Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8916 |
|---|---|
| ensemblid | ENSG00000138641.18 |
| hgncid | 4876 |
| symbol | HERC3 |
| name | HECT and RLD domain containing E3 ubiquitin protein ligase 3 |
| refseq_nuc | NM_014606.3 |
| refseq_prot | NP_055421.1 |
| ensembl_nuc | ENST00000402738.6 |
| ensembl_prot | ENSP00000385684.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 88592480 |
| end | 88708539 |
| strand | + |
| ver | v1.2 |
| region | chr4:88592480-88708539 |
| region5000 | chr4:88587480-88713539 |
| regionname0 | HERC3_chr4_88592480_88708539 |
| regionname5000 | HERC3_chr4_88587480_88713539 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1050 | 223 | 72 | 42 | 89 | 3 | 15 | 62 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002 | 0/0 | 1050 | 70 | 16 | 10 | 38 | 3 | 3 | 33 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0003 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0004 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0005 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3153 | 179 | 54 | 33 | 78 | 2 | 10 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0002 | 0/0 | 3153 | 33 | 0 | 6 | 24 | 3 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0003 | 0/0 | 3153 | 32 | 12 | 4 | 14 | 0 | 2 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0004 | 0/0 | 3153 | 20 | 12 | 2 | 2 | 0 | 4 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0005 | 0/0 | 3153 | 17 | 3 | 3 | 9 | 1 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0006 | 0/0 | 3153 | 5 | 4 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0007 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0008 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0009 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0010 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0011 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0012 | 0/0 | 3153 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| c0013 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1762 | 83 | 10 | 26 | 39 | 1 | 6 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0002 | 0/0 | 1762 | 78 | 28 | 8 | 37 | 3 | 2 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0003 | 0/0 | 1762 | 60 | 11 | 0 | 43 | 0 | 6 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0004 | 0/0 | 1762 | 33 | 23 | 8 | 1 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0005 | 0/0 | 1762 | 11 | 8 | 1 | 0 | 1 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0006 | 0/0 | 1762 | 10 | 3 | 3 | 4 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0007 | 0/1 | 1762 | 3 | 0 | 2 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0008 | 0/0 | 1762 | 3 | 1 | 1 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0009 | 0/0 | 1762 | 2 | 1 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0010 | 0/0 | 1762 | 2 | 0 | 1 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0011 | 0/0 | 1762 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0012 | 0/0 | 1762 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0013 | 0/0 | 1762 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0014 | 0/0 | 1762 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0015 | 0/0 | 1762 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0016 | 0/0 | 1762 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0017 | 0/0 | 1762 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0018 | 0/0 | 1762 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| t0019 | 0/0 | 1726 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3153 | 179 | 54 | 33 | 78 | 2 | 10 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004 | 0/0 | 3153 | 20 | 12 | 2 | 2 | 0 | 4 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005 | 0/0 | 3153 | 17 | 3 | 3 | 9 | 1 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0007 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0008 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0009 | 0/0 | 3153 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0012 | 0/0 | 3153 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0002 | 0/0 | 3153 | 33 | 0 | 6 | 24 | 3 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0003 | 0/0 | 3153 | 32 | 12 | 4 | 14 | 0 | 2 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0006 | 0/0 | 3153 | 5 | 4 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0003c0010 | 0/0 | 3153 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0004c0011 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0005c0013 | 0/0 | 3153 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4914 | 74 | 9 | 23 | 35 | 1 | 5 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0002 | 0/0 | 4914 | 6 | 6 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0003 | 0/0 | 4914 | 46 | 9 | 0 | 35 | 0 | 2 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0004 | 0/0 | 4914 | 22 | 16 | 4 | 1 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0005 | 0/0 | 4914 | 7 | 6 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0006 | 0/0 | 4914 | 9 | 2 | 3 | 4 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0007 | 0/1 | 4914 | 3 | 0 | 2 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0008 | 0/0 | 4914 | 3 | 1 | 1 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0009 | 0/0 | 4914 | 2 | 1 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0010 | 0/0 | 4914 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0011 | 0/0 | 4914 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0012 | 0/0 | 4914 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0016 | 0/0 | 4914 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0001t0019 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0001 | 0/0 | 4914 | 2 | 1 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0002 | 0/0 | 4914 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0003 | 0/0 | 4914 | 6 | 1 | 0 | 1 | 0 | 4 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0004 | 0/0 | 4914 | 6 | 5 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0005 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0006 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0010 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0004t0017 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005t0001 | 0/0 | 4914 | 5 | 0 | 1 | 3 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005t0002 | 0/0 | 4914 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005t0003 | 0/0 | 4914 | 7 | 1 | 0 | 6 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005t0004 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0005t0005 | 0/0 | 4914 | 2 | 0 | 1 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0007t0002 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0007t0004 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0008t0001 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0008t0004 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0009t0004 | 0/0 | 4914 | 2 | 1 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0001c0012t0001 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0002t0002 | 0/0 | 4914 | 32 | 0 | 5 | 24 | 3 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0002t0015 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0003t0002 | 0/0 | 4914 | 30 | 12 | 3 | 13 | 0 | 2 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0003t0013 | 0/0 | 4914 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0003t0014 | 0/0 | 4914 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0006t0002 | 0/0 | 4914 | 4 | 4 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0002c0006t0018 | 0/0 | 4914 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0003c0010t0003 | 0/0 | 4914 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0004c0011t0002 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| a0005c0013t0005 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | copy fasta | chr4 | 88587480 | 88713539 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0007g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0010g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0004t0017g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0005t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0007t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0007t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0008t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0008t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0009t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0009t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0001c0012t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0002t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0013g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0003t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0006t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0006t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0006t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0006t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0002c0006t0018g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0003c0010t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0004c0011t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| a0005c0013t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | GBR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00140 | hp2 | a0001 | c0005 | t0005 | g0106 | EUR | GBR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0087 | EUR | FIN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0257 | EUR | FIN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00438 | hp2 | a0001 | c0004 | t0003 | g0266 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0030 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00639 | hp1 | a0001 | c0007 | t0004 | g0121 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00733 | hp2 | a0001 | c0012 | t0001 | g0270 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00738 | hp1 | a0002 | c0003 | t0014 | g0033 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01081 | hp1 | a0001 | c0008 | t0001 | g0005 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0159 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0241 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01106 | hp2 | a0001 | c0004 | t0010 | g0259 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01109 | hp1 | a0002 | c0002 | t0015 | g0115 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01167 | hp1 | a0001 | c0004 | t0004 | g0277 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0287 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01243 | hp2 | a0001 | c0009 | t0004 | g0132 | AMR | PUR | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0175 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01257 | hp1 | a0001 | c0005 | t0004 | g0091 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0237 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0119 | EUR | IBS | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0135 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0137 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02055 | hp1 | a0005 | c0013 | t0005 | g0264 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02071 | hp2 | a0001 | c0005 | t0001 | g0081 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02080 | hp1 | a0001 | c0005 | t0003 | g0105 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02083 | hp1 | a0001 | c0001 | t0010 | g0210 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02132 | hp1 | a0002 | c0003 | t0002 | g0173 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02135 | hp1 | a0002 | c0003 | t0002 | g0032 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CDX | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02257 | hp2 | a0002 | c0003 | t0002 | g0018 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0265 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02273 | hp2 | a0001 | c0005 | t0001 | g0092 | AMR | PEL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02280 | hp2 | a0004 | c0011 | t0002 | g0017 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02572 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02602 | hp1 | a0001 | c0004 | t0003 | g0258 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0254 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0282 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0251 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02647 | hp2 | a0001 | c0009 | t0004 | g0131 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02723 | hp2 | a0002 | c0003 | t0002 | g0038 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02818 | hp2 | a0002 | c0006 | t0002 | g0272 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02886 | hp1 | a0001 | c0004 | t0004 | g0189 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0103 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0185 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0279 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02897 | hp2 | a0001 | c0004 | t0004 | g0281 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02922 | hp1 | a0002 | c0006 | t0002 | g0191 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02970 | hp2 | a0002 | c0003 | t0002 | g0250 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02976 | hp2 | a0002 | c0006 | t0002 | g0273 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0280 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03130 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0156 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03225 | hp1 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03225 | hp2 | a0001 | c0005 | t0002 | g0096 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0268 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0039 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03453 | hp2 | a0002 | c0003 | t0002 | g0019 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0141 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0078 | SAS | PJL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03516 | hp2 | a0001 | c0004 | t0003 | g0262 | AFR | ESN | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03540 | hp2 | a0001 | c0005 | t0003 | g0110 | AFR | GWD | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03579 | hp2 | a0001 | c0007 | t0002 | g0122 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03831 | hp1 | a0001 | c0004 | t0003 | g0276 | SAS | BEB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03942 | hp1 | a0001 | c0004 | t0003 | g0267 | SAS | BEB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG04115 | hp1 | a0002 | c0006 | t0018 | g0260 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0024 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0082 | SAS | STU | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0186 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | CHB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18906 | hp1 | a0002 | c0006 | t0002 | g0275 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18940 | hp2 | a0002 | c0003 | t0002 | g0181 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18960 | hp1 | a0002 | c0003 | t0013 | g0178 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18961 | hp2 | a0001 | c0005 | t0001 | g0104 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18965 | hp2 | a0002 | c0003 | t0002 | g0031 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0177 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18982 | hp1 | a0001 | c0005 | t0001 | g0100 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18988 | hp1 | a0002 | c0003 | t0002 | g0123 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18988 | hp2 | a0003 | c0010 | t0003 | g0278 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18990 | hp1 | a0001 | c0005 | t0003 | g0065 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18991 | hp2 | a0002 | c0003 | t0002 | g0179 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0192 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19043 | hp1 | a0001 | c0004 | t0006 | g0285 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0263 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19057 | hp2 | a0001 | c0005 | t0003 | g0094 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19063 | hp2 | a0001 | c0005 | t0003 | g0116 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19067 | hp1 | a0001 | c0005 | t0003 | g0063 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19067 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19075 | hp2 | a0002 | c0003 | t0002 | g0283 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19080 | hp2 | a0002 | c0003 | t0002 | g0153 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19081 | hp2 | a0001 | c0005 | t0003 | g0120 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19091 | hp2 | a0002 | c0003 | t0002 | g0029 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0274 | AFR | YRI | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ASW | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ASW | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20905 | hp1 | a0001 | c0005 | t0001 | g0093 | SAS | GIH | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG01123 | hp2 | a0001 | c0005 | t0005 | g0062 | AMR | CLM | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02109 | hp2 | a0001 | c0004 | t0017 | g0187 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02486 | hp1 | a0001 | c0008 | t0004 | g0010 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03471 | hp1 | a0002 | c0003 | t0002 | g0022 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18955 | hp1 | a0001 | c0001 | t0016 | g0184 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | USA | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0220 | AFR | LWK | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0171 | REF | REF | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | HERC3_chr4_88587480_88713539 | HERC3 | chr4 | 88587480 | 88713539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88649918
|
G | A | 1 | a0003 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.305G>A | p.Arg102Gln | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/26 | 487/4914 | 305/3153 | 102/1050 | chr4 | 88649918 | ||
| chr4:88662509
|
G | A | 1 | a0004 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1225G>A | p.Val409Ile | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/26 | 1407/4914 | 1225/3153 | 409/1050 | chr4 | 88662509 | ||
| chr4:88681276
|
G | T | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.2458G>T | p.Val820Leu | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/26 | 2640/4914 | 2458/3153 | 820/1050 | chr4 | 88681276 | ||
| chr4:88704276
|
G | C | 2 | a0002a0004 | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
missense_variant | MODERATE | c.2836G>C | p.Glu946Gln | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 24/26 | 3018/4914 | 2836/3153 | 946/1050 | chr4 | 88704276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88605994
|
A | G | 1 | a0001c0009 | 2 | HG01243.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.171A>G | p.Thr57Thr | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/26 | 353/4914 | 171/3153 | 57/1050 | chr4 | 88605994 | ||
| chr4:88652885
|
C | T | 1 | a0001c0008 | 2 | HG01081.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.480C>T | p.Thr160Thr | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/26 | 662/4914 | 480/3153 | 160/1050 | chr4 | 88652885 | ||
| chr4:88680149
|
T | C | 1 | a0001c0012 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.2253T>C | p.Phe751Phe | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/26 | 2435/4914 | 2253/3153 | 751/1050 | chr4 | 88680149 | ||
| chr4:88686754
|
A | G | 3 | a0001c0005a0002c0002a0003c0010 | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
synonymous_variant | LOW | c.2526A>G | p.Leu842Leu | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/26 | 2708/4914 | 2526/3153 | 842/1050 | chr4 | 88686754 | ||
| chr4:88686763
|
C | T | 1 | a0001c0007 | 2 | HG00639.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2535C>T | p.Pro845Pro | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/26 | 2717/4914 | 2535/3153 | 845/1050 | chr4 | 88686763 | ||
| chr4:88686781
|
G | A | 3 | a0001c0004a0002c0006a0005c0013 | 26 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(23): Show |
synonymous_variant | LOW | c.2553G>A | p.Glu851Glu | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/26 | 2735/4914 | 2553/3153 | 851/1050 | chr4 | 88686781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88707091
|
G | T | 13 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(10): Show | 78 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*131G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 131 | chr4 | 88707091 | |||||
| chr4:88707295
|
A | G | 1 | a0002c0006t0018 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 335 | chr4 | 88707295 | |||||
| chr4:88707396
|
A | G | 1 | a0001c0001t0009 | 2 | HG00323.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*436A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 436 | chr4 | 88707396 | |||||
| chr4:88707401
|
C | T | 1 | a0001c0001t0012 | 2 | HG02723.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*441C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 441 | chr4 | 88707401 | |||||
| chr4:88707408
|
G | A | 7 | a0001c0001t0003a0001c0001t0010a0001c0001t0019others(4): Show | 63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*448G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 448 | chr4 | 88707408 | |||||
| chr4:88707498
|
A | G | 1 | a0001c0004t0017 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 538 | chr4 | 88707498 | |||||
| chr4:88707582
|
T | A | 12 | a0001c0001t0002a0001c0004t0002a0001c0005t0002others(9): Show | 82 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*622T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 622 | chr4 | 88707582 | |||||
| chr4:88707729
|
G | T | 1 | a0002c0002t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*769G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 769 | chr4 | 88707729 | |||||
| chr4:88707762
|
C | T | 1 | a0001c0001t0008 | 3 | HG01071.hp1 HG03490.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*802C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 802 | chr4 | 88707762 | |||||
| chr4:88707849
|
A | G | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(18): Show | 115 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*889A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 889 | chr4 | 88707849 | |||||
| chr4:88707907
|
G | A | 1 | a0002c0003t0013 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*947G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 947 | chr4 | 88707907 | |||||
| chr4:88707915
|
T | C | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*955T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 955 | chr4 | 88707915 | |||||
| chr4:88708226
|
GAGTAAGA others(29): Show |
G | 1 | a0001c0001t0019 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1270_*1305delAAGA others(32): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 1270 | INFO_REALIGN_3_PRIME | chr4 | 88708226 | ||||
| chr4:88708399
|
T | C | 1 | a0001c0001t0016 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 26/26 | 1439 | chr4 | 88708399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88592606
|
G | T | 2 | a0001c0001t0004g0286a0001c0001t0004g0287 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-88+32G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592606 | ||||||
| chr4:88592771
|
C | G | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-88+197C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592771 | ||||||
| chr4:88592787
|
C | T | 1 | a0001c0001t0003g0284 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-88+213C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592787 | ||||||
| chr4:88592827
|
C | G | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-88+253C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592827 | ||||||
| chr4:88592871
|
A | G | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+297A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592871 | ||||||
| chr4:88592881
|
GCCTCCCG others(15): Show |
G | 1 | a0003c0010t0003g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-88+318_-88+339del others(22): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88592881 | |||||
| chr4:88592912
|
C | A | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-88+338C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592912 | ||||||
| chr4:88592921
|
CGGGA | C | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-88+350_-88+353del others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88592921 | |||||
| chr4:88592972
|
C | T | 7 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-88+398C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88592972 | ||||||
| chr4:88593044
|
A | AAATGGGA others(7): Show |
18 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-88+472_-88+485dup others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88593044 | |||||
| chr4:88593185
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-88+611G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593185 | ||||||
| chr4:88593260
|
G | GGT | 21 | a0001c0001t0001g0271a0001c0001t0004g0261a0001c0004t0001g0269others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-88+701_-88+702dup others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88593260 | |||||
| chr4:88593260
|
GGT | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 22 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-88+701_-88+702del others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88593260 | |||||
| chr4:88593344
|
CTT | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88+771_-88+772del others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593344 | ||||||
| chr4:88593379
|
CA | C | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+806delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593379 | ||||||
| chr4:88593421
|
G | A | 72 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0002g0054others(69): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-88+847G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593421 | ||||||
| chr4:88593772
|
C | T | 1 | a0002c0003t0002g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-88+1198C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593772 | ||||||
| chr4:88593881
|
A | C | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+1307A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593881 | ||||||
| chr4:88593929
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-88+1355A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593929 | ||||||
| chr4:88593984
|
G | C | 2 | a0001c0005t0005g0062a0002c0002t0002g0061 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-88+1410G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88593984 | ||||||
| chr4:88594054
|
CCT | C | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+1483_-88+1484d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88594054 | |||||
| chr4:88594101
|
A | G | 18 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-87-1456A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594101 | ||||||
| chr4:88594107
|
A | T | 6 | a0001c0001t0008g0028a0002c0003t0002g0029a0002c0003t0002g0030others(3): Show | 6 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-87-1450A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594107 | ||||||
| chr4:88594618
|
A | G | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-87-939A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594618 | ||||||
| chr4:88594744
|
C | T | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87-813C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594744 | ||||||
| chr4:88594841
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-87-716C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594841 | ||||||
| chr4:88594860
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-87-697G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594860 | ||||||
| chr4:88594966
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-87-591G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88594966 | ||||||
| chr4:88595094
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-87-463C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88595094 | ||||||
| chr4:88595100
|
C | CA | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(70): Show | 74 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-87-434dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88595100 | |||||
| chr4:88595100
|
C | CAA | 8 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(5): Show | 8 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.-87-435_-87-434dup others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88595100 | |||||
| chr4:88595100
|
C | CAAA | 16 | a0001c0001t0002g0034a0001c0001t0008g0028a0001c0001t0011g0020others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-87-436_-87-434dup others(3): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88595100 | |||||
| chr4:88595100
|
CA | C | 10 | a0001c0001t0001g0252a0001c0001t0005g0009a0001c0001t0005g0255others(7): Show | 11 | HG01167.hp1 HG02135.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-87-434delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 88595100 | |||||
| chr4:88595178
|
A | G | 3 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249 | 3 | HG02040.hp2 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-87-379A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88595178 | ||||||
| chr4:88595249
|
A | G | 1 | a0002c0002t0002g0119 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-87-308A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88595249 | ||||||
| chr4:88595288
|
A | G | 2 | a0001c0005t0005g0062a0002c0002t0002g0061 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-87-269A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88595288 | ||||||
| chr4:88595420
|
C | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-87-137C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 1/25 | chr4 | 88595420 | ||||||
| chr4:88595801
|
A | G | 1 | a0002c0003t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-30+187A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88595801 | ||||||
| chr4:88595841
|
C | CT | 21 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0246others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30+254dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CT | C | 76 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0211others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-30+254delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CTT | C | 62 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(59): Show | 64 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-30+253_-30+254del others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CTTT | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 17 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+252_-30+254del others(3): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-30+244_-30+254del others(11): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+243_-30+254del others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595841
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-30+242_-30+254del others(13): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88595841 | |||||
| chr4:88595912
|
G | T | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-30+298G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88595912 | ||||||
| chr4:88595944
|
G | T | 1 | a0001c0001t0010g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-30+330G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88595944 | ||||||
| chr4:88595963
|
C | A | 1 | a0001c0004t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-30+349C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88595963 | ||||||
