 | hp2 | a0001 | c0016 | t0029 | g0164 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03098 | hp1 | a0001 | c0002 | t0009 | g0046 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03130 | hp1 | a0002 | c0003 | t0006 | g0016 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03195 | hp2 | a0007 | c0010 | t0005 | g0154 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0162 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03453 | hp1 | a0006 | c0008 | t0001 | g0005 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0151 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0144 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03579 | hp2 | a0002 | c0003 | t0006 | g0147 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03669 | hp2 | a0001 | c0001 | t0018 | g0029 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | BEB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04228 | hp1 | a0004 | c0007 | t0002 | g0049 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18522 | hp1 | a0001 | c0002 | t0010 | g0023 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18906 | hp1 | a0001 | c0014 | t0024 | g0090 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18948 | hp2 | a0001 | c0002 | t0014 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18963 | hp1 | a0001 | c0001 | t0028 | g0131 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18990 | hp2 | a0001 | c0002 | t0021 | g0057 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19002 | hp2 | a0001 | c0002 | t0011 | g0014 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19004 | hp2 | a0001 | c0002 | t0011 | g0014 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | LWK | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | LWK | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19068 | hp2 | a0008 | c0012 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19085 | hp1 | a0001 | c0002 | t0011 | g0014 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | YRI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0159 | EUR | TSI | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20905 | hp1 | a0003 | c0004 | t0002 | g0068 | SAS | GIH | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02109 | hp1 | a0001 | c0002 | t0010 | g0041 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0003 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0142 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG03471 | hp2 | a0001 | c0009 | t0015 | g0166 | AFR | MSL | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG06807 | hp1 | a0002 | c0003 | t0006 | g0016 | AFR | USA | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | USA | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20300 | hp1 | a0009 | c0015 | t0026 | g0089 | AFR | USA | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | USA | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA21309 | hp1 | a0002 | c0003 | t0006 | g0146 | AFR | LWK | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| homoSapiens | chm13v2 | a0010 | c0013 | t0001 | g0001 | REF | REF | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0020 | REF | REF | ERCC4_chr16_13915154_13957348 | ERCC4 | chr16 | 13915154 | 13957348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:13935176 | G | A | 1 | a0003 | 6 | HG00140.hp2 HG00738.hp1 HG01358.hp2 others(3): Show |
missense_variant | MODERATE | c.1244G>A | p.Arg415Gln | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/11 | 1256/6764 | 1244/2751 | 415/916 | chr16 | 13935176 | |||
| chr16:13935420 | A | T | 1 | a0009 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1488A>T | p.Gln496His | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/11 | 1500/6764 | 1488/2751 | 496/916 | chr16 | 13935420 | |||
| chr16:13935538 | G | C | 1 | a0007 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1606G>C | p.Val536Leu | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/11 | 1618/6764 | 1606/2751 | 536/916 | chr16 | 13935538 | |||
| chr16:13937825 | G | A | 1 | a0005 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp2 |
missense_variant | MODERATE | c.1871G>A | p.Arg624Gln | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/11 | 1883/6764 | 1871/2751 | 624/916 | chr16 | 13937825 | |||
| chr16:13944802 | T | C | 1 | a0002 | 19 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(16): Show |
missense_variant | MODERATE | c.1984T>C | p.Ser662Pro | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/11 | 1996/6764 | 1984/2751 | 662/916 | chr16 | 13944802 | |||
| chr16:13948175 | C | A | 1 | a0009 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.2579C>A | p.Ala860Asp | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2591/6764 | 2579/2751 | 860/916 | chr16 | 13948175 | |||
| chr16:13948213 | A | G | 1 | a0006 | 2 | HG02257.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.2617A>G | p.Ile873Val | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2629/6764 | 2617/2751 | 873/916 | chr16 | 13948213 | |||
| chr16:13948220 | A | G | 1 | a0004 | 3 | HG00280.hp1 HG01496.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.2624A>G | p.Glu875Gly | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2636/6764 | 2624/2751 | 875/916 | chr16 | 13948220 | |||
| chr16:13948330 | G | A | 1 | a0008 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2734G>A | p.Gly912Arg | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2746/6764 | 2734/2751 | 912/916 | chr16 | 13948330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:13922075 | C | T | 1 | a0001c0017 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.252C>T | p.Leu84Leu | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/11 | 264/6764 | 252/2751 | 84/916 | chr16 | 13922075 | |||
| chr16:13926643 | A | G | 1 | a0001c0016 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.471A>G | p.Lys157Lys | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/11 | 483/6764 | 471/2751 | 157/916 | chr16 | 13926643 | |||
| chr16:13935378 | A | G | 2 | a0001c0014 a0009c0015 |
2 | NA18906.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1446A>G | p.Glu482Glu | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/11 | 1458/6764 | 1446/2751 | 482/916 | chr16 | 13935378 | |||
| chr16:13937838 | A | G | 1 | a0001c0005 | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.1884A>G | p.Glu628Glu | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/11 | 1896/6764 | 1884/2751 | 628/916 | chr16 | 13937838 | |||
| chr16:13948023 | G | A | 1 | a0001c0016 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.2427G>A | p.Thr809Thr | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2439/6764 | 2427/2751 | 809/916 | chr16 | 13948023 | |||
| chr16:13948059 | A | G | 1 | a0001c0009 | 2 | HG01167.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.2463A>G | p.Pro821Pro | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2475/6764 | 2463/2751 | 821/916 | chr16 | 13948059 | |||
| chr16:13948101 | T | C | 5 | a0001c0002 a0001c0011 a0001c0016 others(2): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
synonymous_variant | LOW | c.2505T>C | p.Ser835Ser | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2517/6764 | 2505/2751 | 835/916 | chr16 | 13948101 | |||
| chr16:13948113 | C | T | 1 | a0001c0011 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.2517C>T | p.Pro839Pro | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2529/6764 | 2517/2751 | 839/916 | chr16 | 13948113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:13948358 | C | T | 2 | a0001c0001t0005 a0007c0010t0005 |
10 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 11 | chr16 | 13948358 | ||||||
| chr16:13948442 | A | G | 1 | a0001c0016t0029 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 95 | chr16 | 13948442 | ||||||
| chr16:13948535 | T | A | 1 | a0001c0001t0016 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 188 | chr16 | 13948535 | ||||||
| chr16:13948665 | A | T | 1 | a0001c0001t0028 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*318A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 318 | chr16 | 13948665 | ||||||
| chr16:13948831 | G | T | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(19): Show |
140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*484G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 484 | chr16 | 13948831 | ||||||
| chr16:13948905 | A | C | 1 | a0001c0002t0027 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 558 | chr16 | 13948905 | ||||||
| chr16:13949021 | G | C | 1 | a0001c0001t0004 | 10 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*674G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 674 | chr16 | 13949021 | ||||||
| chr16:13949022 | G | T | 1 | a0001c0001t0004 | 10 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 675 | chr16 | 13949022 | ||||||
| chr16:13949026 | C | G | 1 | a0001c0009t0015 | 2 | HG01167.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*679C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 679 | chr16 | 13949026 | ||||||
| chr16:13949048 | A | T | 1 | a0009c0015t0026 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 701 | chr16 | 13949048 | ||||||
| chr16:13949073 | G | C | 11 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0009 others(8): Show |
102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*726G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 726 | chr16 | 13949073 | ||||||
| chr16:13949157 | G | A | 13 | a0001c0001t0003 a0001c0001t0012 a0001c0002t0002 others(10): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 810 | chr16 | 13949157 | ||||||
| chr16:13949318 | C | G | 11 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0009 others(8): Show |
102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*971C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 971 | chr16 | 13949318 | ||||||
