Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8667 |
|---|---|
| ensemblid | ENSG00000147677.12 |
| hgncid | 3273 |
| symbol | EIF3H |
| name | eukaryotic translation initiation factor 3 subunit H |
| refseq_nuc | NM_003756.3 |
| refseq_prot | NP_003747.1 |
| ensembl_nuc | ENST00000521861.6 |
| ensembl_prot | ENSP00000429931.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 116642130 |
| end | 116755823 |
| strand | - |
| ver | v1.2 |
| region | chr8:116642130-116755823 |
| region5000 | chr8:116637130-116760823 |
| regionname0 | EIF3H_chr8_116642130_116755823 |
| regionname5000 | EIF3H_chr8_116637130_116760823 |
| 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 | 352 | 335 | 94 | 60 | 147 | 8 | 24 | 119 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0002 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| 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 | 1059 | 335 | 94 | 60 | 147 | 8 | 24 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| c0002 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| 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 | 0/1 | 2903 | 77 | 25 | 14 | 22 | 2 | 13 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0002 | 0/0 | 2903 | 67 | 1 | 12 | 52 | 1 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0003 | 1/0 | 2903 | 59 | 2 | 9 | 40 | 2 | 5 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0004 | 0/0 | 2903 | 38 | 0 | 16 | 19 | 2 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0005 | 0/0 | 2903 | 20 | 13 | 3 | 0 | 1 | 3 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0006 | 0/0 | 2903 | 16 | 14 | 2 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0007 | 0/0 | 2902 | 13 | 12 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0008 | 0/0 | 2903 | 11 | 0 | 0 | 11 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0009 | 0/0 | 2903 | 5 | 4 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0010 | 0/0 | 2903 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0011 | 0/0 | 2902 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0012 | 0/0 | 2903 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0013 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0014 | 0/0 | 2903 | 3 | 2 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0015 | 0/0 | 2876 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0016 | 0/0 | 2903 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0017 | 0/0 | 2903 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0018 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0019 | 0/0 | 2903 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0020 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0021 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0022 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| t0023 | 0/0 | 2903 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| 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 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| 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 | 1059 | 335 | 94 | 60 | 147 | 8 | 24 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0002c0002 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3961 | 77 | 25 | 14 | 22 | 2 | 13 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0002 | 0/0 | 3961 | 66 | 1 | 12 | 51 | 1 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0003 | 1/0 | 3961 | 59 | 2 | 9 | 40 | 2 | 5 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0004 | 0/0 | 3961 | 38 | 0 | 16 | 19 | 2 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0005 | 0/0 | 3961 | 20 | 13 | 3 | 0 | 1 | 3 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0006 | 0/0 | 3961 | 16 | 14 | 2 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0007 | 0/0 | 3960 | 13 | 12 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0008 | 0/0 | 3961 | 11 | 0 | 0 | 11 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0009 | 0/0 | 3961 | 5 | 4 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0010 | 0/0 | 3961 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0011 | 0/0 | 3960 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0012 | 0/0 | 3961 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0013 | 0/0 | 3961 | 3 | 3 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0014 | 0/0 | 3961 | 3 | 2 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0015 | 0/0 | 3934 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0016 | 0/0 | 3961 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0017 | 0/0 | 3961 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0018 | 0/0 | 3961 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0019 | 0/0 | 3961 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0020 | 0/0 | 3961 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0021 | 0/0 | 3961 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0022 | 0/0 | 3961 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0001c0001t0023 | 0/0 | 3961 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| a0002c0002t0002 | 0/0 | 3961 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | copy fasta | chr8 | 116637130 | 116760823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0014g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0014g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0015g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0017g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0017g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0018g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0019g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0021g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0022g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0001c0001t0023g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | FIN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0197 | EUR | FIN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00558 | hp1 | a0001 | c0001 | t0022 | g0129 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | CHS | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0101 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0095 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0153 | AMR | PUR | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0314 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0258 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0211 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01978 | hp2 | a0001 | c0001 | t0023 | g0164 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0247 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | CDX | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | CDX | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CDX | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CDX | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0007 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0333 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0327 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0331 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02735 | hp2 | a0001 | c0001 | t0019 | g0303 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0332 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0203 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0322 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0326 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0249 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0217 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0319 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0104 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0318 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0105 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0103 | AFR | ESN | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | GWD | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03579 | hp1 | a0001 | c0001 | t0018 | g0157 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0334 | SAS | BEB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | BEB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | YRI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | CHB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | CHB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | CHB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0102 | AFR | YRI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | YRI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18982 | hp1 | a0001 | c0001 | t0021 | g0194 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18985 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18986 | hp2 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0061 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0315 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0076 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19054 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19060 | hp1 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0078 | EAS | JPT | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | ASW | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | ASW | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0174 | EUR | TSI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | TSI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0177 | EUR | TSI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | TSI | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0210 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0154 | AFR | ACB | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | USA | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | USA | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | USA | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | LWK | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0023 | REF | REF | EIF3H_chr8_116637130_116760823 | EIF3H | chr8 | 116637130 | 116760823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:116646503
|
G | A | 1 | a0002 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.929C>T | p.Pro310Leu | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/8 | 955/3961 | 929/1059 | 310/352 | chr8 | 116646503 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:116642223
|
T | C | 1 | a0001c0001t0021 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2783A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2783 | chr8 | 116642223 | |||||
| chr8:116642423
|
TA | T | 1 | a0001c0001t0011 | 4 | HG02615.hp2 HG03540.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2582delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2582 | chr8 | 116642423 | |||||
| chr8:116642459
|
C | T | 1 | a0001c0001t0017 | 2 | HG02615.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2547G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2547 | chr8 | 116642459 | |||||
| chr8:116642463
|
T | A | 4 | a0001c0001t0002a0001c0001t0012a0001c0001t0019others(1): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2543 | chr8 | 116642463 | |||||
| chr8:116642522
|
TATCAATG others(19): Show |
T | 1 | a0001c0001t0015 | 2 | HG01884.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2458_*2483delTTGA others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2458 | chr8 | 116642522 | |||||
| chr8:116642534
|
G | T | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*2472C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 2472 | chr8 | 116642534 | |||||
| chr8:116643097
|
A | G | 2 | a0001c0001t0007a0001c0001t0015 | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1909T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1909 | chr8 | 116643097 | |||||
| chr8:116643142
|
A | C | 2 | a0001c0001t0007a0001c0001t0015 | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1864T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1864 | chr8 | 116643142 | |||||
| chr8:116643160
|
C | T | 1 | a0001c0001t0017 | 2 | HG02615.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1846G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1846 | chr8 | 116643160 | |||||
| chr8:116643197
|
T | C | 2 | a0001c0001t0008a0001c0001t0016 | 13 | HG02129.hp2 NA18950.hp2 NA18964.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1809A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1809 | chr8 | 116643197 | |||||
| chr8:116643251
|
GT | G | 2 | a0001c0001t0007a0001c0001t0015 | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1754delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1754 | chr8 | 116643251 | |||||
| chr8:116643326
|
C | T | 2 | a0001c0001t0009a0001c0001t0018 | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1680G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1680 | chr8 | 116643326 | |||||
| chr8:116643348
|
G | C | 1 | a0001c0001t0019 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1658C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1658 | chr8 | 116643348 | |||||
| chr8:116643356
|
A | G | 1 | a0001c0001t0016 | 2 | NA18986.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1650T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1650 | chr8 | 116643356 | |||||
| chr8:116643575
|
C | T | 1 | a0001c0001t0010 | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1431G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1431 | chr8 | 116643575 | |||||
| chr8:116643740
|
T | C | 1 | a0001c0001t0022 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1266 | chr8 | 116643740 | |||||
| chr8:116643842
|
C | T | 1 | a0001c0001t0007 | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1164G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1164 | chr8 | 116643842 | |||||
| chr8:116643877
|
A | G | 3 | a0001c0001t0007a0001c0001t0015a0001c0001t0018 | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1129T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1129 | chr8 | 116643877 | |||||
| chr8:116643882
|
C | T | 3 | a0001c0001t0004a0001c0001t0021a0001c0001t0023 | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 1124 | chr8 | 116643882 | |||||
| chr8:116644159
|
G | T | 3 | a0001c0001t0007a0001c0001t0015a0001c0001t0018 | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 847 | chr8 | 116644159 | |||||
| chr8:116644250
|
C | T | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0013others(3): Show | 62 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*756G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 756 | chr8 | 116644250 | |||||
| chr8:116644438
|
A | G | 1 | a0001c0001t0013 | 3 | HG02257.hp1 HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*568T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 568 | chr8 | 116644438 | |||||
| chr8:116644456
|
T | C | 1 | a0001c0001t0020 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 550 | chr8 | 116644456 | |||||
| chr8:116644502
|
G | A | 1 | a0001c0001t0005 | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*504C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 504 | chr8 | 116644502 | |||||
| chr8:116644542
|
T | C | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 464 | chr8 | 116644542 | |||||
| chr8:116644632
|
C | T | 3 | a0001c0001t0002a0001c0001t0019a0002c0002t0002 | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*374G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 374 | chr8 | 116644632 | |||||
| chr8:116644892
|
T | A | 1 | a0001c0001t0014 | 3 | HG01109.hp1 HG03195.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 114 | chr8 | 116644892 | |||||
| chr8:116644940
|
T | C | 1 | a0001c0001t0023 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 66 | chr8 | 116644940 | |||||
| chr8:116644942
|
C | G | 3 | a0001c0001t0007a0001c0001t0015a0001c0001t0018 | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*64G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 8/8 | 64 | chr8 | 116644942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:116645138
|
T | C | 21 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.962-35A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645138 | ||||||
| chr8:116645255
|
C | T | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.962-152G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645255 | ||||||
| chr8:116645350
|
T | C | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.962-247A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645350 | ||||||
| chr8:116645608
|
A | G | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.962-505T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645608 | ||||||
| chr8:116645840
|
T | A | 45 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(42): Show | 45 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.961+631A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645840 | ||||||
| chr8:116645943
|
T | G | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.961+528A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645943 | ||||||
| chr8:116645963
|
C | G | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.961+508G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116645963 | ||||||
| chr8:116646038
|
G | A | 14 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(11): Show | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.961+433C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 7/7 | chr8 | 116646038 | ||||||
| chr8:116647100
|
T | C | 14 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(11): Show | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.829-497A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647100 | ||||||
| chr8:116647174
|
CT | C | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-572delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647174 | ||||||
| chr8:116647180
|
G | A | 119 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.829-577C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647180 | ||||||
| chr8:116647261
|
C | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0237 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.829-658G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647261 | ||||||
| chr8:116647303
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.829-700G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647303 | ||||||
| chr8:116647335
|
C | T | 1 | a0001c0001t0021g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.829-732G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647335 | ||||||
| chr8:116647347
|
G | A | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.829-744C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647347 | ||||||
| chr8:116647401
|
ATTG | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.829-801_829-799del others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647401 | ||||||
| chr8:116647414
|
T | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG02615.hp2 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-811A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647414 | ||||||
| chr8:116647740
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.828+1066G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647740 | ||||||
| chr8:116647873
|
C | T | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.828+933G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647873 | ||||||
| chr8:116647964
|
T | C | 3 | a0001c0001t0004g0188a0001c0001t0004g0190a0001c0001t0004g0195 | 3 | NA19003.hp2 NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.828+842A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116647964 | ||||||
| chr8:116648003
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.828+803A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116648003 | ||||||
| chr8:116648270
|
A | G | 21 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.828+536T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116648270 | ||||||
| chr8:116648556
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.828+250A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116648556 | ||||||
| chr8:116648670
|
A | G | 1 | a0001c0001t0004g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.828+136T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 6/7 | chr8 | 116648670 | ||||||
| chr8:116649087
|
T | C | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.708-161A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649087 | ||||||
| chr8:116649138
|
T | C | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.708-212A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649138 | ||||||
| chr8:116649215
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.708-289A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649215 | ||||||
| chr8:116649248
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.708-322A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649248 | ||||||
| chr8:116649327
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.708-401G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649327 | ||||||
| chr8:116649753
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.708-827A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649753 | ||||||
| chr8:116649873
|
G | A | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.708-947C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116649873 | ||||||
| chr8:116650190
|
A | T | 9 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0015others(6): Show | 9 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-1264T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650190 | ||||||
| chr8:116650718
|
A | G | 1 | a0001c0001t0013g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.708-1792T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650718 | ||||||
| chr8:116650795
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.708-1869G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650795 | ||||||
| chr8:116650908
|
C | G | 247 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.708-1982G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650908 | ||||||
| chr8:116650936
|
C | T | 2 | a0001c0001t0009g0152a0001c0001t0009g0153 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.708-2010G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650936 | ||||||
| chr8:116650976
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.708-2050A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116650976 | ||||||
| chr8:116651200
