Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2071 |
| ensemblid | ENSG00000163161.14 |
| hgncid | 3435 |
| symbol | ERCC3 |
| name | ERCC excision repair 3, TFIIH core complex helicase subunit |
| refseq_nuc | NM_000122.2 |
| refseq_prot | NP_000113.1 |
| ensembl_nuc | ENST00000285398.7 |
| ensembl_prot | ENSP00000285398.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 127257290 |
| end | 127294144 |
| strand | - |
| ver | v1.2 |
| region | chr2:127257290-127294144 |
| region5000 | chr2:127252290-127299144 |
| regionname0 | ERCC3_chr2_127257290_127294144 |
| regionname5000 | ERCC3_chr2_127252290_127299144 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 782 | 346 | 91 | 69 | 131 | 8 | 45 | 101 | ERCC3_chr2_127252290_127299144 | ERCC3 | MGKRD others(777): Show |
chr2 | 127252290 | 127299144 |
| a0002 | 0/0 | 782 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | MGKRD others(777): Show |
chr2 | 127252290 | 127299144 |
| a0003 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | MGKRD others(777): Show |
chr2 | 127252290 | 127299144 |
| a0004 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | MGKRD others(777): Show |
chr2 | 127252290 | 127299144 |
| a0005 | 0/0 | 782 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | MGKRD others(777): Show |
chr2 | 127252290 | 127299144 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2346 | 329 | 78 | 67 | 130 | 8 | 44 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0002 | 0/0 | 2346 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0003 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0004 | 0/0 | 2346 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0005 | 0/0 | 2346 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0008 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0001c0010 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0002c0011 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0003c0006 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0004c0009 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 | ||
| a0005c0007 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | ATGGG others(2341): Show |
chr2 | 127252290 | 127299144 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2718 | 315 | 73 | 60 | 128 | 8 | 44 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0001t0002 | 0/0 | 2718 | 5 | 4 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0001t0003 | 0/0 | 2718 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0001t0004 | 0/0 | 2718 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0001t0005 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0002t0001 | 0/0 | 2718 | 6 | 5 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0003t0001 | 0/0 | 2718 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0004t0001 | 0/0 | 2718 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0005t0001 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0008t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0001c0010t0001 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0002c0011t0001 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0003c0006t0002 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0004c0009t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| a0005c0007t0001 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | AGAGC others(2713): Show |
chr2 | 127252290 | 127299144 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 3 | 7 | 11 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 4 | 2 | 2 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0003 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0002t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0003t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0004t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0001c0010t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0002c0011t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0003c0006t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0004c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| a0005c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0215 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01975 | hp2 | a0002 | c0011 | t0001 | g0216 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | KHV | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02738 | hp1 | a0001 | c0010 | t0001 | g0237 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0211 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03209 | hp1 | a0003 | c0006 | t0002 | g0240 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0048 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18991 | hp2 | a0004 | c0009 | t0001 | g0079 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19075 | hp1 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20905 | hp1 | a0005 | c0007 | t0001 | g0171 | SAS | GIH | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | MSL | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | ERCC3_chr2_127252290_127299144 | ERCC3 | chr2 | 127252290 | 127299144 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127259310 | A | G | 1 | a0004 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.2203T>C | p.Ser735Pro | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/15 | 2266/2718 | 2203/2349 | 735/782 | chr2 | 127259310 | |||
| chr2:127261332 | C | T | 1 | a0005 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1960G>A | p.Glu654Lys | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/15 | 2023/2718 | 1960/2349 | 654/782 | chr2 | 127261332 | |||
| chr2:127286997 | C | T | 1 | a0003 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1048G>A | p.Gly350Ser | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/15 | 1111/2718 | 1048/2349 | 350/782 | chr2 | 127286997 | |||
| chr2:127292833 | T | C | 1 | a0002 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.248A>G | p.His83Arg | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/15 | 311/2718 | 248/2349 | 83/782 | chr2 | 127292833 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127259407 | C | T | 1 | a0001c0008 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.2106G>A | p.Ala702Ala | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/15 | 2169/2718 | 2106/2349 | 702/782 | chr2 | 127259407 | |||
| chr2:127280489 | C | T | 1 | a0001c0002 | 6 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.1485G>A | p.Glu495Glu | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/15 | 1548/2718 | 1485/2349 | 495/782 | chr2 | 127280489 | |||
| chr2:127286926 | C | T | 1 | a0001c0003 | 4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.1119G>A | p.Gln373Gln | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/15 | 1182/2718 | 1119/2349 | 373/782 | chr2 | 127286926 | |||
| chr2:127288679 | C | T | 1 | a0001c0005 | 2 | HG02622.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1008G>A | p.Gly336Gly | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/15 | 1071/2718 | 1008/2349 | 336/782 | chr2 | 127288679 | |||
| chr2:127289731 | C | T | 1 | a0001c0004 | 3 | HG01175.hp1 HG02257.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.615G>A | p.Glu205Glu | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/15 | 678/2718 | 615/2349 | 205/782 | chr2 | 127289731 | |||
| chr2:127289818 | G | A | 1 | a0001c0010 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.528C>T | p.Phe176Phe | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/15 | 591/2718 | 528/2349 | 176/782 | chr2 | 127289818 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127257337 | C | T | 1 | a0001c0001t0004 | 3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*259G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 259 | chr2 | 127257337 | ||||||
| chr2:127257419 | T | C | 1 | a0001c0001t0003 | 4 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 177 | chr2 | 127257419 | ||||||
| chr2:127257490 | A | G | 2 | a0001c0001t0002 a0003c0006t0002 |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 15/15 | 106 | chr2 | 127257490 | ||||||
| chr2:127294132 | C | T | 1 | a0001c0001t0005 | 2 | HG02083.hp1 HG02523.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/15 | 51 | chr2 | 127294132 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127257733 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.2218-6C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257733 | |||||||
| chr2:127257791 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
301 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.2218-64G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257791 | |||||||
| chr2:127257818 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0092 others(4): Show |
11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2218-91G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257818 | |||||||
| chr2:127257843 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2218-116A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127257843 | |||||||
| chr2:127258104 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2218-377A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258104 | |||||||
| chr2:127258179 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2218-452G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258179 | |||||||
| chr2:127258224 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2218-497A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258224 | |||||||
| chr2:127258268 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2218-541G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258268 | |||||||
| chr2:127258415 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2218-688C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258415 | |||||||
| chr2:127258631 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+665C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258631 | |||||||
| chr2:127258658 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2217+638C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258658 | |||||||
| chr2:127258827 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+469C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258827 | |||||||
| chr2:127258852 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2217+444T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258852 | |||||||
| chr2:127258988 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+308T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127258988 | |||||||