| chr4:88595968
|
G | A | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+354G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88595968 | ||||||
| chr4:88596007
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-30+393G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88596007 | ||||||
| chr4:88596010
|
C | T | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30+396C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88596010 | ||||||
| chr4:88596115
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(118): Show | 125 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-30+501T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88596115 | ||||||
| chr4:88596690
|
A | G | 10 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0003g0067others(7): Show | 10 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+1076A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88596690 | ||||||
| chr4:88596933
|
A | G | 1 | a0002c0002t0002g0114 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-30+1319A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88596933 | ||||||
| chr4:88597050
|
C | CTG | 6 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(3): Show | 6 | HG00639.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1437_-30+1438i others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88597050 | |||||
| chr4:88597124
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-30+1510T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88597124 | ||||||
| chr4:88597308
|
A | G | 2 | a0001c0001t0008g0028a0002c0003t0014g0033 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-30+1694A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88597308 | ||||||
| chr4:88597462
|
G | T | 7 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+1848G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88597462 | ||||||
| chr4:88597811
|
A | G | 1 | a0001c0004t0004g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+2197A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88597811 | ||||||
| chr4:88597950
|
A | C | 41 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(38): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-30+2336A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88597950 | ||||||
| chr4:88598493
|
A | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01099.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+2879A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88598493 | ||||||
| chr4:88598512
|
C | T | 2 | a0001c0001t0001g0271a0001c0012t0001g0270 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.-30+2898C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88598512 | ||||||
| chr4:88599022
|
A | T | 2 | a0001c0001t0003g0208a0001c0001t0003g0209 | 2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-30+3408A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88599022 | ||||||
| chr4:88599162
|
T | G | 1 | a0002c0002t0002g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-30+3548T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88599162 | ||||||
| chr4:88599514
|
T | G | 1 | a0002c0003t0002g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-30+3900T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88599514 | ||||||
| chr4:88599756
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30+4142G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88599756 | ||||||
| chr4:88600196
|
G | T | 1 | a0001c0001t0003g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-30+4582G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600196 | ||||||
| chr4:88600562
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30+4948C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600562 | ||||||
| chr4:88600632
|
T | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-30+5018T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600632 | ||||||
| chr4:88600746
|
G | A | 1 | a0001c0001t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-5049G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600746 | ||||||
| chr4:88600800
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-29-4995A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600800 | ||||||
| chr4:88600819
|
C | CA | 20 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 22 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29-4975dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88600819 | |||||
| chr4:88600940
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-29-4855C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88600940 | ||||||
| chr4:88601120
|
T | C | 1 | a0002c0006t0018g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-29-4675T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601120 | ||||||
| chr4:88601470
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(119): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-29-4325G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601470 | ||||||
| chr4:88601548
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(119): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-29-4247G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601548 | ||||||
| chr4:88601552
|
A | G | 42 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(39): Show | 44 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29-4243A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601552 | ||||||
| chr4:88601757
|
TAGAAAAG others(308): Show |
T | 122 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(119): Show | 126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-29-4021_-29-3707d others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88601757 | |||||
| chr4:88601782
|
C | T | 3 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113 | 3 | HG02523.hp1 NA18968.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-29-4013C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601782 | ||||||
| chr4:88601839
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-29-3956G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601839 | ||||||
| chr4:88601852
|
C | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG00408.hp2 HG01099.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-3943C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601852 | ||||||
| chr4:88601907
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0006g0135a0001c0001t0006g0137 | 3 | HG01978.hp1 HG02004.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-29-3888T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601907 | ||||||
| chr4:88601926
|
G | C | 1 | a0002c0002t0002g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-29-3869G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88601926 | ||||||
| chr4:88602011
|
C | G | 2 | a0001c0005t0003g0110a0002c0003t0002g0251 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-3784C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602011 | ||||||
| chr4:88602055
|
C | CA | 67 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(64): Show | 69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-29-3722dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88602055 | |||||
| chr4:88602130
|
G | A | 15 | a0001c0001t0004g0002a0001c0001t0004g0040a0001c0001t0004g0041others(12): Show | 16 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-3665G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602130 | ||||||
| chr4:88602344
|
G | A | 4 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0009t0004g0131others(1): Show | 4 | HG01243.hp2 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-3451G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602344 | ||||||
| chr4:88602402
|
C | CA | 48 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0142others(45): Show | 49 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-29-3369dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88602402 | |||||
| chr4:88602402
|
CA | C | 9 | a0001c0001t0001g0130a0001c0001t0001g0239a0001c0001t0002g0034others(6): Show | 9 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-3369delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88602402 | |||||
| chr4:88602527
|
G | C | 3 | a0001c0001t0001g0271a0001c0004t0010g0259a0001c0012t0001g0270 | 3 | HG00733.hp2 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-29-3268G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602527 | ||||||
| chr4:88602540
|
C | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0240a0001c0001t0001g0252 | 3 | HG00408.hp2 HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-29-3255C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602540 | ||||||
| chr4:88602632
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-29-3163C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602632 | ||||||
| chr4:88602716
|
G | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00642.hp2 HG01257.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-3079G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602716 | ||||||
| chr4:88602874
|
A | G | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-2921A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602874 | ||||||
| chr4:88602954
|
G | A | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-2841G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88602954 | ||||||
| chr4:88603085
|
CT | C | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-2708delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88603085 | |||||
| chr4:88603116
|
T | C | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2679T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603116 | ||||||
| chr4:88603117
|
C | A | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2678C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603117 | ||||||
| chr4:88603118
|
A | T | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2677A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603118 | ||||||
| chr4:88603204
|
C | CT | 14 | a0001c0001t0001g0127a0001c0001t0001g0148a0001c0001t0001g0246others(11): Show | 14 | HG00621.hp1 HG01099.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-2571dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88603204 | |||||
| chr4:88603268
|
C | T | 1 | a0002c0002t0002g0108 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-29-2527C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603268 | ||||||
| chr4:88603353
|
A | C | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2442A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603353 | ||||||
| chr4:88603362
|
C | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29-2433C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603362 | ||||||
| chr4:88603453
|
T | TGC | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-2341_-29-2340d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88603453 | |||||
| chr4:88603511
|
G | A | 21 | a0001c0001t0001g0271a0001c0001t0004g0261a0001c0004t0002g0265others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-29-2284G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603511 | ||||||
| chr4:88603534
|
A | C | 3 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113 | 3 | HG02523.hp1 NA18968.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-29-2261A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603534 | ||||||
| chr4:88603544
|
A | G | 57 | a0001c0001t0003g0053a0001c0001t0003g0056a0001c0001t0003g0060others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-29-2251A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603544 | ||||||
| chr4:88603545
|
T | C | 1 | a0001c0005t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-29-2250T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603545 | ||||||
| chr4:88603550
|
T | A | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2245T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603550 | ||||||
| chr4:88603579
|
C | G | 20 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 22 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29-2216C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603579 | ||||||
| chr4:88603671
|
G | A | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2124G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603671 | ||||||
| chr4:88603748
|
C | T | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-2047C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603748 | ||||||
| chr4:88603894
|
A | T | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-1901A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603894 | ||||||
| chr4:88603902
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(90): Show | 97 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-29-1893C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88603902 | ||||||
| chr4:88604058
|
T | G | 1 | a0002c0003t0002g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-29-1737T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604058 | ||||||
| chr4:88604094
|
C | T | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0051 | 3 | HG01109.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-1701C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604094 | ||||||
| chr4:88604113
|
C | T | 6 | a0001c0001t0001g0146a0002c0003t0002g0177a0002c0003t0002g0181others(3): Show | 6 | HG01496.hp2 NA18940.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-1682C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604113 | ||||||
| chr4:88604125
|
A | T | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-1670A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604125 | ||||||
| chr4:88604146
|
G | T | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29-1649G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604146 | ||||||
| chr4:88604176
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-1619C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604176 | ||||||
| chr4:88604177
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-29-1618G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604177 | ||||||
| chr4:88604219
|
A | G | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-1576A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604219 | ||||||
| chr4:88604245
|
C | A | 4 | a0001c0001t0003g0053a0001c0001t0003g0056a0001c0001t0003g0060others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1550C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604245 | ||||||
| chr4:88604249
|
C | T | 1 | a0001c0004t0003g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-29-1546C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604249 | ||||||
| chr4:88604273
|
C | T | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29-1522C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604273 | ||||||
| chr4:88604310
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-29-1485C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604310 | ||||||
| chr4:88604311
|
G | A | 1 | a0001c0001t0011g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-29-1484G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604311 | ||||||
| chr4:88604514
|
G | C | 2 | a0001c0001t0001g0005a0001c0008t0001g0005 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-29-1281G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604514 | ||||||
| chr4:88604535
|
C | T | 1 | a0001c0001t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29-1260C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604535 | ||||||
| chr4:88604594
|
T | C | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-1201T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604594 | ||||||
| chr4:88604889
|
A | G | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01099.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-906A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604889 | ||||||
| chr4:88604934
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-29-861G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604934 | ||||||
| chr4:88604939
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29-856A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604939 | ||||||
| chr4:88604944
|
A | AT | 7 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-842dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr4 | 88604944 | |||||
| chr4:88604992
|
T | C | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(18): Show | 21 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-29-803T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88604992 | ||||||
| chr4:88605090
|
A | T | 18 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29-705A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605090 | ||||||
| chr4:88605095
|
G | T | 18 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29-700G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605095 | ||||||
| chr4:88605184
|
C | T | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-611C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605184 | ||||||
| chr4:88605331
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-29-464C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605331 | ||||||
| chr4:88605575
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-29-220A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605575 | ||||||
| chr4:88605713
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(118): Show | 125 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-29-82A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 2/25 | chr4 | 88605713 | ||||||
| chr4:88606059
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.226+10C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606059 | ||||||
| chr4:88606146
|
C | T | 41 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(38): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.226+97C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606146 | ||||||
| chr4:88606172
|
G | A | 57 | a0001c0001t0003g0053a0001c0001t0003g0056a0001c0001t0003g0060others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.226+123G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606172 | ||||||
| chr4:88606187
|
TC | T | 3 | a0001c0007t0002g0122a0001c0007t0004g0121a0002c0003t0002g0016 | 3 | HG00639.hp1 HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+140delC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88606187 | |||||
| chr4:88606253
|
CT | C | 56 | a0001c0001t0001g0036a0001c0001t0001g0223a0001c0001t0001g0271others(53): Show | 57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.226+220delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88606253 | |||||
| chr4:88606261
|
T | C | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+212T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606261 | ||||||
| chr4:88606283
|
G | A | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+234G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606283 | ||||||
| chr4:88606360
|
T | C | 44 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0150others(41): Show | 46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.226+311T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606360 | ||||||
| chr4:88606445
|
G | A | 1 | a0001c0005t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.226+396G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606445 | ||||||
| chr4:88606514
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(165): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.226+465G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606514 | ||||||
| chr4:88606606
|
G | A | 3 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031 | 3 | HG00544.hp2 NA18965.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.226+557G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606606 | ||||||
| chr4:88606606
|
G | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+557G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606606 | ||||||
| chr4:88606614
|
G | A | 1 | a0002c0003t0002g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.226+565G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606614 | ||||||
| chr4:88606652
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.226+603T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606652 | ||||||
| chr4:88606738
|
A | G | 1 | a0001c0005t0005g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.226+689A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88606738 | ||||||
| chr4:88607172
|
GGT | G | 163 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.226+1146_226+1147d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88607172 | |||||
| chr4:88607172
|
GGTGT | G | 21 | a0001c0001t0001g0147a0001c0001t0002g0034a0001c0001t0004g0025others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.226+1144_226+1147d others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88607172 | |||||
| chr4:88607172
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.226+1138_226+1147d others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88607172 | |||||
| chr4:88607333
|
G | C | 1 | a0001c0001t0006g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+1284G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607333 | ||||||
| chr4:88607352
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.226+1303A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607352 | ||||||
| chr4:88607375
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.226+1326A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607375 | ||||||
| chr4:88607378
|
C | T | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+1329C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607378 | ||||||
| chr4:88607438
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.226+1389C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607438 | ||||||
| chr4:88607609
|
C | A | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226+1560C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607609 | ||||||
| chr4:88607647
|
T | A | 4 | a0001c0001t0003g0053a0001c0001t0003g0056a0001c0001t0003g0060others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+1598T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88607647 | ||||||
| chr4:88608142
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+2093C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608142 | ||||||
| chr4:88608182
|
C | T | 1 | a0001c0004t0004g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226+2133C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608182 | ||||||
| chr4:88608308
|
C | G | 3 | a0001c0001t0005g0009a0002c0003t0002g0250a0002c0003t0002g0251 | 4 | HG02647.hp1 HG02970.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2259C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608308 | ||||||
| chr4:88608444
|
A | C | 1 | a0001c0001t0004g0050 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.226+2395A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608444 | ||||||
| chr4:88608673
|
G | A | 1 | a0001c0001t0009g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226+2624G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608673 | ||||||
| chr4:88608836
|
A | G | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2787A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608836 | ||||||
| chr4:88608869
|
A | G | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+2820A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88608869 | ||||||
| chr4:88609083
|
T | C | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+3034T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609083 | ||||||
| chr4:88609112
|
C | CA | 86 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(83): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.226+3084dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88609112 | |||||
| chr4:88609112
|
C | CAA | 14 | a0001c0001t0003g0056a0001c0001t0003g0067a0001c0001t0003g0204others(11): Show | 14 | HG00438.hp1 HG00639.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.226+3083_226+3084d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88609112 | |||||
| chr4:88609112
|
CA | C | 69 | a0001c0001t0001g0222a0001c0001t0004g0117a0001c0001t0004g0190others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.226+3084delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88609112 | |||||
| chr4:88609112
|
CAA | C | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG00140.hp2 HG01884.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.226+3083_226+3084d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88609112 | |||||
| chr4:88609112
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+3075_226+3084d others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88609112 | |||||
| chr4:88609206
|
C | G | 54 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(51): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.226+3157C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609206 | ||||||
| chr4:88609244
|
T | C | 9 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(6): Show | 9 | HG00639.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.226+3195T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609244 | ||||||
| chr4:88609305
|
C | A | 1 | a0001c0001t0004g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.226+3256C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609305 | ||||||
| chr4:88609674
|
C | G | 50 | a0001c0001t0004g0117a0001c0005t0001g0081a0001c0005t0001g0092others(47): Show | 52 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.226+3625C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609674 | ||||||
| chr4:88609789
|
G | A | 1 | a0002c0002t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.226+3740G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609789 | ||||||
| chr4:88609838
|
A | G | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+3789A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609838 | ||||||
| chr4:88609851
|
A | G | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+3802A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609851 | ||||||
| chr4:88609865
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(185): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.226+3816A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88609865 | ||||||
| chr4:88610043
|
C | T | 2 | a0001c0001t0004g0190a0001c0004t0006g0285 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.226+3994C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610043 | ||||||
| chr4:88610049
|
C | T | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+4000C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610049 | ||||||
| chr4:88610107
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(185): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.226+4058A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610107 | ||||||
| chr4:88610189
|
T | C | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226+4140T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610189 | ||||||
| chr4:88610402
|
G | A | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.226+4353G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610402 | ||||||
| chr4:88610449
|
G | A | 3 | a0001c0001t0005g0027a0001c0001t0011g0020a0002c0003t0002g0021 | 3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.226+4400G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610449 | ||||||
| chr4:88610453
|
C | CA | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(135): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.226+4422dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88610453 | |||||
| chr4:88610453
|
C | CAA | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+4421_226+4422d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88610453 | |||||
| chr4:88610453
|
CAA | C | 47 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(44): Show | 49 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.226+4421_226+4422d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88610453 | |||||
| chr4:88610453
|
CAAA | C | 6 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+4420_226+4422d others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88610453 | |||||
| chr4:88610549
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+4500G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610549 | ||||||
| chr4:88610602
|
C | T | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+4553C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610602 | ||||||
| chr4:88610703
|
T | C | 1 | a0001c0005t0003g0063 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.226+4654T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610703 | ||||||
| chr4:88610816
|
C | T | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+4767C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610816 | ||||||
| chr4:88610941
|
C | T | 1 | a0002c0006t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.226+4892C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610941 | ||||||
| chr4:88610967
|
C | T | 1 | a0001c0004t0017g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226+4918C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610967 | ||||||
| chr4:88610968
|
G | A | 64 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(61): Show | 66 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.226+4919G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88610968 | ||||||
| chr4:88611223
|
C | T | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+5174C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88611223 | ||||||
| chr4:88611430
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+5381C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88611430 | ||||||
| chr4:88611496
|
T | C | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+5447T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88611496 | ||||||
| chr4:88611531
|
G | A | 158 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(155): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.226+5482G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88611531 | ||||||
| chr4:88611853
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0142a0001c0001t0001g0145others(7): Show | 10 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.226+5804G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88611853 | ||||||
| chr4:88612029
|
A | C | 1 | a0001c0001t0003g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.226+5980A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612029 | ||||||
| chr4:88612114
|
C | T | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+6065C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612114 | ||||||
| chr4:88612182
|
G | T | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+6133G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612182 | ||||||
| chr4:88612189
|
T | C | 4 | a0002c0003t0002g0016a0002c0003t0002g0019a0002c0003t0002g0022others(1): Show | 4 | HG00733.hp1 HG01099.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+6140T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612189 | ||||||
| chr4:88612259
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+6210C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612259 | ||||||
| chr4:88612289
|
C | CTG | 13 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0003g0011others(10): Show | 13 | HG00323.hp1 HG00544.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+6277_226+6278d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTG | 14 | a0001c0001t0001g0252a0001c0001t0002g0034a0001c0001t0003g0012others(11): Show | 14 | HG01071.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.226+6275_226+6278d others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTG | 41 | a0001c0001t0004g0040a0001c0001t0004g0043a0001c0001t0004g0048others(38): Show | 43 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.226+6273_226+6278d others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTGT others(1): Show |
29 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0041others(26): Show | 30 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.226+6271_226+6278d others(10): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTGT others(3): Show |