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.708-2274A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116651200 | ||||||
| chr8:116651244
|
CAT | C | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.708-2320_708-2319d others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116651244 | ||||||
| chr8:116651584
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.708-2658C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116651584 | ||||||
| chr8:116651759
|
C | A | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.708-2833G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116651759 | ||||||
| chr8:116651912
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.708-2986A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116651912 | ||||||
| chr8:116652061
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.708-3135C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652061 | ||||||
| chr8:116652384
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.708-3458A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652384 | ||||||
| chr8:116652388
|
T | C | 21 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.708-3462A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652388 | ||||||
| chr8:116652692
|
T | C | 21 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.707+3164A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652692 | ||||||
| chr8:116652886
|
G | A | 1 | a0001c0001t0012g0203 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.707+2970C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652886 | ||||||
| chr8:116652889
|
C | T | 2 | a0001c0001t0014g0103a0001c0001t0014g0104 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.707+2967G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652889 | ||||||
| chr8:116652952
|
G | A | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.707+2904C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116652952 | ||||||
| chr8:116653103
|
C | T | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.707+2753G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653103 | ||||||
| chr8:116653210
|
T | A | 3 | a0001c0001t0013g0007a0001c0001t0013g0102a0001c0001t0013g0105 | 3 | HG02257.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.707+2646A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653210 | ||||||
| chr8:116653251
|
T | C | 1 | a0001c0001t0002g0293 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.707+2605A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653251 | ||||||
| chr8:116653348
|
A | AACACACA others(3): Show |
9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0118others(6): Show | 9 | HG00558.hp1 HG01884.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+2498_707+2507d others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(5): Show |
58 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.707+2496_707+2507d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(7): Show |
13 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0143others(10): Show | 14 | HG01069.hp1 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.707+2494_707+2507d others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(9): Show |
12 | a0001c0001t0001g0125a0001c0001t0001g0204a0001c0001t0001g0206others(9): Show | 12 | HG01074.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.707+2492_707+2507d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(11): Show |
77 | a0001c0001t0001g0196a0001c0001t0001g0207a0001c0001t0001g0229others(74): Show | 77 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.707+2490_707+2507d others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(13): Show |
27 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0001g0221others(24): Show | 27 | HG01167.hp2 HG01981.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.707+2488_707+2507d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(15): Show |
7 | a0001c0001t0001g0079a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG02145.hp2 HG02165.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.707+2486_707+2507d others(24): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(17): Show |
16 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0158others(13): Show | 16 | HG00323.hp2 HG01070.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.707+2507_707+2508i others(26): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(19): Show |
10 | a0001c0001t0004g0166a0001c0001t0004g0171a0001c0001t0004g0181others(7): Show | 10 | HG01074.hp1 HG01081.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.707+2507_707+2508i others(28): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(21): Show |
8 | a0001c0001t0004g0159a0001c0001t0004g0165a0001c0001t0004g0168others(5): Show | 8 | HG01192.hp2 HG01361.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.707+2507_707+2508i others(30): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(23): Show |
1 | a0001c0001t0004g0175 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.707+2507_707+2508i others(32): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(25): Show |
5 | a0001c0001t0004g0085a0001c0001t0004g0180a0001c0001t0004g0185others(2): Show | 5 | NA18941.hp2 NA18979.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.707+2507_707+2508i others(34): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(27): Show |
12 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0163others(9): Show | 12 | HG00609.hp2 HG01358.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.707+2507_707+2508i others(36): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | AACACACA others(29): Show |
3 | a0001c0001t0004g0176a0001c0001t0004g0188a0001c0001t0004g0195 | 3 | NA19003.hp2 NA19004.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.707+2507_707+2508i others(38): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0291 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.707+2507_707+2508i others(21): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653348
|
A | ACACACAC others(16): Show |
1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.707+2507_707+2508i others(25): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653348 | ||||||
| chr8:116653506
|
A | T | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.707+2350T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653506 | ||||||
| chr8:116653667
|
C | CT | 20 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.707+2188dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653667 | ||||||
| chr8:116653757
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.707+2099C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653757 | ||||||
| chr8:116653807
|
A | T | 2 | a0001c0001t0002g0307a0001c0001t0002g0308 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.707+2049T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653807 | ||||||
| chr8:116653902
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.707+1954A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116653902 | ||||||
| chr8:116654085
|
T | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.707+1771A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654085 | ||||||
| chr8:116654123
|
G | A | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.707+1733C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654123 | ||||||
| chr8:116654135
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0120 | 2 | NA18948.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.707+1721G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654135 | ||||||
| chr8:116654224
|
A | G | 247 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.707+1632T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654224 | ||||||
| chr8:116654230
|
G | A | 276 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(273): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.707+1626C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654230 | ||||||
| chr8:116654501
|
T | C | 4 | a0001c0001t0002g0267a0001c0001t0002g0298a0001c0001t0002g0324others(1): Show | 4 | NA18941.hp1 NA18952.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+1355A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654501 | ||||||
| chr8:116654601
|
G | A | 2 | a0001c0001t0009g0152a0001c0001t0009g0153 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.707+1255C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654601 | ||||||
| chr8:116654691
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.707+1165G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654691 | ||||||
| chr8:116654708
|
G | C | 4 | a0001c0001t0002g0267a0001c0001t0002g0298a0001c0001t0002g0324others(1): Show | 4 | NA18941.hp1 NA18952.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+1148C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654708 | ||||||
| chr8:116654792
|
C | T | 1 | a0001c0001t0007g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.707+1064G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654792 | ||||||
| chr8:116654793
|
G | A | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.707+1063C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654793 | ||||||
| chr8:116654824
|
A | T | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.707+1032T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654824 | ||||||
| chr8:116654844
|
T | A | 3 | a0001c0001t0013g0007a0001c0001t0013g0102a0001c0001t0013g0105 | 3 | HG02257.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.707+1012A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654844 | ||||||
| chr8:116654907
|
C | CT | 107 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(104): Show | 107 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.707+948dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654907 | ||||||
| chr8:116654907
|
CT | C | 8 | a0001c0001t0001g0239a0001c0001t0001g0243a0001c0001t0009g0152others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.707+948delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116654907 | ||||||
| chr8:116655094
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.707+762G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116655094 | ||||||
| chr8:116655119
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.707+737C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116655119 | ||||||
| chr8:116655523
|
G | A | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.707+333C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 5/7 | chr8 | 116655523 | ||||||
| chr8:116656150
|
G | A | 247 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.558-145C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656150 | ||||||
| chr8:116656189
|
T | A | 15 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.558-184A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656189 | ||||||
| chr8:116656493
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.558-488A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656493 | ||||||
| chr8:116656578
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.558-573G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656578 | ||||||
| chr8:116656826
|
A | C | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.557+389T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656826 | ||||||
| chr8:116656944
|
A | G | 1 | a0001c0001t0020g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.557+271T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656944 | ||||||
| chr8:116656963
|
C | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.557+252G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116656963 | ||||||
| chr8:116657066
|
G | C | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.557+149C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116657066 | ||||||
| chr8:116657104
|
C | T | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.557+111G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116657104 | ||||||
| chr8:116657134
|
C | T | 1 | a0001c0001t0002g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.557+81G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 4/7 | chr8 | 116657134 | ||||||
| chr8:116657472
|
C | T | 1 | a0001c0001t0015g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.458-158G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657472 | ||||||
| chr8:116657574
|
A | G | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.458-260T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657574 | ||||||
| chr8:116657622
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.458-308G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657622 | ||||||
| chr8:116657635
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.458-321G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657635 | ||||||
| chr8:116657732
|
C | T | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.458-418G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657732 | ||||||
| chr8:116657894
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.458-580A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116657894 | ||||||
| chr8:116658035
|
T | C | 12 | a0001c0001t0003g0066a0001c0001t0004g0166a0001c0001t0004g0167others(9): Show | 12 | HG01074.hp1 HG01081.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.458-721A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658035 | ||||||
| chr8:116658086
|
A | G | 1 | a0001c0001t0006g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.457+727T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658086 | ||||||
| chr8:116658236
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.457+577T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658236 | ||||||
| chr8:116658421
|
T | C | 1 | a0001c0001t0005g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.457+392A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658421 | ||||||
| chr8:116658563
|
A | G | 20 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.457+250T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658563 | ||||||
| chr8:116658597
|
T | C | 1 | a0001c0001t0005g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.457+216A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 3/7 | chr8 | 116658597 | ||||||
| chr8:116659051
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.290-71C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659051 | ||||||
| chr8:116659343
|
G | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-363C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659343 | ||||||
| chr8:116659472
|
T | C | 1 | a0001c0001t0017g0332 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-492A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659472 | ||||||
| chr8:116659569
|
G | A | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.290-589C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659569 | ||||||
| chr8:116659611
|
A | G | 3 | a0001c0001t0004g0170a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01358.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.290-631T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659611 | ||||||
| chr8:116659786
|
G | T | 4 | a0001c0001t0003g0038a0001c0001t0003g0048a0001c0001t0003g0067others(1): Show | 4 | NA18947.hp1 NA18959.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-806C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659786 | ||||||
| chr8:116659869
|
T | C | 1 | a0001c0001t0004g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.290-889A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659869 | ||||||
| chr8:116659901
|
A | G | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-921T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659901 | ||||||
| chr8:116659904
|
G | A | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-924C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659904 | ||||||
| chr8:116659988
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-1008C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116659988 | ||||||
| chr8:116660021
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.290-1041C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660021 | ||||||
| chr8:116660025
|
T | C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-1045A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660025 | ||||||
| chr8:116660042
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.290-1062C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660042 | ||||||
| chr8:116660128
|
G | A | 1 | a0001c0001t0002g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.290-1148C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660128 | ||||||
| chr8:116660302
|
G | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0123 | 3 | NA18982.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.290-1322C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660302 | ||||||
| chr8:116660373
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-1393C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660373 | ||||||
| chr8:116660507
|
C | A | 4 | a0001c0001t0003g0031a0001c0001t0003g0045a0001c0001t0003g0060others(1): Show | 4 | HG02083.hp2 HG02132.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-1527G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660507 | ||||||
| chr8:116660636
|
G | C | 5 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-1656C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116660636 | ||||||
| chr8:116661314
|
A | C | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.290-2334T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116661314 | ||||||
| chr8:116661403
|
T | C | 4 | a0001c0001t0005g0222a0001c0001t0005g0226a0001c0001t0005g0227others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2423A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116661403 | ||||||
| chr8:116661676
|
T | C | 22 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(19): Show | 22 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.290-2696A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116661676 | ||||||
| chr8:116661728
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.290-2748G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116661728 | ||||||
| chr8:116662534
|
C | G | 7 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(4): Show | 7 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-3554G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116662534 | ||||||
| chr8:116662960
|
T | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-3980A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116662960 | ||||||
| chr8:116662981
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-4001T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116662981 | ||||||
| chr8:116663021
|
G | C | 14 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(11): Show | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-4041C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663021 | ||||||
| chr8:116663035
|
A | G | 1 | a0001c0001t0003g0011 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.290-4055T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663035 | ||||||
| chr8:116663170
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.290-4190C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663170 | ||||||
| chr8:116663387
|
A | T | 5 | a0001c0001t0002g0289a0001c0001t0002g0291a0001c0001t0002g0293others(2): Show | 5 | NA18964.hp1 NA18978.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-4407T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663387 | ||||||
| chr8:116663669
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-4689C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663669 | ||||||
| chr8:116663803
|
C | T | 1 | a0001c0001t0004g0165 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.290-4823G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663803 | ||||||
| chr8:116663930
|
C | CA | 104 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(101): Show | 104 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.290-4951dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663930 | ||||||
| chr8:116663930
|
C | CAA | 38 | a0001c0001t0001g0158a0001c0001t0004g0084a0001c0001t0004g0085others(35): Show | 39 | HG00609.hp2 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.290-4952_290-4951d others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663930 | ||||||
| chr8:116663930
|
CA | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0219others(3): Show | 6 | HG01069.hp1 HG02602.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-4951delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116663930 | ||||||
| chr8:116664029
|
G | A | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-5049C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664029 | ||||||
| chr8:116664174
|
T | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-5194A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664174 | ||||||
| chr8:116664267
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-5287G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664267 | ||||||
| chr8:116664276
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-5296G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664276 | ||||||
| chr8:116664320
|
T | C | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-5340A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664320 | ||||||
| chr8:116664332
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.290-5352T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664332 | ||||||
| chr8:116664561
|
C | T | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-5581G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664561 | ||||||
| chr8:116664595
|
G | C | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-5615C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664595 | ||||||
| chr8:116664776
|
AAAC | A | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-5799_290-5797d others(5): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664776 | ||||||
| chr8:116664822
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-5842A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664822 | ||||||
| chr8:116664958
|
C | T | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.290-5978G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116664958 | ||||||