| chr2:127259085 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2217+211C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127259085 | |||||||
| chr2:127259166 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2217+130G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 14/14 | chr2 | 127259166 | |||||||
| chr2:127259608 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2065-160C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259608 | |||||||
| chr2:127259715 | T | C | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2065-267A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259715 | |||||||
| chr2:127259764 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2065-316G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259764 | |||||||
| chr2:127259764 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0228 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2065-316G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259764 | |||||||
| chr2:127259806 | G | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-358C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259806 | |||||||
| chr2:127259915 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0203 a0001c0001t0001g0204 |
5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-467T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127259915 | |||||||
| chr2:127260190 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2065-742C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260190 | |||||||
| chr2:127260208 | C | T | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2065-760G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260208 | |||||||
| chr2:127260487 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2064+741T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260487 | |||||||
| chr2:127260517 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2064+711C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260517 | |||||||
| chr2:127260566 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0126 |
4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+662A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260566 | |||||||
| chr2:127260616 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.2064+612T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260616 | |||||||
| chr2:127260884 | GGAGGCAA others(3): Show |
G | 18 | a0001c0001t0001g0077 a0001c0001t0001g0198 a0001c0001t0001g0199 others(15): Show |
19 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2064+334_2064+343d others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260884 | |||||||
| chr2:127260946 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.2064+282A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260946 | |||||||
| chr2:127260985 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2064+243C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127260985 | |||||||
| chr2:127261169 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2064+59C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 13/14 | chr2 | 127261169 | |||||||
| chr2:127261367 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1946-21G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261367 | |||||||
| chr2:127261416 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-70A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261416 | |||||||
| chr2:127261486 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1946-140C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261486 | |||||||
| chr2:127261602 | G | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-256C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261602 | |||||||
| chr2:127261665 | A | C | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1946-319T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261665 | |||||||
| chr2:127261879 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-533C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127261879 | |||||||
| chr2:127262083 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1946-737G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262083 | |||||||
| chr2:127262139 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1946-793A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262139 | |||||||
| chr2:127262425 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-1079T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262425 | |||||||
| chr2:127262775 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-1429C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262775 | |||||||
| chr2:127262791 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0105 others(3): Show |
8 | HG02165.hp1 NA18945.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1946-1445C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262791 | |||||||
| chr2:127262798 | C | T | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1946-1452G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262798 | |||||||
| chr2:127262970 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(59): Show |
89 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1946-1624C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127262970 | |||||||
| chr2:127263092 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1946-1746A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263092 | |||||||
| chr2:127263181 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1946-1835A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263181 | |||||||
| chr2:127263366 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1946-2020C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263366 | |||||||
| chr2:127263480 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-2134G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263480 | |||||||
| chr2:127263666 | T | C | 7 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1946-2320A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263666 | |||||||
| chr2:127263702 | GTTCT | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
99 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1946-2360_1946-235 others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263702 | |||||||
| chr2:127263738 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1946-2392G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263738 | |||||||
| chr2:127263776 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-2430G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263776 | |||||||
| chr2:127263828 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0001g0198 a0001c0001t0001g0199 others(16): Show |
20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1946-2482G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263828 | |||||||
| chr2:127263868 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1946-2522G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263868 | |||||||
| chr2:127263978 | C | T | 22 | a0001c0001t0001g0077 a0001c0001t0001g0198 a0001c0001t0001g0199 others(19): Show |
24 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1946-2632G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127263978 | |||||||
| chr2:127264053 | A | G | 23 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0198 others(20): Show |
25 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1946-2707T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264053 | |||||||
| chr2:127264143 | T | C | 1 | a0001c0005t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1946-2797A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264143 | |||||||
| chr2:127264189 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1946-2843G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264189 | |||||||
| chr2:127264216 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-2870G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264216 | |||||||
| chr2:127264318 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0092 others(4): Show |
11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1946-2972A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264318 | |||||||
| chr2:127264517 | T | C | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1946-3171A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264517 | |||||||
| chr2:127264528 | T | C | 1 | a0001c0001t0001g0017 | 3 | HG02451.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1946-3182A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264528 | |||||||
| chr2:127264539 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1946-3193A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264539 | |||||||
| chr2:127264639 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1946-3293G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264639 | |||||||
| chr2:127264708 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-3362A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264708 | |||||||
| chr2:127264847 | A | AT | 13 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0075 others(10): Show |
14 | HG01175.hp1 HG01192.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1946-3502dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264847 | |||||||
| chr2:127264847 | AT | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0110 a0001c0001t0001g0112 others(3): Show |
6 | HG01256.hp1 HG01358.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1946-3502delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264847 | |||||||
| chr2:127264871 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0233 |
2 | HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1946-3525C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127264871 | |||||||
| chr2:127265095 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1946-3749G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265095 | |||||||
| chr2:127265189 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0080 others(10): Show |
17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1946-3843C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265189 | |||||||
| chr2:127265192 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0126 |
4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1946-3846G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265192 | |||||||
| chr2:127265320 | G | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0230 |
