Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1161 |
| ensemblid | ENSG00000049167.16 |
| hgncid | 3439 |
| symbol | ERCC8 |
| name | ERCC excision repair 8, CSA ubiquitin ligase complex subunit |
| refseq_nuc | NM_000082.4 |
| refseq_prot | NP_000073.1 |
| ensembl_nuc | ENST00000676185.1 |
| ensembl_prot | ENSP00000501614.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 60866454 |
| end | 60945070 |
| strand | - |
| ver | v1.2 |
| region | chr5:60866454-60945070 |
| region5000 | chr5:60861454-60950070 |
| regionname0 | ERCC8_chr5_60866454_60945070 |
| regionname5000 | ERCC8_chr5_60861454_60950070 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 396 | 301 | 88 | 56 | 104 | 16 | 35 | 82 | ERCC8_chr5_60861454_60950070 | ERCC8 | MLGFL others(391): Show |
chr5 | 60861454 | 60950070 |
| a0002 | 0/0 | 396 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | MLGFL others(391): Show |
chr5 | 60861454 | 60950070 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1188 | 249 | 77 | 37 | 97 | 10 | 26 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0002 | 0/0 | 1188 | 36 | 9 | 15 | 0 | 4 | 8 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0003 | 0/0 | 1188 | 6 | 0 | 3 | 0 | 2 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0004 | 0/0 | 1188 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0005 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0006 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0007 | 0/0 | 1188 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0001c0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 | ||
| a0002c0008 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | ATGCT others(1183): Show |
chr5 | 60861454 | 60950070 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9415 | 38 | 4 | 7 | 21 | 3 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0002 | 1/0 | 9414 | 35 | 0 | 8 | 18 | 1 | 7 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0003 | 0/0 | 9414 | 20 | 0 | 6 | 12 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0004 | 0/0 | 9411 | 14 | 0 | 2 | 12 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9406): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0005 | 0/1 | 9416 | 11 | 9 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0007 | 0/0 | 9412 | 10 | 10 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9407): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0009 | 0/0 | 9415 | 9 | 0 | 3 | 3 | 0 | 3 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0010 | 0/0 | 9413 | 9 | 9 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9408): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0011 | 0/0 | 9415 | 7 | 0 | 0 | 6 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0012 | 0/0 | 9415 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0013 | 0/0 | 9416 | 4 | 0 | 2 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0014 | 0/0 | 9414 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0015 | 0/0 | 9418 | 4 | 2 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9413): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0018 | 0/0 | 9417 | 3 | 2 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0019 | 0/0 | 9414 | 3 | 0 | 1 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0020 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0021 | 0/0 | 9414 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0022 | 0/0 | 9411 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9406): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0023 | 0/0 | 9412 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9407): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0027 | 0/0 | 9416 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0028 | 0/0 | 9418 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9413): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0029 | 0/0 | 9416 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0030 | 0/0 | 9414 | 2 | 0 | 0 | 0 | 2 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0031 | 0/0 | 9412 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9407): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0034 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0035 | 0/0 | 9417 | 2 | 0 | 1 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0036 | 0/0 | 9417 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0037 | 0/0 | 9414 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0038 | 0/0 | 9415 | 2 | 0 | 0 | 1 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0039 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0040 | 0/0 | 9415 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0041 | 0/0 | 9416 | 2 | 0 | 0 | 1 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0042 | 0/0 | 9414 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0043 | 0/0 | 9414 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0044 | 0/0 | 9401 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9396): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0045 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0046 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0047 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0048 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0049 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0050 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0051 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9413): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0058 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0059 | 0/0 | 9418 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9413): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0060 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9412): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0061 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0062 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0063 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0064 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0065 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0066 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0067 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0068 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9413): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0069 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0070 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0071 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0072 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0073 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0074 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0075 | 0/0 | 9415 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0076 | 0/0 | 9391 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9386): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0077 | 0/0 | 9415 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0079 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0080 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0081 | 0/0 | 9409 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9404): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0082 | 0/0 | 9413 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9408): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0083 | 0/0 | 9411 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9406): Show |
chr5 | 60861454 | 60950070 |
| a0001c0001t0084 | 0/0 | 9416 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0006 | 0/0 | 9415 | 10 | 1 | 4 | 0 | 0 | 5 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0008 | 0/0 | 9400 | 8 | 1 | 4 | 0 | 3 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0016 | 0/0 | 9400 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0017 | 0/0 | 9400 | 4 | 0 | 4 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0032 | 0/0 | 9401 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9396): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0033 | 0/0 | 9400 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0052 | 0/0 | 9414 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0053 | 0/0 | 9415 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0054 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0055 | 0/0 | 9400 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0056 | 0/0 | 9400 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| a0001c0002t0057 | 0/0 | 9415 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0003t0024 | 0/0 | 9411 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9406): Show |
chr5 | 60861454 | 60950070 |
| a0001c0003t0025 | 0/0 | 9421 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9416): Show |
chr5 | 60861454 | 60950070 |
| a0001c0003t0026 | 0/0 | 9422 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9417): Show |
chr5 | 60861454 | 60950070 |
| a0001c0004t0001 | 0/0 | 9415 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0004t0039 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0004t0078 | 0/0 | 9415 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9410): Show |
chr5 | 60861454 | 60950070 |
| a0001c0005t0020 | 0/0 | 9414 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0006t0003 | 0/0 | 9414 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9409): Show |
chr5 | 60861454 | 60950070 |
| a0001c0007t0013 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0001c0009t0034 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9411): Show |
chr5 | 60861454 | 60950070 |
| a0002c0008t0008 | 0/0 | 9400 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | AGTCC others(9395): Show |
chr5 | 60861454 | 60950070 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0009g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0013g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0013g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0015g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0018g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0019g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0021g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0021g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0021g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0022g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0022g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0022g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0023g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0023g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0023g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0027g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0027g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0028g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0028g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0029g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0029g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0030g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0030g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0031g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0031g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0034g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0035g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0035g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0036g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0036g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0037g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0037g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0038g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0038g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0039g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0040g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0040g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0041g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0041g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0042g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0042g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0043g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0044g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0045g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0046g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0047g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0048g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0049g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0050g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0051g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0058g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0059g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0060g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0061g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0062g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0063g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0064g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0065g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0066g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0067g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0068g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0069g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0070g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0071g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0072g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0073g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0074g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0075g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0076g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0077g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0079g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0080g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0081g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0082g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0083g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0001t0084g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0008g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0016g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0017g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0017g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0017g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0017g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0032g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0032g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0033g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0033g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0052g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0053g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0054g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0055g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0056g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0002t0057g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0024g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0024g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0025g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0025g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0026g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0003t0026g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0004t0039g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0004t0078g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0005t0020g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0006t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0007t0013g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0001c0009t0034g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| a0002c0008t0008g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0050 | g0274 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00140 | hp1 | a0001 | c0002 | t0008 | g0072 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | GBR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00280 | hp1 | a0001 | c0002 | t0057 | g0051 | EUR | FIN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0167 | EUR | FIN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00558 | hp2 | a0001 | c0001 | t0068 | g0113 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00621 | hp1 | a0001 | c0001 | t0067 | g0140 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00642 | hp1 | a0001 | c0002 | t0006 | g0053 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00642 | hp2 | a0001 | c0002 | t0033 | g0059 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00673 | hp1 | a0001 | c0001 | t0062 | g0091 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | CHS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0180 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00733 | hp2 | a0001 | c0007 | t0013 | g0109 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0181 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00738 | hp1 | a0001 | c0002 | t0008 | g0061 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0070 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01069 | hp2 | a0001 | c0001 | t0019 | g0114 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01099 | hp1 | a0001 | c0002 | t0017 | g0229 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01109 | hp1 | a0001 | c0001 | t0015 | g0252 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01109 | hp2 | a0001 | c0003 | t0024 | g0013 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0271 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01168 | hp1 | a0001 | c0001 | t0069 | g0116 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01168 | hp2 | a0001 | c0002 | t0017 | g0069 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01175 | hp1 | a0001 | c0001 | t0059 | g0256 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01175 | hp2 | a0001 | c0002 | t0017 | g0065 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01192 | hp1 | a0001 | c0002 | t0053 | g0048 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01192 | hp2 | a0001 | c0001 | t0043 | g0018 | AMR | PUR | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01255 | hp2 | a0001 | c0002 | t0006 | g0052 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01257 | hp2 | a0001 | c0003 | t0025 | g0014 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01258 | hp2 | a0001 | c0003 | t0026 | g0015 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01346 | hp1 | a0001 | c0002 | t0017 | g0062 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01358 | hp2 | a0001 | c0002 | t0055 | g0073 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01361 | hp1 | a0001 | c0001 | t0042 | g0042 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0126 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01433 | hp2 | a0001 | c0002 | t0008 | g0064 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0050 | AMR | CLM | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01515 | hp1 | a0001 | c0001 | t0038 | g0154 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01515 | hp2 | a0001 | c0003 | t0025 | g0017 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01516 | hp1 | a0001 | c0002 | t0008 | g0058 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01516 | hp2 | a0001 | c0001 | t0030 | g0246 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01517 | hp1 | a0001 | c0003 | t0026 | g0016 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01517 | hp2 | a0001 | c0001 | t0030 | g0247 | EUR | IBS | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0288 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01928 | hp2 | a0001 | c0001 | t0035 | g0104 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01952 | hp2 | a0001 | c0002 | t0008 | g0074 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01981 | hp1 | a0001 | c0002 | t0006 | g0049 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0127 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02056 | hp1 | a0001 | c0001 | t0074 | g0046 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02056 | hp2 | a0001 | c0001 | t0073 | g0156 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0152 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02080 | hp1 | a0001 | c0001 | t0011 | g0096 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02080 | hp2 | a0001 | c0001 | t0070 | g0099 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0136 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02132 | hp2 | a0001 | c0001 | t0031 | g0234 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02135 | hp2 | a0001 | c0001 | t0041 | g0219 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02145 | hp1 | a0001 | c0001 | t0018 | g0242 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02145 | hp2 | a0001 | c0002 | t0016 | g0071 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02257 | hp1 | a0001 | c0002 | t0056 | g0068 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02257 | hp2 | a0001 | c0001 | t0081 | g0019 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02258 | hp1 | a0001 | c0001 | t0027 | g0249 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02273 | hp2 | a0001 | c0001 | t0013 | g0103 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02280 | hp1 | a0001 | c0001 | t0046 | g0269 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02300 | hp2 | a0001 | c0001 | t0065 | g0122 | AMR | PEL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0083 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02523 | hp2 | a0001 | c0001 | t0038 | g0137 | EAS | KHV | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0039 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02572 | hp2 | a0001 | c0001 | t0044 | g0170 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02602 | hp1 | a0001 | c0001 | t0080 | g0205 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0267 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02615 | hp1 | a0001 | c0001 | t0037 | g0183 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02615 | hp2 | a0001 | c0001 | t0076 | g0047 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02622 | hp1 | a0001 | c0001 | t0082 | g0030 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0172 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0278 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02647 | hp1 | a0001 | c0005 | t0020 | g0005 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02647 | hp2 | a0001 | c0001 | t0084 | g0171 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0207 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02683 | hp2 | a0001 | c0002 | t0033 | g0232 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02717 | hp1 | a0001 | c0001 | t0027 | g0250 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02717 | hp2 | a0001 | c0005 | t0020 | g0005 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02723 | hp2 | a0001 | c0001 | t0029 | g0258 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02735 | hp2 | a0001 | c0001 | t0058 | g0255 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02809 | hp1 | a0001 | c0001 | t0022 | g0280 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02809 | hp2 | a0001 | c0002 | t0016 | g0067 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0176 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02895 | hp2 | a0001 | c0002 | t0016 | g0075 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02896 | hp1 | a0001 | c0002 | t0016 | g0060 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0177 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0223 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02970 | hp1 | a0001 | c0001 | t0037 | g0182 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0254 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03017 | hp1 | a0001 | c0003 | t0024 | g0012 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0253 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03098 | hp2 | a0001 | c0001 | t0083 | g0279 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0080 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0057 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03139 | hp1 | a0001 | c0001 | t0075 | g0086 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0284 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0283 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0173 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03486 | hp1 | a0001 | c0001 | t0060 | g0024 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03486 | hp2 | a0001 | c0001 | t0023 | g0281 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03490 | hp1 | a0001 | c0002 | t0006 | g0003 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03516 | hp1 | a0001 | c0001 | t0034 | g0044 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0079 | AFR | ESN | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03540 | hp1 | a0001 | c0002 | t0032 | g0056 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0081 | AFR | GWD | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03579 | hp1 | a0001 | c0001 | t0048 | g0272 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0285 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03654 | hp1 | a0001 | c0001 | t0061 | g0087 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0134 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03704 | hp2 | a0001 | c0002 | t0006 | g0003 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03710 | hp1 | a0001 | c0001 | t0045 | g0245 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0179 | SAS | PJL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03831 | hp1 | a0001 | c0002 | t0006 | g0055 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0287 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03927 | hp1 | a0001 | c0001 | t0041 | g0194 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03927 | hp2 | a0001 | c0002 | t0006 | g0169 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0275 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03942 | hp2 | a0001 | c0001 | t0036 | g0132 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04115 | hp1 | a0001 | c0001 | t0051 | g0262 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04115 | hp2 | a0002 | c0008 | t0008 | g0066 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04184 | hp1 | a0001 | c0002 | t0054 | g0228 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04184 | hp2 | a0001 | c0001 | t0036 | g0151 | SAS | BEB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04199 | hp1 | a0001 | c0001 | t0013 | g0115 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04199 | hp2 | a0001 | c0002 | t0006 | g0233 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04204 | hp2 | a0001 | c0001 | t0064 | g0106 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04228 | hp1 | a0001 | c0002 | t0052 | g0027 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | CHB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0282 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | YRI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18940 | hp2 | a0001 | c0001 | t0009 | g0196 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18945 | hp2 | a0001 | c0001 | t0079 | g0200 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18953 | hp1 | a0001 | c0001 | t0019 | g0112 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18953 | hp2 | a0001 | c0001 | t0040 | g0214 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18957 | hp1 | a0001 | c0001 | t0021 | g0209 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18964 | hp2 | a0001 | c0001 | t0011 | g0165 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18970 | hp2 | a0001 | c0001 | t0063 | g0111 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18975 | hp1 | a0001 | c0001 | t0021 | g0195 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18975 | hp2 | a0001 | c0001 | t0066 | g0092 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18981 | hp2 | a0001 | c0001 | t0011 | g0161 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA18988 | hp2 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19003 | hp1 | a0001 | c0001 | t0072 | g0093 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19004 | hp1 | a0001 | c0001 | t0011 | g0084 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19004 | hp2 | a0001 | c0004 | t0078 | g0178 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19030 | hp2 | a0001 | c0001 | t0077 | g0026 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0174 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19056 | hp2 | a0001 | c0001 | t0071 | g0166 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19058 | hp1 | a0001 | c0006 | t0003 | g0077 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19076 | hp1 | a0001 | c0001 | t0009 | g0213 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19076 | hp2 | a0001 | c0001 | t0039 | g0100 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19078 | hp1 | a0001 | c0001 | t0021 | g0215 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19081 | hp2 | a0001 | c0001 | t0035 | g0098 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19082 | hp1 | a0001 | c0001 | t0019 | g0108 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19082 | hp2 | a0001 | c0009 | t0034 | g0025 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19083 | hp2 | a0001 | c0001 | t0031 | g0237 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19084 | hp1 | a0001 | c0001 | t0040 | g0216 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0212 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19086 | hp1 | a0001 | c0004 | t0039 | g0153 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ASW | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0054 | AFR | ASW | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0155 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20805 | hp1 | a0001 | c0002 | t0008 | g0231 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02486 | hp1 | a0001 | c0001 | t0029 | g0257 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0082 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0036 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG02559 | hp2 | a0001 | c0002 | t0032 | g0063 | AFR | ACB | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03471 | hp1 | a0001 | c0001 | t0028 | g0277 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG03471 | hp2 | a0001 | c0001 | t0049 | g0266 | AFR | MSL | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| HG06807 | hp2 | a0001 | c0001 | t0047 | g0251 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20300 | hp1 | a0001 | c0002 | t0008 | g0230 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | USA | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0135 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| NA21309 | hp2 | a0001 | c0001 | t0042 | g0029 | AFR | LWK | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0243 | REF | REF | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0268 | REF | REF | ERCC8_chr5_60861454_60950070 | ERCC8 | chr5 | 60861454 | 60950070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:60904864 | C | A | 1 | a0002 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.409G>T | p.Val137Leu | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/12 | 471/9414 | 409/1191 | 137/396 | chr5 | 60904864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:60887482 | A | G | 1 | a0001c0004 | 5 | HG02071.hp1 NA18959.hp2 NA19004.hp2 others(2): Show |
synonymous_variant | LOW | c.1080T>C | p.Ala360Ala | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/12 | 1142/9414 | 1080/1191 | 360/396 | chr5 | 60887482 | |||
| chr5:60891081 | G | A | 1 | a0001c0007 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.849C>T | p.Asn283Asn | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/12 | 911/9414 | 849/1191 | 283/396 | chr5 | 60891081 | |||
| chr5:60902507 | A | T | 1 | a0001c0006 | 1 | NA19058.hp1 | splice_region_variant&synonymous_variant | LOW | c.552T>A | p.Gly184Gly | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/12 | 614/9414 | 552/1191 | 184/396 | chr5 | 60902507 | |||
| chr5:60903694 | T | C | 1 | a0001c0005 | 2 | HG02647.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.504A>G | p.Val168Val | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/12 | 566/9414 | 504/1191 | 168/396 | chr5 | 60903694 | |||
| chr5:60904838 | A | G | 2 | a0001c0002 a0002c0008 |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
synonymous_variant | LOW | c.435T>C | p.Tyr145Tyr | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/12 | 497/9414 | 435/1191 | 145/396 | chr5 | 60904838 | |||
| chr5:60918301 | A | G | 1 | a0001c0003 | 6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
synonymous_variant | LOW | c.363T>C | p.Asp121Asp | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/12 | 425/9414 | 363/1191 | 121/396 | chr5 | 60918301 | |||
| chr5:60922137 | T | C | 1 | a0001c0009 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.192A>G | p.Ser64Ser | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/12 | 254/9414 | 192/1191 | 64/396 | chr5 | 60922137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:60866519 | C | T | 1 | a0001c0001t0071 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8096G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 8096 | chr5 | 60866519 | ||||||
| chr5:60866845 | C | T | 1 | a0001c0002t0053 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7770G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7770 | chr5 | 60866845 | ||||||
| chr5:60866856 | T | G | 13 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0016 others(10): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*7759A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7759 | chr5 | 60866856 | ||||||
| chr5:60866903 | G | C | 1 | a0001c0001t0067 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7712C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7712 | chr5 | 60866903 | ||||||
| chr5:60866945 | C | T | 1 | a0001c0001t0082 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7670G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7670 | chr5 | 60866945 | ||||||
| chr5:60867080 | T | C | 84 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(81): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*7535A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 7535 | chr5 | 60867080 | ||||||
| chr5:60867656 | T | C | 4 | a0001c0001t0043 a0001c0003t0024 a0001c0003t0025 others(1): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6959A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6959 | chr5 | 60867656 | ||||||
| chr5:60867689 | T | G | 1 | a0001c0001t0065 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6926A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6926 | chr5 | 60867689 | ||||||
| chr5:60867768 | CAGA | C | 3 | a0001c0003t0024 a0001c0003t0025 a0001c0003t0026 |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6844_*6846delTCT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6844 | chr5 | 60867768 | ||||||
| chr5:60867843 | C | G | 84 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(81): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*6772G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6772 | chr5 | 60867843 | ||||||
| chr5:60867844 | T | C | 1 | a0001c0001t0047 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6771A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6771 | chr5 | 60867844 | ||||||
| chr5:60867903 | G | A | 1 | a0001c0001t0049 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6712C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6712 | chr5 | 60867903 | ||||||
| chr5:60868018 | T | G | 35 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(32): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*6597A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6597 | chr5 | 60868018 | ||||||
| chr5:60868120 | C | T | 1 | a0001c0001t0066 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6495G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6495 | chr5 | 60868120 | ||||||
| chr5:60868141 | T | C | 1 | a0001c0001t0083 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6474A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6474 | chr5 | 60868141 | ||||||
| chr5:60868452 | T | G | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0081 others(1): Show |
21 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6163A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 6163 | chr5 | 60868452 | ||||||
| chr5:60868715 | T | C | 1 | a0001c0001t0028 | 2 | HG02630.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5900A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5900 | chr5 | 60868715 | ||||||
| chr5:60868786 | G | A | 1 | a0001c0002t0056 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5829 | chr5 | 60868786 | ||||||
| chr5:60868857 | A | G | 1 | a0001c0001t0075 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5758T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5758 | chr5 | 60868857 | ||||||
| chr5:60868949 | C | T | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(31): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*5666G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5666 | chr5 | 60868949 | ||||||
| chr5:60868998 | T | G | 1 | a0001c0002t0017 | 4 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5617A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5617 | chr5 | 60868998 | ||||||
| chr5:60869147 | G | A | 7 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0022 others(4): Show |
28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5468C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5468 | chr5 | 60869147 | ||||||
| chr5:60869373 | G | A | 35 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(32): Show |
114 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5242C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5242 | chr5 | 60869373 | ||||||
| chr5:60869412 | T | A | 2 | a0001c0001t0050 a0001c0001t0051 |
2 | HG00099.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5203A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5203 | chr5 | 60869412 | ||||||
| chr5:60869439 | C | T | 1 | a0001c0001t0064 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5176G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5176 | chr5 | 60869439 | ||||||
| chr5:60869494 | T | A | 1 | a0001c0001t0072 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5121A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5121 | chr5 | 60869494 | ||||||
| chr5:60869555 | T | C | 1 | a0001c0001t0043 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5060A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 5060 | chr5 | 60869555 | ||||||
| chr5:60869623 | C | A | 1 | a0001c0001t0073 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4992G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4992 | chr5 | 60869623 | ||||||
| chr5:60869744 | T | C | 1 | a0001c0004t0078 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4871A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4871 | chr5 | 60869744 | ||||||
| chr5:60869819 | AAAGTG | A | 7 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0022 others(4): Show |
28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4791_*4795delCACT others(1): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4791 | chr5 | 60869819 | ||||||
| chr5:60869875 | C | A | 2 | a0001c0001t0012 a0001c0001t0084 |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4740G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4740 | chr5 | 60869875 | ||||||
| chr5:60869960 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4655G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4655 | chr5 | 60869960 | ||||||
| chr5:60870043 | TTCAAGTG others(17): Show |
T | 1 | a0001c0001t0076 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4548_*4571delGAAA others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4548 | chr5 | 60870043 | ||||||
| chr5:60870091 | TAACAA | T | 2 | a0001c0001t0004 a0001c0001t0031 |
16 | HG00673.hp2 HG02004.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4519_*4523delTTGT others(1): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4519 | chr5 | 60870091 | ||||||
| chr5:60870134 | G | T | 1 | a0001c0001t0074 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4481C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4481 | chr5 | 60870134 | ||||||
| chr5:60870298 | A | G | 1 | a0001c0001t0046 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4317T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4317 | chr5 | 60870298 | ||||||
| chr5:60870355 | G | A | 1 | a0001c0002t0033 | 2 | HG00642.hp2 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4260C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4260 | chr5 | 60870355 | ||||||
| chr5:60870360 | C | G | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(26): Show |
101 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4255G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4255 | chr5 | 60870360 | ||||||
| chr5:60870367 | G | A | 1 | a0001c0001t0037 | 2 | HG02615.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4248C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4248 | chr5 | 60870367 | ||||||
| chr5:60870372 | G | A | 6 | a0001c0001t0028 a0001c0001t0043 a0001c0001t0044 others(3): Show |
10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4243C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4243 | chr5 | 60870372 | ||||||
| chr5:60870381 | C | T | 1 | a0001c0001t0060 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4234G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4234 | chr5 | 60870381 | ||||||
| chr5:60870482 | T | TA | 22 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(19): Show |
90 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4132dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | T | TAA | 19 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(16): Show |
49 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4131_*4132dupTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | T | TAAA | 9 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0023 others(6): Show |
24 | HG01167.hp1 HG01891.hp1 HG01928.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4130_*4132dupTTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | T | TAAAA | 6 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0028 others(3): Show |
18 | HG00558.hp2 HG01109.hp1 HG01175.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4129_*4132dupTTTT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | T | TAAAAAAA others(3): Show |
1 | a0001c0003t0025 | 2 | HG01257.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4123_*4132dupTTTT others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | T | TAAAAAAA others(4): Show |
1 | a0001c0003t0026 | 2 | HG01258.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4122_*4132dupTTTT others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4132 | chr5 | 60870482 | ||||||
| chr5:60870482 | TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0044 a0001c0002t0032 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4120_*4132delTTTT others(9): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4120 | chr5 | 60870482 | ||||||
| chr5:60870482 | TAAAAAAA others(7): Show |
T | 7 | a0001c0002t0008 a0001c0002t0016 a0001c0002t0017 others(4): Show |
21 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4119_*4132delTTTT others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4119 | chr5 | 60870482 | ||||||
| chr5:60870523 | G | A | 7 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0022 others(4): Show |
28 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4092C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 4092 | chr5 | 60870523 | ||||||
| chr5:60870618 | C | T | 6 | a0001c0001t0034 a0001c0001t0058 a0001c0001t0059 others(3): Show |
6 | HG01175.hp1 HG01358.hp2 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3997G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3997 | chr5 | 60870618 | ||||||
| chr5:60870619 | G | A | 1 | a0001c0001t0069 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3996C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3996 | chr5 | 60870619 | ||||||
| chr5:60870946 | T | A | 1 | a0001c0001t0043 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3669 | chr5 | 60870946 | ||||||
| chr5:60870972 | G | GA | 7 | a0001c0001t0036 a0001c0001t0038 a0001c0001t0040 others(4): Show |
11 | HG01515.hp1 HG02080.hp2 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3642dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3642 | chr5 | 60870972 | ||||||
| chr5:60870981 | C | A | 6 | a0001c0002t0008 a0001c0002t0017 a0001c0002t0033 others(3): Show |
17 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3634G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3634 | chr5 | 60870981 | ||||||
| chr5:60871082 | C | T | 4 | a0001c0001t0043 a0001c0003t0024 a0001c0003t0025 others(1): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3533G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3533 | chr5 | 60871082 | ||||||
| chr5:60871115 | A | G | 1 | a0001c0001t0002 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3500T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3500 | chr5 | 60871115 | ||||||
| chr5:60871147 | A | G | 1 | a0001c0001t0021 | 3 | NA18957.hp1 NA18975.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3468T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3468 | chr5 | 60871147 | ||||||
| chr5:60871193 | A | C | 84 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(81): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*3422T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3422 | chr5 | 60871193 | ||||||
| chr5:60871380 | C | T | 3 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0083 |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3235G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 3235 | chr5 | 60871380 | ||||||
| chr5:60871855 | T | C | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2760 | chr5 | 60871855 | ||||||
| chr5:60871888 | C | A | 1 | a0001c0001t0049 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2727 | chr5 | 60871888 | ||||||
| chr5:60872061 | A | C | 19 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0019 others(16): Show |
65 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2554T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2554 | chr5 | 60872061 | ||||||
| chr5:60872084 | G | A | 1 | a0001c0001t0014 | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2531C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2531 | chr5 | 60872084 | ||||||
| chr5:60872213 | A | T | 1 | a0001c0001t0062 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2402T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2402 | chr5 | 60872213 | ||||||
| chr5:60872338 | A | C | 64 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(61): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2277 | chr5 | 60872338 | ||||||
| chr5:60872382 | G | T | 1 | a0001c0001t0079 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2233C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 2233 | chr5 | 60872382 | ||||||
| chr5:60872756 | G | A | 3 | a0001c0001t0039 a0001c0004t0039 a0001c0004t0078 |
3 | NA19004.hp2 NA19076.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1859C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1859 | chr5 | 60872756 | ||||||
| chr5:60872810 | G | C | 5 | a0001c0001t0034 a0001c0001t0058 a0001c0001t0059 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1805C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1805 | chr5 | 60872810 | ||||||
| chr5:60872881 | T | C | 2 | a0001c0001t0050 a0001c0001t0051 |
2 | HG00099.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1734A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1734 | chr5 | 60872881 | ||||||
| chr5:60873068 | G | A | 3 | a0001c0001t0034 a0001c0001t0060 a0001c0009t0034 |
3 | HG03486.hp1 HG03516.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1547C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1547 | chr5 | 60873068 | ||||||
| chr5:60873145 | A | G | 13 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0016 others(10): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1470T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1470 | chr5 | 60873145 | ||||||
| chr5:60873210 | T | C | 1 | a0001c0001t0080 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1405A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1405 | chr5 | 60873210 | ||||||
| chr5:60873273 | T | C | 4 | a0001c0001t0043 a0001c0003t0024 a0001c0003t0025 others(1): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1342A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1342 | chr5 | 60873273 | ||||||
| chr5:60873287 | C | T | 84 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(81): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1328 | chr5 | 60873287 | ||||||
| chr5:60873324 | T | C | 13 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0016 others(10): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1291A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1291 | chr5 | 60873324 | ||||||
| chr5:60873445 | C | T | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1170G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1170 | chr5 | 60873445 | ||||||
| chr5:60873472 | C | T | 4 | a0001c0001t0043 a0001c0003t0024 a0001c0003t0025 others(1): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1143G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1143 | chr5 | 60873472 | ||||||
| chr5:60873500 | C | T | 1 | a0001c0001t0029 | 2 | HG02486.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1115G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1115 | chr5 | 60873500 | ||||||
| chr5:60873533 | C | T | 6 | a0001c0001t0028 a0001c0001t0043 a0001c0001t0044 others(3): Show |
10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1082G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1082 | chr5 | 60873533 | ||||||
| chr5:60873578 | T | G | 48 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(45): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1037A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 1037 | chr5 | 60873578 | ||||||
| chr5:60873655 | C | A | 7 | a0001c0001t0012 a0001c0001t0034 a0001c0001t0058 others(4): Show |
12 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*960G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 960 | chr5 | 60873655 | ||||||
| chr5:60873831 | G | A | 1 | a0001c0002t0057 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 784 | chr5 | 60873831 | ||||||
| chr5:60874032 | A | G | 1 | a0001c0001t0027 | 2 | HG02258.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*583T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 583 | chr5 | 60874032 | ||||||
| chr5:60874096 | G | T | 5 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0042 others(2): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*519C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 519 | chr5 | 60874096 | ||||||
| chr5:60874176 | C | A | 10 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0012 others(7): Show |
37 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*439G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 439 | chr5 | 60874176 | ||||||
| chr5:60874378 | A | G | 5 | a0001c0001t0034 a0001c0001t0058 a0001c0001t0059 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*237T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 237 | chr5 | 60874378 | ||||||
| chr5:60874510 | A | G | 34 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0015 others(31): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 105 | chr5 | 60874510 | ||||||
| chr5:60874579 | G | A | 1 | a0001c0001t0014 | 5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 12/12 | 36 | chr5 | 60874579 | ||||||
| chr5:60945031 | A | C | 4 | a0001c0001t0043 a0001c0003t0024 a0001c0003t0025 others(1): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/12 | 23 | chr5 | 60945031 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:60874731 | T | C | 44 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(41): Show |
46 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1123-48A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60874731 | |||||||
| chr5:60874778 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(103): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1123-95A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60874778 | |||||||
| chr5:60875007 | G | C | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1123-324C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875007 | |||||||
| chr5:60875015 | T | C | 4 | a0001c0001t0002g0189 a0001c0001t0002g0191 a0001c0001t0009g0180 others(1): Show |
4 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1123-332A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875015 | |||||||
| chr5:60875150 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-467G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875150 | |||||||
| chr5:60875243 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1123-560A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875243 | |||||||
| chr5:60875340 | C | G | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-657G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875340 | |||||||