| chr8:116665155
|
G | A | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026 | 3 | HG02135.hp1 HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.290-6175C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116665155 | ||||||
| chr8:116665320
|
G | A | 22 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(19): Show | 22 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.290-6340C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116665320 | ||||||
| chr8:116665518
|
G | A | 1 | a0001c0001t0004g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.290-6538C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116665518 | ||||||
| chr8:116665737
|
A | G | 3 | a0001c0001t0013g0007a0001c0001t0013g0102a0001c0001t0013g0105 | 3 | HG02257.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.290-6757T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116665737 | ||||||
| chr8:116665875
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.290-6895T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116665875 | ||||||
| chr8:116666188
|
T | G | 5 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-7208A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666188 | ||||||
| chr8:116666273
|
A | G | 1 | a0001c0001t0004g0181 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.290-7293T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666273 | ||||||
| chr8:116666394
|
T | C | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-7414A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666394 | ||||||
| chr8:116666413
|
T | C | 107 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(104): Show | 107 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.290-7433A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666413 | ||||||
| chr8:116666749
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290-7769A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666749 | ||||||
| chr8:116666753
|
C | CAAA | 6 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0143others(3): Show | 6 | HG00280.hp1 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-7776_290-7774d others(5): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAA | 115 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.290-7777_290-7774d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAA | 80 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(77): Show | 80 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(77): Show |
intron_variant | MODIFIER | c.290-7778_290-7774d others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAA | 27 | a0001c0001t0001g0196a0001c0001t0001g0225a0001c0001t0001g0240others(24): Show | 27 | HG00323.hp1 HG00423.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.290-7779_290-7774d others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA | 8 | a0001c0001t0004g0185a0001c0001t0005g0218a0001c0001t0005g0233others(5): Show | 8 | HG01123.hp2 HG01167.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-7780_290-7774d others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0009g0154a0001c0001t0018g0157 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.290-7783_290-7774d others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0158a0001c0001t0007g0316a0001c0001t0009g0153 | 3 | HG01243.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.290-7785_290-7774d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0009g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.290-7786_290-7774d others(15): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0007g0325a0001c0001t0007g0327 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290-7790_290-7774d others(19): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0007g0317a0001c0001t0007g0322 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.290-7795_290-7774d others(24): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(20): Show |
2 | a0001c0001t0007g0001a0001c0001t0007g0326 | 3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.290-7774_290-7773i others(29): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0007g0320 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.290-7774_290-7773i others(31): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0007g0321 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.290-7774_290-7773i others(35): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(33): Show |
1 | a0001c0001t0007g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290-7774_290-7773i others(42): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666753
|
C | CAAAAAAA others(39): Show |
1 | a0001c0001t0007g0319 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-7774_290-7773i others(48): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666753 | ||||||
| chr8:116666777
|
T | A | 1 | a0001c0001t0002g0289 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.290-7797A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666777 | ||||||
| chr8:116666820
|
C | G | 3 | a0001c0001t0004g0167a0001c0001t0004g0168a0001c0001t0004g0173 | 3 | HG01934.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.290-7840G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666820 | ||||||
| chr8:116666965
|
A | G | 233 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.290-7985T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666965 | ||||||
| chr8:116666986
|
C | T | 1 | a0001c0001t0015g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-8006G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116666986 | ||||||
| chr8:116667108
|
A | G | 1 | a0001c0001t0008g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.290-8128T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667108 | ||||||
| chr8:116667183
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.290-8203C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667183 | ||||||
| chr8:116667198
|
T | C | 3 | a0001c0001t0004g0188a0001c0001t0004g0190a0001c0001t0004g0195 | 3 | NA19003.hp2 NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.290-8218A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667198 | ||||||
| chr8:116667362
|
T | C | 43 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.290-8382A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667362 | ||||||
| chr8:116667399
|
T | C | 115 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(112): Show | 115 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.290-8419A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667399 | ||||||
| chr8:116667451
|
T | C | 22 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(19): Show | 22 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.290-8471A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667451 | ||||||
| chr8:116667464
|
C | CA | 219 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(216): Show | 219 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.290-8485dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667464 | ||||||
| chr8:116667464
|
C | CAA | 22 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0134others(19): Show | 22 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.290-8486_290-8485d others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667464 | ||||||
| chr8:116667509
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-8529A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667509 | ||||||
| chr8:116667673
|
C | T | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-8693G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116667673 | ||||||
| chr8:116668030
|
T | C | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-9050A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668030 | ||||||
| chr8:116668080
|
A | T | 312 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(309): Show | 313 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.290-9100T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668080 | ||||||
| chr8:116668099
|
T | G | 12 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0262others(9): Show | 12 | HG02165.hp2 NA18969.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.290-9119A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668099 | ||||||
| chr8:116668125
|
C | T | 61 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(58): Show | 61 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.290-9145G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668125 | ||||||
| chr8:116668458
|
G | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.290-9478C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668458 | ||||||
| chr8:116668567
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.290-9587C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668567 | ||||||
| chr8:116668692
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-9712A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668692 | ||||||
| chr8:116668713
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.290-9733C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668713 | ||||||
| chr8:116668723
|
G | A | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-9743C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668723 | ||||||
| chr8:116668743
|
G | T | 2 | a0001c0001t0007g0325a0001c0001t0007g0327 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290-9763C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668743 | ||||||
| chr8:116668792
|
A | G | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-9812T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668792 | ||||||
| chr8:116668973
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.290-9993G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668973 | ||||||
| chr8:116668974
|
G | A | 14 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(11): Show | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-9994C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116668974 | ||||||
| chr8:116669111
|
A | G | 1 | a0001c0001t0004g0083 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.290-10131T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669111 | ||||||
| chr8:116669336
|
C | T | 31 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0161others(28): Show | 31 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.290-10356G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669336 | ||||||
| chr8:116669424
|
C | T | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-10444G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669424 | ||||||
| chr8:116669486
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.290-10506T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669486 | ||||||
| chr8:116669548
|
T | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-10568A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669548 | ||||||
| chr8:116669770
|
G | A | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.290-10790C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116669770 | ||||||
| chr8:116670295
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.290-11315C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670295 | ||||||
| chr8:116670387
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.290-11407A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670387 | ||||||
| chr8:116670429
|
T | A | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.290-11449A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670429 | ||||||
| chr8:116670443
|
C | A | 1 | a0001c0001t0003g0017 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.290-11463G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670443 | ||||||
| chr8:116670618
|
T | G | 1 | a0001c0001t0021g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.290-11638A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670618 | ||||||
| chr8:116670739
|
T | C | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0285 | 3 | HG00609.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.290-11759A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670739 | ||||||
| chr8:116670867
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-11887G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670867 | ||||||
| chr8:116670905
|
A | C | 59 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.290-11925T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670905 | ||||||
| chr8:116670962
|
C | G | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-11982G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670962 | ||||||
| chr8:116670983
|
G | A | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-12003C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670983 | ||||||
| chr8:116670988
|
A | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-12008T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116670988 | ||||||
| chr8:116671216
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.290-12236A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671216 | ||||||
| chr8:116671216
|
T | G | 1 | a0001c0001t0001g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.290-12236A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671216 | ||||||
| chr8:116671443
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.290-12463A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671443 | ||||||
| chr8:116671486
|
C | T | 3 | a0001c0001t0013g0007a0001c0001t0013g0102a0001c0001t0013g0105 | 3 | HG02257.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.290-12506G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671486 | ||||||
| chr8:116671532
|
A | G | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.290-12552T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671532 | ||||||
| chr8:116671607
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-12627G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671607 | ||||||
| chr8:116671914
|
C | T | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.290-12934G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671914 | ||||||
| chr8:116671933
|
A | G | 1 | a0001c0001t0012g0203 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.290-12953T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116671933 | ||||||
| chr8:116672087
|
C | G | 11 | a0001c0001t0004g0166a0001c0001t0004g0167a0001c0001t0004g0168others(8): Show | 11 | HG01074.hp1 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-13107G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672087 | ||||||
| chr8:116672221
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.290-13241A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672221 | ||||||
| chr8:116672543
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.290-13563A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672543 | ||||||
| chr8:116672557
|
T | C | 1 | a0001c0001t0008g0030 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290-13577A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672557 | ||||||
| chr8:116672646
|
G | GA | 8 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-13667dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672646 | ||||||
| chr8:116672692
|
T | C | 2 | a0001c0001t0004g0167a0001c0001t0004g0173 | 2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.290-13712A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116672692 | ||||||
| chr8:116673008
|
C | CA | 126 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(123): Show | 126 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.290-14029dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673008 | ||||||
| chr8:116673008
|
CA | C | 6 | a0001c0001t0003g0064a0001c0001t0007g0325a0001c0001t0007g0327others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-14029delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673008 | ||||||
| chr8:116673026
|
A | C | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.290-14046T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673026 | ||||||
| chr8:116673269
|
A | G | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-14289T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673269 | ||||||
| chr8:116673332
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-14352G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673332 | ||||||
| chr8:116673516
|
CTG | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-14538_290-1453 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673516 | ||||||
| chr8:116673626
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.290-14646C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673626 | ||||||
| chr8:116673668
|
G | A | 3 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.290-14688C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673668 | ||||||
| chr8:116673683
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.290-14703C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673683 | ||||||
| chr8:116673809
|
T | A | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-14829A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673809 | ||||||
| chr8:116673857
|
T | C | 1 | a0001c0001t0006g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-14877A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673857 | ||||||
| chr8:116673962
|
C | T | 1 | a0001c0001t0004g0187 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.290-14982G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116673962 | ||||||
| chr8:116674067
|
C | CA | 16 | a0001c0001t0003g0032a0001c0001t0003g0066a0001c0001t0003g0075others(13): Show | 16 | HG01261.hp1 HG01952.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-15088dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674067
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0009g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.290-15097_290-1508 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674067
|
CA | C | 32 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0125others(29): Show | 32 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.290-15088delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674067
|
CAA | C | 127 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(124): Show | 127 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.290-15089_290-1508 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674067
|
CAAA | C | 74 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0126others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.290-15090_290-1508 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674067
|
CAAAAA | C | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0238others(7): Show | 10 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-15092_290-1508 others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674067 | ||||||
| chr8:116674321
|
T | TG | 157 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0109others(154): Show | 157 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.290-15342dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674321 | ||||||
| chr8:116674321
|
TG | T | 21 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0305others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.290-15342delC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674321 | ||||||
| chr8:116674331
|
T | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0231a0001c0001t0002g0313others(2): Show | 5 | HG01192.hp2 HG02145.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-15351A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674331 | ||||||
| chr8:116674378
|
A | C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-15398T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674378 | ||||||
| chr8:116674382
|
A | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.290-15402T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674382 | ||||||
| chr8:116674412
|
T | G | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-15432A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674412 | ||||||
| chr8:116674448
|
C | T | 1 | a0001c0001t0007g0314 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.290-15468G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674448 | ||||||
| chr8:116674496
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.290-15516A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674496 | ||||||
| chr8:116674714
|
A | G | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.290-15734T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674714 | ||||||
| chr8:116674750
|
C | G | 1 | a0001c0001t0004g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.290-15770G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674750 | ||||||
| chr8:116674818
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.290-15838C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674818 | ||||||
| chr8:116674868
|
T | G | 1 | a0001c0001t0004g0163 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.290-15888A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674868 | ||||||
| chr8:116674893
|
T | G | 11 | a0001c0001t0002g0283a0001c0001t0002g0287a0001c0001t0002g0289others(8): Show | 11 | NA18942.hp2 NA18960.hp2 NA18964.hp1 others(8): Show |
intron_variant | MODIFIER | c.290-15913A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674893 | ||||||
| chr8:116674961
|
A | G | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290-15981T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674961 | ||||||
| chr8:116674979
|
C | A | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.290-15999G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116674979 | ||||||
| chr8:116675001
|
T | C | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.290-16021A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675001 | ||||||
| chr8:116675109
|
AT | A | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.290-16130delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675109 | ||||||
| chr8:116675134
|
A | G | 1 | a0001c0001t0002g0288 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.290-16154T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675134 | ||||||
| chr8:116675143
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.290-16163A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675143 | ||||||
| chr8:116675159
|