12 | a0001c0001t0003g0118a0001c0001t0005g0082a0001c0004t0003g0268others(9): Show | 12 | HG01099.hp1 HG01934.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+6269_226+6278d others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTGT others(5): Show |
9 | a0001c0004t0003g0266a0001c0004t0003g0267a0001c0004t0003g0276others(6): Show | 9 | HG00438.hp2 HG00733.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.226+6267_226+6278d others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTGT others(9): Show |
2 | a0001c0004t0001g0269a0001c0005t0003g0110 | 2 | HG03540.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.226+6263_226+6278d others(18): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
C | CTGTGTGT others(11): Show |
1 | a0001c0004t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+6261_226+6278d others(20): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
CTG | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6277_226+6278d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
CTGTG | C | 3 | a0001c0001t0005g0009a0002c0003t0002g0250a0002c0003t0002g0251 | 4 | HG02647.hp1 HG02970.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+6275_226+6278d others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0005t0003g0063 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.226+6269_226+6278d others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0003g0067a0001c0001t0006g0195 | 2 | HG01884.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.226+6267_226+6278d others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612289
|
CTGTGTGT others(7): Show |
C | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+6265_226+6278d others(16): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612289 | |||||
| chr4:88612380
|
C | CAGGCCCC others(7): Show |
1 | a0001c0004t0004g0280 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.226+6332_226+6345d others(16): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88612380 | |||||
| chr4:88612617
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+6568C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612617 | ||||||
| chr4:88612794
|
C | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+6745C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612794 | ||||||
| chr4:88612949
|
T | G | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+6900T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88612949 | ||||||
| chr4:88613009
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.226+6960A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613009 | ||||||
| chr4:88613032
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.226+6983A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613032 | ||||||
| chr4:88613150
|
A | G | 3 | a0001c0005t0002g0096a0001c0005t0002g0103a0001c0005t0003g0110 | 3 | HG02895.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.226+7101A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613150 | ||||||
| chr4:88613152
|
C | T | 1 | a0001c0001t0003g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.226+7103C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613152 | ||||||
| chr4:88613353
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+7304G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613353 | ||||||
| chr4:88613478
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.226+7429A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613478 | ||||||
| chr4:88613557
|
C | T | 1 | a0004c0011t0002g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.226+7508C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613557 | ||||||
| chr4:88613782
|
G | C | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+7733G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613782 | ||||||
| chr4:88613955
|
C | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0007t0002g0122others(1): Show | 4 | HG00639.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+7906C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88613955 | ||||||
| chr4:88613959
|
A | AT | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.226+7918dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88613959 | |||||
| chr4:88614119
|
G | A | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+8070G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88614119 | ||||||
| chr4:88614133
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.226+8084T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88614133 | ||||||
| chr4:88614251
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+8202A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88614251 | ||||||
| chr4:88614468
|
T | C | 2 | a0001c0001t0011g0186a0001c0001t0012g0185 | 2 | HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.226+8419T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88614468 | ||||||
| chr4:88614822
|
T | G | 2 | a0001c0001t0002g0034a0001c0001t0004g0025 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.226+8773T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88614822 | ||||||
| chr4:88615142
|
G | A | 8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+9093G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615142 | ||||||
| chr4:88615165
|
A | G | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.226+9116A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615165 | ||||||
| chr4:88615223
|
T | TCC | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+9175_226+9176i others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88615223 | |||||
| chr4:88615225
|
T | C | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+9176T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615225 | ||||||
| chr4:88615227
|
G | C | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+9178G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615227 | ||||||
| chr4:88615239
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+9190A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615239 | ||||||
| chr4:88615645
|
T | G | 1 | a0001c0001t0007g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.226+9596T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615645 | ||||||
| chr4:88615681
|
T | G | 65 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(62): Show | 67 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.226+9632T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88615681 | ||||||
| chr4:88616112
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.226+10063T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616112 | ||||||
| chr4:88616118
|
G | A | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+10069G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616118 | ||||||
| chr4:88616195
|
TCTTTA | T | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+10152_226+1015 others(9): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88616195 | |||||
| chr4:88616233
|
T | C | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+10184T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616233 | ||||||
| chr4:88616257
|
T | C | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+10208T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616257 | ||||||
| chr4:88616540
|
A | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+10491A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616540 | ||||||
| chr4:88616670
|
T | TTTTG | 4 | a0001c0001t0001g0035a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00642.hp2 HG01257.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+10645_226+1064 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88616670 | |||||
| chr4:88616707
|
T | C | 1 | a0001c0001t0006g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.226+10658T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616707 | ||||||
| chr4:88616889
|
A | G | 2 | a0001c0001t0011g0186a0001c0001t0012g0185 | 2 | HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.226+10840A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88616889 | ||||||
| chr4:88617017
|
A | G | 4 | a0002c0002t0002g0084a0002c0002t0002g0085a0002c0002t0002g0086others(1): Show | 4 | NA18943.hp2 NA18945.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+10968A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617017 | ||||||
| chr4:88617055
|
A | G | 2 | a0001c0001t0003g0248a0001c0001t0003g0249 | 2 | HG02040.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.226+11006A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617055 | ||||||
| chr4:88617175
|
C | CA | 25 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 26 | HG00140.hp2 HG00423.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.226+11152dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617175 | |||||
| chr4:88617175
|
C | CAA | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+11151_226+1115 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617175 | |||||
| chr4:88617175
|
CA | C | 13 | a0001c0001t0001g0133a0001c0001t0001g0143a0001c0001t0001g0172others(10): Show | 13 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+11152delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617175 | |||||
| chr4:88617200
|
A | AAAT | 46 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.226+11152_226+1115 others(7): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617200 | |||||
| chr4:88617201
|
A | AG | 3 | a0002c0003t0002g0018a0002c0003t0002g0026a0002c0003t0002g0032 | 3 | HG02135.hp1 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.226+11153dupG | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617201 | |||||
| chr4:88617201
|
A | G | 16 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.226+11152A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617201 | ||||||
| chr4:88617218
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(193): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.226+11169T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617218 | ||||||
| chr4:88617273
|
G | T | 71 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(68): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.226+11224G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617273 | ||||||
| chr4:88617672
|
C | T | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226+11623C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617672 | ||||||
| chr4:88617883
|
A | AAG | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+11834_226+1183 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617883 | ||||||
| chr4:88617884
|
G | A | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+11835G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88617884 | ||||||
| chr4:88617884
|
G | GA | 69 | a0001c0001t0004g0117a0001c0001t0004g0190a0001c0001t0004g0244others(66): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.226+11845dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88617884 | |||||
| chr4:88618016
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.226+11967A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618016 | ||||||
| chr4:88618137
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.226+12088G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618137 | ||||||
| chr4:88618168
|
C | T | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+12119C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618168 | ||||||
| chr4:88618430
|
A | G | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+12381A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618430 | ||||||
| chr4:88618536
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+12487T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618536 | ||||||
| chr4:88618798
|
T | C | 19 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+12749T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618798 | ||||||
| chr4:88618913
|
G | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.226+12864G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88618913 | ||||||
| chr4:88618980
|
AG | A | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+12935delG | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88618980 | |||||
| chr4:88619058
|
C | T | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+13009C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619058 | ||||||
| chr4:88619195
|
C | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+13146C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619195 | ||||||
| chr4:88619268
|
A | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+13219A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619268 | ||||||
| chr4:88619336
|
G | C | 2 | a0001c0005t0003g0120a0002c0002t0002g0083 | 2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.226+13287G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619336 | ||||||
| chr4:88619431
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.226+13382T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619431 | ||||||
| chr4:88619445
|
A | G | 4 | a0001c0001t0005g0009a0002c0003t0002g0250a0002c0003t0002g0251others(1): Show | 5 | HG02630.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+13396A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619445 | ||||||
| chr4:88619560
|
A | G | 2 | a0001c0001t0004g0049a0001c0001t0004g0051 | 2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226+13511A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619560 | ||||||
| chr4:88619562
|
C | T | 1 | a0001c0001t0012g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.226+13513C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619562 | ||||||
| chr4:88619577
|
G | A | 1 | a0001c0004t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+13528G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619577 | ||||||
| chr4:88619596
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.226+13547A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619596 | ||||||
| chr4:88619659
|
G | A | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.226+13610G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619659 | ||||||
| chr4:88619703
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+13654C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619703 | ||||||
| chr4:88619704
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.226+13655G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619704 | ||||||
| chr4:88619788
|
T | C | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+13739T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619788 | ||||||
| chr4:88619865
|
G | A | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+13816G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88619865 | ||||||
| chr4:88620333
|
C | T | 1 | a0002c0003t0014g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.226+14284C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620333 | ||||||
| chr4:88620410
|
C | T | 4 | a0001c0001t0005g0009a0002c0003t0002g0250a0002c0003t0002g0251others(1): Show | 5 | HG02630.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+14361C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620410 | ||||||
| chr4:88620468
|
C | A | 1 | a0001c0001t0004g0002 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.226+14419C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620468 | ||||||
| chr4:88620616
|
A | G | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.226+14567A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620616 | ||||||
| chr4:88620619
|
C | A | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+14570C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620619 | ||||||
| chr4:88620631
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+14582T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620631 | ||||||
| chr4:88620877
|
C | T | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+14828C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620877 | ||||||
| chr4:88620878
|
C | G | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+14829C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88620878 | ||||||
| chr4:88621088
|
G | A | 22 | a0001c0001t0004g0002a0001c0001t0004g0040a0001c0001t0004g0041others(19): Show | 23 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.226+15039G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621088 | ||||||
| chr4:88621114
|
A | G | 1 | a0001c0001t0003g0284 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.226+15065A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621114 | ||||||
| chr4:88621130
|
C | T | 85 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(82): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.226+15081C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621130 | ||||||
| chr4:88621147
|
A | T | 1 | a0001c0005t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.226+15098A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621147 | ||||||
| chr4:88621150
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+15101C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621150 | ||||||
| chr4:88621338
|
C | G | 4 | a0001c0001t0005g0027a0001c0001t0011g0020a0001c0004t0004g0282others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+15289C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621338 | ||||||
| chr4:88621413
|
G | A | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226+15364G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621413 | ||||||
| chr4:88621470
|
G | A | 1 | a0002c0003t0002g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.226+15421G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621470 | ||||||
| chr4:88621831
|
C | T | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+15782C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621831 | ||||||
| chr4:88621895
|
A | C | 6 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+15846A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88621895 | ||||||
| chr4:88622039
|
A | G | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+15990A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622039 | ||||||
| chr4:88622236
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.226+16187C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622236 | ||||||
| chr4:88622471
|
CAT | C | 19 | a0001c0001t0002g0034a0001c0004t0001g0269a0001c0004t0002g0265others(16): Show | 19 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.226+16423_226+1642 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622471 | ||||||
| chr4:88622582
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+16533A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622582 | ||||||
| chr4:88622669
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.226+16620G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622669 | ||||||
| chr4:88622767
|
A | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0139others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+16718A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622767 | ||||||
| chr4:88622821
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226+16772C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622821 | ||||||
| chr4:88622890
|
C | T | 1 | a0002c0002t0002g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.226+16841C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622890 | ||||||
| chr4:88622893
|
C | T | 1 | a0002c0002t0002g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.226+16844C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88622893 | ||||||
| chr4:88623112
|
G | A | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.226+17063G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623112 | ||||||
| chr4:88623191
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG00408.hp2 HG02165.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+17142G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623191 | ||||||
| chr4:88623490
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0252 | 2 | HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.226+17441C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623490 | ||||||
| chr4:88623731
|
A | C | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.226+17682A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623731 | ||||||
| chr4:88623847
|
A | T | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.226+17798A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623847 | ||||||
| chr4:88623866
|
G | T | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.226+17817G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623866 | ||||||
| chr4:88623867
|
T | C | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.226+17818T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88623867 | ||||||
| chr4:88624155
|
T | G | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.226+18106T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624155 | ||||||
| chr4:88624193
|
C | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(185): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.226+18144C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624193 | ||||||
| chr4:88624194
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.226+18145G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624194 | ||||||
| chr4:88624251
|
G | T | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.226+18202G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624251 | ||||||
| chr4:88624350
|
A | G | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+18301A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624350 | ||||||
| chr4:88624456
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.226+18407C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624456 | ||||||
| chr4:88624529
|
C | T | 1 | a0001c0001t0006g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+18480C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624529 | ||||||
| chr4:88624695
|
C | T | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | NA18975.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.226+18646C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624695 | ||||||
| chr4:88624728
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+18679A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624728 | ||||||
| chr4:88624787
|
G | A | 2 | a0002c0003t0002g0177a0002c0003t0002g0181 | 2 | NA18940.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.226+18738G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624787 | ||||||
| chr4:88624792
|
G | A | 2 | a0001c0004t0004g0277a0005c0013t0005g0264 | 2 | HG01167.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.226+18743G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624792 | ||||||
| chr4:88624874
|
T | C | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+18825T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624874 | ||||||
| chr4:88624889
|
A | T | 1 | a0001c0001t0003g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226+18840A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624889 | ||||||
| chr4:88624905
|
G | GT | 4 | a0001c0001t0001g0162a0001c0001t0001g0201a0001c0001t0006g0137others(1): Show | 4 | HG01934.hp1 HG02004.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+18863dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88624905 | |||||
| chr4:88624924
|
C | T | 2 | a0001c0001t0004g0049a0001c0001t0004g0051 | 2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226+18875C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88624924 | ||||||
| chr4:88625116
|
G | A | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.226+19067G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625116 | ||||||
| chr4:88625275
|
A | G | 3 | a0001c0001t0007g0159a0001c0001t0007g0171a0001c0001t0007g0241 | 3 | HG01081.hp2 HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.226+19226A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625275 | ||||||
| chr4:88625276
|
A | G | 1 | a0001c0004t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+19227A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625276 | ||||||
| chr4:88625345
|
T | C | 1 | a0002c0003t0002g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.226+19296T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625345 | ||||||
| chr4:88625649
|
T | TGGCTTAT others(7): Show |
1 | a0001c0001t0003g0075 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.226+19601_226+1961 others(18): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88625649 | |||||
| chr4:88625836
|
A | AT | 23 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(20): Show | 23 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.226+19796dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88625836 | |||||
| chr4:88625836
|
AT | A | 13 | a0001c0001t0004g0040a0001c0001t0004g0042a0001c0001t0004g0045others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+19796delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88625836 | |||||
| chr4:88625839
|
T | A | 13 | a0001c0001t0004g0040a0001c0001t0004g0042a0001c0001t0004g0045others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+19790T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625839 | ||||||
| chr4:88625982
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0157 | 2 | HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.226+19933C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625982 | ||||||
| chr4:88625994
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.226+19945C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88625994 | ||||||
| chr4:88626375
|
A | G | 10 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0003g0067others(7): Show | 10 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.226+20326A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626375 | ||||||
| chr4:88626405
|
G | C | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+20356G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626405 | ||||||
| chr4:88626465
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+20416A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626465 | ||||||
| chr4:88626485
|
A | G | 2 | a0001c0001t0004g0190a0001c0004t0006g0285 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.226+20436A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626485 | ||||||
| chr4:88626538
|
A | T | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+20489A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626538 | ||||||
| chr4:88626540
|
A | G | 22 | a0001c0001t0004g0002a0001c0001t0004g0040a0001c0001t0004g0041others(19): Show | 23 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.226+20491A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626540 | ||||||
| chr4:88626739
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+20690C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88626739 | ||||||
| chr4:88626872
|
CTTTTTG | C | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.226+20827_226+2083 others(10): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88626872 | |||||
| chr4:88627170
|
G | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.226+21121G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627170 | ||||||
| chr4:88627189
|
T | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0164others(3): Show | 6 | HG01081.hp2 HG01099.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+21140T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627189 | ||||||
| chr4:88627624
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.226+21575C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627624 | ||||||
| chr4:88627625
|
G | A | 6 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+21576G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627625 | ||||||
| chr4:88627748
|
CA | C | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0051 | 3 | HG01109.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226+21705delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88627748 | |||||
| chr4:88627755
|
G | T | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0051 | 3 | HG01109.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226+21706G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627755 | ||||||
| chr4:88627760
|
CAGGT | C | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.226+21713_226+2171 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88627760 | |||||
| chr4:88627819
|
G | A | 6 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(3): Show | 6 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+21770G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88627819 | ||||||
| chr4:88627904
|
CA | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(113): Show | 120 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.226+21876delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88627904 | |||||
| chr4:88627904
|
CAA | C | 23 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(20): Show | 23 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.226+21875_226+2187 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88627904 | |||||
| chr4:88627904
|
CAAAAAAA others(2): Show |
C | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+21868_226+2187 others(13): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88627904 | |||||
| chr4:88628033
|
G | A | 1 | a0001c0005t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.227-21807G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628033 | ||||||
| chr4:88628304
|
G | A | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-21536G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628304 | ||||||
| chr4:88628597
|
T | C | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-21243T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628597 | ||||||
| chr4:88628673
|
A | G | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-21167A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628673 | ||||||
| chr4:88628757
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-21083A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628757 | ||||||
| chr4:88628900
|
C | T | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.227-20940C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628900 | ||||||
| chr4:88628954
|
G | C | 2 | a0001c0001t0004g0190a0001c0004t0006g0285 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.227-20886G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88628954 | ||||||
| chr4:88629317
|
T | TTA | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.227-20521_227-2052 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88629317 | |||||
| chr4:88629336
|
C | T | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-20504C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629336 | ||||||
| chr4:88629576
|
C | G | 1 | a0001c0001t0003g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.227-20264C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629576 | ||||||
| chr4:88629609
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.227-20231T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629609 | ||||||
| chr4:88629611
|
T | C | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.227-20229T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629611 | ||||||
| chr4:88629647
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-20193A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629647 | ||||||
| chr4:88629890
|
A | G | 1 | a0003c0010t0003g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.227-19950A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88629890 | ||||||
| chr4:88630030
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-19810A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630030 | ||||||
| chr4:88630066
|
T | C | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-19774T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630066 | ||||||
| chr4:88630224
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-19616C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630224 | ||||||
| chr4:88630248
|
A | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-19592A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630248 | ||||||
| chr4:88630402
|
G | A | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-19438G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630402 | ||||||
| chr4:88630855
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.227-18985C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88630855 | ||||||
| chr4:88631053
|
A | T | 1 | a0001c0005t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.227-18787A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631053 | ||||||
| chr4:88631070
|
A | T | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-18770A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631070 | ||||||
| chr4:88631197
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-18643A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631197 | ||||||
| chr4:88631212
|
T | C | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-18628T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631212 | ||||||
| chr4:88631223
|
G | A | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-18617G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631223 | ||||||
| chr4:88631316
|
G | A | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-18524G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631316 | ||||||
| chr4:88631500
|
A | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-18340A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631500 | ||||||
| chr4:88631571
|
G | A | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-18269G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631571 | ||||||
| chr4:88631711
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.227-18129G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631711 | ||||||
| chr4:88631863
|
T | A | 51 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(48): Show | 53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-17977T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631863 | ||||||
| chr4:88631960
|
T | C | 1 | a0002c0003t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.227-17880T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631960 | ||||||
| chr4:88631990
|
A | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-17850A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88631990 | ||||||
| chr4:88632007
|
A | T | 72 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(69): Show | 74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.227-17833A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632007 | ||||||
| chr4:88632033
|
C | A | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-17807C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632033 | ||||||
| chr4:88632141
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.227-17699C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632141 | ||||||
| chr4:88632170
|
C | T | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-17670C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632170 | ||||||
| chr4:88632260
|
A | G | 1 | a0001c0004t0002g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.227-17580A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632260 | ||||||
| chr4:88632349
|
A | C | 58 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(55): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.227-17491A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632349 | ||||||
| chr4:88632474
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0155 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.227-17366T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632474 | ||||||
| chr4:88632577
|
A | G | 1 | a0002c0002t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.227-17263A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632577 | ||||||
| chr4:88632687
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-17153A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632687 | ||||||
| chr4:88632820
|
C | T | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.227-17020C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632820 | ||||||
| chr4:88632821
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.227-17019A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632821 | ||||||
| chr4:88632867
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-16973A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88632867 | ||||||
| chr4:88633321
|
G | A | 2 | a0001c0001t0004g0190a0001c0004t0006g0285 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.227-16519G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633321 | ||||||
| chr4:88633440
|
G | A | 57 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.227-16400G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633440 | ||||||
| chr4:88633456
|
A | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-16384A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633456 | ||||||
| chr4:88633500
|
T | C | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-16340T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633500 | ||||||
| chr4:88633606
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-16234G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633606 | ||||||
| chr4:88633717
|
T | TAGAG | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-16120_227-1611 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88633717 | |||||
| chr4:88633956
|
G | A | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-15884G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633956 | ||||||
| chr4:88633964
|
C | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.227-15876C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88633964 | ||||||
| chr4:88634471
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0003g0228 | 2 | NA19063.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.227-15369G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88634471 | ||||||
| chr4:88634492
|
A | G | 72 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(69): Show | 74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.227-15348A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88634492 | ||||||
| chr4:88634522
|
G | A | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-15318G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88634522 | ||||||
| chr4:88634701
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.227-15139C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88634701 | ||||||
| chr4:88634795
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0005g0082a0002c0003t0002g0078 | 3 | HG03490.hp2 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.227-15045G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88634795 | ||||||
| chr4:88635011
|
C | T | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.227-14829C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635011 | ||||||
| chr4:88635044
|
A | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-14796A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635044 | ||||||
| chr4:88635085
|
G | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-14755G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635085 | ||||||
| chr4:88635161
|
T | C | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-14679T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635161 | ||||||
| chr4:88635310
|
G | A | 2 | a0002c0003t0002g0016a0002c0003t0002g0019 | 2 | HG01099.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.227-14530G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635310 | ||||||
| chr4:88635314
|
T | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-14526T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635314 | ||||||
| chr4:88635532
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.227-14308A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88635532 | ||||||
| chr4:88636069
|
A | G | 3 | a0001c0005t0002g0096a0001c0005t0002g0103a0001c0005t0003g0110 | 3 | HG02895.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.227-13771A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636069 | ||||||
| chr4:88636085
|
A | G | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.227-13755A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636085 | ||||||
| chr4:88636088
|
A | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-13752A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636088 | ||||||
| chr4:88636115
|
G | A | 2 | a0001c0001t0006g0135a0001c0001t0006g0137 | 2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.227-13725G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636115 | ||||||
| chr4:88636385
|
C | A | 2 | a0001c0001t0004g0286a0001c0001t0004g0287 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.227-13455C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636385 | ||||||
| chr4:88636610
|
A | C | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-13230A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636610 | ||||||
| chr4:88636651
|
A | G | 3 | a0001c0001t0005g0027a0001c0001t0011g0020a0002c0003t0002g0021 | 3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.227-13189A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636651 | ||||||
| chr4:88636863
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-12977C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636863 | ||||||
| chr4:88636910
|
C | T | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-12930C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636910 | ||||||
| chr4:88636996
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.227-12844G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88636996 | ||||||
| chr4:88637002
|
G | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-12838G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637002 | ||||||
| chr4:88637139
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.227-12701A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637139 | ||||||
| chr4:88637252
|
C | T | 18 | a0001c0001t0004g0117a0001c0001t0005g0027a0001c0001t0008g0028others(15): Show | 18 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.227-12588C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637252 | ||||||
| chr4:88637404
|
C | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-12436C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637404 | ||||||
| chr4:88637425
|
C | CCAAA | 25 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 26 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.227-12398_227-1239 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88637425 | |||||
| chr4:88637600
|
G | A | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.227-12240G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637600 | ||||||
| chr4:88637610
|
A | G | 1 | a0001c0005t0001g0092 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.227-12230A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637610 | ||||||
| chr4:88637672
|
A | G | 58 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(55): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.227-12168A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637672 | ||||||
| chr4:88637887
|
G | A | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-11953G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637887 | ||||||
| chr4:88637966
|
A | AT | 77 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-11874_227-1187 others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88637966 | ||||||
| chr4:88638021
|
C | A | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.227-11819C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638021 | ||||||
| chr4:88638036
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-11804T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638036 | ||||||
| chr4:88638150
|
T | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-11690T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638150 | ||||||
| chr4:88638279
|
A | T | 1 | a0002c0003t0002g0123 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.227-11561A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638279 | ||||||
| chr4:88638282
|
CA | C | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-11556delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88638282 | |||||
| chr4:88638287
|
A | C | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-11553A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638287 | ||||||
| chr4:88638340
|
T | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-11500T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638340 | ||||||
| chr4:88638469
|
A | G | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.227-11371A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638469 | ||||||
| chr4:88638472
|
C | T | 1 | a0002c0003t0002g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.227-11368C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638472 | ||||||
| chr4:88638491
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.227-11349A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638491 | ||||||
| chr4:88638561
|
C | A | 1 | a0001c0001t0003g0202 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.227-11279C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638561 | ||||||
| chr4:88638630
|
T | C | 1 | a0001c0004t0003g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.227-11210T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638630 | ||||||
| chr4:88638813
|
A | C | 1 | a0002c0002t0015g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.227-11027A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638813 | ||||||
| chr4:88638816
|
C | T | 21 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-11024C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88638816 | ||||||
| chr4:88639324
|
T | C | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.227-10516T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639324 | ||||||
| chr4:88639332
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(282): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.227-10508T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639332 | ||||||
| chr4:88639404
|
T | C | 1 | a0002c0003t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.227-10436T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639404 | ||||||
| chr4:88639431
|
A | ACAC | 77 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-10408_227-1040 others(7): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88639431 | |||||
| chr4:88639841
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.227-9999A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639841 | ||||||
| chr4:88639887
|
GA | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-9943delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88639887 | |||||
| chr4:88639897
|
A | C | 44 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(41): Show | 46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.227-9943A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639897 | ||||||
| chr4:88639898
|
C | A | 1 | a0001c0001t0012g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.227-9942C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639898 | ||||||
| chr4:88639971
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.227-9869G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88639971 | ||||||
| chr4:88640095
|
A | G | 1 | a0002c0003t0002g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.227-9745A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88640095 | ||||||
| chr4:88640524
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.227-9316T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88640524 | ||||||
| chr4:88640687
|
TAACA | T | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.227-9149_227-9146d others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88640687 | |||||
| chr4:88640826
|
A | G | 20 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-9014A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88640826 | ||||||
| chr4:88640940
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(191): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.227-8900T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88640940 | ||||||
| chr4:88640971
|
T | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-8869T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88640971 | ||||||
| chr4:88641069
|
G | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-8771G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641069 | ||||||
| chr4:88641112
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0231 | 2 | HG02083.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.227-8728C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641112 | ||||||
| chr4:88641203
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-8637A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641203 | ||||||
| chr4:88641213
|
G | A | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.227-8627G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641213 | ||||||
| chr4:88641423
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(76): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.227-8417T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641423 | ||||||
| chr4:88641656
|
G | C | 1 | a0002c0003t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.227-8184G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88641656 | ||||||
| chr4:88642015
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.227-7825C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642015 | ||||||
| chr4:88642130
|
C | CA | 98 | a0001c0001t0001g0035a0001c0001t0001g0070a0001c0001t0001g0076others(95): Show | 101 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.227-7688dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88642130 | |||||
| chr4:88642130
|
C | CAA | 9 | a0001c0001t0001g0211a0001c0001t0003g0060a0001c0001t0003g0118others(6): Show | 9 | HG00438.hp2 HG02027.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.227-7689_227-7688d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88642130 | |||||
| chr4:88642130
|
CAAAAAAA others(5): Show |
C | 57 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.227-7699_227-7688d others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88642130 | |||||
| chr4:88642195
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.227-7645C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642195 | ||||||
| chr4:88642287
|
T | G | 1 | a0001c0001t0003g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-7553T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642287 | ||||||
| chr4:88642346
|
A | T | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.227-7494A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642346 | ||||||
| chr4:88642608
|
C | T | 1 | a0001c0001t0006g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.227-7232C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642608 | ||||||
| chr4:88642800
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-7040G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642800 | ||||||
| chr4:88642822
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-7018T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642822 | ||||||
| chr4:88642828
|
A | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-7012A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642828 | ||||||
| chr4:88642916
|
G | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-6924G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642916 | ||||||
| chr4:88642929
|
A | T | 16 | a0001c0001t0005g0027a0001c0001t0008g0028a0001c0001t0011g0020others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.227-6911A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88642929 | ||||||
| chr4:88643097
|
G | A | 4 | a0001c0001t0005g0009a0002c0003t0002g0250a0002c0003t0002g0251others(1): Show | 5 | HG02630.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-6743G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643097 | ||||||
| chr4:88643211
|
A | G | 9 | a0001c0005t0001g0092a0001c0005t0001g0093a0001c0005t0004g0091others(6): Show | 9 | HG00323.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.227-6629A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643211 | ||||||
| chr4:88643258
|
T | C | 46 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(43): Show | 48 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.227-6582T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643258 | ||||||
| chr4:88643284
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.227-6556C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643284 | ||||||
| chr4:88643371
|
T | C | 1 | a0002c0006t0002g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.227-6469T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643371 | ||||||
| chr4:88643451
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.227-6389T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643451 | ||||||
| chr4:88643818
|
T | C | 1 | a0001c0001t0003g0208 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.227-6022T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643818 | ||||||
| chr4:88643968
|
G | T | 1 | a0001c0005t0001g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.227-5872G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643968 | ||||||
| chr4:88643981
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.227-5859A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643981 | ||||||
| chr4:88643993
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.227-5847C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88643993 | ||||||
| chr4:88644072
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.227-5768G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88644072 | ||||||
| chr4:88644136
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-5704G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88644136 | ||||||
| chr4:88644220
|
G | A | 3 | a0001c0001t0005g0027a0001c0001t0011g0020a0002c0003t0002g0021 | 3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.227-5620G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88644220 | ||||||
| chr4:88644419
|
C | T | 4 | a0001c0001t0003g0053a0001c0001t0003g0056a0001c0001t0003g0060others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-5421C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88644419 | ||||||
| chr4:88644692
|
G | C | 1 | a0001c0001t0008g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.227-5148G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88644692 | ||||||
| chr4:88645052
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(82): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.227-4788C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645052 | ||||||
| chr4:88645082
|
T | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.227-4758T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645082 | ||||||
| chr4:88645097
|
T | C | 1 | a0002c0003t0002g0031 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.227-4743T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645097 | ||||||
| chr4:88645223
|
G | A | 22 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(19): Show | 22 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.227-4617G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645223 | ||||||
| chr4:88645350
|
T | A | 1 | a0001c0001t0003g0068 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.227-4490T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645350 | ||||||
| chr4:88645749
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-4091T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88645749 | ||||||
| chr4:88646616
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(193): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.227-3224G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88646616 | ||||||
| chr4:88646622
|
A | G | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-3218A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88646622 | ||||||
| chr4:88646687
|
G | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-3153G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88646687 | ||||||
| chr4:88646995
|
C | G | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.227-2845C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88646995 | ||||||
| chr4:88647231
|
G | C | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-2609G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88647231 | ||||||
| chr4:88647261
|
C | T | 1 | a0001c0001t0012g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.227-2579C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88647261 | ||||||
| chr4:88647677
|
AT | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-2159delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88647677 | |||||
| chr4:88647725
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-2115A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88647725 | ||||||
| chr4:88647808
|
C | CT | 54 | a0001c0001t0001g0238a0001c0001t0004g0190a0001c0001t0005g0255others(51): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.227-2017dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88647808 | |||||
| chr4:88647808
|
C | CTT | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-2018_227-2017d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr4 | 88647808 | |||||
| chr4:88647846
|
A | T | 1 | a0001c0001t0003g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.227-1994A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88647846 | ||||||
| chr4:88647996
|
T | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.227-1844T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88647996 | ||||||
| chr4:88648049
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-1791G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648049 | ||||||
| chr4:88648064
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-1776A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648064 | ||||||
| chr4:88648124
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.227-1716T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648124 | ||||||
| chr4:88648503
|
GA | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.227-1336delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648503 | ||||||
| chr4:88648706
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0155 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.227-1134A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648706 | ||||||
| chr4:88648867
|
T | G | 1 | a0001c0001t0004g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.227-973T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88648867 | ||||||
| chr4:88649065
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(76): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.227-775T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649065 | ||||||
| chr4:88649210
|
C | T | 7 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0046others(4): Show | 7 | HG00642.hp1 HG01243.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-630C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649210 | ||||||
| chr4:88649296
|
C | T | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.227-544C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649296 | ||||||
| chr4:88649444
|
G | A | 58 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(55): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.227-396G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649444 | ||||||
| chr4:88649706
|
T | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.227-134T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649706 | ||||||
| chr4:88649748
|
A | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.227-92A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 3/25 | chr4 | 88649748 | ||||||
| chr4:88650109
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.386+110A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650109 | ||||||
| chr4:88650297
|
G | A | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.386+298G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650297 | ||||||
| chr4:88650600
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+601T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650600 | ||||||
| chr4:88650773
|
C | A | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+774C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650773 | ||||||
| chr4:88650868
|
T | A | 1 | a0001c0001t0003g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.386+869T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650868 | ||||||
| chr4:88650890
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+891T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650890 | ||||||
| chr4:88650980
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386+981T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88650980 | ||||||
| chr4:88651069
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387-943G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651069 | ||||||
| chr4:88651181
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.387-831A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651181 | ||||||
| chr4:88651212
|
A | G | 2 | a0001c0001t0004g0117a0001c0008t0004g0010 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.387-800A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651212 | ||||||
| chr4:88651292
|
G | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.387-720G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651292 | ||||||
| chr4:88651444
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0042 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387-568G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651444 | ||||||
| chr4:88651496
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.387-516T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651496 | ||||||
| chr4:88651506
|
A | T | 1 | a0001c0001t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387-506A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651506 | ||||||
| chr4:88651512
|
A | C | 1 | a0001c0001t0001g0223 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.387-500A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651512 | ||||||
| chr4:88651525
|
A | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387-487A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651525 | ||||||
| chr4:88651545
|
T | C | 1 | a0001c0001t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387-467T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651545 | ||||||
| chr4:88651564
|
G | A | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.387-448G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651564 | ||||||
| chr4:88651687
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.387-325G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651687 | ||||||
| chr4:88651712
|
G | C | 1 | a0001c0004t0004g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.387-300G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651712 | ||||||
| chr4:88651807
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0003g0008a0001c0001t0003g0199others(3): Show | 7 | NA18959.hp2 NA18979.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-205C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651807 | ||||||
| chr4:88651872
|
A | T | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.387-140A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 4/25 | chr4 | 88651872 | ||||||
| chr4:88652119
|
A | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.463+31A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652119 | ||||||
| chr4:88652181
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.463+93G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652181 | ||||||
| chr4:88652316
|
G | C | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+228G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652316 | ||||||
| chr4:88652329