| chr16:13949549 | G | T | 1 | a0001c0001t0020 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1202G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1202 | chr16 | 13949549 | ||||||
| chr16:13949700 | G | A | 1 | a0001c0002t0014 | 2 | HG00438.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1353G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1353 | chr16 | 13949700 | ||||||
| chr16:13949768 | G | T | 1 | a0001c0001t0003 | 11 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1421G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1421 | chr16 | 13949768 | ||||||
| chr16:13950227 | C | T | 3 | a0001c0002t0027 a0001c0009t0015 a0001c0016t0029 |
4 | HG01167.hp1 HG02056.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1880C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1880 | chr16 | 13950227 | ||||||
| chr16:13950241 | G | A | 1 | a0001c0002t0021 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1894G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1894 | chr16 | 13950241 | ||||||
| chr16:13950283 | G | A | 1 | a0001c0001t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 1936 | chr16 | 13950283 | ||||||
| chr16:13950521 | A | G | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(4): Show |
22 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2174A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2174 | chr16 | 13950521 | ||||||
| chr16:13950860 | C | A | 13 | a0001c0001t0003 a0001c0001t0012 a0001c0002t0002 others(10): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2513C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2513 | chr16 | 13950860 | ||||||
| chr16:13950886 | A | G | 1 | a0001c0002t0010 | 3 | HG02109.hp1 HG02257.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2539A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2539 | chr16 | 13950886 | ||||||
| chr16:13950902 | T | G | 1 | a0001c0001t0018 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2555T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2555 | chr16 | 13950902 | ||||||
| chr16:13950918 | GC | G | 13 | a0001c0001t0003 a0001c0001t0012 a0001c0002t0002 others(10): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2577delC | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2577 | INFO_REALIGN_3_PRIME | chr16 | 13950918 | |||||
| chr16:13950924 | C | A | 7 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0010 others(4): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2577C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2577 | chr16 | 13950924 | ||||||
| chr16:13951226 | A | C | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2879A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2879 | chr16 | 13951226 | ||||||
| chr16:13951239 | C | G | 1 | a0001c0014t0024 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2892C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 2892 | chr16 | 13951239 | ||||||
| chr16:13951379 | G | T | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0002t0002 others(7): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*3032G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3032 | chr16 | 13951379 | ||||||
| chr16:13951472 | A | G | 1 | a0002c0003t0006 | 7 | HG02717.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3125A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3125 | chr16 | 13951472 | ||||||
| chr16:13951542 | G | A | 7 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0010 others(4): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3195G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3195 | chr16 | 13951542 | ||||||
| chr16:13951547 | A | G | 1 | a0001c0002t0009 | 4 | HG02109.hp2 HG02559.hp1 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3200A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3200 | chr16 | 13951547 | ||||||
| chr16:13951550 | A | G | 1 | a0001c0009t0015 | 2 | HG01167.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3203A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3203 | chr16 | 13951550 | ||||||
| chr16:13951674 | A | G | 1 | a0001c0002t0023 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3327A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3327 | chr16 | 13951674 | ||||||
| chr16:13951840 | T | C | 6 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(3): Show |
20 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3493T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3493 | chr16 | 13951840 | ||||||
| chr16:13951852 | T | C | 1 | a0001c0011t0022 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3505T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3505 | chr16 | 13951852 | ||||||
| chr16:13951884 | C | T | 2 | a0001c0002t0027 a0001c0009t0015 |
3 | HG01167.hp1 HG02056.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3537C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3537 | chr16 | 13951884 | ||||||
| chr16:13952074 | G | T | 2 | a0001c0016t0029 a0009c0015t0026 |
2 | HG03041.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3727G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3727 | chr16 | 13952074 | ||||||
| chr16:13952148 | C | T | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0025 others(4): Show |
20 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3801C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3801 | chr16 | 13952148 | ||||||
| chr16:13952258 | C | T | 2 | a0001c0016t0029 a0009c0015t0026 |
2 | HG03041.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3911C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3911 | chr16 | 13952258 | ||||||
| chr16:13952260 | G | C | 3 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0025 |
15 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3913G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3913 | chr16 | 13952260 | ||||||
| chr16:13952292 | AT | A | 7 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0010 others(4): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3953delT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 11/11 | 3953 | INFO_REALIGN_3_PRIME | chr16 | 13952292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:13920383 | G | A | 46 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0019g0044 others(43): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.207+11G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920383 | |||||||
| chr16:13920421 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(16): Show |
37 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.207+49G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920421 | |||||||
| chr16:13920451 | G | C | 2 | a0001c0014t0024g0090 a0009c0015t0026g0089 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.207+79G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920451 | |||||||
| chr16:13920607 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.207+235T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920607 | |||||||
| chr16:13920653 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.207+281G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920653 | |||||||
| chr16:13920804 | A | G | 1 | a0001c0001t0003g0039 | 2 | HG01928.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.207+432A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13920804 | |||||||
| chr16:13921040 | G | C | 1 | a0005c0006t0001g0017 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.207+668G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921040 | |||||||
| chr16:13921120 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.207+748A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921120 | |||||||
| chr16:13921160 | GGC | G | 52 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0019g0044 others(49): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.207+791_207+792del others(2): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 13921160 | ||||||
| chr16:13921224 | G | C | 46 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0019g0044 others(43): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.208-807G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921224 | |||||||
| chr16:13921249 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
7 | HG00735.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-782G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921249 | |||||||
| chr16:13921395 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(7): Show |
15 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.208-636C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921395 | |||||||
| chr16:13921433 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.208-598C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921433 | |||||||
| chr16:13921442 | G | C | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208-589G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921442 | |||||||
| chr16:13921453 | C | G | 46 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0019g0044 others(43): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.208-578C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921453 | |||||||
| chr16:13921485 | C | G | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.208-546C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921485 | |||||||
| chr16:13921620 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.208-411A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921620 | |||||||
| chr16:13921720 | C | G | 8 | a0001c0002t0002g0065 a0001c0002t0002g0067 a0001c0002t0002g0070 others(5): Show |
9 | HG00140.hp2 HG00738.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-311C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921720 | |||||||