CT | C | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-16180delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675159 | ||||||
| chr8:116675377
|
T | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-16397A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675377 | ||||||
| chr8:116675471
|
T | C | 1 | a0001c0001t0002g0311 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290-16491A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675471 | ||||||
| chr8:116675484
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-16504G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675484 | ||||||
| chr8:116675745
|
T | C | 2 | a0001c0001t0003g0049a0001c0001t0003g0073 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.290-16765A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675745 | ||||||
| chr8:116675792
|
G | A | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.290-16812C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116675792 | ||||||
| chr8:116676142
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.290-17162G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676142 | ||||||
| chr8:116676155
|
G | T | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-17175C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676155 | ||||||
| chr8:116676312
|
C | T | 45 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(42): Show | 45 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.290-17332G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676312 | ||||||
| chr8:116676405
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-17425C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676405 | ||||||
| chr8:116676429
|
A | G | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-17449T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676429 | ||||||
| chr8:116676952
|
TA | T | 134 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(131): Show | 134 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.290-17973delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116676952 | ||||||
| chr8:116677028
|
T | C | 2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.290-18048A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677028 | ||||||
| chr8:116677204
|
A | C | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.290-18224T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677204 | ||||||
| chr8:116677313
|
CAAAT | C | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.290-18337_290-1833 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677313 | ||||||
| chr8:116677363
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290-18383A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677363 | ||||||
| chr8:116677564
|
G | A | 20 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-18584C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677564 | ||||||
| chr8:116677580
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290-18600A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677580 | ||||||
| chr8:116677597
|
G | A | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.290-18617C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677597 | ||||||
| chr8:116677645
|
G | A | 3 | a0001c0001t0002g0299a0001c0001t0002g0323a0002c0002t0002g0260 | 3 | HG02165.hp2 NA18979.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.290-18665C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677645 | ||||||
| chr8:116677793
|
T | C | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-18813A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677793 | ||||||
| chr8:116677799
|
G | C | 1 | a0001c0001t0012g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290-18819C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116677799 | ||||||
| chr8:116678038
|
G | C | 1 | a0001c0001t0003g0016 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.290-19058C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678038 | ||||||
| chr8:116678077
|
T | C | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.290-19097A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678077 | ||||||
| chr8:116678135
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.290-19155C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678135 | ||||||
| chr8:116678137
|
G | A | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-19157C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678137 | ||||||
| chr8:116678142
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-19162C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678142 | ||||||
| chr8:116678161
|
C | CG | 6 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0134others(3): Show | 6 | HG00280.hp1 HG03098.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-19182dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678161 | ||||||
| chr8:116678162
|
G | GT | 26 | a0001c0001t0001g0204a0001c0001t0001g0221a0001c0001t0001g0232others(23): Show | 26 | HG01175.hp1 HG01243.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.290-19183dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678162 | ||||||
| chr8:116678163
|
T | G | 100 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(97): Show | 100 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.290-19183A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678163 | ||||||
| chr8:116678183
|
C | T | 1 | a0001c0001t0014g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290-19203G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678183 | ||||||
| chr8:116678316
|
G | C | 16 | a0001c0001t0004g0160a0001c0001t0004g0161a0001c0001t0004g0162others(13): Show | 16 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.290-19336C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678316 | ||||||
| chr8:116678338
|
C | T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-19358G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678338 | ||||||
| chr8:116678361
|
C | T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-19381G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678361 | ||||||
| chr8:116678410
|
G | A | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.290-19430C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678410 | ||||||
| chr8:116678432
|
G | A | 15 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(12): Show | 16 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-19452C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678432 | ||||||
| chr8:116678451
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.290-19471G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678451 | ||||||
| chr8:116678526
|
G | A | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.290-19546C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678526 | ||||||
| chr8:116678545
|
G | A | 1 | a0001c0001t0006g0095 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.290-19565C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678545 | ||||||
| chr8:116678606
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | NA18950.hp1 NA19075.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-19626C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678606 | ||||||
| chr8:116678683
|
C | G | 1 | a0001c0001t0020g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.290-19703G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678683 | ||||||
| chr8:116678707
|
C | A | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290-19727G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678707 | ||||||
| chr8:116678709
|
T | G | 1 | a0001c0001t0013g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.290-19729A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678709 | ||||||
| chr8:116678750
|
T | G | 1 | a0001c0001t0003g0050 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.290-19770A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678750 | ||||||
| chr8:116678766
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-19786G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678766 | ||||||
| chr8:116678794
|
C | T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-19814G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678794 | ||||||
| chr8:116678855
|
G | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0279 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.290-19875C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678855 | ||||||
| chr8:116678861
|
T | TG | 29 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0001g0196others(26): Show | 29 | HG01099.hp1 HG01167.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.290-19882dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678861 | ||||||
| chr8:116678863
|
GGGGGGGG others(714): Show |
G | 39 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(36): Show | 39 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.290-20604_290-1988 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678863 | ||||||
| chr8:116678863
|
GGGGGGGG others(988): Show |
G | 1 | a0001c0001t0001g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.290-20878_290-1988 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678863 | ||||||
| chr8:116678864
|
GGGGGGGT others(713): Show |
G | 4 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0136others(1): Show | 4 | HG01175.hp2 HG01192.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-20604_290-1988 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678864 | ||||||
| chr8:116678877
|
C | A | 5 | a0001c0001t0005g0222a0001c0001t0005g0223a0001c0001t0005g0226others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-19897G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678877 | ||||||
| chr8:116678887
|
CCAGCCGC others(989): Show |
C | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.290-20903_290-1990 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678887 | ||||||
| chr8:116678936
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.290-19956T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678936 | ||||||
| chr8:116678944
|
G | C | 1 | a0001c0001t0011g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.290-19964C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678944 | ||||||
| chr8:116678952
|
CCCCTCTG others(120): Show |
C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-20099_290-1997 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116678952 | ||||||
| chr8:116679008
|
G | C | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.290-20028C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679008 | ||||||
| chr8:116679019
|
C | G | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290-20039G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679019 | ||||||
| chr8:116679029
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-20049C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679029 | ||||||
| chr8:116679046
|
T | C | 60 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(57): Show | 60 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20066A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679046 | ||||||
| chr8:116679067
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-20087C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679067 | ||||||
| chr8:116679072
|
T | C | 3 | a0001c0001t0007g0001a0001c0001t0007g0316a0001c0001t0007g0326 | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-20092A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679072 | ||||||
| chr8:116679090
|
G | C | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.290-20110C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679090 | ||||||
| chr8:116679098
|
T | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20118A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679098 | ||||||
| chr8:116679104
|
T | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20124A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679104 | ||||||
| chr8:116679114
|
G | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20134C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679114 | ||||||
| chr8:116679117
|
A | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20137T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679117 | ||||||
| chr8:116679121
|
GGGGTCAG others(41): Show |
G | 49 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0196others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.290-20189_290-2014 others(52): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679121 | ||||||
| chr8:116679122
|
G | GGGGGGTC others(188): Show |
1 | a0001c0001t0011g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.290-20143_290-2014 others(199): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679122 | ||||||
| chr8:116679122
|
G | GGGGGTCA others(187): Show |
4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0008others(1): Show | 4 | HG02257.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-20143_290-2014 others(198): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679122 | ||||||
| chr8:116679122
|
GGGTCAGC others(40): Show |
G | 6 | a0001c0001t0001g0081a0001c0001t0001g0231a0001c0001t0001g0245others(3): Show | 6 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-20189_290-2014 others(51): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679122 | ||||||
| chr8:116679124
|
G | T | 60 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(57): Show | 60 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20144C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679124 | ||||||
| chr8:116679134
|
T | C | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20154A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679134 | ||||||
| chr8:116679134
|
TGCCCGGC others(43): Show |
T | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-20204_290-2015 others(54): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679134 | ||||||
| chr8:116679168
|
GT | G | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20189delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679168 | ||||||
| chr8:116679174
|
G | A | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20194C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679174 | ||||||
| chr8:116679188
|
C | T | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20208G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679188 | ||||||
| chr8:116679188
|
CGGCCAGC others(234): Show |
C | 5 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0001t0002g0270others(2): Show | 5 | NA18959.hp2 NA18965.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20449_290-2020 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679188 | ||||||
| chr8:116679213
|
G | A | 9 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(6): Show | 9 | HG01891.hp2 HG02486.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-20233C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679213 | ||||||
| chr8:116679220
|
G | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-20240C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679220 | ||||||
| chr8:116679267
|
G | A | 63 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.290-20287C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679267 | ||||||
| chr8:116679274
|
C | T | 4 | a0001c0001t0004g0184a0001c0001t0004g0187a0001c0001t0004g0189others(1): Show | 4 | HG02155.hp1 NA18612.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-20294G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679274 | ||||||
| chr8:116679348
|
GGGTCAGC others(9): Show |
G | 83 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.290-20384_290-2036 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679348 | ||||||
| chr8:116679361
|
G | A | 60 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(57): Show | 60 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20381C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679361 | ||||||
| chr8:116679364
|
C | CGGTCAGC others(217): Show |
2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.290-20385_290-2038 others(228): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679364 | ||||||
| chr8:116679364
|
CGGTCAGC others(218): Show |
C | 1 | a0001c0001t0005g0234 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.290-20609_290-2038 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679364 | ||||||
| chr8:116679376
|
C | G | 1 | a0001c0001t0003g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.290-20396G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679376 | ||||||
| chr8:116679383
|
C | A | 2 | a0001c0001t0005g0220a0001c0001t0005g0237 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.290-20403G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679383 | ||||||
| chr8:116679398
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-20418C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679398 | ||||||
| chr8:116679398
|
GGGAGGGA others(660): Show |
G | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-21085_290-2041 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679398 | ||||||
| chr8:116679446
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.290-20466G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679446 | ||||||
| chr8:116679446
|
CGGGAGGT others(660): Show |
C | 5 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-21133_290-2046 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679446 | ||||||
| chr8:116679451
|
G | A | 3 | a0001c0001t0006g0088a0001c0001t0006g0091a0001c0001t0006g0093 | 3 | HG01884.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.290-20471C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679451 | ||||||
| chr8:116679471
|
GGCCGCCC others(218): Show |
G | 2 | a0001c0001t0005g0199a0001c0001t0005g0233 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.290-20716_290-2049 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679471 | ||||||
| chr8:116679479
|
C | G | 60 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(57): Show | 60 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-20499G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679479 | ||||||
| chr8:116679507
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.290-20527G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679507 | ||||||
| chr8:116679508
|
G | A | 5 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0001t0002g0270others(2): Show | 5 | NA18959.hp2 NA18965.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-20528C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679508 | ||||||
| chr8:116679552
|
C | T | 4 | a0001c0001t0003g0038a0001c0001t0003g0048a0001c0001t0003g0067others(1): Show | 4 | NA18947.hp1 NA18959.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-20572G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679552 | ||||||
| chr8:116679560
|
C | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-20580G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679560 | ||||||
| chr8:116679589
|
G | GGGGTCAG others(10): Show |
1 | a0001c0001t0002g0296 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.290-20610_290-2060 others(21): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679589 | ||||||
| chr8:116679589
|
G | GGGTCAGC others(10): Show |
2 | a0001c0001t0001g0205a0001c0001t0002g0276 | 2 | HG02071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.290-20610_290-2060 others(21): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679589 | ||||||
| chr8:116679589
|
G | GGGTCAGC others(9): Show |
117 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.290-20625_290-2061 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679589 | ||||||
| chr8:116679589
|
G | GGGTCAGT others(9): Show |
2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG00609.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.290-20610_290-2060 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679589 | ||||||
| chr8:116679595
|
G | GCCCCCCG others(10): Show |
2 | a0001c0001t0001g0219a0001c0001t0002g0306 | 2 | HG02004.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.290-20616_290-2061 others(21): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679595 | ||||||
| chr8:116679602
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.290-20622C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679602 | ||||||
| chr8:116679605
|
CGGCCAGC others(252): Show |
C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-20884_290-2062 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679605 | ||||||
| chr8:116679608
|
C | A | 1 | a0001c0001t0005g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-20628G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679608 | ||||||
| chr8:116679628
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.290-20648C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679628 | ||||||
| chr8:116679696
|
A | G | 234 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(231): Show | 234 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.290-20716T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679696 | ||||||
| chr8:116679746
|
GTCCGGGA others(42): Show |
G | 1 | a0001c0001t0020g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.290-20815_290-2076 others(53): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679746 | ||||||
| chr8:116679760
|
T | C | 1 | a0001c0001t0004g0181 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.290-20780A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679760 | ||||||
| chr8:116679760
|
T | TG | 20 | a0001c0001t0001g0219a0001c0001t0002g0264a0001c0001t0006g0082others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-20781dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679760 | ||||||
| chr8:116679761
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-20781C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679761 | ||||||
| chr8:116679763
|
GGGGGTCA others(265): Show |
G | 1 | a0001c0001t0004g0181 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.290-21055_290-2078 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679763 | ||||||
| chr8:116679772
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-20792G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679772 | ||||||
| chr8:116679809
|