|
G | A | 6 | a0001c0001t0008g0028a0002c0003t0002g0029a0002c0003t0002g0030others(3): Show | 6 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+241G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652329 | ||||||
| chr4:88652412
|
A | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+324A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652412 | ||||||
| chr4:88652476
|
G | A | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+388G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652476 | ||||||
| chr4:88652622
|
C | A | 1 | a0001c0001t0004g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.464-247C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 5/25 | chr4 | 88652622 | ||||||
| chr4:88653112
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.685+22A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653112 | ||||||
| chr4:88653501
|
A | C | 7 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0168others(4): Show | 7 | HG00423.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.685+411A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653501 | ||||||
| chr4:88653502
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.685+412G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653502 | ||||||
| chr4:88653503
|
G | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.685+413G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653503 | ||||||
| chr4:88653511
|
A | G | 152 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(149): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.685+421A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653511 | ||||||
| chr4:88653563
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.685+473C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653563 | ||||||
| chr4:88653957
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.686-85A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653957 | ||||||
| chr4:88653986
|
T | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.686-56T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 6/25 | chr4 | 88653986 | ||||||
| chr4:88654173
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(191): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.777+40T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654173 | ||||||
| chr4:88654178
|
G | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.777+45G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654178 | ||||||
| chr4:88654189
|
T | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+56T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654189 | ||||||
| chr4:88654348
|
TCATA | T | 14 | a0001c0001t0002g0034a0001c0001t0005g0027a0001c0001t0008g0028others(11): Show | 14 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.777+216_777+219del others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(5): Show |
T | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.777+216_777+227del others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(7): Show |
T | 5 | a0001c0004t0003g0267a0001c0005t0003g0120a0001c0007t0002g0122others(2): Show | 5 | HG00639.hp1 HG03579.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+216_777+229del others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(9): Show |
T | 63 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(60): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.777+216_777+231del others(16): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(11): Show |
T | 1 | a0002c0002t0002g0079 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.777+216_777+233del others(18): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(13): Show |
T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+216_777+235del others(20): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654348
|
TCATATAT others(19): Show |
T | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.777+216_777+241del others(26): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654348 | ||||||
| chr4:88654349
|
C | CAT | 11 | a0001c0001t0001g0128a0001c0001t0001g0157a0001c0001t0003g0228others(8): Show | 12 | HG02055.hp2 HG02056.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.777+254_777+255dup others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
C | CATAT | 10 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0240others(7): Show | 11 | HG00408.hp2 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.777+252_777+255dup others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
C | CATATAT | 11 | a0001c0001t0001g0217a0001c0001t0001g0234a0001c0001t0001g0235others(8): Show | 11 | HG00642.hp1 HG01168.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+250_777+255dup others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
C | CATATATA others(1): Show |
3 | a0001c0001t0004g0040a0002c0003t0002g0078a0002c0003t0002g0251 | 3 | HG02647.hp1 HG03490.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+248_777+255dup others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
C | T | 3 | a0001c0008t0004g0010a0002c0003t0002g0018a0002c0003t0002g0032 | 3 | HG02135.hp1 HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.777+216C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654349 | ||||||
| chr4:88654349
|
CAT | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(52): Show | 56 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.777+254_777+255del others(2): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
CATAT | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0012t0001g0270 | 3 | HG00733.hp2 HG03540.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.777+252_777+255del others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.777+246_777+255del others(10): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654349
|
CATATATA others(5): Show |
C | 11 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 12 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.777+244_777+255del others(12): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654349 | |||||
| chr4:88654383
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+250T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654383 | ||||||
| chr4:88654385
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+252T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654385 | ||||||
| chr4:88654387
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(31): Show | 35 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+254T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654387 | ||||||
| chr4:88654387
|
T | TATATATA others(3): Show |
1 | a0001c0001t0004g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.777+255_777+256ins others(10): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr4 | 88654387 | |||||
| chr4:88654389
|
C | T | 59 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(56): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.777+256C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654389 | ||||||
| chr4:88654403
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0232a0001c0001t0008g0220 | 3 | HG01192.hp1 HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.777+270A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654403 | ||||||
| chr4:88654489
|
T | G | 1 | a0001c0005t0003g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.777+356T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654489 | ||||||
| chr4:88654561
|
A | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.777+428A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654561 | ||||||
| chr4:88654735
|
T | C | 3 | a0002c0002t0002g0080a0002c0002t0002g0097a0002c0002t0002g0098 | 3 | NA18975.hp2 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.778-439T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654735 | ||||||
| chr4:88654794
|
T | G | 7 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0046others(4): Show | 7 | HG00642.hp1 HG01243.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-380T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654794 | ||||||
| chr4:88654797
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.778-377C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654797 | ||||||
| chr4:88654842
|
T | A | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.778-332T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654842 | ||||||
| chr4:88654861
|
G | C | 8 | a0001c0001t0001g0201a0001c0001t0003g0008a0001c0001t0003g0199others(5): Show | 9 | NA18959.hp2 NA18960.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-313G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654861 | ||||||
| chr4:88654924
|
C | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-250C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88654924 | ||||||
| chr4:88655021
|
A | G | 1 | a0001c0004t0003g0262 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.778-153A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88655021 | ||||||
| chr4:88655143
|
G | A | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.778-31G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 7/25 | chr4 | 88655143 | ||||||
| chr4:88655430
|
C | T | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.908+126C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655430 | ||||||
| chr4:88655468
|
G | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+164G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655468 | ||||||
| chr4:88655588
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.908+284T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655588 | ||||||
| chr4:88655597
|
T | C | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.909-278T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655597 | ||||||
| chr4:88655651
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.909-224T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655651 | ||||||
| chr4:88655657
|
A | T | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.909-218A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655657 | ||||||
| chr4:88655793
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.909-82A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655793 | ||||||
| chr4:88655834
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.909-41T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 8/25 | chr4 | 88655834 | ||||||
| chr4:88656063
|
A | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1069+28A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656063 | ||||||
| chr4:88656093
|
A | G | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1069+58A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656093 | ||||||
| chr4:88656156
|
T | G | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1069+121T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656156 | ||||||
| chr4:88656296
|
TGAA | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+265_1069+267d others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 88656296 | |||||
| chr4:88656921
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1069+886A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656921 | ||||||
| chr4:88656947
|
C | A | 1 | a0002c0003t0002g0031 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1069+912C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656947 | ||||||
| chr4:88656989
|
A | T | 152 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(149): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1069+954A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88656989 | ||||||
| chr4:88657051
|
AAGTC | A | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1069+1019_1069+102 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 88657051 | |||||
| chr4:88657264
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1070-1151C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657264 | ||||||
| chr4:88657269
|
A | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1070-1146A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657269 | ||||||
| chr4:88657439
|
T | G | 1 | a0002c0003t0002g0123 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1070-976T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657439 | ||||||
| chr4:88657496
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1070-919C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657496 | ||||||
| chr4:88657764
|
A | G | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1070-651A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657764 | ||||||
| chr4:88657780
|
C | T | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1070-635C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88657780 | ||||||
| chr4:88658025
|
T | G | 1 | a0002c0003t0002g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1070-390T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658025 | ||||||
| chr4:88658032
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1070-383G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658032 | ||||||
| chr4:88658181
|
T | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1070-234T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658181 | ||||||
| chr4:88658183
|
G | C | 1 | a0002c0003t0002g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1070-232G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658183 | ||||||
| chr4:88658199
|
A | G | 2 | a0001c0001t0004g0190a0001c0004t0006g0285 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1070-216A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658199 | ||||||
| chr4:88658318
|
T | C | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1070-97T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 9/25 | chr4 | 88658318 | ||||||
| chr4:88658700
|
T | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+209T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88658700 | ||||||
| chr4:88658841
|
T | C | 1 | a0001c0001t0003g0212 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1146+350T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88658841 | ||||||
| chr4:88659014
|
T | C | 1 | a0001c0001t0004g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1146+523T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659014 | ||||||
| chr4:88659392
|
A | G | 1 | a0002c0003t0002g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1146+901A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659392 | ||||||
| chr4:88659536
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1146+1045G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659536 | ||||||
| chr4:88659671
|
A | G | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1146+1180A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659671 | ||||||
| chr4:88659750
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1146+1259C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659750 | ||||||
| chr4:88659960
|
A | C | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1146+1469A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659960 | ||||||
| chr4:88659995
|
A | T | 6 | a0001c0004t0002g0265a0001c0004t0002g0274a0001c0004t0003g0262others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1146+1504A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659995 | ||||||
| chr4:88659997
|
G | C | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+1506G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88659997 | ||||||
| chr4:88660206
|
A | AT | 21 | a0001c0001t0001g0140a0001c0001t0002g0034a0001c0001t0004g0025others(18): Show | 21 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1146+1728dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr4 | 88660206 | |||||
| chr4:88660240
|
C | T | 9 | a0001c0001t0005g0027a0001c0001t0008g0028a0001c0001t0011g0020others(6): Show | 9 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1146+1749C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660240 | ||||||
| chr4:88660292
|
C | T | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1146+1801C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660292 | ||||||
| chr4:88660424
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1146+1933G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660424 | ||||||
| chr4:88660450
|
C | T | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1146+1959C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660450 | ||||||
| chr4:88660503
|
C | T | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1147-1928C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660503 | ||||||
| chr4:88660527
|
C | T | 2 | a0002c0003t0002g0038a0002c0003t0002g0039 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1147-1904C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660527 | ||||||
| chr4:88660528
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1147-1903T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660528 | ||||||
| chr4:88660661
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1147-1770C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660661 | ||||||
| chr4:88660854
|
T | A | 2 | a0001c0005t0002g0096a0001c0005t0002g0103 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1147-1577T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88660854 | ||||||
| chr4:88661289
|
A | G | 58 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(55): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1147-1142A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88661289 | ||||||
| chr4:88661379
|
A | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1147-1052A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88661379 | ||||||
| chr4:88661543
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1147-888C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88661543 | ||||||
| chr4:88661645
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1147-786G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88661645 | ||||||
| chr4:88661911
|
C | G | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1147-520C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88661911 | ||||||
| chr4:88662087
|
T | G | 25 | a0001c0001t0003g0118a0001c0001t0004g0002a0001c0001t0004g0040others(22): Show | 26 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1147-344T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662087 | ||||||
| chr4:88662099
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0004g0025 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1147-332A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662099 | ||||||
| chr4:88662191
|
A | G | 2 | a0001c0001t0011g0186a0001c0001t0012g0185 | 2 | HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1147-240A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662191 | ||||||
| chr4:88662261
|
T | G | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-170T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662261 | ||||||
| chr4:88662347
|
A | G | 1 | a0001c0001t0010g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1147-84A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662347 | ||||||
| chr4:88662352
|
G | T | 1 | a0003c0010t0003g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1147-79G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 10/25 | chr4 | 88662352 | ||||||
| chr4:88662563
|
G | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
splice_region_variant&intron_variant | LOW | c.1271+8G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88662563 | ||||||
| chr4:88662681
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1271+126C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88662681 | ||||||
| chr4:88662970
|
A | G | 1 | a0001c0001t0004g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1271+415A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88662970 | ||||||
| chr4:88663000
|
G | GA | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1271+458dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 88663000 | |||||
| chr4:88663000
|
GA | G | 53 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(50): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1271+458delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 88663000 | |||||
| chr4:88663220
|
G | A | 4 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0046others(1): Show | 4 | HG02818.hp1 NA18522.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271+665G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663220 | ||||||
| chr4:88663246
|
A | G | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1271+691A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663246 | ||||||
| chr4:88663273
|
G | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(160): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1271+718G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663273 | ||||||
| chr4:88663351
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+796C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663351 | ||||||
| chr4:88663375
|
G | C | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1272-778G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663375 | ||||||
| chr4:88663379
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1272-774C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663379 | ||||||
| chr4:88663416
|
CA | C | 6 | a0001c0001t0001g0076a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG00408.hp1 NA18971.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272-735delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 88663416 | |||||
| chr4:88663484
|
C | A | 19 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0001t0005g0027others(16): Show | 19 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1272-669C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663484 | ||||||
| chr4:88663546
|
C | T | 46 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(43): Show | 48 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1272-607C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663546 | ||||||
| chr4:88663577
|
C | A | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272-576C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663577 | ||||||
| chr4:88663687
|
A | G | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1272-466A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663687 | ||||||
| chr4:88663732
|
A | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1272-421A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663732 | ||||||
| chr4:88663838
|
T | A | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1272-315T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663838 | ||||||
| chr4:88663854
|
C | A | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1272-299C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663854 | ||||||
| chr4:88663867
|
G | A | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1272-286G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663867 | ||||||
| chr4:88663980
|
G | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00642.hp2 HG01257.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272-173G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88663980 | ||||||
| chr4:88664084
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1272-69A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 11/25 | chr4 | 88664084 | ||||||
| chr4:88664285
|
G | A | 1 | a0002c0002t0002g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1331+73G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664285 | ||||||
| chr4:88664613
|
A | T | 1 | a0002c0003t0002g0029 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1331+401A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664613 | ||||||
| chr4:88664630
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1331+418T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664630 | ||||||
| chr4:88664660
|
C | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1331+448C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664660 | ||||||
| chr4:88664700
|
A | G | 2 | a0002c0002t0002g0080a0002c0002t0002g0098 | 2 | NA18975.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1331+488A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664700 | ||||||
| chr4:88664741
|
A | C | 1 | a0001c0008t0004g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1331+529A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88664741 | ||||||
| chr4:88665040
|
C | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1331+828C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88665040 | ||||||
| chr4:88665092
|
G | A | 19 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(16): Show | 19 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1331+880G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88665092 | ||||||
| chr4:88665244
|
A | G | 2 | a0001c0001t0004g0117a0001c0008t0004g0010 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1331+1032A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88665244 | ||||||
| chr4:88665825
|
T | C | 58 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(55): Show | 60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1332-1552T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88665825 | ||||||
| chr4:88666164
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1332-1213T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666164 | ||||||
| chr4:88666174
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 26 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1332-1203G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666174 | ||||||
| chr4:88666226
|
A | T | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1332-1151A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666226 | ||||||
| chr4:88666260
|
G | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1332-1117G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666260 | ||||||
| chr4:88666560
|
T | C | 6 | a0001c0001t0005g0009a0001c0001t0011g0186a0001c0001t0012g0185others(3): Show | 7 | HG02630.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1332-817T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666560 | ||||||
| chr4:88666683
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(82): Show | 88 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1332-694T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666683 | ||||||
| chr4:88666849
|
A | C | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1332-528A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666849 | ||||||
| chr4:88666916
|
G | A | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1332-461G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666916 | ||||||
| chr4:88666961
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332-416C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88666961 | ||||||
| chr4:88667002
|
G | A | 1 | a0002c0003t0002g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1332-375G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88667002 | ||||||
| chr4:88667129
|
G | A | 1 | a0001c0004t0001g0269 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1332-248G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88667129 | ||||||
| chr4:88667264
|
C | T | 2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1332-113C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88667264 | ||||||
| chr4:88667327
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1332-50A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 12/25 | chr4 | 88667327 | ||||||
| chr4:88667536
|
A | G | 1 | a0002c0003t0002g0123 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1443+48A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 13/25 | chr4 | 88667536 | ||||||
| chr4:88667538
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(186): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1443+50C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 13/25 | chr4 | 88667538 | ||||||
| chr4:88668241
|
C | G | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1633+160C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668241 | ||||||
| chr4:88668363
|
C | A | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1633+282C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668363 | ||||||
| chr4:88668417
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1633+336A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668417 | ||||||
| chr4:88668539
|
C | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1633+458C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668539 | ||||||
| chr4:88668566
|
C | T | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1633+485C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668566 | ||||||
| chr4:88668977
|
G | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1634-883G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88668977 | ||||||
| chr4:88669089
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1634-771T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669089 | ||||||
| chr4:88669095
|
T | A | 27 | a0001c0001t0001g0134a0001c0001t0003g0118a0001c0001t0004g0002others(24): Show | 28 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.1634-765T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669095 | ||||||
| chr4:88669198
|
T | C | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1634-662T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669198 | ||||||
| chr4:88669209
|
C | A | 4 | a0001c0004t0002g0274a0002c0006t0002g0272a0002c0006t0002g0273others(1): Show | 4 | HG02818.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-651C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669209 | ||||||
| chr4:88669315
|
C | T | 52 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(49): Show | 54 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1634-545C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669315 | ||||||
| chr4:88669321
|
A | T | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1634-539A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669321 | ||||||
| chr4:88669668
|
C | T | 1 | a0002c0003t0002g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1634-192C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669668 | ||||||
| chr4:88669680
|
T | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(80): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1634-180T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 14/25 | chr4 | 88669680 | ||||||
| chr4:88670416
|
A | G | 1 | a0001c0001t0011g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1911+164A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670416 | ||||||
| chr4:88670630
|
A | G | 1 | a0002c0003t0002g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1911+378A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670630 | ||||||
| chr4:88670631
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1911+379T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670631 | ||||||
| chr4:88670664
|
GA | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1911+415delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88670664 | |||||
| chr4:88670698
|
A | G | 1 | a0001c0005t0003g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1911+446A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670698 | ||||||
| chr4:88670710
|
G | GT | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1911+467dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88670710 | |||||
| chr4:88670712
|
T | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1911+460T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670712 | ||||||
| chr4:88670719
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1911+467T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670719 | ||||||
| chr4:88670749
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1911+497C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88670749 | ||||||
| chr4:88671037
|
A | G | 16 | a0001c0001t0005g0027a0001c0001t0008g0028a0001c0001t0011g0020others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1911+785A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671037 | ||||||
| chr4:88671129