2 | NA18970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1946-3974C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265320 | |||||||
| chr2:127265465 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1946-4119G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265465 | |||||||
| chr2:127265519 | C | G | 1 | a0001c0001t0003g0193 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1946-4173G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265519 | |||||||
| chr2:127265519 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0001g0126 |
5 | HG02647.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1946-4173G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265519 | |||||||
| chr2:127265680 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-4334C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265680 | |||||||
| chr2:127265741 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1946-4395G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265741 | |||||||
| chr2:127265766 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0075 |
3 | HG01884.hp1 HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1946-4420A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265766 | |||||||
| chr2:127265773 | T | C | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1946-4427A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265773 | |||||||
| chr2:127265947 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0064 others(3): Show |
7 | HG00741.hp1 HG01106.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1946-4601G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127265947 | |||||||
| chr2:127266082 | G | GT | 11 | a0001c0001t0001g0102 a0001c0001t0001g0162 a0001c0001t0001g0173 others(8): Show |
11 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1946-4737dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266082 | |||||||
| chr2:127266085 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1946-4739A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266085 | |||||||
| chr2:127266112 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1946-4766G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266112 | |||||||
| chr2:127266196 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1946-4850G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266196 | |||||||
| chr2:127266287 | C | CAAGAAAA others(326): Show |
1 | a0001c0001t0001g0244 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1946-4942_1946-494 others(337): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266287 | |||||||
| chr2:127266287 | C | CAAGAAAA others(327): Show |
3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG03041.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1946-4942_1946-494 others(338): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266287 | |||||||
| chr2:127266308 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1946-4962A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266308 | |||||||
| chr2:127266333 | C | CT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0015 others(44): Show |
61 | HG00423.hp1 HG00735.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1946-4988dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | |||||||
| chr2:127266333 | C | CTT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0205 a0001c0001t0001g0219 others(9): Show |
15 | HG00423.hp2 HG01069.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1946-4989_1946-498 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | |||||||
| chr2:127266333 | CTTTTTTT others(1): Show |
C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(80): Show |
125 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1945+4995_1946-498 others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266333 | |||||||
| chr2:127266354 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4982A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266354 | |||||||
| chr2:127266355 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4981A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266355 | |||||||
| chr2:127266358 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4978C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266358 | |||||||
| chr2:127266362 | G | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1945+4974C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266362 | |||||||
| chr2:127266367 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1945+4969C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266367 | |||||||
| chr2:127266374 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1945+4962A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266374 | |||||||
| chr2:127266398 | C | T | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+4938G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266398 | |||||||
| chr2:127266549 | G | A | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0238 |
3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1945+4787C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266549 | |||||||
| chr2:127266559 | G | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0156 |
2 | NA18939.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1945+4777C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266559 | |||||||
| chr2:127266587 | T | C | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+4749A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266587 | |||||||
| chr2:127266603 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1945+4733G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266603 | |||||||
| chr2:127266605 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
4 | HG00733.hp2 HG01070.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4731C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266605 | |||||||
| chr2:127266621 | G | A | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4715C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266621 | |||||||
| chr2:127266650 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1945+4686G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266650 | |||||||
| chr2:127266663 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1945+4673C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266663 | |||||||
| chr2:127266706 | ATTATTTT others(4): Show |
A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+4619_1945+462 others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266706 | |||||||
| chr2:127266709 | A | AT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
81 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1945+4626dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | A | ATT | 16 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0077 others(13): Show |
16 | HG00423.hp2 HG01243.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1945+4625_1945+462 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0084 others(2): Show |
5 | HG04184.hp2 HG06807.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+4627T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | AT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0037 others(3): Show |
7 | HG00280.hp1 HG00438.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1945+4626delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | ATT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0085 others(3): Show |
8 | NA18951.hp2 NA18953.hp1 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1945+4625_1945+462 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | ATTTTTTT | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(1): Show |
6 | HG01433.hp2 HG02698.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+4620_1945+462 others(11): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266709 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1945+4616_1945+462 others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266709 | |||||||
| chr2:127266717 | T | TA | 3 | a0001c0001t0001g0015 a0001c0001t0001g0203 a0001c0001t0001g0204 |
5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945+4618_1945+461 others(5): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266717 | |||||||
| chr2:127266841 | C | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+4495G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266841 | |||||||
| chr2:127266868 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1945+4468G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266868 | |||||||
| chr2:127266869 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1945+4467C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266869 | |||||||
| chr2:127266881 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1945+4455A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266881 | |||||||
| chr2:127266904 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0235 |
2 | HG03516.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1945+4432G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266904 | |||||||
| chr2:127266915 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1945+4421G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266915 | |||||||
| chr2:127266969 | G | A | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+4367C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127266969 | |||||||
| chr2:127267194 | T | C | 1 | a0001c0005t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1945+4142A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267194 | |||||||
| chr2:127267288 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1945+4048G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267288 | |||||||
| chr2:127267323 | G | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+4013C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267323 | |||||||
| chr2:127267376 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1945+3960G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267376 | |||||||
| chr2:127267429 | C | CT | 4 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0203 others(1): Show |
6 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+3906dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267429 | |||||||
| chr2:127267453 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1945+3883A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267453 | |||||||