T | TG | 18 | a0001c0001t0001g0136a0001c0001t0002g0279a0001c0001t0003g0033others(15): Show | 19 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.290-20830dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679809 | ||||||
| chr8:116679824
|
T | C | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0285 | 3 | HG00609.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.290-20844A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679824 | ||||||
| chr8:116679854
|
G | C | 1 | a0001c0001t0007g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290-20874C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679854 | ||||||
| chr8:116679858
|
T | TG | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0109others(103): Show | 106 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.290-20879dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679858 | ||||||
| chr8:116679858
|
T | TGG | 45 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.290-20880_290-2087 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679858 | ||||||
| chr8:116679858
|
T | TGGG | 62 | a0001c0001t0001g0081a0001c0001t0001g0158a0001c0001t0001g0238others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.290-20881_290-2087 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679858 | ||||||
| chr8:116679858
|
T | TGGGG | 19 | a0001c0001t0001g0239a0001c0001t0002g0250a0001c0001t0002g0252others(16): Show | 19 | HG01934.hp1 HG01981.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.290-20882_290-2087 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679858 | ||||||
| chr8:116679870
|
GC | G | 102 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(99): Show | 102 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.290-20891delG | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679870 | ||||||
| chr8:116679877
|
G | A | 1 | a0001c0001t0015g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.290-20897C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679877 | ||||||
| chr8:116679883
|
T | C | 303 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(300): Show | 304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.290-20903A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679883 | ||||||
| chr8:116679898
|
GGGAGGGA others(160): Show |
G | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-21085_290-2091 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679898 | ||||||
| chr8:116679926
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.290-20946G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679926 | ||||||
| chr8:116679926
|
C | G | 249 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(246): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.290-20946G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679926 | ||||||
| chr8:116679928
|
CT | C | 12 | a0001c0001t0003g0032a0001c0001t0008g0030a0001c0001t0008g0034others(9): Show | 12 | HG01952.hp1 HG02129.hp2 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-20949delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679928 | ||||||
| chr8:116679929
|
T | C | 1 | a0001c0001t0008g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.290-20949A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679929 | ||||||
| chr8:116679961
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-20981C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116679961 | ||||||
| chr8:116680021
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.290-21041C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680021 | ||||||
| chr8:116680021
|
GTCCGGGA others(159): Show |
G | 1 | a0001c0001t0003g0017 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.290-21207_290-2104 others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680021 | ||||||
| chr8:116680035
|
C | CG | 82 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0215others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.290-21056dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680035 | ||||||
| chr8:116680035
|
C | CGG | 26 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(23): Show | 26 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.290-21057_290-2105 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680035 | ||||||
| chr8:116680035
|
C | CGGG | 38 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0158others(35): Show | 38 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.290-21058_290-2105 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680035 | ||||||
| chr8:116680035
|
C | CGGGG | 86 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0112others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.290-21059_290-2105 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680035 | ||||||
| chr8:116680035
|
C | CGGGGG | 26 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(23): Show | 26 | HG00558.hp1 HG00609.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.290-21060_290-2105 others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680035 | ||||||
| chr8:116680064
|
C | T | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.290-21084G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680064 | ||||||
| chr8:116680065
|
A | G | 232 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(229): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.290-21085T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680065 | ||||||
| chr8:116680086
|
GC | G | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.290-21107delG | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680086 | ||||||
| chr8:116680113
|
T | C | 197 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(194): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.290-21133A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680113 | ||||||
| chr8:116680198
|
T | TG | 105 | a0001c0001t0001g0079a0001c0001t0001g0107a0001c0001t0001g0146others(102): Show | 105 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.290-21219dupC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680198 | ||||||
| chr8:116680198
|
T | TGG | 34 | a0001c0001t0001g0108a0001c0001t0001g0139a0001c0001t0001g0142others(31): Show | 35 | HG00323.hp2 HG01099.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.290-21220_290-2121 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680198 | ||||||
| chr8:116680198
|
T | TGGGG | 24 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0111others(21): Show | 24 | HG00558.hp1 HG01070.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.290-21222_290-2121 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680198 | ||||||
| chr8:116680200
|
G | A | 1 | a0001c0001t0003g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.290-21220C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680200 | ||||||
| chr8:116680202
|
G | GGGT | 59 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(56): Show | 59 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.290-21223_290-2122 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680202 | ||||||
| chr8:116680202
|
G | T | 1 | a0001c0001t0004g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.290-21222C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680202 | ||||||
| chr8:116680212
|
A | T | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.290-21232T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680212 | ||||||
| chr8:116680220
|
G | A | 47 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(44): Show | 47 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.290-21240C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680220 | ||||||
| chr8:116680254
|
C | T | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-21274G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680254 | ||||||
| chr8:116680309
|
AC | A | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-21330delG | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680309 | ||||||
| chr8:116680417
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.290-21437C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680417 | ||||||
| chr8:116680428
|
G | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-21448C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680428 | ||||||
| chr8:116680446
|
G | T | 1 | a0001c0001t0003g0055 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.290-21466C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680446 | ||||||
| chr8:116680457
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.290-21477T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680457 | ||||||
| chr8:116680526
|
T | TC | 4 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | NA18948.hp1 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-21547dupG | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680526 | ||||||
| chr8:116680637
|
T | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-21657A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680637 | ||||||
| chr8:116680647
|
T | C | 2 | a0001c0001t0006g0089a0001c0001t0006g0095 | 2 | HG01167.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.290-21667A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680647 | ||||||
| chr8:116680685
|
A | T | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.290-21705T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680685 | ||||||
| chr8:116680713
|
T | G | 1 | a0001c0001t0003g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290-21733A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680713 | ||||||
| chr8:116680749
|
A | G | 11 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(8): Show | 11 | HG02257.hp1 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-21769T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680749 | ||||||
| chr8:116680830
|
A | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.290-21850T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680830 | ||||||
| chr8:116680832
|
AT | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0002g0284others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-21853delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680832 | ||||||
| chr8:116680833
|
T | A | 3 | a0001c0001t0015g0315a0001c0001t0017g0331a0001c0001t0017g0332 | 3 | HG02615.hp1 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.290-21853A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680833 | ||||||
| chr8:116680844
|
AAAT | A | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.290-21867_290-2186 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680844 | ||||||
| chr8:116680847
|
T | TA | 149 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(146): Show | 150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.290-21868dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680847 | ||||||
| chr8:116680973
|
T | TA | 53 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(50): Show | 53 | HG00280.hp2 HG01099.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.290-21994dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680973 | ||||||
| chr8:116680973
|
TA | T | 103 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0125others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.290-21994delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680973 | ||||||
| chr8:116680974
|
A | T | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.290-21994T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116680974 | ||||||
| chr8:116681046
|
T | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-22066A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681046 | ||||||
| chr8:116681091
|
G | C | 1 | a0001c0001t0004g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.290-22111C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681091 | ||||||
| chr8:116681161
|
G | A | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.290-22181C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681161 | ||||||
| chr8:116681183
|
TA | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-22204delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681183 | ||||||
| chr8:116681184
|
A | T | 1 | a0001c0001t0021g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.290-22204T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681184 | ||||||
| chr8:116681225
|
T | C | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-22245A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681225 | ||||||
| chr8:116681240
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-22260C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681240 | ||||||
| chr8:116681255
|
C | G | 3 | a0001c0001t0002g0277a0001c0001t0002g0290a0001c0001t0002g0292 | 3 | NA18943.hp2 NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.290-22275G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681255 | ||||||
| chr8:116681526
|
C | T | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.290-22546G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681526 | ||||||
| chr8:116681591
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-22611C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681591 | ||||||
| chr8:116681614
|
C | T | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-22634G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681614 | ||||||
| chr8:116681621
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.290-22641C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681621 | ||||||
| chr8:116681666
|
C | CA | 80 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(77): Show | 81 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.290-22687dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681666 | ||||||
| chr8:116681666
|
C | CAA | 40 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0196others(37): Show | 40 | HG00280.hp2 HG01123.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-22688_290-2268 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681666 | ||||||
| chr8:116681666
|
C | CAAA | 23 | a0001c0001t0001g0079a0001c0001t0005g0197a0001c0001t0005g0198others(20): Show | 23 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.290-22689_290-2268 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681666 | ||||||
| chr8:116681666
|
CA | C | 20 | a0001c0001t0001g0120a0001c0001t0001g0134a0001c0001t0004g0083others(17): Show | 20 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-22687delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681666 | ||||||
| chr8:116681736
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.290-22756A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681736 | ||||||
| chr8:116681809
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.290-22829T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681809 | ||||||
| chr8:116681905
|
T | C | 3 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249 | 3 | HG02055.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.290-22925A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116681905 | ||||||
| chr8:116682098
|
G | A | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.290-23118C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682098 | ||||||
| chr8:116682121
|
A | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.290-23141T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682121 | ||||||
| chr8:116682257
|
T | C | 1 | a0001c0001t0004g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.290-23277A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682257 | ||||||
| chr8:116682279
|
G | C | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.290-23299C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682279 | ||||||
| chr8:116682302
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.290-23322G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682302 | ||||||
| chr8:116682460
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-23480G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682460 | ||||||
| chr8:116682566
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.290-23586G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682566 | ||||||
| chr8:116682610
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.290-23630G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682610 | ||||||
| chr8:116682643
|
G | A | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.290-23663C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682643 | ||||||
| chr8:116682655
|
T | A | 14 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(11): Show | 14 | HG00639.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-23675A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682655 | ||||||
| chr8:116682833
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.290-23853A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116682833 | ||||||
| chr8:116683017
|
A | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.290-24037T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683017 | ||||||
| chr8:116683167
|
T | C | 1 | a0001c0001t0004g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.290-24187A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683167 | ||||||
| chr8:116683340
|
C | T | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.290-24360G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683340 | ||||||
| chr8:116683406
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.290-24426C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683406 | ||||||
| chr8:116683420
|
G | A | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.290-24440C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683420 | ||||||
| chr8:116683639
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.290-24659T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683639 | ||||||
| chr8:116683708
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.290-24728T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683708 | ||||||
| chr8:116683765
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.290-24785G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116683765 | ||||||
| chr8:116684075
|
G | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-25095C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116684075 | ||||||
| chr8:116684286
|
T | C | 6 | a0001c0001t0005g0197a0001c0001t0005g0213a0001c0001t0005g0216others(3): Show | 6 | HG00323.hp1 HG01123.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-25306A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116684286 | ||||||
| chr8:116684318
|
T | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0237 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.290-25338A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116684318 | ||||||
| chr8:116685060
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.290-26080A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685060 | ||||||
| chr8:116685096
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290-26116G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685096 | ||||||
| chr8:116685107
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-26127C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685107 | ||||||
| chr8:116685313
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290-26333C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685313 | ||||||
| chr8:116685335
|
G | C | 247 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.290-26355C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685335 | ||||||
| chr8:116685659
|
C | T | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.290-26679G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685659 | ||||||
| chr8:116685682
|
T | C | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-26702A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685682 | ||||||
| chr8:116685876
|
C | A | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.290-26896G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685876 | ||||||
| chr8:116685938
|
T | C | 114 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.290-26958A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116685938 | ||||||
| chr8:116686202
|
T | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG03491.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.290-27222A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686202 | ||||||
| chr8:116686379
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-27399C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686379 | ||||||
| chr8:116686389
|
T | C | 1 | a0001c0001t0022g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.290-27409A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686389 | ||||||
| chr8:116686568
|
A | G | 11 | a0001c0001t0002g0250a0001c0001t0002g0255a0001c0001t0002g0275others(8): Show | 11 | HG01123.hp1 HG01346.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-27588T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686568 | ||||||
| chr8:116686790
|
AAAAAAAT | A | 66 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(63): Show | 66 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.290-27817_290-2781 others(11): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686790 | ||||||
| chr8:116686803
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.290-27823T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686803 | ||||||
| chr8:116686811
|
T | G | 1 | a0001c0001t0002g0273 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.290-27831A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686811 | ||||||
| chr8:116686846
|
C | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.290-27866G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686846 | ||||||
| chr8:116686907
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.290-27927A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116686907 | ||||||
| chr8:116687476
|
G | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-28496C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116687476 | ||||||
| chr8:116687536
|
T | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-28556A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116687536 | ||||||
| chr8:116687541
|
TA | T | 12 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0262others(9): Show | 12 | HG02165.hp2 NA18969.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.290-28562delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116687541 | ||||||
| chr8:116687639
|