| chr5:60875711 | T | C | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1123-1028A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875711 | |||||||
| chr5:60875855 | C | T | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-1172G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875855 | |||||||
| chr5:60875886 | A | C | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-1203T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875886 | |||||||
| chr5:60875893 | C | CT | 48 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(45): Show |
49 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1123-1211dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875893 | |||||||
| chr5:60875893 | C | CTT | 83 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(80): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1123-1212_1123-121 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875893 | |||||||
| chr5:60875937 | G | A | 1 | a0001c0001t0036g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1123-1254C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60875937 | |||||||
| chr5:60876029 | T | C | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1346A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876029 | |||||||
| chr5:60876053 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1123-1370C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876053 | |||||||
| chr5:60876080 | G | C | 90 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1123-1397C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876080 | |||||||
| chr5:60876083 | G | A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-1400C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876083 | |||||||
| chr5:60876341 | C | T | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-1658G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876341 | |||||||
| chr5:60876369 | T | A | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1123-1686A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876369 | |||||||
| chr5:60876392 | C | T | 1 | a0001c0001t0065g0122 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1123-1709G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876392 | |||||||
| chr5:60876547 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1864G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876547 | |||||||
| chr5:60876558 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1875A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876558 | |||||||
| chr5:60876565 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1882G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876565 | |||||||
| chr5:60876566 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1883T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876566 | |||||||
| chr5:60876572 | C | G | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1889G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876572 | |||||||
| chr5:60876583 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1123-1900C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876583 | |||||||
| chr5:60876692 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-2009A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876692 | |||||||
| chr5:60876763 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1123-2080C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876763 | |||||||
| chr5:60876787 | G | C | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2104C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876787 | |||||||
| chr5:60876819 | A | T | 12 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(9): Show |
12 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1123-2136T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876819 | |||||||
| chr5:60876884 | A | G | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123-2201T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876884 | |||||||
| chr5:60876913 | T | G | 90 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1123-2230A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876913 | |||||||
| chr5:60876990 | C | A | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-2307G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60876990 | |||||||
| chr5:60877195 | T | C | 2 | a0001c0001t0037g0182 a0001c0001t0037g0183 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1123-2512A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877195 | |||||||
| chr5:60877219 | G | C | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2536C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877219 | |||||||
| chr5:60877230 | T | A | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1123-2547A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877230 | |||||||
| chr5:60877360 | C | T | 1 | a0001c0001t0012g0173 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1123-2677G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877360 | |||||||
| chr5:60877408 | G | A | 1 | a0001c0001t0079g0200 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1123-2725C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877408 | |||||||
| chr5:60877448 | C | CATGGCAT others(5): Show |
1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2766_1123-276 others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877448 | |||||||
| chr5:60877481 | A | C | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2798T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877481 | |||||||
| chr5:60877482 | C | A | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2799G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877482 | |||||||
| chr5:60877496 | C | A | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2813G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877496 | |||||||
| chr5:60877548 | C | A | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2865G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877548 | |||||||
| chr5:60877551 | T | G | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2868A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877551 | |||||||
| chr5:60877552 | G | T | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2869C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877552 | |||||||
| chr5:60877568 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1123-2885T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877568 | |||||||
| chr5:60877576 | G | A | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2893C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877576 | |||||||
| chr5:60877577 | A | G | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2894T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877577 | |||||||
| chr5:60877580 | A | C | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2897T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877580 | |||||||
| chr5:60877585 | C | T | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2902G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877585 | |||||||
| chr5:60877588 | C | A | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-2905G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877588 | |||||||
| chr5:60877623 | A | G | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1123-2940T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877623 | |||||||
| chr5:60877710 | C | T | 1 | a0001c0001t0041g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1123-3027G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877710 | |||||||
| chr5:60877758 | A | G | 1 | a0001c0001t0019g0114 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1123-3075T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877758 | |||||||
| chr5:60877784 | G | T | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1123-3101C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877784 | |||||||
| chr5:60877792 | A | T | 10 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0043g0018 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1123-3109T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877792 | |||||||
| chr5:60877950 | T | A | 1 | a0001c0001t0049g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1123-3267A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877950 | |||||||
| chr5:60877967 | C | G | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-3284G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60877967 | |||||||
| chr5:60878041 | G | A | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1123-3358C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878041 | |||||||
| chr5:60878164 | C | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 |
3 | NA18939.hp2 NA18962.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1123-3481G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878164 | |||||||
| chr5:60878230 | C | A | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-3547G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878230 | |||||||
| chr5:60878385 | T | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0225 |
3 | NA18963.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1123-3702A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878385 | |||||||
| chr5:60878480 | G | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-3797C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878480 | |||||||
| chr5:60878486 | C | G | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1123-3803G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878486 | |||||||
| chr5:60878502 | G | A | 1 | a0001c0001t0063g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1123-3819C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878502 | |||||||
| chr5:60878507 | T | C | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1123-3824A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878507 | |||||||
| chr5:60878572 | A | T | 2 | a0001c0001t0058g0255 a0001c0001t0059g0256 |
2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1123-3889T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878572 | |||||||
| chr5:60878595 | C | G | 1 | a0001c0001t0029g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1123-3912G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878595 | |||||||
| chr5:60878656 | C | G | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1123-3973G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878656 | |||||||
| chr5:60878716 | T | A | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1123-4033A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878716 | |||||||
| chr5:60878733 | T | TA | 36 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1123-4051_1123-405 others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878733 | |||||||
| chr5:60878875 | C | G | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1123-4192G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878875 | |||||||
| chr5:60878904 | C | T | 1 | a0001c0001t0031g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1123-4221G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878904 | |||||||
| chr5:60878948 | T | C | 36 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1123-4265A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60878948 | |||||||
| chr5:60879146 | G | C | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1123-4463C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879146 | |||||||
| chr5:60879168 | G | T | 38 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(35): Show |
40 | HG00099.hp1 HG00673.hp2 HG01516.hp2 others(37): Show |
intron_variant | MODIFIER | c.1123-4485C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879168 | |||||||
| chr5:60879174 | C | T | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1123-4491G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879174 | |||||||
| chr5:60879180 | T | C | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-4497A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879180 | |||||||
| chr5:60879203 | T | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-4520A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879203 | |||||||
| chr5:60879205 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(102): Show |
111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1123-4522G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879205 | |||||||
| chr5:60879549 | G | C | 1 | a0001c0002t0016g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1123-4866C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879549 | |||||||
| chr5:60879596 | T | C | 1 | a0001c0004t0078g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1123-4913A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879596 | |||||||
| chr5:60879748 | C | G | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-5065G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879748 | |||||||
| chr5:60879896 | G | C | 1 | a0001c0001t0072g0093 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1123-5213C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879896 | |||||||
| chr5:60879907 | G | T | 80 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123-5224C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879907 | |||||||
| chr5:60879919 | T | C | 1 | a0001c0007t0013g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1123-5236A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60879919 | |||||||
| chr5:60880002 | A | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0260 |
3 | NA18968.hp1 NA18973.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1123-5319T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880002 | |||||||
| chr5:60880194 | C | A | 1 | a0001c0001t0031g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1123-5511G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880194 | |||||||
| chr5:60880271 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1123-5588G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880271 | |||||||
| chr5:60880297 | C | T | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-5614G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880297 | |||||||
| chr5:60880317 | C | T | 1 | a0001c0001t0013g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1123-5634G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880317 | |||||||
| chr5:60880372 | T | C | 5 | a0001c0001t0007g0037 a0001c0001t0010g0002 a0001c0001t0010g0034 others(2): Show |
6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-5689A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880372 | |||||||
| chr5:60880401 | A | T | 1 | a0001c0004t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1123-5718T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880401 | |||||||
| chr5:60880409 | C | T | 80 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123-5726G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880409 | |||||||
| chr5:60880507 | A | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(103): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1123-5824T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880507 | |||||||
| chr5:60880536 | C | T | 8 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(5): Show |
8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-5853G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880536 | |||||||
| chr5:60880590 | C | T | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-5907G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880590 | |||||||
| chr5:60880674 | A | G | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1123-5991T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880674 | |||||||
| chr5:60880684 | C | T | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1123-6001G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880684 | |||||||
| chr5:60880721 | C | A | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1123-6038G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880721 | |||||||
| chr5:60880721 | C | T | 44 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(41): Show |
46 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1123-6038G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880721 | |||||||
| chr5:60880725 | A | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1123-6042T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880725 | |||||||
| chr5:60880808 | A | G | 1 | a0001c0001t0060g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1123-6125T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880808 | |||||||
| chr5:60880841 | G | A | 2 | a0001c0001t0001g0125 a0001c0002t0052g0027 |
2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1123-6158C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880841 | |||||||
| chr5:60880865 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-6182G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880865 | |||||||
| chr5:60880940 | C | G | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1123-6257G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880940 | |||||||
| chr5:60880944 | C | G | 12 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0202 others(9): Show |
14 | NA18940.hp2 NA18942.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1123-6261G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880944 | |||||||
| chr5:60880967 | G | T | 6 | a0001c0001t0005g0263 a0001c0001t0018g0057 a0001c0001t0027g0249 others(3): Show |
6 | HG00099.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-6284C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880967 | |||||||
| chr5:60880968 | C | T | 6 | a0001c0001t0005g0263 a0001c0001t0018g0057 a0001c0001t0027g0249 others(3): Show |
6 | HG00099.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123-6285G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60880968 | |||||||
| chr5:60881026 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1123-6343C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881026 | |||||||
| chr5:60881150 | ATCAG | A | 44 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(41): Show |
46 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1122+6286_1122+628 others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881150 | |||||||
| chr5:60881162 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1122+6278T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881162 | |||||||
| chr5:60881192 | A | C | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1122+6248T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881192 | |||||||
| chr5:60881263 | C | G | 1 | a0001c0001t0002g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1122+6177G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881263 | |||||||
| chr5:60881288 | A | G | 2 | a0001c0001t0037g0182 a0001c0001t0037g0183 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1122+6152T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881288 | |||||||
| chr5:60881319 | G | A | 5 | a0001c0001t0014g0079 a0001c0001t0014g0080 a0001c0001t0014g0081 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+6121C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881319 | |||||||
| chr5:60881328 | G | C | 5 | a0001c0001t0014g0079 a0001c0001t0014g0080 a0001c0001t0014g0081 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+6112C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881328 | |||||||
| chr5:60881475 | C | T | 44 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(41): Show |
46 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1122+5965G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881475 | |||||||
| chr5:60881510 | A | T | 1 | a0001c0005t0020g0005 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1122+5930T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881510 | |||||||
| chr5:60881613 | T | C | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+5827A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881613 | |||||||
| chr5:60881624 | T | C | 6 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122+5816A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881624 | |||||||
| chr5:60881642 | C | A | 1 | a0001c0001t0007g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1122+5798G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881642 | |||||||
| chr5:60881643 | G | A | 43 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(40): Show |
44 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.1122+5797C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881643 | |||||||
| chr5:60881663 | C | T | 1 | a0001c0003t0024g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1122+5777G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881663 | |||||||
| chr5:60881700 | C | G | 13 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(10): Show |
14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+5740G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881700 | |||||||
| chr5:60881752 | G | A | 2 | a0001c0001t0034g0044 a0001c0001t0060g0024 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1122+5688C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881752 | |||||||
| chr5:60881785 | A | G | 1 | a0001c0001t0067g0140 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1122+5655T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881785 | |||||||
| chr5:60881794 | C | T | 1 | a0001c0001t0022g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1122+5646G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881794 | |||||||
| chr5:60881796 | C | T | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+5644G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881796 | |||||||
| chr5:60881851 | C | A | 41 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(38): Show |
42 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1122+5589G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881851 | |||||||
| chr5:60881852 | G | A | 2 | a0001c0001t0005g0263 a0001c0001t0018g0057 |
2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1122+5588C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881852 | |||||||
| chr5:60881924 | G | C | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+5516C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881924 | |||||||
| chr5:60881954 | C | T | 2 | a0001c0001t0004g0244 a0001c0001t0004g0265 |
2 | HG00673.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1122+5486G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60881954 | |||||||
| chr5:60882010 | T | G | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+5430A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882010 | |||||||
| chr5:60882031 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1122+5409G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882031 | |||||||
| chr5:60882043 | G | A | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1122+5397C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882043 | |||||||
| chr5:60882260 | G | A | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1122+5180C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882260 | |||||||
| chr5:60882268 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1122+5172T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882268 | |||||||
| chr5:60882301 | G | A | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1122+5139C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882301 | |||||||
| chr5:60882309 | T | A | 7 | a0001c0001t0001g0089 a0001c0001t0039g0100 a0001c0004t0001g0090 others(4): Show |
7 | HG02071.hp1 NA18944.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+5131A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882309 | |||||||
| chr5:60882348 | A | T | 12 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0202 others(9): Show |
14 | NA18940.hp2 NA18942.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+5092T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882348 | |||||||
| chr5:60882462 | T | C | 1 | a0001c0001t0022g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1122+4978A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882462 | |||||||
| chr5:60882662 | C | T | 2 | a0001c0002t0006g0055 a0001c0002t0054g0228 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1122+4778G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882662 | |||||||
| chr5:60882666 | C | T | 5 | a0001c0001t0005g0270 a0001c0001t0014g0080 a0001c0001t0014g0081 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+4774G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882666 | |||||||
| chr5:60882671 | G | C | 1 | a0001c0001t0002g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1122+4769C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882671 | |||||||
| chr5:60882834 | A | C | 1 | a0001c0002t0006g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1122+4606T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882834 | |||||||
| chr5:60882911 | A | G | 1 | a0001c0001t0005g0276 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1122+4529T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882911 | |||||||
| chr5:60882970 | A | AAC | 61 | a0001c0001t0001g0004 a0001c0001t0001g0085 a0001c0001t0001g0117 others(58): Show |
63 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1122+4468_1122+446 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60882970 | A | AACAC | 14 | a0001c0001t0001g0088 a0001c0001t0001g0150 a0001c0001t0002g0191 others(11): Show |
14 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+4466_1122+446 others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60882970 | A | AACACAC | 26 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(23): Show |
27 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1122+4464_1122+446 others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60882970 | A | AACACACA others(1): Show |
9 | a0001c0001t0007g0035 a0001c0001t0007g0038 a0001c0001t0015g0253 others(6): Show |
9 | HG02630.hp1 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+4462_1122+446 others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60882970 | A | AACACACA others(3): Show |
1 | a0001c0001t0023g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1122+4460_1122+446 others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60882970 | AAC | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+4468_1122+446 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60882970 | |||||||
| chr5:60883004 | CAT | C | 3 | a0001c0001t0027g0249 a0001c0001t0027g0250 a0001c0001t0028g0278 |
3 | HG02258.hp1 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1122+4434_1122+443 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883004 | |||||||
| chr5:60883006 | T | C | 90 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1122+4434A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883006 | |||||||