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1911+877T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671129 | ||||||
| chr4:88671276
|
T | C | 1 | a0002c0003t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1911+1024T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671276 | ||||||
| chr4:88671348
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0239 | 3 | NA18959.hp1 NA18965.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1911+1096G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671348 | ||||||
| chr4:88671400
|
T | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1911+1148T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671400 | ||||||
| chr4:88671751
|
T | A | 2 | a0001c0005t0002g0096a0001c0005t0002g0103 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1911+1499T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671751 | ||||||
| chr4:88671785
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1911+1533A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671785 | ||||||
| chr4:88671814
|
G | C | 2 | a0001c0001t0001g0218a0001c0001t0006g0175 | 2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1911+1562G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671814 | ||||||
| chr4:88671870
|
C | A | 1 | a0001c0001t0010g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1911+1618C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671870 | ||||||
| chr4:88671895
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1911+1643G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88671895 | ||||||
| chr4:88672005
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(186): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1911+1753A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88672005 | ||||||
| chr4:88672075
|
A | G | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1911+1823A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88672075 | ||||||
| chr4:88672621
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(54): Show | 60 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1911+2369T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88672621 | ||||||
| chr4:88672884
|
C | CAG | 162 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1911+2633_1911+263 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88672884 | |||||
| chr4:88672892
|
A | G | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0051 | 3 | HG01109.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1911+2640A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88672892 | ||||||
| chr4:88673382
|
AT | A | 4 | a0001c0001t0003g0196a0001c0001t0003g0206a0001c0001t0003g0212others(1): Show | 4 | NA18940.hp1 NA18991.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1912-2833delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88673382 | |||||
| chr4:88673488
|
C | T | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1912-2730C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673488 | ||||||
| chr4:88673513
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-2705A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673513 | ||||||
| chr4:88673588
|
C | G | 1 | a0001c0001t0003g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1912-2630C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673588 | ||||||
| chr4:88673599
|
A | C | 1 | a0002c0003t0002g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1912-2619A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673599 | ||||||
| chr4:88673668
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-2550T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673668 | ||||||
| chr4:88673694
|
A | G | 3 | a0001c0001t0003g0118a0001c0001t0005g0082a0002c0003t0002g0078 | 3 | HG03490.hp2 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1912-2524A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673694 | ||||||
| chr4:88673872
|
T | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-2346T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88673872 | ||||||
| chr4:88674045
|
CAG | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-2167_1912-216 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88674045 | |||||
| chr4:88674197
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1912-2021G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88674197 | ||||||
| chr4:88674309
|
GCTGATTG others(13): Show |
G | 1 | a0002c0003t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1912-1905_1912-188 others(24): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88674309 | |||||
| chr4:88674577
|
T | G | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1912-1641T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88674577 | ||||||
| chr4:88674687
|
G | GT | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1912-1524dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88674687 | |||||
| chr4:88674838
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1912-1380T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88674838 | ||||||
| chr4:88674882
|
G | T | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1912-1336G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88674882 | ||||||
| chr4:88675192
|
C | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1912-1026C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88675192 | ||||||
| chr4:88675496
|
C | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1912-722C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88675496 | ||||||
| chr4:88675804
|
A | ATG | 5 | a0001c0004t0004g0282a0001c0005t0001g0100a0002c0002t0002g0099others(2): Show | 5 | HG01109.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1912-400_1912-399d others(4): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr4 | 88675804 | |||||
| chr4:88676161
|
G | A | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1912-57G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 16/25 | chr4 | 88676161 | ||||||
| chr4:88676582
|
A | C | 46 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2025+159A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88676582 | ||||||
| chr4:88676676
|
G | C | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2025+253G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88676676 | ||||||
| chr4:88677027
|
C | T | 20 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2025+604C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677027 | ||||||
| chr4:88677368
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(139): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2026-596G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677368 | ||||||
| chr4:88677512
|
T | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2026-452T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677512 | ||||||
| chr4:88677521
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2026-443A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677521 | ||||||
| chr4:88677589
|
A | G | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2026-375A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677589 | ||||||
| chr4:88677753
|
A | C | 1 | a0002c0006t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2026-211A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677753 | ||||||
| chr4:88677759
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2026-205T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677759 | ||||||
| chr4:88677820
|
T | G | 3 | a0001c0001t0005g0027a0001c0001t0011g0020a0002c0003t0002g0021 | 3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2026-144T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677820 | ||||||
| chr4:88677869
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2026-95G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677869 | ||||||
| chr4:88677879
|
C | T | 1 | a0002c0003t0002g0124 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2026-85C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 18/25 | chr4 | 88677879 | ||||||
| chr4:88678270
|
A | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2196+136A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678270 | ||||||
| chr4:88678326
|
G | A | 16 | a0001c0001t0005g0027a0001c0001t0008g0028a0001c0001t0011g0020others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.2196+192G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678326 | ||||||
| chr4:88678419
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(139): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2196+285G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678419 | ||||||
| chr4:88678464
|
G | A | 55 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(52): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2196+330G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678464 | ||||||
| chr4:88678688
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(139): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2196+554A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678688 | ||||||
| chr4:88678756
|
A | T | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2196+622A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678756 | ||||||
| chr4:88678853
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2196+719C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88678853 | ||||||
| chr4:88679072
|
T | C | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2196+938T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679072 | ||||||
| chr4:88679103
|
G | A | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2196+969G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679103 | ||||||
| chr4:88679352
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2197-741T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679352 | ||||||
| chr4:88679444
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2197-649A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679444 | ||||||
| chr4:88679522
|
CT | C | 27 | a0001c0004t0001g0188a0001c0004t0001g0269a0001c0004t0002g0265others(24): Show | 27 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.2197-556delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 88679522 | |||||
| chr4:88679669
|
C | A | 137 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(134): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.2197-424C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679669 | ||||||
| chr4:88679674
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2197-419T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679674 | ||||||
| chr4:88679738
|
G | A | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2197-355G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679738 | ||||||
| chr4:88679767
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2197-326C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679767 | ||||||
| chr4:88679769
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2197-324C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679769 | ||||||
| chr4:88679808
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(186): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2197-285A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679808 | ||||||
| chr4:88679883
|
C | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2197-210C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679883 | ||||||
| chr4:88679897
|
T | A | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2197-196T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679897 | ||||||
| chr4:88679898
|
A | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2197-195A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 19/25 | chr4 | 88679898 | ||||||
| chr4:88680259
|
A | T | 28 | a0001c0004t0001g0188a0001c0004t0001g0269a0001c0004t0002g0265others(25): Show | 28 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.2340+23A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88680259 | ||||||
| chr4:88680309
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2340+73A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88680309 | ||||||
| chr4:88680435
|
T | G | 1 | a0001c0001t0003g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2340+199T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88680435 | ||||||
| chr4:88680448
|
C | T | 1 | a0001c0001t0008g0028 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2340+212C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88680448 | ||||||
| chr4:88681093
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG00642.hp2 HG01257.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2341-66G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88681093 | ||||||
| chr4:88681118
|
A | G | 1 | a0001c0001t0004g0002 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2341-41A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 20/25 | chr4 | 88681118 | ||||||
| chr4:88681479
|
A | T | 4 | a0001c0001t0003g0068a0001c0001t0003g0072a0001c0001t0003g0073others(1): Show | 4 | HG00408.hp1 NA18971.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2507+154A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681479 | ||||||
| chr4:88681528
|
C | T | 2 | a0001c0001t0001g0005a0001c0008t0001g0005 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2507+203C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681528 | ||||||
| chr4:88681547
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2507+222G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681547 | ||||||
| chr4:88681614
|
T | C | 27 | a0001c0001t0001g0134a0001c0001t0003g0118a0001c0001t0004g0002others(24): Show | 28 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.2507+289T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681614 | ||||||
| chr4:88681737
|
G | T | 1 | a0002c0003t0002g0031 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2507+412G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681737 | ||||||
| chr4:88681828
|
C | T | 1 | a0001c0001t0006g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2507+503C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681828 | ||||||
| chr4:88681934
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(139): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2507+609C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88681934 | ||||||
| chr4:88682147
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(186): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2507+822A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682147 | ||||||
| chr4:88682150
|
G | A | 18 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.2507+825G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682150 | ||||||
| chr4:88682266
|
C | T | 1 | a0001c0004t0004g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2507+941C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682266 | ||||||
| chr4:88682339
|
T | C | 1 | a0001c0005t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2507+1014T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682339 | ||||||
| chr4:88682355
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(194): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.2507+1030A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682355 | ||||||
| chr4:88682368
|
A | T | 1 | a0001c0004t0002g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2507+1043A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682368 | ||||||
| chr4:88682369
|
C | T | 1 | a0001c0004t0002g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2507+1044C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682369 | ||||||
| chr4:88682444
|
A | T | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2507+1119A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682444 | ||||||
| chr4:88682465
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2507+1140T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682465 | ||||||
| chr4:88682471
|
G | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2507+1146G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682471 | ||||||
| chr4:88682472
|
A | C | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2507+1147A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682472 | ||||||
| chr4:88682473
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2507+1148C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682473 | ||||||
| chr4:88682507
|
G | A | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2507+1182G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682507 | ||||||
| chr4:88682512
|
G | C | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2507+1187G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682512 | ||||||
| chr4:88682772
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2507+1447G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682772 | ||||||
| chr4:88682793
|
G | T | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2507+1468G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682793 | ||||||
| chr4:88682852
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(200): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2507+1527C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682852 | ||||||
| chr4:88682892
|
C | T | 1 | a0001c0001t0010g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2507+1567C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682892 | ||||||
| chr4:88682936
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2507+1611T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88682936 | ||||||
| chr4:88683008
|
C | T | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2507+1683C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683008 | ||||||
| chr4:88683017
|
G | A | 1 | a0001c0001t0003g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2507+1692G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683017 | ||||||
| chr4:88683335
|
T | G | 1 | a0001c0001t0006g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2507+2010T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683335 | ||||||
| chr4:88683363
|
G | T | 2 | a0002c0003t0002g0018a0002c0003t0002g0026 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2507+2038G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683363 | ||||||
| chr4:88683485
|
GC | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2507+2161delC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683485 | ||||||
| chr4:88683758
|
T | A | 1 | a0001c0001t0008g0028 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2507+2433T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683758 | ||||||
| chr4:88683763
|
T | G | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2507+2438T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683763 | ||||||
| chr4:88683791
|
T | C | 1 | a0002c0003t0014g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2507+2466T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683791 | ||||||
| chr4:88683922
|
C | T | 1 | a0001c0001t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2507+2597C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683922 | ||||||
| chr4:88683963
|
A | G | 46 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2507+2638A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88683963 | ||||||
| chr4:88684120
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(133): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.2508-2616C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684120 | ||||||
| chr4:88684198
|
G | A | 2 | a0001c0001t0001g0271a0001c0012t0001g0270 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2508-2538G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684198 | ||||||
| chr4:88684270
|
TATAGACC others(15): Show |
T | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2508-2464_2508-244 others(26): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 88684270 | |||||
| chr4:88684354
|
C | T | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2508-2382C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684354 | ||||||
| chr4:88684361
|
T | C | 2 | a0001c0001t0004g0117a0001c0008t0004g0010 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2508-2375T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684361 | ||||||
| chr4:88684465
|
C | T | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2508-2271C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684465 | ||||||
| chr4:88684491
|
T | A | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2508-2245T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684491 | ||||||
| chr4:88684539
|
A | G | 1 | a0002c0003t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2508-2197A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684539 | ||||||
| chr4:88684672
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2508-2064C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684672 | ||||||
| chr4:88684845
|
T | A | 27 | a0001c0001t0003g0197a0001c0001t0004g0117a0001c0001t0005g0027others(24): Show | 27 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2508-1891T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684845 | ||||||
| chr4:88684846
|
C | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(183): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2508-1890C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684846 | ||||||
| chr4:88684998
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508-1738C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88684998 | ||||||
| chr4:88685049
|
A | G | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2508-1687A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685049 | ||||||
| chr4:88685056
|
G | T | 26 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2508-1680G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685056 | ||||||
| chr4:88685061
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2508-1675T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685061 | ||||||
| chr4:88685180
|
G | A | 1 | a0001c0001t0008g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2508-1556G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685180 | ||||||
| chr4:88685253
|
C | T | 46 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2508-1483C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685253 | ||||||
| chr4:88685270
|
A | T | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2508-1466A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685270 | ||||||
| chr4:88685354
|
C | T | 19 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0274others(16): Show | 19 | HG00438.hp2 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2508-1382C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685354 | ||||||
| chr4:88685448
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2508-1288G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685448 | ||||||
| chr4:88685511
|
A | G | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2508-1225A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685511 | ||||||
| chr4:88685763
|
A | AAATAAT | 48 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(45): Show | 50 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2508-958_2508-953d others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 88685763 | |||||
| chr4:88685829
|
A | G | 5 | a0001c0004t0004g0277a0001c0004t0004g0282a0001c0004t0005g0263others(2): Show | 5 | HG01167.hp1 HG02055.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2508-907A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685829 | ||||||
| chr4:88685951
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2508-785A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88685951 | ||||||
| chr4:88686206
|
A | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508-530A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88686206 | ||||||
| chr4:88686301
|
G | A | 3 | a0002c0003t0002g0124a0002c0003t0002g0153a0002c0003t0002g0182 | 3 | NA18968.hp1 NA19067.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2508-435G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88686301 | ||||||
| chr4:88686640
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2508-96T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88686640 | ||||||
| chr4:88686670
|
A | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508-66A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 21/25 | chr4 | 88686670 | ||||||
| chr4:88686965
|
G | A | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2574+163G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/25 | chr4 | 88686965 | ||||||
| chr4:88687074
|
C | T | 49 | a0001c0005t0001g0081a0001c0005t0001g0092a0001c0005t0001g0093others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2575-143C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/25 | chr4 | 88687074 | ||||||
| chr4:88687113
|
C | T | 1 | a0001c0005t0003g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2575-104C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 22/25 | chr4 | 88687113 | ||||||
| chr4:88687441
|
C | T | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2657+142C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88687441 | ||||||
| chr4:88687607
|
T | C | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2657+308T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88687607 | ||||||
| chr4:88687761
|
T | G | 22 | a0001c0001t0005g0027a0001c0001t0008g0028a0001c0001t0011g0020others(19): Show | 22 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2657+462T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88687761 | ||||||
| chr4:88687900
|
A | G | 2 | a0001c0009t0004g0131a0001c0009t0004g0132 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2657+601A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88687900 | ||||||
| chr4:88688123
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2657+824G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88688123 | ||||||
| chr4:88688189
|
T | TTAGGCAC others(63): Show |
1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2657+893_2657+962d others(72): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88688189 | |||||
| chr4:88688289
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+990G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88688289 | ||||||
| chr4:88688342
|
T | C | 1 | a0002c0003t0002g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2657+1043T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88688342 | ||||||
| chr4:88688770
|
C | T | 1 | a0001c0005t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2657+1471C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88688770 | ||||||
| chr4:88688818
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2657+1519G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88688818 | ||||||
| chr4:88688921
|
TC | T | 3 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0051 | 3 | HG01109.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2657+1624delC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88688921 | |||||
| chr4:88689003
|
G | A | 2 | a0001c0007t0002g0122a0001c0007t0004g0121 | 2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2657+1704G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689003 | ||||||
| chr4:88689015
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02080.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2657+1716T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689015 | ||||||
| chr4:88689106
|
T | G | 1 | a0001c0005t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2657+1807T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689106 | ||||||
| chr4:88689252
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(192): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.2657+1953T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689252 | ||||||
| chr4:88689304
|
A | G | 2 | a0001c0004t0004g0189a0001c0004t0017g0187 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2657+2005A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689304 | ||||||
| chr4:88689349
|
T | TA | 19 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0142others(16): Show | 20 | HG00544.hp2 HG01106.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.2657+2068dupA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689349 | |||||
| chr4:88689349
|
TA | T | 80 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(77): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.2657+2068delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689349 | |||||
| chr4:88689532
|
CA | C | 144 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0134others(141): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2657+2249delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689532 | |||||
| chr4:88689573
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+2274C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689573 | ||||||
| chr4:88689642
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+2343A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689642 | ||||||
| chr4:88689647
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2657+2348G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689647 | ||||||
| chr4:88689695
|
G | A | 7 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0004g0279others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2657+2396G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689695 | ||||||
| chr4:88689703
|
G | A | 2 | a0001c0001t0001g0005a0001c0008t0001g0005 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2657+2404G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689703 | ||||||
| chr4:88689732
|
C | T | 2 | a0001c0001t0004g0117a0001c0008t0004g0010 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2657+2433C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689732 | ||||||
| chr4:88689743
|
A | G | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2657+2444A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689743 | ||||||
| chr4:88689940
|
A | AT | 10 | a0001c0001t0001g0221a0001c0001t0003g0011a0001c0001t0003g0012others(7): Show | 10 | HG00639.hp1 HG01192.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2657+2651dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689940 | |||||
| chr4:88689940
|
A | ATT | 5 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+2650_2657+265 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689940 | |||||
| chr4:88689940
|
AT | A | 24 | a0001c0001t0001g0134a0001c0001t0004g0002a0001c0001t0004g0040others(21): Show | 25 | HG00642.hp1 HG01109.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.2657+2651delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88689940 | |||||
| chr4:88689995
|
G | T | 26 | a0001c0001t0002g0034a0001c0001t0004g0025a0001c0001t0004g0117others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2657+2696G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88689995 | ||||||
| chr4:88690011
|
A | G | 46 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(43): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2657+2712A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690011 | ||||||
| chr4:88690254
|
C | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(159): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2657+2955C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690254 | ||||||
| chr4:88690283
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2657+2984A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690283 | ||||||
| chr4:88690401
|
C | T | 45 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(42): Show | 47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2657+3102C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690401 | ||||||
| chr4:88690790
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+3491T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690790 | ||||||
| chr4:88690813
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2657+3514G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88690813 | ||||||
| chr4:88691051
|
T | A | 3 | a0001c0004t0001g0188a0001c0004t0004g0189a0001c0004t0017g0187 | 3 | HG02109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2657+3752T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691051 | ||||||