| chr2:127267829 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1945+3507A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267829 | |||||||
| chr2:127267857 | A | T | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945+3479T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267857 | |||||||
| chr2:127267950 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1945+3386A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127267950 | |||||||
| chr2:127268023 | G | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+3313C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268023 | |||||||
| chr2:127268076 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3260G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268076 | |||||||
| chr2:127268118 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3218A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268118 | |||||||
| chr2:127268173 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1945+3163C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268173 | |||||||
| chr2:127268255 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3081C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268255 | |||||||
| chr2:127268262 | T | C | 2 | a0001c0001t0002g0242 a0001c0001t0002g0243 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1945+3074A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268262 | |||||||
| chr2:127268285 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+3051T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268285 | |||||||
| chr2:127268295 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1945+3041C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268295 | |||||||
| chr2:127268368 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+2968G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268368 | |||||||
| chr2:127268509 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1945+2827A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268509 | |||||||
| chr2:127268549 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1945+2787G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268549 | |||||||
| chr2:127268550 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1945+2786C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268550 | |||||||
| chr2:127268850 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1945+2486G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268850 | |||||||
| chr2:127268984 | TG | T | 18 | a0001c0001t0001g0077 a0001c0001t0001g0198 a0001c0001t0001g0199 others(15): Show |
19 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1945+2351delC | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127268984 | |||||||
| chr2:127269098 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1945+2238A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269098 | |||||||
| chr2:127269209 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+2127T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269209 | |||||||
| chr2:127269335 | T | A | 4 | a0001c0001t0001g0210 a0001c0003t0001g0047 a0001c0003t0001g0209 others(1): Show |
5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+2001A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269335 | |||||||
| chr2:127269417 | C | CT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(20): Show |
27 | HG01069.hp2 HG01109.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1945+1918dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269417 | |||||||
| chr2:127269417 | CT | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(74): Show |
109 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1945+1918delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269417 | |||||||
| chr2:127269482 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1945+1854G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269482 | |||||||
| chr2:127269522 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0222 a0001c0001t0001g0228 others(1): Show |
8 | HG01346.hp1 HG02683.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1945+1814G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269522 | |||||||
| chr2:127269657 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0175 |
2 | HG01074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1945+1679T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269657 | |||||||
| chr2:127269672 | G | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1945+1664C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269672 | |||||||
| chr2:127269706 | C | A | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG01256.hp1 HG01358.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945+1630G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269706 | |||||||
| chr2:127269711 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1945+1625C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269711 | |||||||
| chr2:127269756 | C | A | 12 | a0001c0001t0001g0077 a0001c0001t0001g0244 a0001c0001t0001g0245 others(9): Show |
13 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1945+1580G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269756 | |||||||
| chr2:127269904 | G | C | 19 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0198 others(16): Show |
20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1945+1432C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127269904 | |||||||
| chr2:127270018 | C | CTCAA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(68): Show |
111 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1945+1314_1945+131 others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | |||||||
| chr2:127270018 | C | CTCAATCA others(1): Show |
4 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
5 | HG01261.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+1310_1945+131 others(12): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | |||||||
| chr2:127270018 | C | CTCAATCA others(5): Show |
1 | a0001c0001t0001g0141 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1945+1306_1945+131 others(16): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270018 | |||||||
| chr2:127270048 | A | C | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945+1288T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270048 | |||||||
| chr2:127270049 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1945+1287T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270049 | |||||||
| chr2:127270075 | A | G | 1 | a0001c0004t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1945+1261T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270075 | |||||||
| chr2:127270173 | A | ACACACCA others(10): Show |
3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1945+1146_1945+116 others(21): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270173 | |||||||
| chr2:127270197 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1945+1139A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270197 | |||||||
| chr2:127270276 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1945+1060A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270276 | |||||||
| chr2:127270304 | T | C | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+1032A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270304 | |||||||
| chr2:127270554 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1945+782C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270554 | |||||||
| chr2:127270906 | G | A | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+430C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270906 | |||||||
| chr2:127270919 | G | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945+417C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270919 | |||||||
| chr2:127270962 | T | A | 1 | a0001c0005t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1945+374A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127270962 | |||||||
| chr2:127271216 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1945+120A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 12/14 | chr2 | 127271216 | |||||||
| chr2:127271489 | GA | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
140 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1828-37delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271489 | |||||||
| chr2:127271689 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0203 a0001c0001t0001g0204 |
5 | HG01106.hp2 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1828-236G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271689 | |||||||
| chr2:127271732 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-279C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271732 | |||||||
| chr2:127271927 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1828-474G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271927 | |||||||
| chr2:127271938 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-485C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271938 | |||||||
| chr2:127271983 | C | A | 1 | a0004c0009t0001g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1828-530G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127271983 | |||||||
| chr2:127272007 | C | CT | 14 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0055 others(11): Show |
16 | HG00741.hp1 HG01106.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1828-555dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | |||||||
| chr2:127272007 | CT | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1828-555delA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | |||||||
| chr2:127272007 | CTT | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
46 | HG00639.hp1 HG01175.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.1828-556_1828-555d others(4): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | |||||||
| chr2:127272007 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-567_1828-555d others(15): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | |||||||
| chr2:127272007 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1828-570_1828-555d others(18): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272007 | |||||||
| chr2:127272041 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1828-588C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272041 | |||||||
| chr2:127272049 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1828-596C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272049 | |||||||