| chr5:60883007 | G | A | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+4433C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883007 | |||||||
| chr5:60883023 | G | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+4417C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883023 | |||||||
| chr5:60883132 | T | A | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1122+4308A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883132 | |||||||
| chr5:60883227 | G | A | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1122+4213C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883227 | |||||||
| chr5:60883319 | G | A | 1 | a0001c0001t0009g0213 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4121C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883319 | |||||||
| chr5:60883320 | T | G | 1 | a0001c0001t0009g0213 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4120A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883320 | |||||||
| chr5:60883321 | A | T | 1 | a0001c0001t0009g0213 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1122+4119T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883321 | |||||||
| chr5:60883335 | T | C | 1 | a0001c0001t0042g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1122+4105A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883335 | |||||||
| chr5:60883468 | T | C | 1 | a0001c0001t0023g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1122+3972A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883468 | |||||||
| chr5:60883474 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(243): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1122+3966T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883474 | |||||||
| chr5:60883491 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1122+3949A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883491 | |||||||
| chr5:60883533 | C | A | 17 | a0001c0002t0008g0058 a0001c0002t0008g0061 a0001c0002t0008g0064 others(14): Show |
17 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1122+3907G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883533 | |||||||
| chr5:60883555 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1122+3885C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60883555 | |||||||
| chr5:60884111 | T | C | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1122+3329A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884111 | |||||||
| chr5:60884173 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+3267G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884173 | |||||||
| chr5:60884250 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0248 a0001c0001t0005g0273 |
4 | HG02886.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+3190G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884250 | |||||||
| chr5:60884252 | G | A | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1122+3188C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884252 | |||||||
| chr5:60884312 | T | C | 1 | a0001c0003t0024g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1122+3128A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884312 | |||||||
| chr5:60884408 | G | A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+3032C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884408 | |||||||
| chr5:60884424 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1122+3016G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884424 | |||||||
| chr5:60884448 | C | A | 1 | a0001c0002t0016g0075 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1122+2992G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884448 | |||||||
| chr5:60884475 | C | CA | 12 | a0001c0001t0002g0041 a0001c0001t0002g0203 a0001c0001t0009g0196 others(9): Show |
12 | HG00621.hp2 HG01099.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1122+2964dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884475 | |||||||
| chr5:60884475 | CA | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(185): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1122+2964delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884475 | |||||||
| chr5:60884487 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1122+2953T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884487 | |||||||
| chr5:60884523 | G | GT | 52 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(49): Show |
54 | HG00099.hp1 HG00673.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.1122+2916dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | |||||||
| chr5:60884523 | G | GTTT | 30 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(27): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122+2914_1122+291 others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | |||||||
| chr5:60884523 | GT | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(98): Show |
107 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1122+2916delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884523 | |||||||
| chr5:60884532 | T | G | 1 | a0001c0001t0014g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1122+2908A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884532 | |||||||
| chr5:60884647 | C | T | 22 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(19): Show |
23 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.1122+2793G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884647 | |||||||
| chr5:60884786 | T | C | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122+2654A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60884786 | |||||||
| chr5:60885014 | CT | C | 48 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(45): Show |
49 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1122+2425delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885014 | |||||||
| chr5:60885039 | A | ACAGGTGA others(4): Show |
4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+2400_1122+240 others(15): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885039 | |||||||
| chr5:60885040 | T | A | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122+2400A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885040 | |||||||
| chr5:60885107 | G | C | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1122+2333C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885107 | |||||||
| chr5:60885155 | G | C | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+2285C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885155 | |||||||
| chr5:60885221 | G | A | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+2219C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885221 | |||||||
| chr5:60885307 | C | A | 90 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1122+2133G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885307 | |||||||
| chr5:60885419 | G | T | 1 | a0001c0001t0039g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1122+2021C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885419 | |||||||
| chr5:60885613 | T | C | 1 | a0001c0001t0003g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1122+1827A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885613 | |||||||
| chr5:60885673 | T | C | 80 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1122+1767A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885673 | |||||||
| chr5:60885779 | T | C | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+1661A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885779 | |||||||
| chr5:60885861 | G | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+1579C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60885861 | |||||||
| chr5:60886066 | G | GTA | 36 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(33): Show |
38 | HG00099.hp1 HG00673.hp2 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.1122+1372_1122+137 others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886066 | |||||||
| chr5:60886182 | T | C | 1 | a0001c0002t0006g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1122+1258A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886182 | |||||||
| chr5:60886395 | G | A | 119 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1122+1045C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886395 | |||||||
| chr5:60886470 | G | C | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1122+970C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886470 | |||||||
| chr5:60886497 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(116): Show |
125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1122+943A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886497 | |||||||
| chr5:60886571 | G | A | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+869C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886571 | |||||||
| chr5:60886573 | G | A | 1 | a0001c0001t0031g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1122+867C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886573 | |||||||
| chr5:60886651 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1122+789T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886651 | |||||||
| chr5:60886687 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1122+753A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886687 | |||||||
| chr5:60886703 | A | AAAAAAT | 52 | a0001c0001t0002g0184 a0001c0001t0002g0198 a0001c0001t0004g0226 others(49): Show |
54 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1122+731_1122+736d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | |||||||
| chr5:60886703 | A | AAAAAATA others(5): Show |
25 | a0001c0001t0005g0261 a0001c0001t0007g0020 a0001c0001t0007g0021 others(22): Show |
26 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1122+725_1122+736d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | |||||||
| chr5:60886703 | AAAAAAT | A | 15 | a0001c0001t0004g0010 a0001c0001t0004g0236 a0001c0001t0004g0238 others(12): Show |
16 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1122+731_1122+736d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | |||||||
| chr5:60886703 | AAAAAATA others(5): Show |
A | 9 | a0001c0001t0001g0089 a0001c0001t0012g0172 a0001c0001t0012g0173 others(6): Show |
9 | HG02257.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+725_1122+736d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886703 | |||||||
| chr5:60886881 | T | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122+559A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886881 | |||||||
| chr5:60886893 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1122+547G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886893 | |||||||
| chr5:60886970 | T | G | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1122+470A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886970 | |||||||
| chr5:60886984 | G | T | 5 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(2): Show |
5 | HG01109.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122+456C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60886984 | |||||||
| chr5:60887061 | C | A | 3 | a0001c0001t0007g0035 a0001c0001t0007g0038 a0001c0001t0007g0286 |
3 | HG02280.hp2 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+379G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60887061 | |||||||
| chr5:60887247 | C | T | 11 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(8): Show |
11 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1122+193G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 11/11 | chr5 | 60887247 | |||||||
| chr5:60887717 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-197A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60887717 | |||||||
| chr5:60887847 | G | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042-327C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60887847 | |||||||
| chr5:60888402 | T | C | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-882A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888402 | |||||||
| chr5:60888561 | T | A | 1 | a0001c0001t0060g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1042-1041A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888561 | |||||||
| chr5:60888591 | T | G | 1 | a0001c0001t0010g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1042-1071A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888591 | |||||||
| chr5:60888701 | T | A | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-1181A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888701 | |||||||
| chr5:60888730 | T | A | 2 | a0001c0001t0001g0101 a0001c0001t0065g0122 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1042-1210A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888730 | |||||||
| chr5:60888762 | C | T | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1042-1242G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60888762 | |||||||
| chr5:60889029 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1042-1509T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889029 | |||||||
| chr5:60889029 | A | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-1509T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889029 | |||||||
| chr5:60889069 | C | T | 11 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(8): Show |
11 | HG01175.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1042-1549G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889069 | |||||||
| chr5:60889429 | C | A | 1 | a0001c0004t0001g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1041+1460G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889429 | |||||||
| chr5:60889456 | C | T | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1041+1433G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889456 | |||||||
| chr5:60889519 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1370A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889519 | |||||||
| chr5:60889598 | G | A | 90 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(87): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1041+1291C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889598 | |||||||
| chr5:60889670 | T | C | 1 | a0001c0001t0014g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1041+1219A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889670 | |||||||
| chr5:60889955 | C | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(283): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1041+934G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60889955 | |||||||
| chr5:60890005 | C | A | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1041+884G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890005 | |||||||
| chr5:60890425 | A | T | 3 | a0001c0002t0016g0060 a0001c0002t0016g0067 a0001c0002t0016g0071 |
3 | HG02145.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1041+464T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890425 | |||||||
| chr5:60890517 | CCA | C | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+370_1041+371d others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890517 | |||||||
| chr5:60890523 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1041+366T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890523 | |||||||
| chr5:60890667 | C | T | 1 | a0001c0002t0016g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1041+222G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890667 | |||||||
| chr5:60890791 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1041+98G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 10/11 | chr5 | 60890791 | |||||||
| chr5:60891148 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.844-62G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891148 | |||||||
| chr5:60891385 | G | A | 4 | a0001c0001t0058g0255 a0001c0001t0059g0256 a0001c0001t0060g0024 others(1): Show |
4 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-299C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891385 | |||||||
| chr5:60891394 | T | A | 4 | a0001c0001t0003g0043 a0001c0001t0003g0076 a0001c0001t0003g0078 others(1): Show |
4 | NA18612.hp2 NA18945.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-308A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891394 | |||||||
| chr5:60891442 | T | C | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-356A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891442 | |||||||
| chr5:60891469 | T | C | 1 | a0001c0001t0011g0165 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-383A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891469 | |||||||
| chr5:60891653 | G | C | 1 | a0001c0002t0057g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.844-567C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891653 | |||||||
| chr5:60891662 | C | CT | 94 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(91): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.844-577dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891662 | |||||||
| chr5:60891662 | CT | C | 33 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(30): Show |
34 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-577delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60891662 | |||||||
| chr5:60892115 | C | A | 1 | a0001c0001t0020g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.844-1029G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892115 | |||||||
| chr5:60892140 | G | GT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(102): Show |
111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.844-1055dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892140 | |||||||
| chr5:60892245 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0164 |
2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.844-1159G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892245 | |||||||
| chr5:60892395 | C | T | 91 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(88): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.844-1309G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892395 | |||||||
| chr5:60892443 | G | A | 7 | a0001c0002t0008g0070 a0001c0002t0008g0074 a0001c0002t0033g0059 others(4): Show |
7 | HG00642.hp2 HG01069.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-1357C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892443 | |||||||
| chr5:60892492 | C | T | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.844-1406G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892492 | |||||||
| chr5:60892663 | C | T | 1 | a0001c0009t0034g0025 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.844-1577G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892663 | |||||||
| chr5:60892771 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0164 |
2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.844-1685C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892771 | |||||||
| chr5:60892921 | G | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-1835C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60892921 | |||||||
| chr5:60893199 | G | C | 45 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(42): Show |
47 | HG00099.hp1 HG00673.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.844-2113C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893199 | |||||||
| chr5:60893479 | C | A | 2 | a0001c0001t0002g0204 a0001c0001t0009g0213 |
2 | NA19076.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.844-2393G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893479 | |||||||
| chr5:60893716 | C | A | 1 | a0001c0005t0020g0005 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.844-2630G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893716 | |||||||
| chr5:60893760 | G | A | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-2674C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893760 | |||||||
| chr5:60893984 | CT | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(232): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.844-2899delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60893984 | |||||||
| chr5:60894001 | T | C | 6 | a0001c0001t0005g0011 a0001c0001t0005g0248 a0001c0001t0005g0261 others(3): Show |
7 | HG02145.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-2915A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894001 | |||||||
| chr5:60894070 | C | T | 22 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(19): Show |
23 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.844-2984G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894070 | |||||||
| chr5:60894108 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.844-3022G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894108 | |||||||
| chr5:60894135 | C | T | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.844-3049G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894135 | |||||||
| chr5:60894197 | G | A | 1 | a0001c0001t0022g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.844-3111C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894197 | |||||||
| chr5:60894250 | C | A | 1 | a0001c0001t0003g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.844-3164G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894250 | |||||||
| chr5:60894498 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0038g0154 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.844-3412C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894498 | |||||||
| chr5:60894579 | T | C | 1 | a0001c0001t0007g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844-3493A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894579 | |||||||
| chr5:60894603 | G | GA | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-3518dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894603 | |||||||
| chr5:60894767 | A | G | 36 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.843+3509T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894767 | |||||||
| chr5:60894791 | G | A | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0041g0194 |
3 | HG03490.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.843+3485C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894791 | |||||||
| chr5:60894937 | G | A | 9 | a0001c0001t0003g0138 a0001c0001t0003g0146 a0001c0001t0003g0147 others(6): Show |
9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+3339C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894937 | |||||||
| chr5:60894952 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.843+3324G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60894952 | |||||||
| chr5:60895011 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843+3265T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895011 | |||||||
| chr5:60895169 | C | CA | 15 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0150 others(12): Show |
15 | HG01981.hp2 HG02004.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.843+3106dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895169 | |||||||
| chr5:60895169 | CA | C | 148 | a0001c0001t0001g0125 a0001c0001t0002g0006 a0001c0001t0002g0007 others(145): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.843+3106delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895169 | |||||||
| chr5:60895368 | C | A | 1 | a0001c0001t0063g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.843+2908G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895368 | |||||||
| chr5:60895633 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+2643T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895633 | |||||||
| chr5:60895892 | T | C | 1 | a0001c0001t0043g0018 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.843+2384A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895892 | |||||||
| chr5:60895977 | A | ATTTCT | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.843+2294_843+2298d others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60895977 | |||||||
| chr5:60896007 | C | T | 4 | a0001c0001t0012g0172 a0001c0001t0012g0174 a0001c0001t0012g0176 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+2269G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896007 | |||||||
| chr5:60896075 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+2201G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896075 | |||||||
| chr5:60896279 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+1997G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896279 | |||||||
| chr5:60896377 | A | AT | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.843+1898dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896377 | |||||||
| chr5:60896442 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(102): Show |
111 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.843+1834G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896442 | |||||||
| chr5:60896500 | G | A | 1 | a0001c0002t0052g0027 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.843+1776C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896500 | |||||||
| chr5:60896537 | T | G | 1 | a0001c0003t0025g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.843+1739A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896537 | |||||||
| chr5:60896630 | G | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+1646C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896630 | |||||||
| chr5:60896716 | T | C | 1 | a0001c0001t0048g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.843+1560A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896716 | |||||||
| chr5:60896828 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.843+1448T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896828 | |||||||
| chr5:60896840 | T | C | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.843+1436A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896840 | |||||||
| chr5:60896926 | C | G | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.843+1350G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896926 | |||||||
| chr5:60896941 | T | C | 1 | a0001c0001t0015g0252 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843+1335A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60896941 | |||||||
| chr5:60897253 | G | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+1023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897253 | |||||||
| chr5:60897440 | G | C | 2 | a0001c0001t0004g0238 a0001c0001t0004g0240 |
2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.843+836C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897440 | |||||||
| chr5:60897469 | A | G | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+807T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897469 | |||||||
| chr5:60897511 | A | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+765T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897511 | |||||||
| chr5:60897512 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.843+764A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897512 | |||||||