| chr16:13921820 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.208-211C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921820 | |||||||
| chr16:13921833 | G | A | 1 | a0001c0002t0002g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.208-198G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 1/10 | chr16 | 13921833 | |||||||
| chr16:13922307 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.388+96C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13922307 | |||||||
| chr16:13922328 | C | T | 1 | a0001c0001t0005g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.388+117C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13922328 | |||||||
| chr16:13922920 | T | C | 3 | a0001c0001t0008g0038 a0001c0001t0008g0150 a0001c0001t0008g0151 |
4 | HG01243.hp1 HG01884.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+709T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13922920 | |||||||
| chr16:13923023 | A | AT | 79 | a0001c0001t0001g0043 a0001c0001t0003g0021 a0001c0001t0003g0039 others(76): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.388+819dupT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 13923023 | ||||||
| chr16:13923099 | A | C | 2 | a0001c0001t0008g0038 a0001c0001t0008g0151 |
3 | HG01884.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.388+888A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923099 | |||||||
| chr16:13923254 | A | G | 1 | a0001c0002t0002g0064 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.388+1043A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923254 | |||||||
| chr16:13923427 | A | AC | 63 | a0001c0001t0001g0043 a0001c0001t0003g0021 a0001c0001t0003g0039 others(60): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.388+1216_388+1217i others(3): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923427 | |||||||
| chr16:13923433 | A | G | 3 | a0001c0009t0015g0166 a0001c0009t0015g0167 a0001c0016t0029g0164 |
3 | HG01167.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.388+1222A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923433 | |||||||
| chr16:13923506 | G | A | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.388+1295G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923506 | |||||||
| chr16:13923524 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0003g0021 a0001c0001t0003g0039 others(60): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.388+1313C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923524 | |||||||
| chr16:13923591 | G | A | 77 | a0001c0001t0001g0043 a0001c0001t0003g0021 a0001c0001t0003g0039 others(74): Show |
143 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.388+1380G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923591 | |||||||
| chr16:13923608 | C | G | 1 | a0003c0004t0002g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.388+1397C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923608 | |||||||
| chr16:13923702 | T | C | 45 | a0001c0001t0001g0043 a0001c0001t0019g0044 a0001c0002t0002g0002 others(42): Show |
97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.388+1491T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923702 | |||||||
| chr16:13923721 | AGTGCCTG others(1): Show |
A | 7 | a0001c0002t0002g0063 a0002c0003t0001g0007 a0002c0003t0001g0143 others(4): Show |
14 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1511_388+1518d others(10): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923721 | |||||||
| chr16:13923730 | T | C | 7 | a0001c0002t0002g0063 a0002c0003t0001g0007 a0002c0003t0001g0143 others(4): Show |
14 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1519T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923730 | |||||||
| chr16:13923862 | A | T | 58 | a0001c0001t0001g0043 a0001c0001t0001g0140 a0001c0001t0003g0021 others(55): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.388+1651A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923862 | |||||||
| chr16:13923868 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.388+1657A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923868 | |||||||
| chr16:13923869 | T | A | 1 | a0001c0001t0001g0026 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.388+1658T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923869 | |||||||
| chr16:13923911 | T | G | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.388+1700T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923911 | |||||||
| chr16:13923984 | G | A | 18 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(15): Show |
24 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.388+1773G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13923984 | |||||||
| chr16:13924045 | C | G | 87 | a0001c0001t0001g0043 a0001c0001t0003g0021 a0001c0001t0003g0039 others(84): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.388+1834C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924045 | |||||||
| chr16:13924160 | C | G | 1 | a0001c0014t0024g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.388+1949C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924160 | |||||||
| chr16:13924225 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.388+2014T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924225 | |||||||
| chr16:13924334 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.388+2123T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924334 | |||||||
| chr16:13924431 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.389-2130T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924431 | |||||||
| chr16:13924658 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.389-1903A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924658 | |||||||
| chr16:13924682 | A | G | 3 | a0002c0003t0006g0145 a0002c0003t0006g0146 a0002c0003t0006g0147 |
3 | HG02717.hp1 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.389-1879A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924682 | |||||||
| chr16:13924703 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.389-1858T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13924703 | |||||||
| chr16:13925267 | T | C | 1 | a0001c0002t0002g0012 | 3 | HG02965.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.389-1294T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925267 | |||||||
| chr16:13925317 | C | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.389-1244C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925317 | |||||||
| chr16:13925380 | T | G | 51 | a0001c0001t0001g0043 a0001c0001t0019g0044 a0001c0002t0002g0002 others(48): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.389-1181T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925380 | |||||||
| chr16:13925552 | T | TA | 42 | a0001c0001t0001g0043 a0001c0001t0019g0044 a0001c0002t0002g0002 others(39): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.389-1006dupA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 13925552 | ||||||
| chr16:13925702 | C | T | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.389-859C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925702 | |||||||
| chr16:13925707 | T | G | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.389-854T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925707 | |||||||
| chr16:13925724 | G | C | 49 | a0001c0001t0001g0043 a0001c0001t0019g0044 a0001c0002t0002g0002 others(46): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.389-837G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925724 | |||||||
| chr16:13925732 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.389-829C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925732 | |||||||
| chr16:13925847 | T | G | 53 | a0001c0001t0001g0043 a0001c0001t0001g0140 a0001c0001t0019g0044 others(50): Show |
108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.389-714T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925847 | |||||||
| chr16:13925960 | G | A | 1 | a0001c0005t0001g0008 | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.389-601G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925960 | |||||||
| chr16:13925961 | T | C | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.389-600T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13925961 | |||||||
| chr16:13926015 | A | G | 1 | a0001c0001t0008g0038 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.389-546A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926015 | |||||||
| chr16:13926035 | G | A | 2 | a0001c0014t0024g0090 a0009c0015t0026g0089 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.389-526G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926035 | |||||||
| chr16:13926242 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.389-319G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926242 | |||||||
| chr16:13926322 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.389-239C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926322 | |||||||
| chr16:13926355 | C | T | 3 | a0001c0002t0027g0165 a0001c0009t0015g0166 a0001c0009t0015g0167 |
3 | HG01167.hp1 HG02056.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.389-206C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926355 | |||||||
| chr16:13926361 | G | A | 5 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(2): Show |
7 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.389-200G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926361 | |||||||
| chr16:13926387 | AT | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.389-172delT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 13926387 | ||||||
| chr16:13926395 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.389-166T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926395 | |||||||