T | G | 61 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(58): Show | 61 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.290-28659A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116687639 | ||||||
| chr8:116687996
|
T | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0125others(1): Show | 4 | HG01069.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-29016A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116687996 | ||||||
| chr8:116688119
|
A | T | 1 | a0001c0001t0003g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.290-29139T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688119 | ||||||
| chr8:116688663
|
A | C | 1 | a0001c0001t0008g0042 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.290-29683T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688663 | ||||||
| chr8:116688732
|
T | TATTA | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.290-29756_290-2975 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688732 | ||||||
| chr8:116688749
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-29769C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688749 | ||||||
| chr8:116688855
|
G | T | 2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.290-29875C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688855 | ||||||
| chr8:116688963
|
G | A | 1 | a0001c0001t0002g0263 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.290-29983C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116688963 | ||||||
| chr8:116689077
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290-30097T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689077 | ||||||
| chr8:116689333
|
C | A | 1 | a0001c0001t0005g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.290-30353G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689333 | ||||||
| chr8:116689391
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.290-30411C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689391 | ||||||
| chr8:116689777
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | NA18948.hp1 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-30797A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689777 | ||||||
| chr8:116689895
|
A | G | 20 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-30915T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689895 | ||||||
| chr8:116689935
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-30955C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116689935 | ||||||
| chr8:116690080
|
T | G | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.290-31100A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690080 | ||||||
| chr8:116690379
|
GA | G | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.290-31400delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690379 | ||||||
| chr8:116690396
|
A | G | 1 | a0001c0001t0003g0029 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.290-31416T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690396 | ||||||
| chr8:116690404
|
A | G | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.290-31424T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690404 | ||||||
| chr8:116690426
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-31446C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690426 | ||||||
| chr8:116690650
|
T | C | 20 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-31670A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690650 | ||||||
| chr8:116690674
|
T | G | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-31694A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690674 | ||||||
| chr8:116690748
|
G | A | 39 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(36): Show | 39 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.290-31768C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116690748 | ||||||
| chr8:116691270
|
T | G | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-32290A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691270 | ||||||
| chr8:116691360
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.290-32380C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691360 | ||||||
| chr8:116691461
|
A | G | 2 | a0001c0001t0009g0152a0001c0001t0009g0153 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.290-32481T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691461 | ||||||
| chr8:116691556
|
G | GA | 84 | a0001c0001t0001g0126a0001c0001t0001g0214a0001c0001t0001g0215others(81): Show | 84 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.290-32577dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691556 | ||||||
| chr8:116691692
|
T | C | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-32712A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691692 | ||||||
| chr8:116691785
|
T | C | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-32805A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691785 | ||||||
| chr8:116691803
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.290-32823G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691803 | ||||||
| chr8:116691869
|
C | CA | 191 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(188): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.290-32890dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691869 | ||||||
| chr8:116691869
|
C | CAA | 47 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0219others(44): Show | 47 | HG00609.hp2 HG01070.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.290-32891_290-3289 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116691869 | ||||||
| chr8:116692014
|
T | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33034A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692014 | ||||||
| chr8:116692015
|
T | G | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33035A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692015 | ||||||
| chr8:116692016
|
C | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33036G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692016 | ||||||
| chr8:116692017
|
C | G | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33037G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692017 | ||||||
| chr8:116692018
|
C | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33038G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692018 | ||||||
| chr8:116692019
|
T | G | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.290-33039A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692019 | ||||||
| chr8:116692994
|
T | C | 132 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.289+33022A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116692994 | ||||||
| chr8:116693156
|
TG | T | 20 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.289+32859delC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693156 | ||||||
| chr8:116693177
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+32839G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693177 | ||||||
| chr8:116693349
|
C | G | 1 | a0001c0001t0003g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.289+32667G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693349 | ||||||
| chr8:116693360
|
C | A | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.289+32656G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693360 | ||||||
| chr8:116693365
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.289+32651A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693365 | ||||||
| chr8:116693446
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.289+32570A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693446 | ||||||
| chr8:116693630
|
T | C | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+32386A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693630 | ||||||
| chr8:116693633
|
C | G | 4 | a0001c0001t0004g0184a0001c0001t0004g0187a0001c0001t0004g0189others(1): Show | 4 | HG02155.hp1 NA18612.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+32383G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693633 | ||||||
| chr8:116693789
|
C | T | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+32227G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693789 | ||||||
| chr8:116693850
|
A | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+32166T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693850 | ||||||
| chr8:116693897
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.289+32119G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693897 | ||||||
| chr8:116693907
|
T | G | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+32109A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693907 | ||||||
| chr8:116693973
|
GTATCA | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+32038_289+3204 others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693973 | ||||||
| chr8:116693979
|
T | C | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.289+32037A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116693979 | ||||||
| chr8:116694144
|
CT | C | 43 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.289+31871delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694144 | ||||||
| chr8:116694226
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+31790C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694226 | ||||||
| chr8:116694293
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02717.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.289+31723T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694293 | ||||||
| chr8:116694418
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.289+31598G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694418 | ||||||
| chr8:116694659
|
G | A | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.289+31357C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694659 | ||||||
| chr8:116694809
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0120 | 2 | NA18948.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.289+31207C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694809 | ||||||
| chr8:116694985
|
G | A | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0002g0312 | 3 | NA18960.hp2 NA19076.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.289+31031C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116694985 | ||||||
| chr8:116695067
|
C | CT | 30 | a0001c0001t0001g0116a0001c0001t0001g0142a0001c0001t0001g0205others(27): Show | 31 | HG00280.hp2 HG02145.hp1 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.289+30948dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695067 | ||||||
| chr8:116695067
|
C | T | 1 | a0001c0001t0011g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289+30949G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695067 | ||||||
| chr8:116695067
|
CT | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0140a0001c0001t0004g0169others(5): Show | 8 | HG01069.hp1 HG01943.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+30948delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695067 | ||||||
| chr8:116695180
|
G | A | 40 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+30836C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695180 | ||||||
| chr8:116695300
|
T | A | 1 | a0001c0001t0002g0266 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.289+30716A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695300 | ||||||
| chr8:116695320
|
C | T | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(6): Show | 9 | HG00280.hp2 HG02602.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+30696G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695320 | ||||||
| chr8:116695364
|
C | T | 16 | a0001c0001t0002g0289a0001c0001t0002g0291a0001c0001t0002g0293others(13): Show | 17 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+30652G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695364 | ||||||
| chr8:116695489
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG03491.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.289+30527C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695489 | ||||||
| chr8:116695656
|
T | C | 5 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0001t0002g0270others(2): Show | 5 | NA18959.hp2 NA18965.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+30360A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695656 | ||||||
| chr8:116695800
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+30216T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116695800 | ||||||
| chr8:116696143
|
C | G | 1 | a0001c0001t0004g0166 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.289+29873G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696143 | ||||||
| chr8:116696668
|
T | C | 3 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.289+29348A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696668 | ||||||
| chr8:116696700
|
G | T | 15 | a0001c0001t0001g0158a0001c0001t0004g0195a0001c0001t0005g0197others(12): Show | 15 | HG00323.hp1 HG01123.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.289+29316C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696700 | ||||||
| chr8:116696770
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+29246A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696770 | ||||||
| chr8:116696830
|
A | G | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+29186T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696830 | ||||||
| chr8:116696887
|
A | C | 1 | a0001c0001t0012g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.289+29129T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116696887 | ||||||
| chr8:116697069
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.289+28947A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697069 | ||||||
| chr8:116697069
|
T | G | 21 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+28947A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697069 | ||||||
| chr8:116697128
|
T | A | 1 | a0001c0001t0015g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+28888A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697128 | ||||||
| chr8:116697214
|
A | G | 34 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(31): Show | 35 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.289+28802T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697214 | ||||||
| chr8:116697336
|
G | A | 57 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(54): Show | 57 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.289+28680C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697336 | ||||||
| chr8:116697358
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.289+28658A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697358 | ||||||
| chr8:116697448
|
T | C | 8 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0006g0082others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.289+28568A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697448 | ||||||
| chr8:116697496
|
C | T | 3 | a0001c0001t0017g0331a0001c0001t0017g0332a0001c0001t0020g0076 | 3 | HG02615.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.289+28520G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697496 | ||||||
| chr8:116697799
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+28217C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697799 | ||||||
| chr8:116697974
|
G | A | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+28042C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116697974 | ||||||
| chr8:116698093
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.289+27923G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698093 | ||||||
| chr8:116698184
|
G | GT | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+27831dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698184 | ||||||
| chr8:116698418
|
A | G | 2 | a0001c0001t0007g0001a0001c0001t0007g0326 | 3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.289+27598T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698418 | ||||||
| chr8:116698429
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+27587G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698429 | ||||||
| chr8:116698430
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.289+27586C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698430 | ||||||
| chr8:116698456
|
T | G | 1 | a0001c0001t0004g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.289+27560A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698456 | ||||||
| chr8:116698527
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.289+27489G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698527 | ||||||
| chr8:116698540
|
T | C | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+27476A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698540 | ||||||
| chr8:116698716
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18994.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.289+27300T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698716 | ||||||
| chr8:116698821
|
A | G | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+27195T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698821 | ||||||
| chr8:116698905
|
T | C | 61 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(58): Show | 61 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.289+27111A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116698905 | ||||||
| chr8:116699134
|
CA | C | 172 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(169): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.289+26881delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699134 | ||||||
| chr8:116699150
|
AT | A | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+26865delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699150 | ||||||
| chr8:116699418
|
T | C | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+26598A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699418 | ||||||
| chr8:116699529
|
A | G | 1 | a0001c0001t0004g0187 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.289+26487T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699529 | ||||||
| chr8:116699722
|
T | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.289+26294A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699722 | ||||||
| chr8:116699736
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.289+26280A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699736 | ||||||
| chr8:116699793
|
A | AGG | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.289+26221_289+2622 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699793 | ||||||
| chr8:116699796
|
T | A | 108 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(105): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.289+26220A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699796 | ||||||
| chr8:116699803
|
G | GT | 70 | a0001c0001t0001g0136a0001c0001t0001g0231a0001c0001t0002g0250others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.289+26212dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699803 | ||||||
| chr8:116699803
|
G | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0004g0167others(1): Show | 4 | HG01169.hp1 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+26213C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699803 | ||||||
| chr8:116699808
|
T | TTTTG | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+26204_289+2620 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699808 | ||||||
| chr8:116699936
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+26080C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699936 | ||||||
| chr8:116699986
|
A | G | 1 | a0001c0001t0003g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.289+26030T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116699986 | ||||||
| chr8:116700052
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.289+25964A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700052 | ||||||
| chr8:116700255
|
A | G | 2 | a0001c0001t0006g0089a0001c0001t0006g0095 | 2 | HG01167.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.289+25761T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700255 | ||||||
| chr8:116700333
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+25683C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700333 | ||||||
| chr8:116700371
|
G | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.289+25645C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700371 | ||||||
| chr8:116700522
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+25494C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700522 | ||||||
| chr8:116700582
|
T | C | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.289+25434A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700582 | ||||||
| chr8:116700758
|
C | T | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.289+25258G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700758 | ||||||
| chr8:116700946
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+25070T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700946 | ||||||
| chr8:116700998
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+25018A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700998 | ||||||
| chr8:116700999
|
A | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+25017T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116700999 | ||||||
| chr8:116701195
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+24821G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701195 | ||||||
| chr8:116701331
|
C | A | 3 | a0001c0001t0003g0027a0001c0001t0003g0047a0001c0001t0003g0066 | 3 | NA18943.hp1 NA18957.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.289+24685G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701331 | ||||||
| chr8:116701441
|
C | T | 5 | a0001c0001t0005g0222a0001c0001t0005g0223a0001c0001t0005g0226others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+24575G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701441 | ||||||
| chr8:116701802
|
A | C | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.289+24214T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701802 | ||||||
| chr8:116701862
|
A | G | 11 | a0001c0001t0006g0088a0001c0001t0006g0090a0001c0001t0006g0091others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+24154T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701862 | ||||||