| chr5:60897527 | A | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+749T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897527 | |||||||
| chr5:60897566 | G | A | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.843+710C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897566 | |||||||
| chr5:60897593 | A | C | 40 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(37): Show |
41 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.843+683T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897593 | |||||||
| chr5:60897951 | T | A | 1 | a0001c0009t0034g0025 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.843+325A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60897951 | |||||||
| chr5:60898003 | T | C | 1 | a0001c0001t0069g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.843+273A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60898003 | |||||||
| chr5:60898269 | C | T | 1 | a0001c0001t0007g0286 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.843+7G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 9/11 | chr5 | 60898269 | |||||||
| chr5:60898649 | G | A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.719-249C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898649 | |||||||
| chr5:60898742 | C | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-342G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898742 | |||||||
| chr5:60898795 | G | A | 1 | a0001c0001t0084g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.719-395C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | |||||||
| chr5:60898795 | G | GA | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(221): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.719-396dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | |||||||
| chr5:60898795 | G | GAA | 10 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(7): Show |
10 | HG01175.hp1 HG02622.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.719-397_719-396dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898795 | |||||||
| chr5:60898842 | A | G | 1 | a0001c0001t0045g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.719-442T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898842 | |||||||
| chr5:60898842 | A | T | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.719-442T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60898842 | |||||||
| chr5:60899024 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.718+603A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899024 | |||||||
| chr5:60899178 | A | G | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+449T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899178 | |||||||
| chr5:60899408 | T | G | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.718+219A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899408 | |||||||
| chr5:60899480 | T | C | 1 | a0001c0002t0006g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.718+147A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899480 | |||||||
| chr5:60899544 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.718+83G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 8/11 | chr5 | 60899544 | |||||||
| chr5:60899792 | C | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-65G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899792 | |||||||
| chr5:60899792 | C | T | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.618-65G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899792 | |||||||
| chr5:60899933 | A | C | 4 | a0001c0001t0012g0172 a0001c0001t0012g0174 a0001c0001t0012g0176 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-206T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899933 | |||||||
| chr5:60899950 | C | T | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-223G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60899950 | |||||||
| chr5:60900187 | T | C | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-460A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900187 | |||||||
| chr5:60900383 | G | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-656C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900383 | |||||||
| chr5:60900401 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-674G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900401 | |||||||
| chr5:60900448 | G | A | 5 | a0001c0001t0007g0037 a0001c0001t0010g0002 a0001c0001t0010g0034 others(2): Show |
6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-721C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900448 | |||||||
| chr5:60900538 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(246): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.618-811A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900538 | |||||||
| chr5:60900605 | C | T | 36 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.618-878G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900605 | |||||||
| chr5:60900884 | A | C | 1 | a0001c0002t0006g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.618-1157T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60900884 | |||||||
| chr5:60901111 | GTAA | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+1328_617+1330d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901111 | |||||||
| chr5:60901252 | C | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+1190G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901252 | |||||||
| chr5:60901273 | T | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.617+1169A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901273 | |||||||
| chr5:60901306 | A | C | 1 | a0001c0002t0006g0052 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.617+1136T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901306 | |||||||
| chr5:60901570 | C | G | 1 | a0001c0001t0073g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.617+872G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901570 | |||||||
| chr5:60901888 | C | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.617+554G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901888 | |||||||
| chr5:60901895 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.617+547A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901895 | |||||||
| chr5:60901963 | AT | A | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+478delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60901963 | |||||||
| chr5:60902020 | T | C | 2 | a0001c0001t0004g0238 a0001c0001t0004g0240 |
2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.617+422A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902020 | |||||||
| chr5:60902199 | A | T | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+243T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902199 | |||||||
| chr5:60902246 | G | A | 1 | a0001c0001t0005g0273 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.617+196C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 7/11 | chr5 | 60902246 | |||||||
| chr5:60902610 | T | A | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.551-102A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902610 | |||||||
| chr5:60902686 | G | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-178C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902686 | |||||||
| chr5:60902885 | A | G | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.551-377T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60902885 | |||||||
| chr5:60903080 | GCTAT | G | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.550+564_550+567del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903080 | |||||||
| chr5:60903374 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.550+274G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903374 | |||||||
| chr5:60903536 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.550+112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903536 | |||||||
| chr5:60903556 | A | G | 2 | a0001c0003t0025g0014 a0001c0003t0026g0015 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.550+92T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 6/11 | chr5 | 60903556 | |||||||
| chr5:60903913 | G | C | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-197C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60903913 | |||||||
| chr5:60903919 | T | A | 1 | a0001c0001t0004g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.482-203A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60903919 | |||||||
| chr5:60904373 | C | A | 1 | a0001c0001t0042g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.481+419G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904373 | |||||||
| chr5:60904439 | T | G | 1 | a0001c0001t0079g0200 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.481+353A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904439 | |||||||
| chr5:60904621 | A | AGT | 3 | a0001c0001t0015g0275 a0001c0001t0018g0271 a0001c0001t0028g0278 |
3 | HG01167.hp1 HG02630.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.481+169_481+170dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | |||||||
| chr5:60904621 | AGT | A | 29 | a0001c0001t0001g0097 a0001c0001t0001g0110 a0001c0001t0001g0141 others(26): Show |
30 | HG00280.hp2 HG00738.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.481+169_481+170del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | |||||||
| chr5:60904621 | AGTGT | A | 17 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0224 others(14): Show |
17 | HG01074.hp2 HG01168.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.481+167_481+170del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | |||||||
| chr5:60904621 | AGTGTGT | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0120 others(10): Show |
16 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+165_481+170del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904621 | |||||||
| chr5:60904622 | G | T | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+170C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904622 | |||||||
| chr5:60904623 | T | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+169A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904623 | |||||||
| chr5:60904628 | G | GTA | 3 | a0001c0001t0001g0101 a0001c0001t0003g0168 a0001c0001t0013g0115 |
3 | HG01433.hp1 HG04199.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.481+163_481+164ins others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(1): Show |
G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0123 others(15): Show |
19 | HG01256.hp1 HG01258.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.481+156_481+163del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(3): Show |
G | 16 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0105 others(13): Show |
16 | HG00639.hp1 HG02071.hp1 HG03486.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+154_481+163del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(5): Show |
G | 10 | a0001c0001t0001g0102 a0001c0001t0001g0107 a0001c0001t0001g0119 others(7): Show |
10 | HG02080.hp1 HG02523.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+152_481+163del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(7): Show |
G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0003g0158 others(6): Show |
10 | HG00673.hp1 HG02132.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+150_481+163del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(9): Show |
G | 7 | a0001c0001t0007g0023 a0001c0001t0022g0280 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+148_481+163del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0007g0223 a0001c0001t0042g0029 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481+146_481+163del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(13): Show |
G | 3 | a0001c0001t0007g0021 a0001c0001t0010g0022 a0001c0001t0042g0042 |
3 | HG01361.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481+144_481+163del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(15): Show |
G | 5 | a0001c0001t0007g0035 a0001c0001t0007g0038 a0001c0001t0007g0286 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+142_481+163del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(17): Show |
G | 12 | a0001c0001t0007g0020 a0001c0001t0007g0028 a0001c0001t0007g0031 others(9): Show |
13 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.481+140_481+163del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(23): Show |
G | 4 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0060g0024 others(1): Show |
4 | HG02735.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+134_481+163del others(30): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904628 | GTGTGTGT others(27): Show |
G | 1 | a0001c0001t0059g0256 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.481+130_481+163del others(34): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904628 | |||||||
| chr5:60904630 | G | A | 8 | a0001c0001t0001g0101 a0001c0001t0003g0168 a0001c0001t0011g0084 others(5): Show |
8 | HG01433.hp1 HG02056.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+162C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | G | GTA | 3 | a0001c0001t0002g0006 a0001c0001t0002g0188 a0001c0001t0002g0192 |
3 | HG00639.hp2 HG03490.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.481+161_481+162ins others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTA | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0199 a0001c0001t0002g0221 others(1): Show |
4 | HG02683.hp1 NA19064.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+161del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTAT others(1): Show |
G | 9 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0002g0208 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+154_481+161del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0002g0007 a0001c0001t0009g0212 |
3 | NA18942.hp2 NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.481+152_481+161del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTAT others(5): Show |
G | 2 | a0001c0001t0002g0203 a0001c0001t0021g0195 |
2 | HG00621.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.481+150_481+161del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTAT others(17): Show |
G | 1 | a0001c0007t0013g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.481+138_481+161del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904630 | GTGTGTAT others(23): Show |
G | 1 | a0001c0001t0002g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.481+132_481+161del others(30): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904630 | |||||||
| chr5:60904632 | G | A | 36 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0110 others(33): Show |
36 | HG00280.hp2 HG00639.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.481+160C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | |||||||
| chr5:60904632 | GTGTA | G | 3 | a0001c0001t0002g0191 a0001c0001t0003g0009 a0001c0001t0003g0225 |
4 | HG00140.hp2 NA18963.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+159del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | |||||||
| chr5:60904632 | GTGTATA | G | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0009g0179 |
3 | HG00735.hp2 HG01074.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.481+154_481+159del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | |||||||
| chr5:60904632 | GTGTATAT others(21): Show |
G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+132_481+159del others(28): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | |||||||
| chr5:60904632 | GTGTATAT others(29): Show |
G | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+124_481+159del others(36): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904632 | |||||||
| chr5:60904634 | G | A | 58 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0110 others(55): Show |
59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.481+158C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | G | GTA | 3 | a0001c0001t0005g0241 a0001c0002t0006g0169 a0001c0002t0054g0228 |
3 | HG02451.hp2 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.481+156_481+157dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | G | GTATA | 3 | a0001c0001t0005g0248 a0001c0001t0005g0270 a0001c0002t0006g0055 |
3 | HG01884.hp1 HG02922.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.481+154_481+157dup others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | G | GTATATAT others(3): Show |
1 | a0001c0001t0018g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.481+148_481+157dup others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | G | GTATATAT others(5): Show |
2 | a0001c0001t0005g0011 a0001c0001t0027g0249 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.481+146_481+157dup others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0005g0011 a0001c0001t0005g0276 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.481+157_481+158ins others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTA | G | 4 | a0001c0001t0015g0253 a0001c0001t0015g0254 a0001c0001t0028g0277 others(1): Show |
4 | HG01192.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+156_481+157del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATA | G | 4 | a0001c0001t0045g0245 a0001c0001t0046g0269 a0001c0002t0006g0052 others(1): Show |
4 | HG00642.hp1 HG01255.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+152_481+157del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(1): Show |
G | 5 | a0001c0001t0029g0257 a0001c0002t0006g0049 a0001c0002t0006g0050 others(2): Show |
5 | HG00280.hp1 HG01496.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+150_481+157del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(3): Show |
G | 3 | a0001c0002t0006g0003 a0001c0002t0006g0233 a0001c0002t0008g0070 |
4 | HG01069.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+148_481+157del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(5): Show |
G | 2 | a0001c0002t0016g0067 a0001c0002t0052g0027 |
2 | HG02809.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.481+146_481+157del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(7): Show |
G | 5 | a0001c0002t0008g0072 a0001c0002t0016g0060 a0001c0002t0017g0229 others(2): Show |
5 | HG00140.hp1 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+144_481+157del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(9): Show |
G | 13 | a0001c0002t0008g0058 a0001c0002t0008g0061 a0001c0002t0008g0064 others(10): Show |
13 | HG00642.hp2 HG00738.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.481+142_481+157del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(11): Show |
G | 2 | a0001c0002t0016g0075 a0001c0002t0032g0063 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.481+140_481+157del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(15): Show |
G | 3 | a0001c0001t0004g0240 a0001c0001t0018g0242 a0001c0002t0017g0065 |
3 | HG01175.hp2 HG02004.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.481+136_481+157del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(17): Show |
G | 14 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(11): Show |
15 | HG00673.hp2 HG02132.hp2 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.481+134_481+157del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904634 | GTATATAT others(29): Show |
G | 1 | a0001c0001t0029g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+122_481+157del others(36): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904634 | |||||||
| chr5:60904636 | A | G | 1 | a0001c0001t0028g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.481+156T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904636 | |||||||
| chr5:60904638 | A | G | 1 | a0001c0001t0028g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+154T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904638 | |||||||
| chr5:60904658 | A | G | 1 | a0001c0001t0018g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.481+134T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904658 | |||||||
| chr5:60904666 | A | G | 1 | a0001c0001t0009g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481+126T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904666 | |||||||
| chr5:60904668 | A | G | 1 | a0001c0001t0009g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481+124T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904668 | |||||||
| chr5:60904683 | T | A | 1 | a0001c0001t0002g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.481+109A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904683 | |||||||
| chr5:60904685 | A | T | 1 | a0001c0004t0001g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481+107T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 5/11 | chr5 | 60904685 | |||||||
| chr5:60904915 | T | C | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-42A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60904915 | |||||||
| chr5:60904929 | T | A | 1 | a0001c0001t0002g0218 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.400-56A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60904929 | |||||||
| chr5:60905029 | A | T | 4 | a0001c0003t0025g0014 a0001c0003t0025g0017 a0001c0003t0026g0015 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-156T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905029 | |||||||
| chr5:60905166 | G | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-293C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905166 | |||||||
| chr5:60905285 | TTTCAG | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(116): Show |
125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.400-417_400-413del others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905285 | |||||||
| chr5:60905300 | A | G | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.400-427T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905300 | |||||||
| chr5:60905498 | T | C | 4 | a0001c0001t0020g0135 a0001c0001t0037g0182 a0001c0001t0037g0183 others(1): Show |
5 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-625A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905498 | |||||||
| chr5:60905877 | G | A | 2 | a0001c0002t0033g0059 a0001c0002t0033g0232 |
2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.400-1004C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905877 | |||||||
| chr5:60905888 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.400-1015A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905888 | |||||||
| chr5:60905950 | C | G | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.400-1077G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905950 | |||||||
| chr5:60905953 | C | G | 2 | a0001c0001t0039g0100 a0001c0004t0039g0153 |
2 | NA19076.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.400-1080G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60905953 | |||||||
| chr5:60906076 | C | T | 1 | a0001c0002t0006g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.400-1203G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906076 | |||||||
| chr5:60906163 | T | C | 1 | a0001c0001t0023g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-1290A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906163 | |||||||
| chr5:60906217 | G | A | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400-1344C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906217 | |||||||
| chr5:60906350 | T | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-1477A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906350 | |||||||
| chr5:60906418 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400-1545C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906418 | |||||||
| chr5:60906420 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(103): Show |
112 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.400-1547T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906420 | |||||||
| chr5:60906587 | G | T | 1 | a0001c0001t0014g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-1714C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906587 | |||||||
| chr5:60906710 | C | T | 1 | a0001c0001t0065g0122 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.400-1837G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906710 | |||||||
| chr5:60906730 | AAAAT | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.400-1861_400-1858d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906730 | |||||||
| chr5:60906758 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.400-1885A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906758 | |||||||
| chr5:60906812 | A | G | 1 | a0001c0001t0071g0166 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.400-1939T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906812 | |||||||
| chr5:60906912 | T | C | 9 | a0001c0001t0003g0138 a0001c0001t0003g0146 a0001c0001t0003g0147 others(6): Show |
9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-2039A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60906912 | |||||||
| chr5:60907029 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.400-2156A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907029 | |||||||
| chr5:60907079 | A | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.400-2206T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907079 | |||||||
| chr5:60907150 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400-2277G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907150 | |||||||
| chr5:60907168 | C | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-2295G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907168 | |||||||
| chr5:60907186 | A | G | 1 | a0001c0001t0013g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.400-2313T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907186 | |||||||
| chr5:60907303 | C | T | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-2430G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907303 | |||||||
| chr5:60907355 | C | CT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.400-2483dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907355 | |||||||
| chr5:60907355 | C | CTTT | 28 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(25): Show |
29 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.400-2485_400-2483d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907355 | |||||||
| chr5:60907387 | C | G | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.400-2514G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907387 | |||||||
| chr5:60907388 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0133 |
2 | NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.400-2515A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907388 | |||||||
| chr5:60907513 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0119 others(1): Show |