| chr16:13926433 | G | C | 1 | a0001c0001t0008g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.389-128G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926433 | |||||||
| chr16:13926525 | C | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.389-36C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 2/10 | chr16 | 13926525 | |||||||
| chr16:13926942 | TTTTA | T | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.584+191_584+194del others(4): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 13926942 | ||||||
| chr16:13927291 | G | A | 2 | a0001c0001t0013g0036 a0001c0001t0013g0142 |
3 | HG03453.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.584+535G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927291 | |||||||
| chr16:13927292 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.584+536C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927292 | |||||||
| chr16:13927296 | C | T | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.584+540C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927296 | |||||||
| chr16:13927419 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.585-609C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927419 | |||||||
| chr16:13927545 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.585-483G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927545 | |||||||
| chr16:13927557 | C | CA | 19 | a0001c0001t0001g0076 a0001c0001t0001g0105 a0001c0001t0001g0106 others(16): Show |
25 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.585-450dupA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 13927557 | ||||||
| chr16:13927557 | C | CAAA | 7 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(4): Show |
10 | HG01496.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.585-452_585-450dup others(3): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 13927557 | ||||||
| chr16:13927557 | CA | C | 21 | a0001c0001t0001g0035 a0001c0001t0001g0085 a0001c0001t0001g0086 others(18): Show |
24 | HG01167.hp1 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.585-450delA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 13927557 | ||||||
| chr16:13927633 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.585-395A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927633 | |||||||
| chr16:13927635 | A | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.585-393A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927635 | |||||||
| chr16:13927658 | A | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.585-370A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927658 | |||||||
| chr16:13927771 | G | T | 1 | a0001c0001t0008g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.585-257G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927771 | |||||||
| chr16:13927810 | G | A | 1 | a0002c0003t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.585-218G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 3/10 | chr16 | 13927810 | |||||||
| chr16:13928550 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.792+315G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13928550 | |||||||
| chr16:13928582 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.792+347A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13928582 | |||||||
| chr16:13928921 | C | G | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.792+686C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13928921 | |||||||
| chr16:13929085 | G | A | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.792+850G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929085 | |||||||
| chr16:13929087 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.792+852G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929087 | |||||||
| chr16:13929148 | T | C | 19 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(16): Show |
32 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.792+913T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929148 | |||||||
| chr16:13929194 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.792+959G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929194 | |||||||
| chr16:13929261 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.792+1026A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929261 | |||||||
| chr16:13929290 | G | T | 1 | a0007c0010t0005g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.792+1055G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929290 | |||||||
| chr16:13929331 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.792+1096G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929331 | |||||||
| chr16:13929392 | A | G | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.792+1157A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929392 | |||||||
| chr16:13929530 | T | G | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.793-1180T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929530 | |||||||
| chr16:13929617 | C | A | 5 | a0001c0002t0027g0165 a0001c0009t0015g0166 a0001c0009t0015g0167 others(2): Show |
5 | HG01167.hp1 HG02056.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-1093C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929617 | |||||||
| chr16:13929664 | T | C | 19 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(16): Show |
32 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.793-1046T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929664 | |||||||
| chr16:13929704 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG00323.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.793-1006G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929704 | |||||||
| chr16:13929781 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.793-929C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929781 | |||||||
| chr16:13929795 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-915C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929795 | |||||||
| chr16:13929845 | T | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-865T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929845 | |||||||
| chr16:13929870 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.793-840A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929870 | |||||||
| chr16:13929990 | A | G | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.793-720A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13929990 | |||||||
| chr16:13930097 | A | G | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.793-613A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930097 | |||||||
| chr16:13930362 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.793-348C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930362 | |||||||
| chr16:13930427 | A | G | 1 | a0001c0014t0024g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-283A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930427 | |||||||
| chr16:13930550 | C | T | 85 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(82): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.793-160C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930550 | |||||||
| chr16:13930577 | A | G | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.793-133A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930577 | |||||||
| chr16:13930641 | G | T | 3 | a0001c0002t0027g0165 a0001c0009t0015g0166 a0001c0009t0015g0167 |
3 | HG01167.hp1 HG02056.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.793-69G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 4/10 | chr16 | 13930641 | |||||||
| chr16:13930901 | A | T | 2 | a0001c0002t0002g0058 a0001c0002t0021g0057 |
2 | HG00423.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.973+11A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13930901 | |||||||
| chr16:13931114 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.973+224C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931114 | |||||||
| chr16:13931265 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.973+375G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931265 | |||||||
| chr16:13931378 | G | A | 1 | a0003c0004t0002g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.973+488G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931378 | |||||||
| chr16:13931494 | A | G | 1 | a0001c0005t0001g0008 | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+604A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931494 | |||||||
| chr16:13931543 | C | T | 3 | a0001c0002t0027g0165 a0001c0009t0015g0166 a0001c0009t0015g0167 |
3 | HG01167.hp1 HG02056.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.974-614C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931543 | |||||||
| chr16:13931699 | CAG | C | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-455_974-454del others(2): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 13931699 | ||||||
| chr16:13931709 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-448C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931709 | |||||||
| chr16:13931720 | A | G | 1 | a0001c0001t0028g0131 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.974-437A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931720 | |||||||
| chr16:13931733 | C | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-424C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931733 | |||||||
| chr16:13931733 | C | G | 33 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(30): Show |
51 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.974-424C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931733 | |||||||
| chr16:13931854 | T | G | 19 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(16): Show |
32 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.974-303T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931854 | |||||||
| chr16:13931978 | C | T | 2 | a0001c0001t0008g0038 a0001c0001t0008g0151 |