| chr8:116701878
|
G | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.289+24138C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701878 | ||||||
| chr8:116701900
|
AT | A | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0285 | 3 | HG00609.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.289+24115delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701900 | ||||||
| chr8:116701995
|
A | AT | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.289+24020dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701995 | ||||||
| chr8:116701995
|
A | T | 1 | a0001c0001t0008g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.289+24021T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116701995 | ||||||
| chr8:116702166
|
T | C | 1 | a0001c0001t0002g0266 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.289+23850A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702166 | ||||||
| chr8:116702182
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.289+23834C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702182 | ||||||
| chr8:116702812
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+23204T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702812 | ||||||
| chr8:116702889
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+23127C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702889 | ||||||
| chr8:116702905
|
C | T | 281 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(278): Show | 282 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.289+23111G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702905 | ||||||
| chr8:116702923
|
C | T | 106 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(103): Show | 106 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.289+23093G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702923 | ||||||
| chr8:116702980
|
C | A | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+23036G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116702980 | ||||||
| chr8:116703218
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(4): Show | 7 | NA18950.hp1 NA18954.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.289+22798C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703218 | ||||||
| chr8:116703250
|
C | T | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+22766G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703250 | ||||||
| chr8:116703272
|
C | T | 1 | a0001c0001t0004g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.289+22744G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703272 | ||||||
| chr8:116703346
|
ACCGGGAA others(9): Show |
A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.289+22654_289+2266 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703346 | ||||||
| chr8:116703366
|
T | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.289+22650A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703366 | ||||||
| chr8:116703444
|
G | A | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+22572C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703444 | ||||||
| chr8:116703461
|
C | T | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+22555G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703461 | ||||||
| chr8:116703488
|
G | A | 12 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0262others(9): Show | 12 | HG02165.hp2 NA18969.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+22528C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703488 | ||||||
| chr8:116703492
|
C | T | 64 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.289+22524G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703492 | ||||||
| chr8:116703660
|
G | A | 1 | a0001c0001t0004g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.289+22356C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703660 | ||||||
| chr8:116703762
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.289+22254G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703762 | ||||||
| chr8:116703848
|
T | C | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+22168A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703848 | ||||||
| chr8:116703868
|
C | G | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.289+22148G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703868 | ||||||
| chr8:116703881
|
G | A | 1 | a0001c0001t0004g0184 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.289+22135C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703881 | ||||||
| chr8:116703977
|
G | A | 1 | a0001c0001t0002g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.289+22039C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116703977 | ||||||
| chr8:116704057
|
T | C | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.289+21959A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704057 | ||||||
| chr8:116704232
|
C | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+21784G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704232 | ||||||
| chr8:116704254
|
A | C | 1 | a0001c0001t0007g0316 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.289+21762T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704254 | ||||||
| chr8:116704298
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+21718A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704298 | ||||||
| chr8:116704552
|
A | G | 1 | a0001c0001t0015g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.289+21464T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704552 | ||||||
| chr8:116704696
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.289+21320T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704696 | ||||||
| chr8:116704724
|
T | C | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+21292A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704724 | ||||||
| chr8:116704833
|
AT | A | 247 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.289+21182delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704833 | ||||||
| chr8:116704892
|
A | G | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+21124T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704892 | ||||||
| chr8:116704895
|
T | C | 1 | a0001c0001t0006g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.289+21121A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704895 | ||||||
| chr8:116704936
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+21080G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116704936 | ||||||
| chr8:116705224
|
G | A | 1 | a0001c0001t0004g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.289+20792C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705224 | ||||||
| chr8:116705423
|
T | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+20593A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705423 | ||||||
| chr8:116705491
|
A | AC | 39 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0111others(36): Show | 39 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.289+20524dupG | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705491 | ||||||
| chr8:116705491
|
A | ACC | 18 | a0001c0001t0001g0080a0001c0001t0001g0112a0001c0001t0001g0135others(15): Show | 18 | HG01169.hp2 HG01192.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.289+20523_289+2052 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705491 | ||||||
| chr8:116705493
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.289+20523G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705493 | ||||||
| chr8:116705494
|
C | G | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.289+20522G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705494 | ||||||
| chr8:116705494
|
C | T | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+20522G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705494 | ||||||
| chr8:116705500
|
CA | C | 92 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0204others(89): Show | 92 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.289+20515delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705500 | ||||||
| chr8:116705501
|
A | C | 190 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(187): Show | 191 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.289+20515T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705501 | ||||||
| chr8:116705502
|
C | G | 4 | a0001c0001t0002g0267a0001c0001t0002g0298a0001c0001t0002g0324others(1): Show | 4 | NA18941.hp1 NA18952.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+20514G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705502 | ||||||
| chr8:116705999
|
G | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.289+20017C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116705999 | ||||||
| chr8:116706011
|
C | G | 5 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+20005G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706011 | ||||||
| chr8:116706235
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.289+19781A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706235 | ||||||
| chr8:116706313
|
T | C | 13 | a0001c0001t0003g0003a0001c0001t0008g0030a0001c0001t0008g0034others(10): Show | 13 | HG02129.hp2 NA18950.hp2 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+19703A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706313 | ||||||
| chr8:116706366
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.289+19650G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706366 | ||||||
| chr8:116706367
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.289+19649C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706367 | ||||||
| chr8:116706584
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0123 | 2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.289+19432C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706584 | ||||||
| chr8:116706588
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.289+19428C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706588 | ||||||
| chr8:116706714
|
T | TAAAAATA others(1): Show |
6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+19301_289+1930 others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706714 | ||||||
| chr8:116706737
|
G | A | 172 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(169): Show | 172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.289+19279C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706737 | ||||||
| chr8:116706840
|
C | T | 66 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(63): Show | 66 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.289+19176G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706840 | ||||||
| chr8:116706990
|
C | T | 1 | a0001c0001t0017g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.289+19026G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116706990 | ||||||
| chr8:116707020
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.289+18996C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707020 | ||||||
| chr8:116707127
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.289+18889G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707127 | ||||||
| chr8:116707128
|
G | A | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.289+18888C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707128 | ||||||
| chr8:116707370
|
T | C | 172 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(169): Show | 172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.289+18646A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707370 | ||||||
| chr8:116707473
|
T | C | 6 | a0001c0001t0004g0167a0001c0001t0004g0168a0001c0001t0004g0169others(3): Show | 6 | HG01081.hp1 HG01192.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+18543A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707473 | ||||||
| chr8:116707480
|
G | C | 2 | a0001c0001t0005g0200a0001c0001t0005g0201 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.289+18536C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707480 | ||||||
| chr8:116707565
|
C | CTTAAG | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+18450_289+1845 others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707565 | ||||||
| chr8:116707689
|
T | G | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+18327A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707689 | ||||||
| chr8:116707991
|
T | G | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+18025A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116707991 | ||||||
| chr8:116708011
|
C | T | 2 | a0001c0001t0002g0280a0001c0001t0002g0286 | 2 | HG00323.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.289+18005G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708011 | ||||||
| chr8:116708094
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0134 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.289+17922A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708094 | ||||||
| chr8:116708098
|
GA | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.289+17917delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708098 | ||||||
| chr8:116708104
|
C | T | 1 | a0001c0001t0011g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.289+17912G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708104 | ||||||
| chr8:116708249
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.289+17767T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708249 | ||||||
| chr8:116708393
|
A | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.289+17623T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708393 | ||||||
| chr8:116708427
|
A | C | 2 | a0001c0001t0005g0216a0001c0001t0005g0217 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.289+17589T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708427 | ||||||
| chr8:116708476
|
A | T | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+17540T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708476 | ||||||
| chr8:116708544
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.289+17472A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708544 | ||||||
| chr8:116708918
|
G | C | 1 | a0001c0001t0017g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.289+17098C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708918 | ||||||
| chr8:116708995
|
TA | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0140a0001c0001t0001g0142others(6): Show | 9 | HG01256.hp1 HG03041.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+17020delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116708995 | ||||||
| chr8:116709010
|
A | AT | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+17005dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709010 | ||||||
| chr8:116709102
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.289+16914C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709102 | ||||||
| chr8:116709176
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.289+16840A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709176 | ||||||
| chr8:116709389
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.289+16627G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709389 | ||||||
| chr8:116709494
|
C | T | 1 | a0001c0001t0012g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.289+16522G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709494 | ||||||
| chr8:116709516
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.289+16500T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116709516 | ||||||
| chr8:116710316
|
G | T | 276 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(273): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.289+15700C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710316 | ||||||
| chr8:116710475
|
A | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+15541T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710475 | ||||||
| chr8:116710529
|
C | T | 1 | a0001c0001t0004g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.289+15487G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710529 | ||||||
| chr8:116710570
|
T | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | NA18948.hp1 NA18951.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+15446A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710570 | ||||||
| chr8:116710636
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.289+15380G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710636 | ||||||
| chr8:116710638
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.289+15378T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710638 | ||||||
| chr8:116710915
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.289+15101G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116710915 | ||||||
| chr8:116711955
|
GCA | G | 104 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.289+14059_289+1406 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116711955 | ||||||
| chr8:116712002
|
GAAGA | G | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+14010_289+1401 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116712002 | ||||||
| chr8:116712106
|
G | A | 19 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(16): Show | 19 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.289+13910C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116712106 | ||||||
| chr8:116712118
|
G | A | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(6): Show | 9 | HG00280.hp2 HG02602.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+13898C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116712118 | ||||||
| chr8:116712227
|
G | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+13789C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116712227 | ||||||
| chr8:116712936
|
A | C | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.289+13080T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116712936 | ||||||
| chr8:116713029
|
T | A | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(6): Show | 9 | HG00280.hp2 HG02602.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+12987A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713029 | ||||||
| chr8:116713161
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.289+12855A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713161 | ||||||
| chr8:116713562
|
A | T | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+12454T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713562 | ||||||
| chr8:116713563
|
A | C | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+12453T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713563 | ||||||
| chr8:116713565
|
C | CT | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+12450dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713565 | ||||||
| chr8:116713628
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+12388G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713628 | ||||||
| chr8:116713635
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.289+12381A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713635 | ||||||
| chr8:116713641
|
C | G | 1 | a0001c0001t0002g0335 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.289+12375G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713641 | ||||||
| chr8:116713763
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.289+12253A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713763 | ||||||
| chr8:116713779
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+12237A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713779 | ||||||
| chr8:116713828
|
T | C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+12188A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713828 | ||||||
| chr8:116713831
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.289+12185C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116713831 | ||||||
| chr8:116714028
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.289+11988T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714028 | ||||||
| chr8:116714091
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.289+11925C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714091 | ||||||
| chr8:116714170
|
G | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+11846C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714170 | ||||||
| chr8:116714230
|
A | C | 1 | a0001c0001t0003g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.289+11786T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714230 | ||||||
| chr8:116714250
|
A | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+11766T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714250 | ||||||
| chr8:116714392
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.289+11624A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714392 | ||||||
| chr8:116714442
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+11574G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714442 | ||||||
| chr8:116714704
|
T | A | 13 | a0001c0001t0006g0100a0001c0001t0007g0001a0001c0001t0007g0314others(10): Show | 14 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.289+11312A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714704 | ||||||
| chr8:116714722
|
AAG | A | 6 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0015others(3): Show | 6 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+11292_289+1129 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714722 | ||||||
| chr8:116714915
|
T | C | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+11101A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116714915 | ||||||
| chr8:116715083
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.289+10933G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715083 | ||||||
| chr8:116715168
|
T | C | 1 | a0001c0001t0003g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.289+10848A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715168 | ||||||
| chr8:116715199
|
T | C | 1 | a0001c0001t0003g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.289+10817A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715199 | ||||||
| chr8:116715341
|
G | GA | 71 | a0001c0001t0001g0158a0001c0001t0002g0250a0001c0001t0002g0251others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.289+10674dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715341 | ||||||