4 | NA18973.hp1 NA19054.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-2640G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907513 | |||||||
| chr5:60907532 | T | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-2659A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907532 | |||||||
| chr5:60907543 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.400-2670T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907543 | |||||||
| chr5:60907640 | A | T | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400-2767T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60907640 | |||||||
| chr5:60908310 | C | A | 1 | a0001c0001t0045g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.400-3437G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908310 | |||||||
| chr5:60908359 | G | C | 6 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-3486C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908359 | |||||||
| chr5:60908391 | A | G | 1 | a0001c0001t0074g0046 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.400-3518T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908391 | |||||||
| chr5:60908533 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0011g0127 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.400-3660G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908533 | |||||||
| chr5:60908564 | C | CAT | 3 | a0001c0001t0059g0256 a0001c0002t0017g0229 a0001c0002t0052g0027 |
3 | HG01099.hp1 HG01175.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.400-3693_400-3692d others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908564 | |||||||
| chr5:60908564 | C | CATAT | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-3695_400-3692d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908564 | |||||||
| chr5:60908579 | A | AT | 7 | a0001c0001t0001g0120 a0001c0001t0022g0280 a0001c0001t0022g0283 others(4): Show |
7 | HG01256.hp2 HG02071.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-3707dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908579 | |||||||
| chr5:60908581 | A | AT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(56): Show |
64 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.400-3709dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | |||||||
| chr5:60908581 | A | ATT | 6 | a0001c0001t0002g0191 a0001c0001t0034g0044 a0001c0001t0058g0255 others(3): Show |
6 | HG00140.hp2 HG02735.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-3709_400-3708i others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | |||||||
| chr5:60908581 | A | ATTT | 34 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0041 others(31): Show |
36 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.400-3709_400-3708i others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | |||||||
| chr5:60908581 | A | T | 8 | a0001c0001t0001g0120 a0001c0001t0022g0280 a0001c0001t0022g0283 others(5): Show |
8 | HG01256.hp2 HG02071.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-3708T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908581 | |||||||
| chr5:60908583 | A | AT | 36 | a0001c0001t0001g0117 a0001c0001t0001g0157 a0001c0001t0003g0009 others(33): Show |
37 | HG00280.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.400-3711dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | |||||||
| chr5:60908583 | A | ATTTT | 11 | a0001c0001t0002g0008 a0001c0001t0002g0202 a0001c0001t0002g0208 others(8): Show |
12 | HG03710.hp2 NA18940.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.400-3714_400-3711d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | |||||||
| chr5:60908583 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(114): Show |
124 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.400-3710T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908583 | |||||||
| chr5:60908584 | T | TA | 24 | a0001c0001t0001g0118 a0001c0001t0003g0162 a0001c0001t0003g0163 others(21): Show |
25 | HG01074.hp2 HG01255.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.400-3712_400-3711i others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908584 | |||||||
| chr5:60908585 | T | A | 4 | a0001c0001t0005g0270 a0001c0001t0018g0057 a0001c0001t0018g0271 others(1): Show |
4 | HG01167.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-3712A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908585 | |||||||
| chr5:60908586 | T | A | 12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(9): Show |
12 | HG01361.hp1 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-3713A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908586 | |||||||
| chr5:60908649 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.400-3776G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908649 | |||||||
| chr5:60908676 | G | C | 1 | a0001c0002t0056g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400-3803C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908676 | |||||||
| chr5:60908696 | AG | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-3824delC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908696 | |||||||
| chr5:60908704 | CATT | C | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.400-3834_400-3832d others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908704 | |||||||
| chr5:60908759 | T | A | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-3886A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908759 | |||||||
| chr5:60908769 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-3896G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908769 | |||||||
| chr5:60908891 | A | T | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4018T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908891 | |||||||
| chr5:60908900 | T | C | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.400-4027A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60908900 | |||||||
| chr5:60909094 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0119 |
2 | NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.400-4221A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909094 | |||||||
| chr5:60909114 | T | A | 1 | a0001c0001t0005g0273 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.400-4241A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909114 | |||||||
| chr5:60909196 | A | G | 4 | a0001c0001t0001g0101 a0001c0001t0013g0103 a0001c0001t0035g0104 others(1): Show |
4 | HG01433.hp1 HG01928.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4323T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909196 | |||||||
| chr5:60909243 | G | GAAAAAAA others(1): Show |
13 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0235 others(10): Show |
13 | HG01517.hp2 HG02004.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-4378_400-4371d others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(2): Show |
5 | a0001c0001t0004g0010 a0001c0001t0004g0239 a0001c0001t0004g0265 others(2): Show |
6 | HG00673.hp2 HG01361.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-4379_400-4371d others(11): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(3): Show |
3 | a0001c0001t0007g0223 a0001c0001t0010g0033 a0001c0001t0027g0249 |
3 | HG02258.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.400-4380_400-4371d others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(4): Show |
12 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0031 others(9): Show |
13 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-4381_400-4371d others(13): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(5): Show |
4 | a0001c0001t0007g0023 a0001c0001t0007g0037 a0001c0001t0007g0038 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-4382_400-4371d others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(6): Show |
1 | a0001c0001t0010g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.400-4383_400-4371d others(15): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAAAAAA others(9): Show |
2 | a0001c0001t0007g0028 a0001c0001t0010g0039 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.400-4386_400-4371d others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | G | GAAGAAAA others(3): Show |
4 | a0001c0003t0025g0014 a0001c0003t0025g0017 a0001c0003t0026g0015 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4371_400-4370i others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | GAAAA | G | 38 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0143 others(35): Show |
38 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.400-4374_400-4371d others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | GAAAAA | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(98): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.400-4375_400-4371d others(7): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | GAAAAAA | G | 53 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0139 others(50): Show |
56 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.400-4376_400-4371d others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | GAAAAAAA | G | 11 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(8): Show |
12 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.400-4377_400-4371d others(9): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909243 | GAAAAAAA others(14): Show |
G | 3 | a0001c0001t0037g0182 a0001c0001t0037g0183 a0001c0005t0020g0005 |
4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4391_400-4371d others(23): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909243 | |||||||
| chr5:60909278 | A | G | 4 | a0001c0003t0025g0014 a0001c0003t0025g0017 a0001c0003t0026g0015 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-4405T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909278 | |||||||
| chr5:60909706 | C | T | 1 | a0001c0002t0017g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.400-4833G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909706 | |||||||
| chr5:60909910 | C | T | 1 | a0001c0002t0016g0075 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.400-5037G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909910 | |||||||
| chr5:60909935 | T | C | 1 | a0001c0001t0045g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.400-5062A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909935 | |||||||
| chr5:60909961 | GA | G | 10 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(7): Show |
10 | HG00642.hp2 HG01884.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-5089delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909961 | |||||||
| chr5:60909972 | A | T | 72 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(69): Show |
76 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.400-5099T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909972 | |||||||
| chr5:60909974 | AT | A | 19 | a0001c0002t0008g0058 a0001c0002t0008g0061 a0001c0002t0008g0064 others(16): Show |
19 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-5102delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909974 | |||||||
| chr5:60909975 | T | A | 32 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(29): Show |
34 | HG00280.hp1 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.400-5102A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909975 | |||||||
| chr5:60909978 | T | A | 1 | a0001c0002t0017g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.400-5105A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60909978 | |||||||
| chr5:60910195 | T | A | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.400-5322A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910195 | |||||||
| chr5:60910295 | T | C | 1 | a0001c0001t0005g0270 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.400-5422A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910295 | |||||||
| chr5:60910298 | A | G | 9 | a0001c0001t0003g0138 a0001c0001t0003g0146 a0001c0001t0003g0147 others(6): Show |
9 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-5425T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910298 | |||||||
| chr5:60910850 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.400-5977G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60910850 | |||||||
| chr5:60911139 | C | T | 2 | a0001c0001t0037g0182 a0001c0001t0037g0183 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.400-6266G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911139 | |||||||
| chr5:60911262 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.400-6389A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911262 | |||||||
| chr5:60911304 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.400-6431A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911304 | |||||||
| chr5:60911397 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG00639.hp1 HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.400-6524A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911397 | |||||||
| chr5:60911436 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0003g0158 |
2 | NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400-6563C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911436 | |||||||
| chr5:60911438 | G | T | 6 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(3): Show |
6 | HG01109.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-6565C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911438 | |||||||
| chr5:60911438 | GT | G | 6 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-6566delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911438 | |||||||
| chr5:60911615 | T | C | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.399+6650A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911615 | |||||||
| chr5:60911774 | GT | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.399+6490delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911774 | |||||||
| chr5:60911791 | G | T | 2 | a0001c0001t0027g0249 a0001c0001t0027g0250 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.399+6474C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60911791 | |||||||
| chr5:60912267 | T | G | 1 | a0001c0001t0014g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.399+5998A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912267 | |||||||
| chr5:60912498 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0009g0207 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.399+5767G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912498 | |||||||
| chr5:60912601 | T | G | 1 | a0001c0001t0043g0018 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.399+5664A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912601 | |||||||
| chr5:60912650 | G | A | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.399+5615C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912650 | |||||||
| chr5:60912650 | G | C | 1 | a0001c0001t0081g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.399+5615C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912650 | |||||||
| chr5:60912769 | A | C | 6 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+5496T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912769 | |||||||
| chr5:60912854 | C | T | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+5411G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912854 | |||||||
| chr5:60912978 | G | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.399+5287C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60912978 | |||||||
| chr5:60913143 | A | T | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+5122T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913143 | |||||||
| chr5:60913339 | G | T | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+4926C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913339 | |||||||
| chr5:60913888 | C | T | 1 | a0001c0001t0070g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.399+4377G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60913888 | |||||||
| chr5:60914168 | T | A | 2 | a0001c0001t0005g0261 a0001c0001t0018g0242 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.399+4097A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914168 | |||||||
| chr5:60914204 | C | T | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.399+4061G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914204 | |||||||
| chr5:60914304 | G | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(204): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.399+3961C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914304 | |||||||
| chr5:60914595 | G | A | 3 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0233 |
4 | HG01981.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+3670C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914595 | |||||||
| chr5:60914605 | G | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3660C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914605 | |||||||
| chr5:60914713 | G | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3552C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914713 | |||||||
| chr5:60914744 | G | A | 1 | a0001c0001t0020g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.399+3521C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914744 | |||||||
| chr5:60914789 | T | TA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(114): Show |
124 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.399+3475dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914789 | |||||||
| chr5:60914789 | TA | T | 16 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0005g0267 others(13): Show |
16 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+3475delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914789 | |||||||
| chr5:60914810 | G | C | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+3455C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914810 | |||||||
| chr5:60914844 | A | G | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.399+3421T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914844 | |||||||
| chr5:60914901 | T | C | 8 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(5): Show |
8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+3364A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60914901 | |||||||
| chr5:60915002 | A | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+3263T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915002 | |||||||
| chr5:60915046 | C | G | 1 | a0001c0001t0009g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.399+3219G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915046 | |||||||
| chr5:60915109 | A | G | 41 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(38): Show |
44 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.399+3156T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915109 | |||||||
| chr5:60915194 | G | T | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+3071C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915194 | |||||||
| chr5:60915565 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.399+2700T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915565 | |||||||
| chr5:60915598 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.399+2667A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915598 | |||||||
| chr5:60915657 | T | C | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+2608A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915657 | |||||||
| chr5:60915669 | A | G | 13 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(10): Show |
14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+2596T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915669 | |||||||
| chr5:60915819 | C | A | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.399+2446G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915819 | |||||||
| chr5:60915825 | C | A | 2 | a0001c0001t0002g0191 a0001c0001t0009g0180 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.399+2440G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60915825 | |||||||
| chr5:60916274 | A | G | 1 | a0001c0001t0031g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.399+1991T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916274 | |||||||
| chr5:60916493 | T | C | 1 | a0001c0001t0028g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+1772A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916493 | |||||||
| chr5:60916507 | A | G | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+1758T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916507 | |||||||
| chr5:60916623 | T | A | 1 | a0001c0001t0037g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.399+1642A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916623 | |||||||
| chr5:60916736 | T | G | 2 | a0001c0003t0024g0012 a0001c0003t0024g0013 |
2 | HG01109.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.399+1529A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60916736 | |||||||
| chr5:60917065 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0164 |
2 | NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.399+1200C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917065 | |||||||
| chr5:60917317 | C | T | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+948G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917317 | |||||||
| chr5:60917370 | A | G | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+895T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917370 | |||||||
| chr5:60917436 | T | G | 1 | a0001c0001t0041g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.399+829A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917436 | |||||||
| chr5:60917516 | T | C | 2 | a0001c0001t0042g0029 a0001c0001t0042g0042 |
2 | HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.399+749A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917516 | |||||||
| chr5:60917588 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.399+677A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917588 | |||||||
| chr5:60917657 | T | C | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+608A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917657 | |||||||
| chr5:60917779 | A | G | 1 | a0001c0001t0007g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.399+486T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60917779 | |||||||
| chr5:60918134 | T | G | 2 | a0001c0001t0003g0009 a0001c0001t0003g0225 |
3 | NA18963.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.399+131A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60918134 | |||||||
| chr5:60918142 | A | C | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.399+123T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 4/11 | chr5 | 60918142 | |||||||
| chr5:60918432 | G | T | 1 | a0001c0001t0010g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276-44C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918432 | |||||||
| chr5:60918482 | G | A | 1 | a0001c0002t0008g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.276-94C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918482 | |||||||
| chr5:60918513 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.276-125A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918513 | |||||||
| chr5:60918622 | G | T | 1 | a0001c0001t0084g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.276-234C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918622 | |||||||
| chr5:60918676 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(282): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.276-288A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918676 | |||||||
| chr5:60918920 | A | C | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.276-532T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918920 | |||||||
| chr5:60918922 | C | T | 1 | a0001c0001t0049g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.276-534G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918922 | |||||||
| chr5:60918929 | T | C | 1 | a0001c0001t0042g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.276-541A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60918929 | |||||||
| chr5:60919062 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.276-674T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919062 | |||||||
| chr5:60919089 | C | T | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.276-701G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919089 | |||||||
| chr5:60919216 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.276-828G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919216 | |||||||
| chr5:60919229 | G | A | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276-841C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919229 | |||||||
| chr5:60919344 | T | C | 1 | a0001c0004t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.276-956A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919344 | |||||||
| chr5:60919353 | G | C | 1 | a0001c0001t0029g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.276-965C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919353 | |||||||
| chr5:60919412 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.276-1024A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919412 | |||||||
| chr5:60919500 | C | T | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.276-1112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919500 | |||||||
| chr5:60919557 | A | T | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.276-1169T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919557 | |||||||
| chr5:60919644 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.276-1256A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919644 | |||||||
| chr5:60919654 | A | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.276-1266T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919654 | |||||||
| chr5:60919894 | G | C | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.276-1506C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919894 | |||||||
| chr5:60919977 | A | G | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.276-1589T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60919977 | |||||||
| chr5:60920089 | G | A | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.276-1701C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920089 | |||||||
| chr5:60920216 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.276-1828A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920216 | |||||||
| chr5:60920577 | T | C | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.275+1477A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920577 | |||||||
| chr5:60920757 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+1297G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920757 | |||||||
| chr5:60920806 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.275+1248G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920806 | |||||||