3 | HG01884.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.974-179C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13931978 | |||||||
| chr16:13932035 | C | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-122C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13932035 | |||||||
| chr16:13932085 | A | G | 2 | a0003c0004t0002g0068 a0003c0004t0002g0069 |
2 | HG01358.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.974-72A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13932085 | |||||||
| chr16:13932150 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
splice_region_variant&intron_variant | LOW | c.974-7G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13932150 | |||||||
| chr16:13932151 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0018g0029 |
2 | HG02683.hp1 HG03669.hp2 |
splice_region_variant&intron_variant | LOW | c.974-6T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 5/10 | chr16 | 13932151 | |||||||
| chr16:13932298 | G | T | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1102+13G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932298 | |||||||
| chr16:13932330 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1102+45A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932330 | |||||||
| chr16:13932479 | C | T | 1 | a0002c0003t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102+194C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932479 | |||||||
| chr16:13932504 | G | A | 16 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(13): Show |
28 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1102+219G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932504 | |||||||
| chr16:13932522 | C | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1102+237C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932522 | |||||||
| chr16:13932592 | G | A | 44 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(41): Show |
67 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.1102+307G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932592 | |||||||
| chr16:13932698 | G | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1102+413G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932698 | |||||||
| chr16:13932725 | A | G | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1102+440A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932725 | |||||||
| chr16:13932757 | T | A | 3 | a0001c0009t0015g0166 a0001c0009t0015g0167 a0009c0015t0026g0089 |
3 | HG01167.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1102+472T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932757 | |||||||
| chr16:13932782 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1102+497C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932782 | |||||||
| chr16:13932783 | G | A | 1 | a0001c0002t0021g0057 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1102+498G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932783 | |||||||
| chr16:13932790 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1102+505A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932790 | |||||||
| chr16:13932821 | G | A | 1 | a0001c0002t0002g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1102+536G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932821 | |||||||
| chr16:13932907 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1102+622G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932907 | |||||||
| chr16:13932938 | C | A | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1102+653C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13932938 | |||||||
| chr16:13933045 | C | CA | 9 | a0001c0001t0001g0030 a0001c0001t0001g0106 a0001c0001t0001g0108 others(6): Show |
12 | HG00323.hp1 HG02056.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102+782dupA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933045 | C | CAA | 7 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(4): Show |
10 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1102+781_1102+782d others(4): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933045 | C | CAAA | 7 | a0001c0001t0003g0158 a0001c0002t0002g0015 a0001c0002t0002g0060 others(4): Show |
10 | HG01346.hp2 HG01496.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1102+780_1102+782d others(5): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933045 | CA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(82): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1102+782delA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933045 | CAA | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0002g0002 others(8): Show |
40 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1102+781_1102+782d others(4): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933045 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0008g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1102+772_1102+782d others(13): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 13933045 | ||||||
| chr16:13933062 | A | C | 1 | a0002c0003t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102+777A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933062 | |||||||
| chr16:13933066 | A | C | 1 | a0001c0002t0011g0014 | 3 | NA19002.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1102+781A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933066 | |||||||
| chr16:13933094 | G | T | 69 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(66): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1102+809G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933094 | |||||||
| chr16:13933097 | G | A | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1102+812G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933097 | |||||||
| chr16:13933158 | G | T | 14 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(11): Show |
19 | HG01167.hp1 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1102+873G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933158 | |||||||
| chr16:13933176 | C | T | 1 | a0002c0003t0006g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1102+891C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933176 | |||||||
| chr16:13933177 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1102+892A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933177 | |||||||
| chr16:13933209 | G | A | 1 | a0001c0002t0002g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1102+924G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933209 | |||||||
| chr16:13933348 | C | T | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1103-844C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933348 | |||||||
| chr16:13933428 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1103-764G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933428 | |||||||
| chr16:13933482 | G | T | 2 | a0001c0002t0002g0063 a0002c0003t0006g0016 |
4 | HG02970.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-710G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933482 | |||||||
| chr16:13933682 | G | A | 1 | a0001c0001t0008g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1103-510G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933682 | |||||||
| chr16:13933764 | T | C | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1103-428T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933764 | |||||||
| chr16:13933774 | C | T | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1103-418C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933774 | |||||||
| chr16:13933775 | G | A | 29 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(26): Show |
47 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.1103-417G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933775 | |||||||
| chr16:13933781 | G | A | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1103-411G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933781 | |||||||
| chr16:13933828 | T | C | 1 | a0002c0003t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1103-364T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933828 | |||||||
| chr16:13933875 | C | T | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1103-317C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933875 | |||||||
| chr16:13933881 | C | G | 9 | a0001c0002t0002g0015 a0001c0002t0002g0060 a0001c0002t0002g0061 others(6): Show |
14 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1103-311C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933881 | |||||||
| chr16:13933974 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1103-218A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13933974 | |||||||
| chr16:13934102 | T | C | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1103-90T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 6/10 | chr16 | 13934102 | |||||||
| chr16:13934386 | A | G | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1213+84A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934386 | |||||||
| chr16:13934516 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0135 |
5 | HG00738.hp2 HG00741.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213+214G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934516 | |||||||
| chr16:13934522 | G | A | 40 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(37): Show |
63 | HG00280.hp2 HG00323.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.1213+220G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934522 | |||||||
| chr16:13934574 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG00544.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1213+272G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934574 | |||||||