| chr4:88691105
|
T | C | 1 | a0002c0003t0002g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2657+3806T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691105 | ||||||
| chr4:88691168
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2657+3869G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691168 | ||||||
| chr4:88691229
|
G | A | 76 | a0001c0001t0005g0255a0001c0004t0001g0188a0001c0004t0001g0269others(73): Show | 78 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2657+3930G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691229 | ||||||
| chr4:88691276
|
C | G | 6 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2657+3977C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691276 | ||||||
| chr4:88691293
|
T | C | 149 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0200others(146): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.2657+3994T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691293 | ||||||
| chr4:88691432
|
C | T | 57 | a0001c0004t0001g0269a0001c0004t0003g0258a0001c0004t0003g0266others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2657+4133C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691432 | ||||||
| chr4:88691444
|
A | G | 2 | a0001c0001t0003g0196a0001c0001t0019g0192 | 2 | NA19011.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2657+4145A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691444 | ||||||
| chr4:88691450
|
C | T | 3 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0046 | 3 | NA18522.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2657+4151C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691450 | ||||||
| chr4:88691458
|
AT | A | 3 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2657+4160delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691458 | ||||||
| chr4:88691517
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(123): Show | 131 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.2657+4218T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691517 | ||||||
| chr4:88691722
|
G | C | 3 | a0001c0004t0004g0277a0002c0003t0002g0047a0005c0013t0005g0264 | 3 | HG01167.hp1 HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2657+4423G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691722 | ||||||
| chr4:88691745
|
G | A | 22 | a0001c0001t0001g0134a0001c0001t0004g0152a0001c0001t0004g0154others(19): Show | 22 | HG01106.hp2 HG01167.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.2657+4446G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691745 | ||||||
| chr4:88691758
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2657+4459C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691758 | ||||||
| chr4:88691790
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0235others(20): Show | 24 | HG00642.hp1 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2657+4491A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88691790 | ||||||
| chr4:88692232
|
C | T | 1 | a0001c0004t0003g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2657+4933C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692232 | ||||||
| chr4:88692234
|
CAT | C | 10 | a0001c0001t0004g0025a0001c0001t0004g0244a0001c0004t0004g0279others(7): Show | 10 | HG01243.hp2 HG02486.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2657+4938_2657+493 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88692234 | |||||
| chr4:88692399
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2657+5100A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692399 | ||||||
| chr4:88692428
|
T | A | 109 | a0001c0001t0001g0134a0001c0001t0001g0218a0001c0001t0003g0011others(106): Show | 113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2657+5129T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692428 | ||||||
| chr4:88692643
|
T | C | 20 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0004t0002g0265others(17): Show | 20 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2657+5344T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692643 | ||||||
| chr4:88692649
|
G | A | 6 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2657+5350G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692649 | ||||||
| chr4:88692824
|
G | A | 1 | a0001c0005t0001g0081 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2657+5525G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692824 | ||||||
| chr4:88692935
|
C | T | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2657+5636C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88692935 | ||||||
| chr4:88692992
|
TA | T | 7 | a0001c0001t0004g0025a0001c0004t0004g0279a0001c0004t0004g0280others(4): Show | 7 | HG01243.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2657+5695delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88692992 | |||||
| chr4:88693238
|
C | T | 1 | a0001c0005t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2657+5939C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88693238 | ||||||
| chr4:88693375
|
T | C | 1 | a0001c0004t0002g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2657+6076T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88693375 | ||||||
| chr4:88693772
|
G | A | 3 | a0002c0003t0002g0038a0002c0003t0002g0039a0004c0011t0002g0017 | 3 | HG02280.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2657+6473G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88693772 | ||||||
| chr4:88693797
|
G | A | 1 | a0001c0005t0003g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2657+6498G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88693797 | ||||||
| chr4:88693838
|
C | A | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2657+6539C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88693838 | ||||||
| chr4:88694023
|
T | C | 55 | a0001c0001t0004g0180a0001c0005t0003g0105a0001c0005t0003g0116others(52): Show | 57 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2657+6724T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694023 | ||||||
| chr4:88694199
|
A | G | 1 | a0001c0005t0004g0091 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2657+6900A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694199 | ||||||
| chr4:88694365
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2657+7066A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694365 | ||||||
| chr4:88694487
|
G | T | 5 | a0001c0001t0002g0034a0001c0001t0011g0186a0001c0001t0012g0044others(2): Show | 5 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2657+7188G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694487 | ||||||
| chr4:88694542
|
A | G | 1 | a0001c0001t0006g0253 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2657+7243A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694542 | ||||||
| chr4:88694547
|
C | G | 35 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0040others(32): Show | 36 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.2657+7248C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694547 | ||||||
| chr4:88694578
|
C | A | 63 | a0001c0001t0001g0070a0001c0001t0002g0034a0001c0001t0002g0054others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2657+7279C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694578 | ||||||
| chr4:88694791
|
C | A | 1 | a0001c0004t0003g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2657+7492C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88694791 | ||||||
| chr4:88695177
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037 | 4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2657+7878T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88695177 | ||||||
| chr4:88695487
|
T | C | 1 | a0001c0004t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2657+8188T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88695487 | ||||||
| chr4:88695741
|
A | G | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-8357A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88695741 | ||||||
| chr4:88695817
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0133 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2658-8281C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88695817 | ||||||
| chr4:88695836
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-8262G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88695836 | ||||||
| chr4:88696168
|
C | A | 1 | a0001c0001t0003g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2658-7930C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696168 | ||||||
| chr4:88696236
|
A | G | 98 | a0001c0001t0001g0070a0001c0001t0003g0007a0001c0001t0003g0008others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.2658-7862A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696236 | ||||||
| chr4:88696290
|
C | A | 9 | a0001c0001t0004g0040a0001c0001t0004g0042a0001c0001t0004g0048others(6): Show | 9 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-7808C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696290 | ||||||
| chr4:88696302
|
T | C | 2 | a0002c0002t0002g0111a0002c0002t0002g0112 | 2 | NA18968.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2658-7796T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696302 | ||||||
| chr4:88696350
|
C | T | 1 | a0001c0004t0010g0259 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2658-7748C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696350 | ||||||
| chr4:88696518
|
CAT | C | 55 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(52): Show | 57 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2658-7577_2658-757 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88696518 | |||||
| chr4:88696631
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2658-7467C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696631 | ||||||
| chr4:88696727
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2658-7371A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696727 | ||||||
| chr4:88696780
|
G | A | 7 | a0001c0001t0005g0009a0001c0001t0005g0027a0001c0004t0004g0277others(4): Show | 8 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658-7318G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696780 | ||||||
| chr4:88696813
|
G | A | 3 | a0001c0001t0001g0005a0001c0005t0001g0093a0001c0008t0001g0005 | 3 | HG00738.hp2 HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2658-7285G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88696813 | ||||||
| chr4:88697296
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-6802G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88697296 | ||||||
| chr4:88697416
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2658-6682A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88697416 | ||||||
| chr4:88697658
|
G | C | 1 | a0001c0004t0003g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2658-6440G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88697658 | ||||||
| chr4:88697681
|
TCCTCTGC others(5): Show |
T | 2 | a0001c0001t0003g0118a0001c0001t0004g0048 | 2 | HG01109.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2658-6412_2658-640 others(16): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88697681 | |||||
| chr4:88697686
|
T | C | 181 | a0001c0001t0001g0070a0001c0001t0001g0145a0001c0001t0001g0155others(178): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.2658-6412T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88697686 | ||||||
| chr4:88698103
|
A | G | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-5995A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698103 | ||||||
| chr4:88698125
|
A | G | 158 | a0001c0001t0001g0070a0001c0001t0002g0034a0001c0001t0002g0054others(155): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2658-5973A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698125 | ||||||
| chr4:88698157
|
C | T | 1 | a0001c0001t0012g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2658-5941C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698157 | ||||||
| chr4:88698171
|
C | T | 2 | a0002c0003t0002g0177a0002c0003t0002g0181 | 2 | NA18940.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2658-5927C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698171 | ||||||
| chr4:88698239
|
C | G | 1 | a0001c0004t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2658-5859C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698239 | ||||||
| chr4:88698312
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0157 | 2 | HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2658-5786C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698312 | ||||||
| chr4:88698439
|
C | A | 34 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0040others(31): Show | 35 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.2658-5659C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698439 | ||||||
| chr4:88698532
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2658-5566C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698532 | ||||||
| chr4:88698572
|
GCAAGTCT others(31): Show |
G | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2658-5524_2658-548 others(42): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698572 | |||||
| chr4:88698617
|
A | G | 34 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0040others(31): Show | 35 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.2658-5481A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698617 | ||||||
| chr4:88698652
|
G | T | 1 | a0002c0003t0002g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2658-5446G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698652 | ||||||
| chr4:88698739
|
T | C | 1 | a0002c0003t0002g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2658-5359T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698739 | ||||||
| chr4:88698810
|
T | G | 47 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(44): Show | 49 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2658-5288T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698810 | ||||||
| chr4:88698811
|
T | C | 47 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(44): Show | 49 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2658-5287T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698811 | ||||||
| chr4:88698891
|
CCACCCTC others(26): Show |
C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-5197_2658-516 others(37): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698891 | |||||
| chr4:88698939
|
C | A | 1 | a0002c0003t0002g0179 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2658-5159C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88698939 | ||||||
| chr4:88698973
|
T | TC | 192 | a0001c0001t0001g0070a0001c0001t0001g0221a0001c0001t0001g0232others(189): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.2658-5119dupC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698973 | |||||
| chr4:88698989
|
T | TTTCCTCA others(41): Show |
52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0125others(49): Show | 53 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2658-4912_2658-486 others(52): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(89): Show |
22 | a0001c0001t0001g0035a0001c0001t0001g0134a0001c0001t0001g0170others(19): Show | 23 | HG00639.hp1 HG00642.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2658-4960_2658-486 others(100): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(137): Show |
1 | a0001c0001t0002g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2658-5008_2658-486 others(148): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(281): Show |
1 | a0001c0001t0008g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2658-4865_2658-486 others(292): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(329): Show |
8 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658-4865_2658-486 others(340): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(41): Show |
3 | a0002c0002t0002g0061a0002c0003t0002g0021a0002c0003t0002g0047 | 3 | HG00140.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2658-5071_2658-507 others(52): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
T | TTTCCTCA others(89): Show |
1 | a0002c0002t0002g0090 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2658-5071_2658-507 others(100): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88698989
|
TTTCCTCA others(41): Show |
T | 19 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0128others(16): Show | 20 | HG00733.hp1 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.2658-4912_2658-486 others(52): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88698989 | |||||
| chr4:88699028
|
C | CACCCTCT others(89): Show |
5 | a0001c0001t0003g0067a0001c0001t0003g0069a0001c0001t0003g0197others(2): Show | 5 | HG00438.hp2 HG00621.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658-4975_2658-497 others(100): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699028 | |||||
| chr4:88699028
|
C | CACCCTCT others(41): Show |
3 | a0002c0006t0002g0272a0002c0006t0002g0273a0002c0006t0002g0275 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2658-5023_2658-502 others(52): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699028 | |||||
| chr4:88699028
|
C | T | 74 | a0001c0001t0004g0117a0001c0001t0005g0009a0001c0001t0005g0027others(71): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2658-5070C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699028 | ||||||
| chr4:88699074
|
TTCACCCT others(17): Show |
T | 4 | a0001c0004t0004g0279a0001c0004t0004g0280a0001c0004t0004g0281others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2658-5004_2658-498 others(28): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699074 | |||||
| chr4:88699076
|
C | CACCCTCT others(41): Show |
48 | a0001c0001t0001g0070a0001c0001t0003g0007a0001c0001t0003g0008others(45): Show | 50 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2658-4975_2658-497 others(52): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699076 | |||||
| chr4:88699076
|
C | T | 3 | a0002c0002t0002g0113a0002c0003t0002g0023a0002c0003t0002g0283 | 3 | HG00733.hp1 HG02523.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2658-5022C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699076 | ||||||
| chr4:88699082
|
C | T | 1 | a0001c0001t0005g0255 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2658-5016C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699082 | ||||||
| chr4:88699090
|
T | C | 7 | a0001c0001t0004g0025a0001c0001t0005g0082a0001c0004t0004g0189others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2658-5008T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699090 | ||||||
| chr4:88699093
|
CG | C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-5004delG | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699093 | ||||||
| chr4:88699094
|
G | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-5004G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699094 | ||||||
| chr4:88699095
|
CTCCTCAC others(8): Show |
C | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2658-4988_2658-497 others(19): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699095 | |||||
| chr4:88699096
|
T | C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-5002T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699096 | ||||||
| chr4:88699096
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-5002T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699096 | ||||||
| chr4:88699099
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4999T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699099 | ||||||
| chr4:88699100
|
C | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4998C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699100 | ||||||
| chr4:88699101
|
A | G | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4997A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699101 | ||||||
| chr4:88699102
|
C | CCCTCTTC others(40): Show |
1 | a0001c0001t0003g0203 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2658-4975_2658-497 others(51): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699102 | |||||
| chr4:88699104
|
CTCTTCTT others(3): Show |
C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4993_2658-498 others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699104 | ||||||
| chr4:88699110
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4988T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699110 | ||||||
| chr4:88699111
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4987T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699111 | ||||||
| chr4:88699112
|
C | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4986C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699112 | ||||||
| chr4:88699114
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4984T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699114 | ||||||
| chr4:88699120
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4978T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699120 | ||||||
| chr4:88699122
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4976T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699122 | ||||||
| chr4:88699123
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4975T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699123 | ||||||
| chr4:88699123
|
T | TCC | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4974_2658-497 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699123 | |||||
| chr4:88699124
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2658-4974C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699124 | ||||||
| chr4:88699125
|
A | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4973A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699125 | ||||||
| chr4:88699128
|
C | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4970C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699128 | ||||||
| chr4:88699129
|
T | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4969T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699129 | ||||||
| chr4:88699129
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4969T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699129 | ||||||
| chr4:88699130
|
CTTCTT | C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4967_2658-496 others(9): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699130 | ||||||
| chr4:88699137
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4961C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699137 | ||||||
| chr4:88699138
|
T | C | 25 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(22): Show | 25 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2658-4960T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699138 | ||||||
| chr4:88699140
|
ACGC | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4957_2658-495 others(7): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699140 | ||||||
| chr4:88699141
|
C | CCCCCTAG others(82): Show |
3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4957_2658-495 others(93): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699141 | ||||||
| chr4:88699142
|
G | C | 17 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(14): Show | 17 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2658-4956G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699142 | ||||||
| chr4:88699143
|
C | CCCTA | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4955_2658-495 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699143 | ||||||
| chr4:88699144
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4954T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699144 | ||||||
| chr4:88699144
|
T | G | 22 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(19): Show | 22 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-4954T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699144 | ||||||
| chr4:88699145
|
CCT | C | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4951_2658-495 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699145 | |||||
| chr4:88699147
|
T | C | 22 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(19): Show | 22 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-4951T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699147 | ||||||
| chr4:88699149
|
A | G | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4949A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699149 | ||||||
| chr4:88699152
|
C | T | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4946C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699152 | ||||||
| chr4:88699153
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4945T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699153 | ||||||
| chr4:88699156
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4942T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699156 | ||||||
| chr4:88699158
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4940T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699158 | ||||||
| chr4:88699158
|
T | C | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4940T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699158 | ||||||
| chr4:88699159
|
T | C | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4939T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699159 | ||||||
| chr4:88699159
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4939T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699159 | ||||||
| chr4:88699160
|
C | A | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4938C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699160 | ||||||
| chr4:88699162
|
T | C | 26 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(23): Show | 26 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.2658-4936T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699162 | ||||||
| chr4:88699166
|
C | CGACCCA | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4932_2658-493 others(10): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699166 | ||||||
| chr4:88699166
|
CCTCTT | C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4930_2658-492 others(9): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699166 | |||||
| chr4:88699167
|
C | CCCA | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2658-4931_2658-493 others(7): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699167 | ||||||
| chr4:88699167
|
C | CCCAGCCC others(52): Show |
2 | a0001c0001t0004g0117a0001c0001t0011g0020 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2658-4931_2658-493 others(63): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699167 | ||||||
| chr4:88699168
|
T | C | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4930T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699168 | ||||||
| chr4:88699168
|
T | G | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4930T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699168 | ||||||
| chr4:88699170
|
T | C | 17 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(14): Show | 17 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2658-4928T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699170 | ||||||
| chr4:88699171
|
T | C | 16 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(13): Show | 16 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2658-4927T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699171 | ||||||
| chr4:88699171
|
TC | T | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4926delC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699171 | ||||||
| chr4:88699173
|
A | G | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2658-4925A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699173 | ||||||
| chr4:88699175
|
C | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4923C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699175 | ||||||
| chr4:88699176
|
C | T | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2658-4922C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699176 | ||||||
| chr4:88699177
|
T | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4921T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699177 | ||||||
| chr4:88699178
|
CTTCTTCC others(3): Show |
C | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4919_2658-491 others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699178 | ||||||
| chr4:88699179
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4919T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699179 | ||||||
| chr4:88699182
|
T | C | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4916T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699182 | ||||||
| chr4:88699182
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4916T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699182 | ||||||
| chr4:88699183
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-4915T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699183 | ||||||
| chr4:88699183
|
T | C | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4915T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699183 | ||||||
| chr4:88699184
|
C | CA | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4914_2658-491 others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699184 | ||||||
| chr4:88699186
|
T | C | 23 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(20): Show | 24 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.2658-4912T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699186 | ||||||
| chr4:88699189
|
C | CCCACCCA others(27): Show |
4 | a0001c0001t0005g0027a0001c0001t0005g0255a0001c0004t0004g0277others(1): Show | 4 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2658-4909_2658-490 others(38): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699189 | ||||||
| chr4:88699189
|
C | CCCCCTAG others(304): Show |
1 | a0001c0001t0003g0206 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2658-4909_2658-490 others(315): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699189 | ||||||
| chr4:88699190
|
G | A | 2 | a0001c0001t0004g0117a0001c0001t0011g0020 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2658-4908G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699190 | ||||||
| chr4:88699190
|
G | C | 22 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 23 | HG00140.hp2 HG01123.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2658-4908G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699190 | ||||||
| chr4:88699191
|
C | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4907C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699191 | ||||||
| chr4:88699191
|
C | CACCCACC others(2): Show |
8 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2658-4907_2658-490 others(13): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699191 | ||||||
| chr4:88699191
|
C | CACCCACC others(146): Show |
2 | a0001c0001t0005g0219a0001c0001t0005g0233 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2658-4907_2658-490 others(157): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699191 | ||||||
| chr4:88699191
|
C | CCCTA | 3 | a0001c0001t0002g0034a0001c0001t0005g0009a0001c0004t0002g0265 | 4 | HG02258.hp1 HG03195.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2658-4907_2658-490 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699191 | ||||||
| chr4:88699192
|
T | A | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4906T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699192 | ||||||
| chr4:88699192
|
T | C | 2 | a0001c0001t0004g0117a0001c0001t0011g0020 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2658-4906T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699192 | ||||||
| chr4:88699192
|
T | G | 19 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(16): Show | 20 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2658-4906T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699192 | ||||||
| chr4:88699193
|
CCT | C | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4903_2658-490 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699193 | |||||