| chr5:60920997 | G | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.275+1057C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60920997 | |||||||
| chr5:60921001 | C | T | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.275+1053G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921001 | |||||||
| chr5:60921150 | C | T | 4 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
4 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+904G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921150 | |||||||
| chr5:60921211 | G | A | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.275+843C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921211 | |||||||
| chr5:60921600 | T | C | 6 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(3): Show |
6 | HG02809.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+454A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921600 | |||||||
| chr5:60921612 | T | C | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+442A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921612 | |||||||
| chr5:60921660 | T | C | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.275+394A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921660 | |||||||
| chr5:60921733 | A | T | 1 | a0001c0002t0006g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.275+321T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921733 | |||||||
| chr5:60921824 | A | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.275+230T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921824 | |||||||
| chr5:60921841 | C | A | 1 | a0001c0001t0002g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.275+213G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 3/11 | chr5 | 60921841 | |||||||
| chr5:60922592 | G | A | 1 | a0001c0001t0043g0018 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.174-437C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60922592 | |||||||
| chr5:60922843 | T | C | 1 | a0001c0001t0003g0159 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.174-688A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60922843 | |||||||
| chr5:60923019 | C | T | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.174-864G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923019 | |||||||
| chr5:60923095 | T | TG | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(204): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.174-941dupC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923095 | |||||||
| chr5:60923224 | A | G | 1 | a0001c0001t0007g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.174-1069T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923224 | |||||||
| chr5:60923541 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.174-1386T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923541 | |||||||
| chr5:60923653 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(247): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.174-1498T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923653 | |||||||
| chr5:60923669 | A | T | 4 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 others(1): Show |
4 | HG01109.hp1 HG01167.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-1514T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923669 | |||||||
| chr5:60923919 | A | G | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-1764T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923919 | |||||||
| chr5:60923973 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.174-1818C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60923973 | |||||||
| chr5:60924051 | T | A | 1 | a0001c0001t0022g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.174-1896A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924051 | |||||||
| chr5:60924267 | C | T | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.174-2112G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924267 | |||||||
| chr5:60924597 | A | G | 1 | a0001c0002t0006g0049 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.174-2442T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924597 | |||||||
| chr5:60924813 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.174-2658C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924813 | |||||||
| chr5:60924834 | C | T | 1 | a0001c0001t0013g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.174-2679G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924834 | |||||||
| chr5:60924923 | T | C | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174-2768A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924923 | |||||||
| chr5:60924932 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-2777A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60924932 | |||||||
| chr5:60925102 | C | T | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-2947G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925102 | |||||||
| chr5:60925204 | C | T | 1 | a0001c0001t0007g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.174-3049G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925204 | |||||||
| chr5:60925394 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.174-3239G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925394 | |||||||
| chr5:60925467 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(246): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.174-3312C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925467 | |||||||
| chr5:60925965 | G | A | 1 | a0001c0001t0065g0122 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.173+2899C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925965 | |||||||
| chr5:60925970 | C | T | 1 | a0001c0001t0031g0234 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.173+2894G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60925970 | |||||||
| chr5:60926013 | C | T | 2 | a0001c0001t0034g0044 a0001c0001t0060g0024 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173+2851G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926013 | |||||||
| chr5:60926071 | C | T | 2 | a0001c0001t0003g0146 a0001c0001t0003g0147 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.173+2793G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926071 | |||||||
| chr5:60926077 | G | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.173+2787C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926077 | |||||||
| chr5:60926132 | T | C | 4 | a0001c0003t0025g0014 a0001c0003t0025g0017 a0001c0003t0026g0015 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+2732A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926132 | |||||||
| chr5:60926216 | A | G | 1 | a0001c0001t0049g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.173+2648T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926216 | |||||||
| chr5:60926296 | C | T | 1 | a0001c0001t0021g0209 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.173+2568G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926296 | |||||||
| chr5:60926342 | T | C | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.173+2522A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926342 | |||||||
| chr5:60926575 | T | C | 1 | a0001c0001t0018g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.173+2289A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60926575 | |||||||
| chr5:60927182 | C | T | 1 | a0001c0001t0011g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.173+1682G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927182 | |||||||
| chr5:60927337 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.173+1527A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927337 | |||||||
| chr5:60927384 | T | G | 1 | a0001c0001t0003g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.173+1480A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927384 | |||||||
| chr5:60927546 | G | A | 1 | a0001c0001t0023g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.173+1318C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927546 | |||||||
| chr5:60927695 | C | T | 1 | a0001c0001t0045g0245 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.173+1169G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927695 | |||||||
| chr5:60927706 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+1158A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927706 | |||||||
| chr5:60927736 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.173+1128T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927736 | |||||||
| chr5:60927914 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.173+950T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60927914 | |||||||
| chr5:60928029 | C | G | 36 | a0001c0001t0018g0057 a0001c0002t0006g0003 a0001c0002t0006g0049 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.173+835G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928029 | |||||||
| chr5:60928618 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.173+246G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928618 | |||||||
| chr5:60928715 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+149G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928715 | |||||||
| chr5:60928731 | C | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | NA18940.hp1 NA18942.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+133G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 2/11 | chr5 | 60928731 | |||||||
| chr5:60929069 | T | G | 1 | a0001c0001t0042g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.78-110A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929069 | |||||||
| chr5:60929087 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.78-128G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929087 | |||||||
| chr5:60929190 | C | T | 2 | a0001c0001t0037g0182 a0001c0001t0037g0183 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.78-231G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929190 | |||||||
| chr5:60929465 | G | A | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-506C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929465 | |||||||
| chr5:60929696 | A | G | 9 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0189 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-737T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929696 | |||||||
| chr5:60929783 | T | C | 1 | a0001c0002t0016g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.78-824A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60929783 | |||||||
| chr5:60930205 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.78-1246C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930205 | |||||||
| chr5:60930214 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-1255T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930214 | |||||||
| chr5:60930325 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.78-1366C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930325 | |||||||
| chr5:60930556 | T | TAAAAAC | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(281): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.78-1603_78-1598dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930556 | |||||||
| chr5:60930578 | C | G | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-1619G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930578 | |||||||
| chr5:60930759 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-1800A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930759 | |||||||
| chr5:60930888 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.78-1929G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930888 | |||||||
| chr5:60930926 | G | A | 1 | a0001c0001t0013g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.78-1967C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60930926 | |||||||
| chr5:60931119 | C | CA | 8 | a0001c0001t0005g0267 a0001c0001t0028g0277 a0001c0001t0028g0278 others(5): Show |
8 | HG01516.hp2 HG01517.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-2161dupT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931119 | |||||||
| chr5:60931194 | G | T | 1 | a0001c0001t0021g0209 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.78-2235C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931194 | |||||||
| chr5:60931303 | T | A | 1 | a0001c0001t0005g0270 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78-2344A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931303 | |||||||
| chr5:60931570 | A | T | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-2611T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931570 | |||||||
| chr5:60931600 | C | T | 1 | a0001c0001t0072g0093 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.78-2641G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931600 | |||||||
| chr5:60931790 | A | G | 1 | a0001c0001t0012g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.78-2831T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60931790 | |||||||
| chr5:60932096 | A | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.78-3137T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932096 | |||||||
| chr5:60932189 | A | C | 20 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(17): Show |
21 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.78-3230T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932189 | |||||||
| chr5:60932196 | A | C | 1 | a0001c0001t0038g0154 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.78-3237T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932196 | |||||||
| chr5:60932252 | T | C | 1 | a0001c0001t0077g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-3293A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932252 | |||||||
| chr5:60932331 | G | T | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-3372C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932331 | |||||||
| chr5:60932627 | A | G | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-3668T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932627 | |||||||
| chr5:60932688 | TCA | T | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-3731_78-3730del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932688 | |||||||
| chr5:60932789 | A | G | 8 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(5): Show |
8 | HG03490.hp2 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3830T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932789 | |||||||
| chr5:60932792 | G | A | 13 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(10): Show |
14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-3833C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932792 | |||||||
| chr5:60932908 | G | C | 1 | a0001c0001t0011g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.78-3949C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60932908 | |||||||
| chr5:60933160 | T | C | 1 | a0001c0001t0034g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.78-4201A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933160 | |||||||
| chr5:60933215 | T | C | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-4256A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933215 | |||||||
| chr5:60933216 | C | CT | 34 | a0001c0001t0004g0235 a0001c0001t0015g0252 a0001c0001t0018g0057 others(31): Show |
35 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.78-4258dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | |||||||
| chr5:60933216 | C | T | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.78-4257G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | |||||||
| chr5:60933216 | CT | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(172): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.78-4258delA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | |||||||
| chr5:60933216 | CTT | C | 14 | a0001c0001t0001g0128 a0001c0001t0002g0188 a0001c0001t0012g0172 others(11): Show |
14 | HG01175.hp1 HG02615.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-4259_78-4258del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933216 | |||||||
| chr5:60933222 | T | C | 12 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(9): Show |
12 | HG01175.hp1 HG02735.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-4263A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933222 | |||||||
| chr5:60933238 | A | T | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-4279T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933238 | |||||||
| chr5:60933323 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.78-4364T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933323 | |||||||
| chr5:60933340 | A | C | 1 | a0001c0001t0009g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.78-4381T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933340 | |||||||
| chr5:60933436 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.78-4477G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933436 | |||||||
| chr5:60933439 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(201): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.78-4480T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933439 | |||||||
| chr5:60933642 | T | G | 6 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(3): Show |
6 | HG02622.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-4683A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933642 | |||||||
| chr5:60933772 | T | C | 1 | a0001c0001t0047g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-4813A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933772 | |||||||
| chr5:60933938 | T | TAC | 3 | a0001c0001t0018g0271 a0001c0001t0084g0171 a0001c0002t0016g0075 |
3 | HG01167.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.78-4981_78-4980dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | |||||||
| chr5:60933938 | T | TACACAC | 40 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
43 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.78-4985_78-4980dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | |||||||
| chr5:60933938 | T | TACACACA others(1): Show |
9 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0189 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-4987_78-4980dup others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60933938 | |||||||
| chr5:60934389 | G | A | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.78-5430C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934389 | |||||||
| chr5:60934487 | T | C | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-5528A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934487 | |||||||
| chr5:60934494 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(201): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.78-5535C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934494 | |||||||
| chr5:60934504 | T | C | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0149 others(2): Show |
5 | NA18957.hp2 NA18961.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-5545A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934504 | |||||||
| chr5:60934523 | T | C | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.78-5564A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934523 | |||||||
| chr5:60934600 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.78-5641C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934600 | |||||||
| chr5:60934758 | A | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-5799T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934758 | |||||||
| chr5:60934886 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.78-5927G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60934886 | |||||||
| chr5:60935104 | G | T | 1 | a0001c0001t0014g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-6145C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935104 | |||||||
| chr5:60935130 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.78-6171A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935130 | |||||||
| chr5:60935259 | G | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.78-6300C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935259 | |||||||
| chr5:60935354 | T | C | 1 | a0001c0002t0052g0027 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.78-6395A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935354 | |||||||
| chr5:60935797 | A | G | 1 | a0001c0001t0047g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-6838T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935797 | |||||||
| chr5:60935867 | C | A | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.78-6908G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935867 | |||||||
| chr5:60935910 | A | G | 29 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(26): Show |
30 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.78-6951T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935910 | |||||||
| chr5:60935993 | G | C | 1 | a0001c0002t0033g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78-7034C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60935993 | |||||||
| chr5:60936316 | T | C | 1 | a0001c0001t0036g0132 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.78-7357A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936316 | |||||||
| chr5:60936483 | A | T | 1 | a0001c0001t0020g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-7524T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936483 | |||||||
| chr5:60936515 | A | G | 37 | a0001c0001t0018g0057 a0001c0002t0006g0003 a0001c0002t0006g0049 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.78-7556T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936515 | |||||||
| chr5:60936564 | G | A | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.78-7605C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936564 | |||||||
| chr5:60936710 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(241): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.78-7751G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936710 | |||||||
| chr5:60936749 | T | C | 1 | a0001c0001t0005g0263 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78-7790A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936749 | |||||||
| chr5:60936928 | C | T | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.78-7969G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936928 | |||||||
| chr5:60936942 | T | C | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.78-7983A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60936942 | |||||||
| chr5:60937148 | G | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+7784C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937148 | |||||||
| chr5:60937709 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.77+7223A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937709 | |||||||
| chr5:60937748 | C | T | 1 | a0001c0001t0011g0134 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.77+7184G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937748 | |||||||
| chr5:60937859 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.77+7073C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60937859 | |||||||
| chr5:60938009 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(193): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.77+6923C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938009 | |||||||
| chr5:60938011 | G | A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+6921C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938011 | |||||||
| chr5:60938024 | TATACATA others(1): Show |
T | 4 | a0001c0001t0002g0206 a0001c0001t0009g0181 a0001c0001t0080g0205 others(1): Show |
4 | HG00735.hp1 HG02602.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6900_77+6907del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938024 | |||||||
| chr5:60938040 | C | T | 4 | a0001c0001t0022g0284 a0001c0001t0023g0281 a0001c0001t0023g0282 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6892G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(3): Show |
C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0186 others(11): Show |
15 | HG03831.hp2 NA18939.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+6882_77+6891del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(5): Show |
C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0193 a0001c0001t0002g0208 others(1): Show |
4 | HG03491.hp1 HG03927.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6880_77+6891del others(12): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(7): Show |
C | 4 | a0001c0001t0002g0192 a0001c0001t0042g0029 a0001c0001t0042g0042 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6878_77+6891del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(9): Show |
C | 4 | a0001c0001t0001g0139 a0001c0001t0007g0035 a0001c0001t0010g0034 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6876_77+6891del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(11): Show |
C | 24 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(21): Show |
25 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.77+6874_77+6891del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(13): Show |
C | 15 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0007g0020 others(12): Show |
15 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+6872_77+6891del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(15): Show |
C | 8 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0010g0039 others(5): Show |
8 | HG02071.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+6870_77+6891del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(17): Show |
C | 14 | a0001c0001t0003g0162 a0001c0001t0003g0163 a0001c0001t0003g0164 others(11): Show |
15 | HG01255.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+6868_77+6891del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938040 | CATACATA others(19): Show |
C | 2 | a0001c0001t0009g0213 a0001c0001t0012g0175 |
2 | HG02818.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.77+6866_77+6891del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938040 | |||||||
| chr5:60938042 | TACATAC | T | 14 | a0001c0001t0002g0041 a0001c0001t0002g0184 a0001c0001t0002g0197 others(11): Show |
14 | HG00738.hp2 HG01099.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+6884_77+6889del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938042 | |||||||
| chr5:60938044 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(79): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.77+6888G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | |||||||
| chr5:60938044 | CATACATA others(1): Show |
C | 5 | a0001c0001t0029g0257 a0001c0003t0025g0014 a0001c0003t0025g0017 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+6880_77+6887del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | |||||||
| chr5:60938044 | CATACATA others(7): Show |