| chr16:13934598 | A | G | 1 | a0001c0002t0002g0012 | 3 | HG02965.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1213+296A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934598 | |||||||
| chr16:13934776 | G | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(5): Show |
11 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214-370G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934776 | |||||||
| chr16:13934840 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1214-306A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934840 | |||||||
| chr16:13934893 | A | G | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1214-253A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 7/10 | chr16 | 13934893 | |||||||
| chr16:13935859 | A | G | 1 | a0001c0002t0002g0012 | 3 | HG02965.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1811+116A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13935859 | |||||||
| chr16:13935885 | A | C | 1 | a0001c0014t0024g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1811+142A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13935885 | |||||||
| chr16:13935886 | A | G | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1811+143A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13935886 | |||||||
| chr16:13935968 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
2 | NA18962.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1811+225C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13935968 | |||||||
| chr16:13935977 | G | A | 19 | a0001c0001t0001g0108 a0001c0001t0005g0010 a0001c0001t0005g0152 others(16): Show |
32 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1811+234G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13935977 | |||||||
| chr16:13936093 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1811+350G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936093 | |||||||
| chr16:13936270 | A | G | 1 | a0001c0002t0002g0064 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1811+527A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936270 | |||||||
| chr16:13936413 | A | G | 1 | a0001c0014t0024g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1811+670A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936413 | |||||||
| chr16:13936499 | G | A | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1811+756G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936499 | |||||||
| chr16:13936503 | C | T | 78 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(75): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1811+760C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936503 | |||||||
| chr16:13936639 | C | T | 1 | a0001c0001t0016g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1811+896C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936639 | |||||||
| chr16:13936898 | C | CT | 9 | a0001c0002t0002g0012 a0001c0002t0027g0165 a0001c0009t0015g0166 others(6): Show |
11 | HG01167.hp1 HG02056.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1812-856dupT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13936898 | ||||||
| chr16:13936898 | CT | C | 42 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0013 others(39): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1812-856delT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13936898 | ||||||
| chr16:13936913 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1812-853T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13936913 | |||||||
| chr16:13937018 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1812-748C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937018 | |||||||
| chr16:13937086 | A | AT | 13 | a0001c0001t0001g0108 a0001c0001t0001g0139 a0001c0001t0003g0021 others(10): Show |
18 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1812-664dupT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13937086 | ||||||
| chr16:13937086 | A | ATTTTTTT others(2): Show |
39 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0015 others(36): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1812-672_1812-664d others(11): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13937086 | ||||||
| chr16:13937086 | A | ATTTTTTT others(3): Show |
2 | a0001c0002t0002g0013 a0001c0002t0002g0052 |
4 | NA18975.hp2 NA18999.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1812-673_1812-664d others(12): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13937086 | ||||||
| chr16:13937086 | AT | A | 22 | a0001c0001t0001g0077 a0001c0001t0001g0092 a0001c0001t0005g0010 others(19): Show |
36 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1812-664delT | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 13937086 | ||||||
| chr16:13937108 | G | A | 1 | a0001c0001t0001g0033 | 2 | NA18974.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1812-658G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937108 | |||||||
| chr16:13937174 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1812-592C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937174 | |||||||
| chr16:13937206 | G | A | 81 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(78): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1812-560G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937206 | |||||||
| chr16:13937309 | T | C | 6 | a0002c0003t0001g0007 a0002c0003t0001g0143 a0002c0003t0001g0144 others(3): Show |
13 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1812-457T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937309 | |||||||
| chr16:13937663 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1812-103G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 8/10 | chr16 | 13937663 | |||||||
| chr16:13937909 | G | C | 1 | a0001c0001t0019g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1904+51G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13937909 | |||||||
| chr16:13937960 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1904+102C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13937960 | |||||||
| chr16:13938014 | A | C | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904+156A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938014 | |||||||
| chr16:13938048 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1904+190G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938048 | |||||||
| chr16:13938236 | T | G | 88 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(85): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1904+378T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938236 | |||||||
| chr16:13938287 | C | T | 1 | a0002c0003t0006g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1904+429C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938287 | |||||||
| chr16:13938384 | G | A | 2 | a0002c0003t0001g0148 a0002c0003t0001g0149 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1904+526G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938384 | |||||||
| chr16:13938446 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1904+588T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938446 | |||||||
| chr16:13938510 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1904+652C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938510 | |||||||
| chr16:13938597 | T | G | 87 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0039 others(84): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1904+739T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938597 | |||||||
| chr16:13938665 | G | A | 1 | a0001c0014t0024g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1904+807G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938665 | |||||||
| chr16:13938731 | G | A | 2 | a0002c0003t0001g0148 a0002c0003t0001g0149 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1904+873G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938731 | |||||||
| chr16:13938899 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG00323.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1904+1041C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938899 | |||||||
| chr16:13938967 | G | A | 2 | a0002c0003t0001g0148 a0002c0003t0001g0149 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1904+1109G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13938967 | |||||||
| chr16:13939019 | A | G | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(47): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1904+1161A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939019 | |||||||
| chr16:13939087 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1904+1229G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939087 | |||||||
| chr16:13939163 | G | A | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1904+1305G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939163 | |||||||
| chr16:13939210 | G | T | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(47): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1904+1352G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939210 | |||||||
| chr16:13939272 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1904+1414G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939272 | |||||||
| chr16:13939294 | A | C | 1 | a0001c0002t0002g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1904+1436A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939294 | |||||||
| chr16:13939401 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1904+1543G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939401 | |||||||
| chr16:13939437 | A | G | 1 | a0001c0002t0023g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1904+1579A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939437 | |||||||
| chr16:13939439 | A | T | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(47): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1904+1581A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939439 | |||||||