| chr2:127272101 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1828-648G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272101 | |||||||
| chr2:127272109 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1828-656A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272109 | |||||||
| chr2:127272153 | T | C | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828-700A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272153 | |||||||
| chr2:127272165 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1827+700G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272165 | |||||||
| chr2:127272170 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1827+695C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272170 | |||||||
| chr2:127272213 | C | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(55): Show |
85 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1827+652G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272213 | |||||||
| chr2:127272259 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1827+606G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272259 | |||||||
| chr2:127272262 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1827+603A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272262 | |||||||
| chr2:127272272 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0092 others(4): Show |
11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1827+593C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272272 | |||||||
| chr2:127272461 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1827+404G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272461 | |||||||
| chr2:127272502 | G | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
16 | HG01081.hp1 HG01358.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1827+363C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272502 | |||||||
| chr2:127272589 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1827+276T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272589 | |||||||
| chr2:127272801 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1827+64A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 11/14 | chr2 | 127272801 | |||||||
| chr2:127272993 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1731-32C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127272993 | |||||||
| chr2:127273020 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1731-59T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273020 | |||||||
| chr2:127273109 | T | G | 4 | a0001c0001t0001g0210 a0001c0003t0001g0047 a0001c0003t0001g0209 others(1): Show |
5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-148A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273109 | |||||||
| chr2:127273157 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
4 | HG00733.hp2 HG01070.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-196G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273157 | |||||||
| chr2:127273196 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1731-235C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273196 | |||||||
| chr2:127273212 | A | C | 4 | a0001c0001t0001g0210 a0001c0003t0001g0047 a0001c0003t0001g0209 others(1): Show |
5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-251T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273212 | |||||||
| chr2:127273303 | A | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1731-342T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273303 | |||||||
| chr2:127273409 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-448T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273409 | |||||||
| chr2:127273475 | C | T | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1731-514G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273475 | |||||||
| chr2:127273512 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1731-551A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273512 | |||||||
| chr2:127273540 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1731-579C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273540 | |||||||
| chr2:127273622 | G | A | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-661C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273622 | |||||||
| chr2:127273641 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1731-680G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273641 | |||||||
| chr2:127273673 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG01192.hp2 HG01261.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1731-712C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273673 | |||||||
| chr2:127273720 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1731-759G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273720 | |||||||
| chr2:127273749 | C | CA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(91): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1731-789dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273749 | C | CAA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0135 others(15): Show |
24 | HG01106.hp2 HG01109.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1731-790_1731-789d others(4): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273749 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-800_1731-789d others(14): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273749 | CA | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
16 | HG02109.hp2 HG02257.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.1731-789delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273749 | CAAAAAA | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-794_1731-789d others(8): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273749 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1731-799_1731-789d others(13): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273749 | |||||||
| chr2:127273842 | T | C | 1 | a0001c0010t0001g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1731-881A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273842 | |||||||
| chr2:127273962 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1731-1001T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127273962 | |||||||
| chr2:127274040 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0002g0050 a0001c0001t0002g0241 others(3): Show |
7 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1079C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274040 | |||||||
| chr2:127274079 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1118C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274079 | |||||||
| chr2:127274088 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1127A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274088 | |||||||
| chr2:127274123 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1731-1162C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274123 | |||||||
| chr2:127274222 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1731-1261C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274222 | |||||||
| chr2:127274309 | C | T | 14 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(11): Show |
15 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1731-1348G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274309 | |||||||
| chr2:127274316 | GA | G | 10 | a0001c0001t0001g0133 a0001c0001t0001g0196 a0001c0001t0001g0198 others(7): Show |
10 | HG01169.hp2 HG01256.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1731-1356delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274316 | |||||||
| chr2:127274380 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1731-1419A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274380 | |||||||
| chr2:127274441 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1731-1480C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274441 | |||||||
| chr2:127274503 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1731-1542G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274503 | |||||||
| chr2:127274729 | G | T | 19 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0198 others(16): Show |
20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1731-1768C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274729 | |||||||
| chr2:127274754 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1793G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274754 | |||||||
| chr2:127274810 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
6 | HG00733.hp2 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1731-1849C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274810 | |||||||
| chr2:127274820 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-1859G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274820 | |||||||
| chr2:127274833 | G | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0193 a0001c0001t0003g0194 |
4 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731-1872C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274833 | |||||||
| chr2:127274951 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0111 |
5 | HG00280.hp1 HG00733.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-1990C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274951 | |||||||
| chr2:127274970 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1731-2009C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127274970 | |||||||
| chr2:127275129 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2168C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275129 | |||||||
| chr2:127275246 | A | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1731-2285T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275246 | |||||||
| chr2:127275383 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0036 others(5): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1731-2422G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275383 | |||||||
| chr2:127275448 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1731-2487G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275448 | |||||||
| chr2:127275559 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2598T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275559 | |||||||
| chr2:127275639 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1731-2678G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275639 | |||||||