C | 1 | a0001c0002t0006g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.77+6874_77+6887del others(14): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | |||||||
| chr5:60938044 | CATACATA others(9): Show |
C | 1 | a0001c0002t0016g0075 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.77+6872_77+6887del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | |||||||
| chr5:60938044 | CATACATA others(11): Show |
C | 1 | a0001c0002t0008g0074 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.77+6870_77+6887del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938044 | |||||||
| chr5:60938048 | C | CAT | 7 | a0001c0001t0004g0240 a0001c0001t0004g0264 a0001c0001t0004g0265 others(4): Show |
8 | HG00673.hp2 HG02004.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6882_77+6883dup others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | C | CATAT | 8 | a0001c0001t0004g0227 a0001c0001t0004g0235 a0001c0001t0004g0236 others(5): Show |
8 | HG02273.hp1 HG02965.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+6880_77+6883dup others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | C | CATATAT | 3 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0031g0234 |
4 | HG02132.hp2 NA18973.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6878_77+6883dup others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(127): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.77+6884G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | CAT | C | 5 | a0001c0001t0005g0241 a0001c0001t0005g0248 a0001c0001t0005g0273 others(2): Show |
5 | HG02451.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6882_77+6883del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | CATATATA others(3): Show |
C | 1 | a0001c0001t0015g0275 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.77+6874_77+6883del others(10): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | CATATATA others(11): Show |
C | 2 | a0001c0001t0027g0249 a0001c0001t0027g0250 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.77+6866_77+6883del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938048 | CATATATA others(17): Show |
C | 1 | a0001c0001t0005g0276 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.77+6860_77+6883del others(24): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938048 | |||||||
| chr5:60938052 | T | C | 2 | a0001c0001t0050g0274 a0001c0001t0051g0262 |
2 | HG00099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.77+6880A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938052 | |||||||
| chr5:60938063 | ATATATAT others(21): Show |
A | 5 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0011g0165 others(2): Show |
5 | HG00280.hp2 HG04184.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6841_77+6868del others(28): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938063 | |||||||
| chr5:60938065 | ATATATAT others(19): Show |
A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(55): Show |
62 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.77+6841_77+6866del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938065 | |||||||
| chr5:60938065 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0003g0009 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.77+6840_77+6866del others(27): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938065 | |||||||
| chr5:60938067 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+6844_77+6864del others(21): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | |||||||
| chr5:60938067 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0097 a0001c0001t0011g0096 |
2 | HG01346.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.77+6840_77+6864del others(25): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | |||||||
| chr5:60938067 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0003g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.77+6839_77+6864del others(26): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938067 | |||||||
| chr5:60938068 | TATATATA others(15): Show |
T | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+6842_77+6863del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938068 | |||||||
| chr5:60938069 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(1): Show |
4 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6841_77+6862del others(22): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938069 | |||||||
| chr5:60938070 | TATATATA others(13): Show |
T | 15 | a0001c0002t0008g0061 a0001c0002t0008g0064 a0001c0002t0008g0070 others(12): Show |
15 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+6842_77+6861del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938070 | |||||||
| chr5:60938072 | TATATATA others(11): Show |
T | 9 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(6): Show |
9 | HG00280.hp1 HG01496.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+6842_77+6859del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938072 | |||||||
| chr5:60938073 | ATATATAT others(11): Show |
A | 2 | a0001c0002t0006g0003 a0001c0002t0016g0067 |
2 | HG02809.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.77+6841_77+6858del others(18): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938073 | |||||||
| chr5:60938073 | ATATATAT others(13): Show |
A | 1 | a0001c0009t0034g0025 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.77+6839_77+6858del others(20): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938073 | |||||||
| chr5:60938074 | TATATATA others(9): Show |
T | 9 | a0001c0001t0018g0057 a0001c0002t0006g0052 a0001c0002t0006g0053 others(6): Show |
9 | HG00642.hp1 HG01192.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+6842_77+6857del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938074 | |||||||
| chr5:60938075 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+6841_77+6856del others(16): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938075 | |||||||
| chr5:60938080 | TATATA | T | 3 | a0001c0001t0023g0281 a0001c0001t0023g0282 a0001c0003t0024g0013 |
3 | HG01109.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.77+6847_77+6851del others(5): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938080 | |||||||
| chr5:60938082 | TATATTTT others(1): Show |
T | 3 | a0001c0001t0002g0202 a0001c0001t0009g0180 a0001c0001t0079g0200 |
3 | HG00733.hp1 NA18945.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.77+6842_77+6849del others(8): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938082 | |||||||
| chr5:60938084 | TATTTTA | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0199 a0001c0001t0002g0204 |
3 | NA19065.hp1 NA19086.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.77+6842_77+6847del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938084 | |||||||
| chr5:60938085 | A | T | 1 | a0001c0001t0007g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.77+6847T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | |||||||
| chr5:60938085 | ATTT | A | 5 | a0001c0001t0002g0208 a0001c0001t0003g0164 a0001c0001t0020g0135 others(2): Show |
5 | HG03927.hp1 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+6844_77+6846del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | |||||||
| chr5:60938085 | ATTTTAT | A | 21 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(18): Show |
21 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.77+6841_77+6846del others(6): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938085 | |||||||
| chr5:60938086 | TTTTA | T | 34 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0002g0006 others(31): Show |
36 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.77+6842_77+6845del others(4): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938086 | |||||||
| chr5:60938087 | T | A | 5 | a0001c0001t0002g0189 a0001c0001t0002g0203 a0001c0001t0002g0289 others(2): Show |
5 | HG00621.hp2 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+6845A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938087 | |||||||
| chr5:60938087 | TTTA | T | 12 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0197 others(9): Show |
12 | HG00738.hp2 HG01255.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+6842_77+6844del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938087 | |||||||
| chr5:60938088 | TTA | T | 22 | a0001c0001t0002g0189 a0001c0001t0002g0203 a0001c0001t0002g0211 others(19): Show |
23 | HG00621.hp2 HG01074.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+6842_77+6843del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938088 | |||||||
| chr5:60938089 | T | A | 1 | a0001c0001t0023g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.77+6843A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938089 | |||||||
| chr5:60938089 | TA | T | 18 | a0001c0001t0002g0289 a0001c0001t0007g0020 a0001c0001t0007g0021 others(15): Show |
18 | HG01361.hp1 HG01884.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+6842delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938089 | |||||||
| chr5:60938090 | A | T | 20 | a0001c0001t0007g0037 a0001c0001t0010g0002 a0001c0001t0010g0032 others(17): Show |
21 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6842T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938090 | |||||||
| chr5:60938095 | T | A | 1 | a0001c0001t0047g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+6837A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938095 | |||||||
| chr5:60938339 | T | C | 17 | a0001c0001t0001g0157 a0001c0001t0003g0009 a0001c0001t0003g0045 others(14): Show |
18 | HG00280.hp2 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+6593A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938339 | |||||||
| chr5:60938348 | GA | G | 52 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0189 others(49): Show |
53 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.77+6583delT | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938348 | |||||||
| chr5:60938349 | AAT | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(114): Show |
125 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.77+6581_77+6582del others(2): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938349 | |||||||
| chr5:60938349 | AATT | A | 19 | a0001c0001t0001g0157 a0001c0001t0003g0009 a0001c0001t0003g0045 others(16): Show |
20 | HG00280.hp2 HG00558.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.77+6580_77+6582del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938349 | |||||||
| chr5:60938350 | A | AT | 24 | a0001c0001t0005g0261 a0001c0001t0015g0252 a0001c0001t0018g0242 others(21): Show |
25 | HG00280.hp1 HG00642.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+6581dupA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938350 | |||||||
| chr5:60938350 | A | T | 9 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(6): Show |
9 | HG01981.hp2 HG02257.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+6582T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938350 | |||||||
| chr5:60938377 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+6555G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938377 | |||||||
| chr5:60938394 | G | A | 1 | a0001c0001t0041g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.77+6538C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938394 | |||||||
| chr5:60938415 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(116): Show |
125 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.77+6517T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938415 | |||||||
| chr5:60938502 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+6430A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938502 | |||||||
| chr5:60938512 | C | G | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.77+6420G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938512 | |||||||
| chr5:60938513 | C | A | 1 | a0001c0003t0024g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6419G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938513 | |||||||
| chr5:60938514 | C | A | 1 | a0001c0003t0024g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6418G>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938514 | |||||||
| chr5:60938542 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.77+6390G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938542 | |||||||
| chr5:60938588 | A | G | 1 | a0001c0003t0024g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+6344T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938588 | |||||||
| chr5:60938602 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(241): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.77+6330A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938602 | |||||||
| chr5:60938634 | G | T | 2 | a0001c0001t0012g0176 a0001c0001t0012g0177 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.77+6298C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938634 | |||||||
| chr5:60938644 | G | T | 1 | a0001c0001t0004g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.77+6288C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938644 | |||||||
| chr5:60938762 | A | T | 1 | a0001c0001t0005g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+6170T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938762 | |||||||
| chr5:60938876 | G | A | 1 | a0001c0004t0001g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.77+6056C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938876 | |||||||
| chr5:60938909 | G | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+6023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60938909 | |||||||
| chr5:60939005 | G | T | 13 | a0001c0002t0006g0003 a0001c0002t0006g0049 a0001c0002t0006g0050 others(10): Show |
14 | HG00280.hp1 HG00642.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+5927C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939005 | |||||||
| chr5:60939076 | G | C | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+5856C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939076 | |||||||
| chr5:60939327 | G | A | 1 | a0001c0004t0039g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.77+5605C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939327 | |||||||
| chr5:60939362 | G | A | 2 | a0001c0001t0012g0176 a0001c0001t0012g0177 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.77+5570C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939362 | |||||||
| chr5:60939413 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(201): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.77+5519C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939413 | |||||||
| chr5:60939478 | CTTT | C | 37 | a0001c0001t0018g0057 a0001c0002t0006g0003 a0001c0002t0006g0049 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.77+5451_77+5453del others(3): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939478 | |||||||
| chr5:60939487 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(200): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.77+5445T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939487 | |||||||
| chr5:60939554 | G | C | 2 | a0001c0002t0006g0003 a0001c0002t0006g0233 |
3 | HG03490.hp1 HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.77+5378C>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939554 | |||||||
| chr5:60939639 | C | T | 1 | a0001c0001t0075g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.77+5293G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939639 | |||||||
| chr5:60939645 | C | T | 6 | a0001c0003t0024g0012 a0001c0003t0024g0013 a0001c0003t0025g0014 others(3): Show |
6 | HG01109.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+5287G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939645 | |||||||
| chr5:60939656 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.77+5276G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939656 | |||||||
| chr5:60939762 | C | T | 7 | a0001c0001t0022g0280 a0001c0001t0022g0283 a0001c0001t0022g0284 others(4): Show |
7 | HG02809.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+5170G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60939762 | |||||||
| chr5:60940109 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.77+4823A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940109 | |||||||
| chr5:60940207 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.77+4725T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940207 | |||||||
| chr5:60940379 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(241): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.77+4553T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940379 | |||||||
| chr5:60940512 | A | T | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4420T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940512 | |||||||
| chr5:60940513 | G | T | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4419C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940513 | |||||||
| chr5:60940514 | A | C | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4418T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940514 | |||||||
| chr5:60940515 | A | T | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4417T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940515 | |||||||
| chr5:60940522 | A | C | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4410T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940522 | |||||||
| chr5:60940606 | T | C | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+4326A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940606 | |||||||
| chr5:60940635 | G | A | 5 | a0001c0001t0034g0044 a0001c0001t0058g0255 a0001c0001t0059g0256 others(2): Show |
5 | HG01175.hp1 HG02735.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+4297C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940635 | |||||||
| chr5:60940653 | A | C | 12 | a0001c0001t0004g0010 a0001c0001t0004g0226 a0001c0001t0004g0227 others(9): Show |
13 | HG02004.hp1 HG02132.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.77+4279T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940653 | |||||||
| chr5:60940703 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.77+4229G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940703 | |||||||
| chr5:60940848 | G | A | 1 | a0001c0001t0044g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+4084C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940848 | |||||||
| chr5:60940909 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+4023C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60940909 | |||||||
| chr5:60941075 | T | G | 1 | a0001c0005t0020g0005 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.77+3857A>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941075 | |||||||
| chr5:60941122 | C | T | 1 | a0001c0001t0011g0084 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.77+3810G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941122 | |||||||
| chr5:60941284 | T | A | 2 | a0001c0001t0003g0155 a0001c0001t0038g0154 |
2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.77+3648A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941284 | |||||||
| chr5:60941325 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02523.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.77+3607C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941325 | |||||||
| chr5:60941609 | T | A | 1 | a0001c0001t0073g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.77+3323A>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941609 | |||||||
| chr5:60941792 | A | C | 5 | a0001c0001t0014g0079 a0001c0001t0014g0080 a0001c0001t0014g0081 others(2): Show |
5 | HG02451.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+3140T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941792 | |||||||
| chr5:60941869 | G | T | 37 | a0001c0001t0018g0057 a0001c0002t0006g0003 a0001c0002t0006g0049 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.77+3063C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941869 | |||||||
| chr5:60941944 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2988T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941944 | |||||||
| chr5:60941946 | A | G | 1 | a0001c0001t0009g0287 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.77+2986T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60941946 | |||||||
| chr5:60942059 | A | G | 2 | a0001c0001t0004g0226 a0001c0001t0004g0227 |
2 | NA18612.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.77+2873T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942059 | |||||||
| chr5:60942141 | C | G | 1 | a0001c0002t0053g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.77+2791G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942141 | |||||||
| chr5:60942157 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2775G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942157 | |||||||
| chr5:60942299 | T | C | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+2633A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942299 | |||||||
| chr5:60942425 | A | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+2507T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942425 | |||||||
| chr5:60942680 | A | C | 2 | a0001c0001t0029g0257 a0001c0001t0029g0258 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.77+2252T>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942680 | |||||||
| chr5:60942763 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(165): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+2169T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942763 | |||||||
| chr5:60942831 | G | A | 17 | a0001c0001t0001g0157 a0001c0001t0003g0009 a0001c0001t0003g0045 others(14): Show |
18 | HG00280.hp2 HG00558.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+2101C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942831 | |||||||
| chr5:60942869 | C | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+2063G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942869 | |||||||
| chr5:60942908 | A | T | 22 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0023 others(19): Show |
23 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.77+2024T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942908 | |||||||
| chr5:60942934 | A | G | 1 | a0001c0001t0009g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.77+1998T>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942934 | |||||||
| chr5:60942979 | A | T | 1 | a0001c0001t0009g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.77+1953T>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60942979 | |||||||
| chr5:60943006 | C | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0076 a0001c0001t0003g0078 others(1): Show |
4 | NA18612.hp2 NA18945.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+1926G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943006 | |||||||
| chr5:60943038 | AG | A | 3 | a0001c0001t0028g0277 a0001c0001t0028g0278 a0001c0001t0044g0170 |
3 | HG02572.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+1893delC | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943038 | |||||||
| chr5:60943067 | T | C | 1 | a0001c0001t0007g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.77+1865A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943067 | |||||||
| chr5:60943107 | C | T | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1825G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943107 | |||||||
| chr5:60943616 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+1316C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943616 | |||||||
| chr5:60943734 | G | A | 1 | a0001c0001t0076g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.77+1198C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943734 | |||||||
| chr5:60943871 | C | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+1061G>C | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943871 | |||||||
| chr5:60943973 | G | A | 7 | a0001c0001t0043g0018 a0001c0003t0024g0012 a0001c0003t0024g0013 others(4): Show |
7 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+959C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60943973 | |||||||
| chr5:60944016 | C | T | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG01109.hp1 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.77+916G>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944016 | |||||||
| chr5:60944135 | ATC | A | 7 | a0001c0001t0012g0172 a0001c0001t0012g0173 a0001c0001t0012g0174 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+795_77+796delGA | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944135 | |||||||
| chr5:60944216 | T | C | 1 | a0001c0001t0042g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.77+716A>G | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944216 | |||||||
| chr5:60944337 | G | A | 1 | a0001c0004t0078g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.77+595C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944337 | |||||||
| chr5:60944641 | G | T | 1 | a0001c0001t0009g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.77+291C>A | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944641 | |||||||
| chr5:60944705 | A | AC | 30 | a0001c0001t0001g0224 a0001c0001t0003g0009 a0001c0001t0003g0225 others(27): Show |
33 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.77+226dupG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | |||||||
| chr5:60944705 | AC | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(119): Show |
127 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.77+226delG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | |||||||
| chr5:60944705 | ACC | A | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
72 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.77+225_77+226delGG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944705 | |||||||
| chr5:60944706 | CCCCCCCC others(14): Show |
C | 2 | a0001c0001t0028g0277 a0001c0001t0028g0278 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.77+205_77+225delTT others(19): Show |
ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944706 | |||||||
| chr5:60944727 | A | AC | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0085 others(194): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.77+204dupG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944727 | |||||||
| chr5:60944727 | A | ACC | 27 | a0001c0001t0002g0041 a0001c0001t0002g0289 a0001c0001t0007g0020 others(24): Show |
28 | HG01099.hp2 HG01361.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.77+203_77+204dupGG | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944727 | |||||||
| chr5:60944916 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0009g0288 |
2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.77+16C>T | ERCC8 | ENSG00000049167.16 | transcript | ENST00000676185.1 | protein_coding | 1/11 | chr5 | 60944916 |