| chr16:13939448 | T | C | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904+1590T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939448 | |||||||
| chr16:13939578 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1904+1720G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939578 | |||||||
| chr16:13939592 | A | G | 1 | a0001c0001t0013g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1904+1734A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939592 | |||||||
| chr16:13939728 | C | T | 1 | a0001c0002t0009g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1904+1870C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939728 | |||||||
| chr16:13939910 | T | G | 2 | a0001c0016t0029g0164 a0009c0015t0026g0089 |
2 | HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1904+2052T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939910 | |||||||
| chr16:13939992 | T | G | 1 | a0003c0004t0002g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1904+2134T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13939992 | |||||||
| chr16:13940033 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1904+2175A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940033 | |||||||
| chr16:13940070 | A | G | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1904+2212A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940070 | |||||||
| chr16:13940124 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1904+2266G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940124 | |||||||
| chr16:13940216 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1904+2358G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940216 | |||||||
| chr16:13940279 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1904+2421C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940279 | |||||||
| chr16:13940282 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1904+2424G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940282 | |||||||
| chr16:13940360 | C | G | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1904+2502C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940360 | |||||||
| chr16:13940372 | A | AG | 2 | a0001c0002t0010g0023 a0001c0002t0010g0041 |
3 | HG02109.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1904+2515dupG | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 13940372 | ||||||
| chr16:13940382 | G | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(5): Show |
11 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1904+2524G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940382 | |||||||
| chr16:13940383 | T | C | 13 | a0001c0002t0002g0012 a0001c0009t0015g0166 a0001c0009t0015g0167 others(10): Show |
22 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1904+2525T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940383 | |||||||
| chr16:13940386 | C | CA | 15 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(12): Show |
21 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1904+2540dupA | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 13940386 | ||||||
| chr16:13940404 | A | T | 12 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(9): Show |
17 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1904+2546A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940404 | |||||||
| chr16:13940475 | G | A | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1904+2617G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940475 | |||||||
| chr16:13940619 | A | G | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1904+2761A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940619 | |||||||
| chr16:13940642 | A | G | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(47): Show |
105 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1904+2784A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940642 | |||||||
| chr16:13940697 | C | T | 1 | a0001c0002t0002g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1904+2839C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940697 | |||||||
| chr16:13940763 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1904+2905T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940763 | |||||||
| chr16:13940844 | T | C | 50 | a0001c0001t0017g0118 a0001c0002t0002g0002 a0001c0002t0002g0003 others(47): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1904+2986T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940844 | |||||||
| chr16:13940916 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1904+3058G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940916 | |||||||
| chr16:13940989 | G | C | 1 | a0001c0002t0007g0099 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1904+3131G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13940989 | |||||||
| chr16:13941029 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1904+3171A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941029 | |||||||
| chr16:13941077 | G | C | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1904+3219G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941077 | |||||||
| chr16:13941367 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1905-3356C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941367 | |||||||
| chr16:13941368 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1905-3355C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941368 | |||||||
| chr16:13941369 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1905-3354A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941369 | |||||||
| chr16:13941540 | T | C | 1 | a0001c0002t0002g0012 | 3 | HG02965.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1905-3183T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941540 | |||||||
| chr16:13941614 | C | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1905-3109C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941614 | |||||||
| chr16:13941620 | A | C | 1 | a0005c0006t0001g0017 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1905-3103A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941620 | |||||||
| chr16:13941642 | G | C | 2 | a0001c0001t0025g0162 a0001c0014t0024g0090 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1905-3081G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941642 | |||||||
| chr16:13941735 | A | C | 1 | a0001c0002t0002g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1905-2988A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13941735 | |||||||
| chr16:13942000 | C | G | 1 | a0001c0001t0017g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1905-2723C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942000 | |||||||
| chr16:13942174 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1905-2549G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942174 | |||||||
| chr16:13942430 | T | A | 1 | a0001c0005t0001g0008 | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1905-2293T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942430 | |||||||
| chr16:13942463 | C | T | 1 | a0001c0009t0015g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1905-2260C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942463 | |||||||
| chr16:13942477 | C | A | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1905-2246C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942477 | |||||||
| chr16:13942477 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(7): Show |
15 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1905-2246C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942477 | |||||||
| chr16:13942614 | T | C | 12 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(9): Show |
18 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1905-2109T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942614 | |||||||
| chr16:13942673 | C | T | 2 | a0001c0002t0010g0023 a0001c0002t0010g0041 |
3 | HG02109.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1905-2050C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942673 | |||||||
| chr16:13942706 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1905-2017C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942706 | |||||||
| chr16:13942732 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1905-1991C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942732 | |||||||
| chr16:13942739 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1905-1984A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13942739 | |||||||
| chr16:13943031 | A | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1905-1692A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13943031 | |||||||
| chr16:13943278 | C | T | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1905-1445C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13943278 | |||||||
| chr16:13943710 | C | T | 1 | a0002c0003t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1905-1013C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13943710 | |||||||
| chr16:13943711 | G | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1905-1012G>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13943711 | |||||||
| chr16:13943795 | A | AG | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(40): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1905-927dupG | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 13943795 | ||||||
| chr16:13943873 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1905-850A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13943873 | |||||||
| chr16:13944182 | T | C | 1 | a0001c0016t0029g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1905-541T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944182 | |||||||