| chr2:127275751 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
300 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.1731-2790G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275751 | |||||||
| chr2:127275829 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1731-2868C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127275829 | |||||||
| chr2:127276023 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18944.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1731-3062G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276023 | |||||||
| chr2:127276156 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+3017G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276156 | |||||||
| chr2:127276406 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1730+2767T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276406 | |||||||
| chr2:127276771 | G | GA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1730+2401dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276771 | |||||||
| chr2:127276845 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1730+2328G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276845 | |||||||
| chr2:127276925 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1730+2248T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276925 | |||||||
| chr2:127276963 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1730+2210T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127276963 | |||||||
| chr2:127277263 | AGAAATTA others(3): Show |
A | 12 | a0001c0001t0001g0077 a0001c0001t0001g0244 a0001c0001t0001g0245 others(9): Show |
13 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1730+1900_1730+190 others(14): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277263 | |||||||
| chr2:127277448 | T | G | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0238 |
3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1730+1725A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277448 | |||||||
| chr2:127277517 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0001g0198 a0001c0001t0001g0199 others(16): Show |
20 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1730+1656G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277517 | |||||||
| chr2:127277521 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+1652G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277521 | |||||||
| chr2:127277609 | T | G | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+1564A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277609 | |||||||
| chr2:127277666 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1730+1507C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277666 | |||||||
| chr2:127277749 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1730+1424G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277749 | |||||||
| chr2:127277762 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1730+1411G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127277762 | |||||||
| chr2:127278084 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1730+1089T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278084 | |||||||
| chr2:127278238 | C | CA | 7 | a0001c0001t0001g0054 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+934dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278238 | |||||||
| chr2:127278238 | CA | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
277 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.1730+934delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278238 | |||||||
| chr2:127278272 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1730+901T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278272 | |||||||
| chr2:127278307 | C | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0060 a0001c0002t0001g0061 |
6 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+866G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278307 | |||||||
| chr2:127278307 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1730+866G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278307 | |||||||
| chr2:127278388 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+785G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278388 | |||||||
| chr2:127278575 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0092 others(4): Show |
11 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1730+598C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278575 | |||||||
| chr2:127278633 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+540C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278633 | |||||||
| chr2:127278685 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1730+488G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278685 | |||||||
| chr2:127278725 | G | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0117 others(1): Show |
7 | NA18944.hp2 NA18951.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1730+448C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278725 | |||||||
| chr2:127278907 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0002g0050 a0001c0001t0002g0241 others(5): Show |
9 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730+266C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278907 | |||||||
| chr2:127278911 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1730+262G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278911 | |||||||
| chr2:127278912 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1730+261T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127278912 | |||||||
| chr2:127279095 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1730+78T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 10/14 | chr2 | 127279095 | |||||||
| chr2:127279567 | G | T | 8 | a0001c0001t0001g0077 a0001c0001t0002g0050 a0001c0001t0002g0241 others(5): Show |
9 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1528-192C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279567 | |||||||
| chr2:127279625 | G | A | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1528-250C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279625 | |||||||
| chr2:127279670 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1528-295C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279670 | |||||||
| chr2:127279759 | T | TA | 7 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0002g0050 others(4): Show |
8 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1528-385dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279759 | |||||||
| chr2:127279863 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1528-488A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279863 | |||||||
| chr2:127279871 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1528-496A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279871 | |||||||
| chr2:127279902 | C | T | 23 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0198 others(20): Show |
25 | HG01243.hp2 HG01256.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1528-527G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279902 | |||||||
| chr2:127279956 | T | A | 1 | a0001c0001t0001g0017 | 3 | HG02451.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1527+491A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279956 | |||||||
| chr2:127279984 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1527+463T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127279984 | |||||||
| chr2:127280178 | C | A | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+269G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127280178 | |||||||
| chr2:127280328 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1527+119T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 9/14 | chr2 | 127280328 | |||||||
| chr2:127280795 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1343-164C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127280795 | |||||||
| chr2:127280968 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(88): Show |
135 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1343-337A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127280968 | |||||||
| chr2:127281077 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00423.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1343-446C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281077 | |||||||
| chr2:127281119 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1343-488A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281119 | |||||||
| chr2:127281160 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0080 others(10): Show |
17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1343-529T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281160 | |||||||
| chr2:127281162 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-531G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281162 | |||||||
| chr2:127281362 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1343-731T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281362 | |||||||
| chr2:127281469 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1343-838A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281469 | |||||||
| chr2:127281958 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1343-1327T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127281958 | |||||||
| chr2:127282008 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0214 |
3 | HG01069.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1343-1377C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282008 | |||||||
| chr2:127282022 | C | T | 1 | a0001c0001t0001g0008 | 4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343-1391G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282022 | |||||||
| chr2:127282123 | C | T | 1 | a0001c0005t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1343-1492G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282123 | |||||||
| chr2:127282215 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1343-1584G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282215 | |||||||
| chr2:127282293 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1343-1662A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282293 | |||||||
| chr2:127282386 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1343-1755G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282386 | |||||||