| chr4:88699195
|
T | C | 22 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 23 | HG00140.hp2 HG01123.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2658-4903T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699195 | ||||||
| chr4:88699196
|
C | CT | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4902_2658-490 others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699196 | ||||||
| chr4:88699201
|
T | C | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4897T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699201 | ||||||
| chr4:88699201
|
T | G | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4897T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699201 | ||||||
| chr4:88699202
|
C | A | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4896C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699202 | ||||||
| chr4:88699203
|
T | C | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4895T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699203 | ||||||
| chr4:88699206
|
T | A | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4892T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699206 | ||||||
| chr4:88699206
|
T | C | 5 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0001t0005g0009others(2): Show | 6 | HG02258.hp1 HG03098.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4892T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699206 | ||||||
| chr4:88699207
|
T | C | 5 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0001t0005g0009others(2): Show | 6 | HG02258.hp1 HG03098.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4891T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699207 | ||||||
| chr4:88699208
|
C | A | 3 | a0001c0001t0002g0034a0001c0001t0005g0009a0001c0004t0002g0265 | 4 | HG02258.hp1 HG03195.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2658-4890C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699208 | ||||||
| chr4:88699209
|
C | G | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4889C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699209 | ||||||
| chr4:88699210
|
T | A | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4888T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699210 | ||||||
| chr4:88699210
|
T | C | 16 | a0001c0001t0002g0034a0001c0001t0003g0206a0001c0001t0004g0117others(13): Show | 17 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2658-4888T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699210 | ||||||
| chr4:88699211
|
CA | C | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4886delA | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699211 | ||||||
| chr4:88699215
|
C | A | 14 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2658-4883C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699215 | ||||||
| chr4:88699215
|
C | CACCCACC others(2): Show |
5 | a0001c0001t0005g0219a0001c0001t0005g0233a0001c0004t0005g0263others(2): Show | 5 | HG00140.hp2 HG01123.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658-4883_2658-488 others(13): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699215 | ||||||
| chr4:88699215
|
C | CCCAGCCC others(52): Show |
2 | a0001c0001t0002g0034a0001c0004t0002g0265 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2658-4883_2658-488 others(63): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699215 | ||||||
| chr4:88699215
|
C | G | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4883C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699215 | ||||||
| chr4:88699216
|
T | A | 8 | a0001c0001t0003g0206a0001c0001t0004g0117a0001c0001t0005g0027others(5): Show | 8 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2658-4882T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699216 | ||||||
| chr4:88699216
|
T | G | 22 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 23 | HG00140.hp2 HG01123.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2658-4882T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699216 | ||||||
| chr4:88699218
|
T | C | 14 | a0001c0001t0003g0206a0001c0001t0004g0117a0001c0001t0005g0009others(11): Show | 15 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2658-4880T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699218 | ||||||
| chr4:88699219
|
T | C | 30 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 31 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2658-4879T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699219 | ||||||
| chr4:88699220
|
C | A | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4878C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699220 | ||||||
| chr4:88699221
|
A | C | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4877A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699221 | ||||||
| chr4:88699221
|
A | G | 1 | a0001c0001t0005g0009 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2658-4877A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699221 | ||||||
| chr4:88699224
|
C | T | 1 | a0001c0001t0005g0009 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2658-4874C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699224 | ||||||
| chr4:88699225
|
T | G | 2 | a0001c0001t0004g0117a0001c0001t0011g0020 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2658-4873T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699225 | ||||||
| chr4:88699225
|
T | TAC | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4873_2658-487 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699225 | ||||||
| chr4:88699226
|
C | A | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4872C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699226 | ||||||
| chr4:88699227
|
T | C | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4871T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699227 | ||||||
| chr4:88699230
|
T | C | 3 | a0001c0004t0005g0263a0001c0005t0005g0062a0001c0005t0005g0106 | 3 | HG00140.hp2 HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2658-4868T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699230 | ||||||
| chr4:88699234
|
C | T | 2 | a0001c0001t0001g0166a0002c0002t0002g0085 | 2 | NA18945.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2658-4864C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699234 | ||||||
| chr4:88699238
|
C | CG | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4860_2658-485 others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699238 | ||||||
| chr4:88699238
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4860C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699238 | ||||||
| chr4:88699239
|
C | A | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4859C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699239 | ||||||
| chr4:88699239
|
C | CA | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4859_2658-485 others(5): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699239 | ||||||
| chr4:88699239
|
C | CACCCA | 7 | a0001c0001t0004g0117a0001c0001t0005g0219a0001c0001t0005g0233others(4): Show | 7 | HG00140.hp2 HG01123.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2658-4859_2658-485 others(9): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699239 | ||||||
| chr4:88699239
|
C | CACCCACC others(142): Show |
1 | a0001c0001t0005g0009 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2658-4859_2658-485 others(153): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699239 | ||||||
| chr4:88699239
|
C | CTCCTCAC others(9): Show |
1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4859_2658-485 others(20): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699239 | ||||||
| chr4:88699242
|
T | C | 30 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(27): Show | 31 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2658-4856T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699242 | ||||||
| chr4:88699243
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4855A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699243 | ||||||
| chr4:88699244
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4854G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699244 | ||||||
| chr4:88699244
|
G | C | 22 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 22 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-4854G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699244 | ||||||
| chr4:88699248
|
C | T | 22 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(19): Show | 22 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-4850C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699248 | ||||||
| chr4:88699253
|
T | G | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4845T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699253 | ||||||
| chr4:88699256
|
T | C | 2 | a0001c0001t0004g0117a0001c0001t0011g0020 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2658-4842T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699256 | ||||||
| chr4:88699256
|
T | TC | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4839dupC | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699256 | |||||
| chr4:88699256
|
T | TCTTC | 11 | a0001c0001t0005g0009a0001c0001t0005g0027a0001c0001t0005g0082others(8): Show | 12 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2658-4841_2658-484 others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699256 | |||||
| chr4:88699258
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4840C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699258 | ||||||
| chr4:88699259
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4839C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699259 | ||||||
| chr4:88699260
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4838A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699260 | ||||||
| chr4:88699264
|
ACC | A | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4830_2658-482 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699264 | |||||
| chr4:88699266
|
C | CCA | 14 | a0001c0001t0003g0206a0001c0001t0004g0117a0001c0001t0005g0009others(11): Show | 15 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2658-4831_2658-483 others(6): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699266 | |||||
| chr4:88699271
|
G | C | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4827G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699271 | ||||||
| chr4:88699275
|
C | T | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4823C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699275 | ||||||
| chr4:88699276
|
G | A | 31 | a0001c0001t0001g0166a0001c0001t0002g0034a0001c0001t0003g0011others(28): Show | 32 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.2658-4822G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699276 | ||||||
| chr4:88699279
|
T | C | 31 | a0001c0001t0001g0166a0001c0001t0002g0034a0001c0001t0003g0011others(28): Show | 32 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.2658-4819T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699279 | ||||||
| chr4:88699280
|
T | G | 16 | a0001c0001t0002g0034a0001c0001t0003g0011a0001c0001t0003g0012others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-4818T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699280 | ||||||
| chr4:88699281
|
C | A | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4817C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699281 | ||||||
| chr4:88699285
|
T | C | 6 | a0001c0001t0003g0206a0001c0001t0005g0027a0001c0001t0005g0082others(3): Show | 6 | HG01167.hp1 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-4813T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699285 | ||||||
| chr4:88699285
|
T | TTCCCCAC others(359): Show |
38 | a0001c0001t0001g0070a0001c0001t0003g0007a0001c0001t0003g0053others(35): Show | 39 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(370): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(392): Show |
2 | a0001c0001t0003g0118a0001c0004t0003g0258 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(403): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(392): Show |
6 | a0001c0001t0003g0008a0001c0001t0003g0202a0001c0001t0003g0203others(3): Show | 7 | HG01106.hp2 HG03540.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(403): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(359): Show |
1 | a0001c0004t0003g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2658-4786_2658-478 others(370): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(281): Show |
1 | a0001c0001t0003g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2658-4786_2658-478 others(292): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(137): Show |
1 | a0001c0001t0003g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2658-4786_2658-478 others(148): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(137): Show |
1 | a0001c0001t0004g0261 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2658-4786_2658-478 others(148): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(170): Show |
17 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0042others(14): Show | 17 | HG00639.hp1 HG01071.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(181): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(203): Show |
3 | a0001c0001t0004g0152a0001c0001t0004g0154a0001c0001t0008g0220 | 3 | HG01168.hp2 HG03239.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(214): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
T | TTCCCCAC others(236): Show |
1 | a0001c0001t0004g0002 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(247): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699285
|
TTCCCCAC others(26): Show |
T | 3 | a0001c0001t0001g0140a0001c0001t0001g0222a0001c0001t0001g0252 | 3 | HG02083.hp2 HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2658-4797_2658-476 others(37): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699285 | |||||
| chr4:88699288
|
C | CCCACCCA others(104): Show |
5 | a0001c0001t0004g0190a0001c0004t0004g0279a0001c0004t0004g0280others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(115): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699288 | |||||
| chr4:88699288
|
C | CCCACCCA others(326): Show |
6 | a0001c0001t0003g0067a0001c0001t0003g0069a0001c0001t0003g0197others(3): Show | 6 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(337): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699288 | |||||
| chr4:88699288
|
C | T | 13 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2658-4810C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699288 | ||||||
| chr4:88699304
|
G | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0158a0001c0001t0001g0162others(2): Show | 5 | HG01106.hp1 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658-4794G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699304 | ||||||
| chr4:88699305
|
C | CCCCACCC others(104): Show |
1 | a0002c0003t0002g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2658-4786_2658-478 others(115): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699305 | |||||
| chr4:88699308
|
C | CACCCCAC others(71): Show |
68 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(65): Show | 70 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(82): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699308 | |||||
| chr4:88699308
|
C | CACCCCAC others(71): Show |
12 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(9): Show | 12 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2658-4786_2658-478 others(82): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699308 | |||||
| chr4:88699308
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0158a0001c0001t0001g0162others(2): Show | 5 | HG01106.hp1 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2658-4790C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699308 | ||||||
| chr4:88699309
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4789A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699309 | ||||||
| chr4:88699312
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2658-4786C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699312 | ||||||
| chr4:88699313
|
T | G | 85 | a0001c0001t0001g0128a0001c0001t0001g0158a0001c0001t0001g0162others(82): Show | 87 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2658-4785T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699313 | ||||||
| chr4:88699314
|
C | A | 12 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(9): Show | 12 | HG01884.hp2 HG02040.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.2658-4784C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699314 | ||||||
| chr4:88699318
|
C | T | 99 | a0001c0001t0001g0128a0001c0001t0001g0158a0001c0001t0001g0162others(96): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2658-4780C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699318 | ||||||
| chr4:88699321
|
C | T | 86 | a0001c0001t0001g0128a0001c0001t0001g0158a0001c0001t0001g0162others(83): Show | 88 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2658-4777C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699321 | ||||||
| chr4:88699334
|
G | C | 191 | a0001c0001t0001g0070a0001c0001t0002g0034a0001c0001t0002g0054others(188): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.2658-4764G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699334 | ||||||
| chr4:88699338
|
C | A | 73 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0004g0279others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.2658-4760C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699338 | ||||||
| chr4:88699338
|
C | CCCCACCC others(17): Show |
1 | a0001c0001t0001g0243 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2658-4753_2658-473 others(28): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88699338 | |||||
| chr4:88699423
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2658-4675C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699423 | ||||||
| chr4:88699425
|
T | A | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2658-4673T>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699425 | ||||||
| chr4:88699921
|
A | G | 98 | a0001c0001t0001g0070a0001c0001t0002g0034a0001c0001t0003g0007others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.2658-4177A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88699921 | ||||||
| chr4:88700002
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0161 | 2 | HG00621.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2658-4096G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700002 | ||||||
| chr4:88700090
|
CT | C | 117 | a0001c0001t0001g0070a0001c0001t0002g0054a0001c0001t0002g0055others(114): Show | 121 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2658-3997delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88700090 | |||||
| chr4:88700176
|
T | C | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2658-3922T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700176 | ||||||
| chr4:88700250
|
C | G | 1 | a0001c0001t0003g0151 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2658-3848C>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700250 | ||||||
| chr4:88700255
|
A | T | 3 | a0002c0003t0002g0038a0002c0003t0002g0039a0004c0011t0002g0017 | 3 | HG02280.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2658-3843A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700255 | ||||||
| chr4:88700515
|
C | T | 159 | a0001c0001t0001g0070a0001c0001t0002g0034a0001c0001t0002g0054others(156): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2658-3583C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700515 | ||||||
| chr4:88700688
|
G | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-3410G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700688 | ||||||
| chr4:88700700
|
G | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2658-3398G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700700 | ||||||
| chr4:88700867
|
T | C | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2658-3231T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700867 | ||||||
| chr4:88700871
|
A | T | 1 | a0001c0001t0006g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2658-3227A>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700871 | ||||||
| chr4:88700992
|
A | G | 2 | a0001c0001t0002g0034a0001c0004t0002g0265 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2658-3106A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700992 | ||||||
| chr4:88700995
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0161 | 2 | HG00621.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2658-3103T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88700995 | ||||||
| chr4:88701216
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2658-2882A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701216 | ||||||
| chr4:88701570
|
T | C | 157 | a0001c0001t0002g0034a0001c0001t0002g0054a0001c0001t0002g0055others(154): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2658-2528T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701570 | ||||||
| chr4:88701638
|
C | T | 2 | a0001c0001t0002g0034a0001c0004t0002g0265 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2658-2460C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701638 | ||||||
| chr4:88701639
|
G | A | 6 | a0001c0001t0004g0025a0001c0004t0004g0189a0001c0004t0017g0187others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2658-2459G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701639 | ||||||
| chr4:88701639
|
G | T | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2658-2459G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701639 | ||||||
| chr4:88701677
|
G | T | 1 | a0002c0002t0002g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2658-2421G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701677 | ||||||
| chr4:88701753
|
T | G | 157 | a0001c0001t0002g0034a0001c0001t0002g0054a0001c0001t0002g0055others(154): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2658-2345T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701753 | ||||||
| chr4:88701803
|
A | AT | 76 | a0001c0001t0001g0164a0001c0001t0002g0034a0001c0001t0003g0007others(73): Show | 79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2658-2278dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88701803 | |||||
| chr4:88701803
|
AT | A | 34 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0040others(31): Show | 35 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.2658-2278delT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88701803 | |||||
| chr4:88701893
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2658-2205C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701893 | ||||||
| chr4:88701976
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2658-2122G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701976 | ||||||
| chr4:88701982
|
A | G | 1 | a0002c0003t0002g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2658-2116A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88701982 | ||||||
| chr4:88702579
|
G | T | 1 | a0001c0001t0001g0130 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2658-1519G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702579 | ||||||
| chr4:88702642
|
G | T | 1 | a0001c0001t0004g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2658-1456G>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702642 | ||||||
| chr4:88702702
|
G | C | 2 | a0001c0001t0002g0034a0001c0004t0002g0265 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2658-1396G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702702 | ||||||
| chr4:88702806
|
A | C | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2658-1292A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702806 | ||||||
| chr4:88702824
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2658-1274A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702824 | ||||||
| chr4:88702949
|
G | A | 5 | a0001c0001t0003g0068a0001c0001t0003g0072a0001c0001t0003g0073others(2): Show | 5 | HG00408.hp1 NA18612.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658-1149G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88702949 | ||||||
| chr4:88703034
|
G | C | 154 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(151): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2658-1064G>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703034 | ||||||
| chr4:88703068
|
G | A | 10 | a0001c0001t0005g0009a0001c0001t0005g0027a0001c0001t0005g0082others(7): Show | 11 | HG00140.hp2 HG01123.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2658-1030G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703068 | ||||||
| chr4:88703228
|
A | G | 35 | a0001c0001t0004g0002a0001c0001t0004g0025a0001c0001t0004g0040others(32): Show | 36 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.2658-870A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703228 | ||||||
| chr4:88703544
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2658-554G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703544 | ||||||
| chr4:88703550
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2658-548A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703550 | ||||||
| chr4:88703637
|
T | C | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2658-461T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703637 | ||||||
| chr4:88703679
|
T | G | 1 | a0001c0004t0010g0259 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2658-419T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703679 | ||||||
| chr4:88703702
|
A | AGGATAG | 154 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(151): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.2658-393_2658-392i others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr4 | 88703702 | |||||
| chr4:88703725
|
T | C | 1 | a0001c0001t0012g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2658-373T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88703725 | ||||||
| chr4:88704062
|
T | G | 3 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0004t0002g0265 | 3 | HG02258.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2658-36T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 23/25 | chr4 | 88704062 | ||||||
| chr4:88704366
|
C | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0141a0001c0001t0008g0220 | 3 | HG01071.hp1 HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2841+85C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 24/25 | chr4 | 88704366 | ||||||
| chr4:88704495
|
C | CT | 24 | a0001c0001t0004g0002a0001c0001t0004g0040a0001c0001t0004g0041others(21): Show | 25 | HG00639.hp1 HG00642.hp1 HG01071.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.2842-7dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 88704495 | |||||
| chr4:88704721
|
G | A | 1 | a0002c0003t0013g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2944+111G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88704721 | ||||||
| chr4:88704770
|
A | G | 69 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0061others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2944+160A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88704770 | ||||||
| chr4:88704862
|
T | G | 1 | a0002c0003t0002g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2944+252T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88704862 | ||||||
| chr4:88704863
|
C | CTTTCTTT others(5): Show |
4 | a0001c0001t0011g0020a0001c0001t0011g0186a0001c0001t0012g0044others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2944+256_2944+257i others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTCTTT others(5): Show |
12 | a0001c0001t0003g0203a0001c0001t0005g0009a0001c0001t0005g0027others(9): Show | 13 | HG00140.hp2 HG01123.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2944+256_2944+257i others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTCTTT others(6): Show |
53 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0011others(50): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2944+256_2944+257i others(15): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTCTTT others(7): Show |
6 | a0001c0001t0003g0012a0001c0001t0003g0067a0001c0001t0003g0196others(3): Show | 6 | HG02056.hp2 NA18991.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.2944+256_2944+257i others(16): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTTTT | 10 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2944+263_2944+268d others(8): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTTTTT others(5): Show |
1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2944+257_2944+268d others(14): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704863
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0034a0001c0004t0002g0265 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2944+256_2944+268d others(15): Show |
HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88704863 | |||||
| chr4:88704878
|
T | G | 1 | a0001c0001t0012g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2944+268T>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88704878 | ||||||
| chr4:88704922
|
G | A | 3 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0004t0002g0265 | 3 | HG02258.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2944+312G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88704922 | ||||||
| chr4:88705118
|
T | C | 3 | a0001c0001t0002g0034a0001c0001t0004g0117a0001c0004t0002g0265 | 3 | HG02258.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2944+508T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705118 | ||||||
| chr4:88705240
|
A | G | 76 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0011others(73): Show | 79 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.2944+630A>G | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705240 | ||||||
| chr4:88705325
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2944+715T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705325 | ||||||
| chr4:88705458
|
C | T | 3 | a0002c0002t0002g0080a0002c0002t0002g0097a0002c0002t0002g0098 | 3 | NA18975.hp2 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2944+848C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705458 | ||||||
| chr4:88705610
|
C | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0140a0001c0001t0001g0217others(4): Show | 7 | HG00408.hp2 HG02083.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2944+1000C>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705610 | ||||||
| chr4:88705720
|
T | C | 1 | a0001c0004t0006g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2945-1032T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705720 | ||||||
| chr4:88705769
|
G | A | 61 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0011others(58): Show | 63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2945-983G>A | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705769 | ||||||
| chr4:88705887
|
A | C | 55 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0053others(52): Show | 57 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2945-865A>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88705887 | ||||||
| chr4:88706392
|
C | T | 1 | a0001c0004t0010g0259 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2945-360C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88706392 | ||||||
| chr4:88706553
|
T | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2945-199T>C | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88706553 | ||||||
| chr4:88706571
|
C | CT | 9 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0057others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2945-171dupT | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 88706571 | |||||
| chr4:88706623
|
C | T | 9 | a0001c0001t0005g0009a0001c0001t0005g0027a0001c0001t0005g0219others(6): Show | 10 | HG00140.hp2 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2945-129C>T | HERC3 | ENSG00000138641.18 | transcript | ENST00000402738.6 | protein_coding | 25/25 | chr4 | 88706623 |