| chr16:13944194 | T | A | 1 | a0001c0002t0002g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1905-529T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944194 | |||||||
| chr16:13944313 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1905-410A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944313 | |||||||
| chr16:13944317 | G | A | 80 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(77): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1905-406G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944317 | |||||||
| chr16:13944344 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0020g0122 |
2 | HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1905-379A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944344 | |||||||
| chr16:13944482 | T | C | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1905-241T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944482 | |||||||
| chr16:13944503 | AAGT | A | 10 | a0002c0003t0001g0007 a0002c0003t0001g0143 a0002c0003t0001g0144 others(7): Show |
19 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1905-215_1905-213d others(5): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 13944503 | ||||||
| chr16:13944505 | G | A | 1 | a0001c0002t0002g0002 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1905-218G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944505 | |||||||
| chr16:13944583 | A | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1905-140A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944583 | |||||||
| chr16:13944613 | C | A | 1 | a0001c0001t0001g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1905-110C>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944613 | |||||||
| chr16:13944688 | T | C | 70 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(67): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1905-35T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944688 | |||||||
| chr16:13944695 | G | A | 42 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(39): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1905-28G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 9/10 | chr16 | 13944695 | |||||||
| chr16:13945009 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2017+174T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945009 | |||||||
| chr16:13945011 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2017+176T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945011 | |||||||
| chr16:13945058 | G | A | 8 | a0002c0003t0001g0007 a0002c0003t0001g0143 a0002c0003t0001g0144 others(5): Show |
17 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2017+223G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945058 | |||||||
| chr16:13945165 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2017+330G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945165 | |||||||
| chr16:13945166 | G | C | 2 | a0001c0001t0004g0110 a0001c0001t0004g0112 |
2 | HG01261.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2017+331G>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945166 | |||||||
| chr16:13945168 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2017+333G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945168 | |||||||
| chr16:13945249 | C | G | 1 | a0003c0004t0002g0069 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2017+414C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945249 | |||||||
| chr16:13945318 | A | G | 1 | a0001c0002t0014g0050 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2017+483A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945318 | |||||||
| chr16:13945329 | T | C | 1 | a0002c0003t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2017+494T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945329 | |||||||
| chr16:13945582 | C | G | 12 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(9): Show |
18 | HG00280.hp2 HG00323.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2017+747C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945582 | |||||||
| chr16:13945624 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2017+789A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945624 | |||||||
| chr16:13945751 | C | T | 10 | a0002c0003t0001g0007 a0002c0003t0001g0143 a0002c0003t0001g0144 others(7): Show |
19 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2017+916C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945751 | |||||||
| chr16:13945791 | C | G | 49 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(46): Show |
102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2017+956C>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945791 | |||||||
| chr16:13945867 | C | T | 3 | a0001c0014t0024g0090 a0001c0016t0029g0164 a0009c0015t0026g0089 |
3 | HG03041.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2017+1032C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945867 | |||||||
| chr16:13945952 | A | C | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2017+1117A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13945952 | |||||||
| chr16:13946267 | G | A | 1 | a0001c0002t0002g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2018-1347G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946267 | |||||||
| chr16:13946285 | A | G | 1 | a0001c0002t0002g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2018-1329A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946285 | |||||||
| chr16:13946296 | C | T | 43 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(40): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.2018-1318C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946296 | |||||||
| chr16:13946357 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2018-1257A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946357 | |||||||
| chr16:13946381 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0106 |
4 | NA18939.hp1 NA18945.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-1233A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946381 | |||||||
| chr16:13946414 | C | T | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2018-1200C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946414 | |||||||
| chr16:13946425 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2018-1189T>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946425 | |||||||
| chr16:13946494 | C | T | 15 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(12): Show |
21 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.2018-1120C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946494 | |||||||
| chr16:13946534 | C | T | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2018-1080C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946534 | |||||||
| chr16:13946544 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2018-1070C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946544 | |||||||
| chr16:13946740 | G | GGTTT | 10 | a0001c0001t0005g0010 a0001c0001t0005g0152 a0001c0001t0005g0153 others(7): Show |
14 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.2018-874_2018-873i others(6): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946740 | |||||||
| chr16:13946741 | T | G | 64 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0157 others(61): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2018-873T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946741 | |||||||
| chr16:13946744 | T | G | 11 | a0001c0001t0001g0037 a0001c0001t0005g0010 a0001c0001t0005g0152 others(8): Show |
16 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2018-870T>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946744 | |||||||
| chr16:13946744 | TTTTG | T | 8 | a0001c0001t0008g0038 a0001c0001t0008g0151 a0001c0002t0010g0023 others(5): Show |
10 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2018-842_2018-839d others(6): Show |
ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 13946744 | ||||||
| chr16:13946865 | A | G | 2 | a0001c0009t0015g0166 a0001c0009t0015g0167 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2018-749A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946865 | |||||||
| chr16:13946865 | A | T | 49 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0012 others(46): Show |
102 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2018-749A>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946865 | |||||||
| chr16:13946883 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18957.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2018-731C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13946883 | |||||||
| chr16:13947004 | C | T | 1 | a0001c0002t0027g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2018-610C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947004 | |||||||
| chr16:13947053 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2018-561C>T | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947053 | |||||||
| chr16:13947087 | A | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0138 |
2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2018-527A>C | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947087 | |||||||
| chr16:13947139 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2018-475T>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947139 | |||||||
| chr16:13947194 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2018-420A>G | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947194 | |||||||
| chr16:13947250 | G | A | 1 | a0004c0007t0002g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2018-364G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947250 | |||||||
| chr16:13947353 | G | A | 1 | a0009c0015t0026g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2018-261G>A | ERCC4 | ENSG00000175595.16 | transcript | ENST00000311895.8 | protein_coding | 10/10 | chr16 | 13947353 |