| chr2:127282503 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1343-1872T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282503 | |||||||
| chr2:127282571 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1343-1940T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282571 | |||||||
| chr2:127282615 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-1984C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282615 | |||||||
| chr2:127282653 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1343-2022A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282653 | |||||||
| chr2:127282687 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1343-2056T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282687 | |||||||
| chr2:127282687 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1343-2056T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282687 | |||||||
| chr2:127282754 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1343-2123A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282754 | |||||||
| chr2:127282795 | C | T | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343-2164G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282795 | |||||||
| chr2:127282909 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0126 |
4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343-2278C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127282909 | |||||||
| chr2:127283094 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1343-2463A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283094 | |||||||
| chr2:127283141 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1343-2510C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283141 | |||||||
| chr2:127283143 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1343-2512A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283143 | |||||||
| chr2:127283288 | C | T | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1343-2657G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283288 | |||||||
| chr2:127283339 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
137 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1343-2708A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283339 | |||||||
| chr2:127283622 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-2991G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283622 | |||||||
| chr2:127283631 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1343-3000A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283631 | |||||||
| chr2:127283805 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1342+2898T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283805 | |||||||
| chr2:127283869 | A | C | 2 | a0001c0001t0005g0052 a0001c0001t0005g0053 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1342+2834T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283869 | |||||||
| chr2:127283891 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0092 |
3 | HG02109.hp2 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1342+2812G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283891 | |||||||
| chr2:127283995 | TGA | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1342+2706_1342+270 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127283995 | |||||||
| chr2:127284037 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1342+2666G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284037 | |||||||
| chr2:127284061 | T | C | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1342+2642A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284061 | |||||||
| chr2:127284258 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0080 others(10): Show |
17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1342+2445A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284258 | |||||||
| chr2:127284354 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1342+2349C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284354 | |||||||
| chr2:127284465 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+2238C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284465 | |||||||
| chr2:127284485 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1342+2218G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284485 | |||||||
| chr2:127284524 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1342+2179G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284524 | |||||||
| chr2:127284533 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1342+2170G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284533 | |||||||
| chr2:127284565 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1342+2138T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284565 | |||||||
| chr2:127284687 | A | AT | 8 | a0001c0001t0001g0086 a0001c0001t0001g0149 a0001c0001t0001g0198 others(5): Show |
8 | HG01884.hp2 HG02922.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1342+2015dupA | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284687 | |||||||
| chr2:127284687 | A | ATT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
34 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1342+2014_1342+201 others(6): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284687 | |||||||
| chr2:127284895 | C | T | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342+1808G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284895 | |||||||
| chr2:127284912 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1342+1791G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127284912 | |||||||
| chr2:127285055 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0085 others(4): Show |
11 | HG00438.hp1 NA18612.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1342+1648C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285055 | |||||||
| chr2:127285056 | C | T | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342+1647G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285056 | |||||||
| chr2:127285145 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1342+1558C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285145 | |||||||
| chr2:127285229 | A | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1342+1474T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285229 | |||||||
| chr2:127285250 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+1453G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285250 | |||||||
| chr2:127285296 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1342+1407T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285296 | |||||||
| chr2:127285297 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1342+1406G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285297 | |||||||
| chr2:127285403 | T | C | 1 | a0001c0005t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1342+1300A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285403 | |||||||
| chr2:127285509 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0182 a0001c0001t0001g0183 |
4 | NA18953.hp2 NA18955.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1342+1194C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285509 | |||||||
| chr2:127285573 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1342+1130G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285573 | |||||||
| chr2:127285709 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1342+994C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285709 | |||||||
| chr2:127285754 | G | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01884.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1342+949C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285754 | |||||||
| chr2:127285776 | T | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1342+927A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285776 | |||||||
| chr2:127285794 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1342+909A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285794 | |||||||
| chr2:127285982 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1342+721A>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285982 | |||||||
| chr2:127285982 | T | TA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1342+720dupT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127285982 | |||||||
| chr2:127286169 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1342+534A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286169 | |||||||
| chr2:127286288 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1342+415G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286288 | |||||||
| chr2:127286419 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0126 |
4 | HG02970.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342+284C>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286419 | |||||||
| chr2:127286472 | G | T | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0238 |
3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1342+231C>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286472 | |||||||
| chr2:127286545 | CA | C | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
10 | HG01081.hp1 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1342+157delT | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286545 | |||||||
| chr2:127286617 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1342+86G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 8/14 | chr2 | 127286617 | |||||||
| chr2:127287354 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1028-337T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287354 | |||||||
| chr2:127287486 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1028-469A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287486 | |||||||
| chr2:127287558 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 |
4 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-541G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287558 | |||||||
| chr2:127287589 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1028-572C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287589 | |||||||
| chr2:127287679 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1028-662A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287679 | |||||||
| chr2:127287727 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1028-710G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287727 | |||||||
| chr2:127287787 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1028-770C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287787 | |||||||
| chr2:127287794 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0059 |
4 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-777T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287794 | |||||||
| chr2:127287839 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1027+821C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287839 | |||||||
| chr2:127287847 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0235 a0001c0001t0001g0236 |
4 | HG03041.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+813C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287847 | |||||||
| chr2:127287912 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1027+748G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127287912 | |||||||
| chr2:127288391 | C | T | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+269G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127288391 | |||||||
| chr2:127288657 | T | C | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1027+3A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 7/14 | chr2 | 127288657 | |||||||
| chr2:127288972 | C | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
280 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.823-108G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127288972 | |||||||
| chr2:127289012 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.823-148T>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289012 | |||||||
| chr2:127289041 | C | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-177G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289041 | |||||||
| chr2:127289062 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02056.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.823-198A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289062 | |||||||
| chr2:127289074 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823-210T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 6/14 | chr2 | 127289074 | |||||||
| chr2:127289525 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG01261.hp1 HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.658-24G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 5/14 | chr2 | 127289525 | |||||||
| chr2:127290044 | G | A | 9 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
10 | HG01099.hp2 HG01943.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.521+180C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290044 | |||||||
| chr2:127290066 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.521+158C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290066 | |||||||
| chr2:127290094 | TTTCTC | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.521+125_521+129del others(5): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290094 | |||||||
| chr2:127290176 | G | A | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.521+48C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290176 | |||||||
| chr2:127290181 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.521+43T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 4/14 | chr2 | 127290181 | |||||||
| chr2:127290372 | C | A | 1 | a0001c0001t0001g0037 | 2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.472-99G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290372 | |||||||
| chr2:127290422 | C | T | 1 | a0001c0001t0001g0008 | 4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-149G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290422 | |||||||
| chr2:127290473 | C | T | 3 | a0001c0003t0001g0047 a0001c0003t0001g0209 a0001c0003t0001g0213 |
4 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-200G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290473 | |||||||
| chr2:127290566 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG01192.hp2 HG01261.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-293G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290566 | |||||||
| chr2:127290698 | C | A | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.472-425G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290698 | |||||||
| chr2:127290713 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-440A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290713 | |||||||
| chr2:127290848 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18994.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.472-575C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290848 | |||||||
| chr2:127290938 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.472-665G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290938 | |||||||
| chr2:127290973 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.472-700A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127290973 | |||||||
| chr2:127291013 | T | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0002c0011t0001g0216 |
3 | HG01169.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.472-740A>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291013 | |||||||
| chr2:127291017 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.472-744C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291017 | |||||||
| chr2:127291019 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.472-746A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291019 | |||||||
| chr2:127291098 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.472-825T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291098 | |||||||
| chr2:127291332 | T | C | 3 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0238 |
3 | HG01256.hp1 HG01358.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.472-1059A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291332 | |||||||
| chr2:127291535 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
10 | HG00408.hp1 HG00438.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+1075T>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291535 | |||||||
| chr2:127291631 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+979G>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291631 | |||||||
| chr2:127291720 | G | A | 4 | a0001c0001t0001g0210 a0001c0003t0001g0047 a0001c0003t0001g0209 others(1): Show |
5 | HG02717.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+890C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291720 | |||||||
| chr2:127291798 | A | G | 1 | a0001c0001t0004g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+812T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127291798 | |||||||
| chr2:127292027 | G | A | 2 | a0001c0005t0001g0211 a0001c0005t0001g0212 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.471+583C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292027 | |||||||
| chr2:127292055 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
162 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.471+555A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292055 | |||||||
| chr2:127292180 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
7 | HG02015.hp1 HG03688.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+430G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292180 | |||||||
| chr2:127292200 | T | C | 1 | a0001c0003t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.471+410A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292200 | |||||||
| chr2:127292281 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+329G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292281 | |||||||
| chr2:127292341 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.471+269G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292341 | |||||||
| chr2:127292369 | GTGGCCTC others(48): Show |
G | 6 | a0001c0001t0001g0077 a0001c0001t0002g0050 a0001c0001t0002g0241 others(3): Show |
7 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+186_471+240del others(55): Show |
ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292369 | |||||||
| chr2:127292424 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
291 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.471+186T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292424 | |||||||
| chr2:127292492 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG00639.hp2 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+118G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292492 | |||||||
| chr2:127292558 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.471+52A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292558 | |||||||
| chr2:127292580 | G | A | 2 | a0001c0004t0001g0048 a0001c0004t0001g0215 |
3 | HG01175.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.471+30C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 3/14 | chr2 | 127292580 | |||||||
| chr2:127292907 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
36 | HG00423.hp1 HG00423.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.235-61A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127292907 | |||||||
| chr2:127293190 | T | C | 1 | a0001c0001t0004g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+323A>G | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127293190 | |||||||
| chr2:127293256 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.234+257G>A | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 2/14 | chr2 | 127293256 | |||||||
| chr2:127293733 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-15G>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293733 | |||||||
| chr2:127293805 | G | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0241 a0001c0001t0002g0242 others(2): Show |
6 | HG01243.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-87C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293805 | |||||||
| chr2:127293843 | G | A | 1 | a0001c0001t0001g0051 | 2 | NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.29-125C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293843 | |||||||
| chr2:127293998 | G | A | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+56C>T | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127293998 | |||||||
| chr2:127294014 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.28+40T>C | ERCC3 | ENSG00000163161.14 | transcript | ENST00000285398.7 | protein_coding | 1/14 | chr2 | 127294014 |