| chr8:116715355
|
T | A | 73 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(70): Show | 73 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.289+10661A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715355 | ||||||
| chr8:116715432
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+10584A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715432 | ||||||
| chr8:116715565
|
T | A | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+10451A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715565 | ||||||
| chr8:116715611
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.289+10405G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715611 | ||||||
| chr8:116715732
|
G | A | 4 | a0001c0001t0004g0186a0001c0001t0004g0188a0001c0001t0004g0190others(1): Show | 4 | HG00609.hp2 NA19003.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+10284C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715732 | ||||||
| chr8:116715895
|
CTT | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+10119_289+1012 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715895 | ||||||
| chr8:116715916
|
A | G | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+10100T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116715916 | ||||||
| chr8:116716006
|
G | A | 1 | a0001c0001t0015g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.289+10010C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716006 | ||||||
| chr8:116716037
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289+9979T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716037 | ||||||
| chr8:116716040
|
AAG | A | 52 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(49): Show | 52 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.289+9974_289+9975d others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716040 | ||||||
| chr8:116716057
|
C | T | 179 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(176): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.289+9959G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716057 | ||||||
| chr8:116716161
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.289+9855C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716161 | ||||||
| chr8:116716182
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.289+9834T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716182 | ||||||
| chr8:116716237
|
T | C | 3 | a0001c0001t0006g0088a0001c0001t0006g0091a0001c0001t0006g0093 | 3 | HG01884.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.289+9779A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716237 | ||||||
| chr8:116716349
|
A | G | 66 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(63): Show | 66 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.289+9667T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716349 | ||||||
| chr8:116716448
|
G | A | 2 | a0001c0001t0003g0049a0001c0001t0003g0073 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.289+9568C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716448 | ||||||
| chr8:116716743
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.289+9273A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716743 | ||||||
| chr8:116716822
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.289+9194A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116716822 | ||||||
| chr8:116717173
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+8843A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116717173 | ||||||
| chr8:116717246
|
T | C | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+8770A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116717246 | ||||||
| chr8:116717512
|
T | C | 74 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(71): Show | 74 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.289+8504A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116717512 | ||||||
| chr8:116717887
|
A | T | 1 | a0001c0001t0012g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.289+8129T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116717887 | ||||||
| chr8:116718062
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.289+7954A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718062 | ||||||
| chr8:116718145
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.289+7871T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718145 | ||||||
| chr8:116718509
|
C | CAT | 16 | a0001c0001t0002g0267a0001c0001t0005g0223a0001c0001t0006g0086others(13): Show | 16 | HG00639.hp2 HG01167.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.289+7505_289+7506d others(4): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718509 | ||||||
| chr8:116718510
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.289+7506T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718510 | ||||||
| chr8:116718511
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.289+7505A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718511 | ||||||
| chr8:116718607
|
G | A | 1 | a0001c0001t0004g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.289+7409C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718607 | ||||||
| chr8:116718654
|
A | G | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.289+7362T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718654 | ||||||
| chr8:116718717
|
T | C | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.289+7299A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718717 | ||||||
| chr8:116718797
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+7219C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116718797 | ||||||
| chr8:116719199
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.289+6817G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719199 | ||||||
| chr8:116719277
|
C | T | 5 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0264others(2): Show | 5 | HG00323.hp2 NA18969.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+6739G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719277 | ||||||
| chr8:116719304
|
G | A | 20 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(17): Show | 20 | HG00323.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.289+6712C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719304 | ||||||
| chr8:116719336
|
C | T | 2 | a0001c0001t0009g0152a0001c0001t0009g0153 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.289+6680G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719336 | ||||||
| chr8:116719351
|
G | C | 1 | a0001c0001t0006g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.289+6665C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719351 | ||||||
| chr8:116719441
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+6575A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719441 | ||||||
| chr8:116719502
|
T | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+6514A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719502 | ||||||
| chr8:116719771
|
G | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.289+6245C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719771 | ||||||
| chr8:116719789
|
G | GA | 334 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(331): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.289+6226dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719789 | ||||||
| chr8:116719861
|
G | A | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+6155C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719861 | ||||||
| chr8:116719965
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.289+6051A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116719965 | ||||||
| chr8:116720087
|
GACCTTCA | G | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.289+5922_289+5928d others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720087 | ||||||
| chr8:116720303
|
T | G | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.289+5713A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720303 | ||||||
| chr8:116720398
|
T | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+5618A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720398 | ||||||
| chr8:116720550
|
T | A | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+5466A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720550 | ||||||
| chr8:116720599
|
A | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0334 | 2 | HG03834.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.289+5417T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720599 | ||||||
| chr8:116720670
|
C | G | 1 | a0001c0001t0002g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.289+5346G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720670 | ||||||
| chr8:116720761
|
A | G | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | NA18977.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.289+5255T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720761 | ||||||
| chr8:116720953
|
C | T | 1 | a0001c0001t0004g0163 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.289+5063G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116720953 | ||||||
| chr8:116721303
|
AG | A | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0285 | 3 | HG00609.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.289+4712delC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721303 | ||||||
| chr8:116721330
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0006g0082 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.289+4686G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721330 | ||||||
| chr8:116721437
|
A | G | 1 | a0001c0001t0004g0163 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.289+4579T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721437 | ||||||
| chr8:116721509
|
C | T | 4 | a0001c0001t0004g0170a0001c0001t0004g0175a0001c0001t0004g0177others(1): Show | 4 | HG01256.hp1 HG01358.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+4507G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721509 | ||||||
| chr8:116721551
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.289+4465T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721551 | ||||||
| chr8:116721797
|
T | A | 61 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(58): Show | 61 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.289+4219A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721797 | ||||||
| chr8:116721878
|
T | C | 1 | a0001c0001t0006g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.289+4138A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721878 | ||||||
| chr8:116721904
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+4112C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116721904 | ||||||
| chr8:116722330
|
T | C | 1 | a0001c0001t0013g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.289+3686A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722330 | ||||||
| chr8:116722350
|
C | A | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(6): Show | 9 | HG00280.hp2 HG02602.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+3666G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722350 | ||||||
| chr8:116722541
|
C | T | 3 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249 | 3 | HG02055.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.289+3475G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722541 | ||||||
| chr8:116722684
|
C | T | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.289+3332G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722684 | ||||||
| chr8:116722755
|
T | A | 14 | a0001c0001t0003g0027a0001c0001t0007g0001a0001c0001t0007g0314others(11): Show | 15 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+3261A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722755 | ||||||
| chr8:116722769
|
T | A | 1 | a0001c0001t0007g0314 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.289+3247A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722769 | ||||||
| chr8:116722828
|
A | T | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.289+3188T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722828 | ||||||
| chr8:116722860
|
C | T | 40 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.289+3156G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722860 | ||||||
| chr8:116722950
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+3066G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722950 | ||||||
| chr8:116722970
|
A | G | 44 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.289+3046T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116722970 | ||||||
| chr8:116723353
|
G | A | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.289+2663C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723353 | ||||||
| chr8:116723425
|
AG | A | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.289+2590delC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723425 | ||||||
| chr8:116723427
|
G | T | 162 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(159): Show | 163 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.289+2589C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723427 | ||||||
| chr8:116723430
|
A | T | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.289+2586T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723430 | ||||||
| chr8:116723598
|
G | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.289+2418C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723598 | ||||||
| chr8:116723629
|
G | C | 5 | a0001c0001t0014g0101a0001c0001t0014g0103a0001c0001t0014g0104others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+2387C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723629 | ||||||
| chr8:116723829
|
T | C | 82 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(79): Show | 83 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.289+2187A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723829 | ||||||
| chr8:116723872
|
C | A | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.289+2144G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723872 | ||||||
| chr8:116723980
|
T | A | 1 | a0001c0001t0002g0274 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.289+2036A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723980 | ||||||
| chr8:116723981
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.289+2035C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723981 | ||||||
| chr8:116723989
|
A | T | 1 | a0001c0001t0011g0006 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.289+2027T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116723989 | ||||||
| chr8:116724517
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.289+1499A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724517 | ||||||
| chr8:116724528
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.289+1488T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724528 | ||||||
| chr8:116724629
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1387T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724629 | ||||||
| chr8:116724661
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.289+1355G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724661 | ||||||
| chr8:116724763
|
C | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+1253G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724763 | ||||||
| chr8:116724880
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1136C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724880 | ||||||
| chr8:116724881
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1135A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724881 | ||||||
| chr8:116724883
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1133G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724883 | ||||||
| chr8:116724892
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.289+1124T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724892 | ||||||
| chr8:116724902
|
G | A | 13 | a0001c0001t0006g0088a0001c0001t0006g0089a0001c0001t0006g0090others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.289+1114C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724902 | ||||||
| chr8:116724910
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1106T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724910 | ||||||
| chr8:116724929
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289+1087A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116724929 | ||||||
| chr8:116725187
|
T | C | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+829A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725187 | ||||||
| chr8:116725476
|
T | C | 1 | a0001c0001t0007g0316 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.289+540A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725476 | ||||||
| chr8:116725494
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.289+522G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725494 | ||||||
| chr8:116725628
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.289+388A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725628 | ||||||
| chr8:116725812
|
TAAGTA | T | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.289+199_289+203del others(5): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725812 | ||||||
| chr8:116725869
|
T | C | 1 | a0001c0001t0006g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.289+147A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725869 | ||||||
| chr8:116725912
|
C | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0237 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.289+104G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 2/7 | chr8 | 116725912 | ||||||
| chr8:116726352
|
T | C | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.133-180A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726352 | ||||||
| chr8:116726538
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133-366A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726538 | ||||||
| chr8:116726587
|
G | A | 1 | a0001c0001t0004g0165 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.133-415C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726587 | ||||||
| chr8:116726591
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.133-419G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726591 | ||||||
| chr8:116726639
|
C | T | 1 | a0001c0001t0015g0258 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133-467G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726639 | ||||||
| chr8:116726716
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0232 | 2 | NA18999.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.133-544T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726716 | ||||||
| chr8:116726822
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-650T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116726822 | ||||||
| chr8:116727201
|
C | T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-1029G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116727201 | ||||||
| chr8:116727693
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-1521G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116727693 | ||||||
| chr8:116727882
|
T | C | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-1710A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116727882 | ||||||
| chr8:116727932
|
G | A | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-1760C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116727932 | ||||||
| chr8:116728212
|
C | T | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-2040G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728212 | ||||||
| chr8:116728289
|
TA | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.133-2118delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728289 | ||||||
| chr8:116728349
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-2177C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728349 | ||||||
| chr8:116728602
|
A | G | 114 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.133-2430T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728602 | ||||||
| chr8:116728629
|
C | A | 1 | a0001c0001t0003g0028 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.133-2457G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728629 | ||||||
| chr8:116728632
|
A | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.133-2460T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728632 | ||||||
| chr8:116728668
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133-2496C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728668 | ||||||
| chr8:116728885
|
T | C | 1 | a0001c0001t0010g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133-2713A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116728885 | ||||||
| chr8:116729134
|
T | A | 1 | a0001c0001t0013g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.133-2962A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729134 | ||||||
| chr8:116729336
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-3164C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729336 | ||||||
| chr8:116729479
|
G | C | 1 | a0001c0001t0018g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.133-3307C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729479 | ||||||
| chr8:116729567
|
C | T | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-3395G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729567 | ||||||
| chr8:116729666
|
A | C | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-3494T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729666 | ||||||
| chr8:116729674
|
T | C | 174 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(171): Show | 174 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.133-3502A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729674 | ||||||
| chr8:116729808
|
G | T | 1 | a0001c0001t0015g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.133-3636C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116729808 | ||||||
| chr8:116730041
|
C | A | 29 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(26): Show | 29 | HG00423.hp2 HG02027.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.133-3869G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730041 | ||||||
| chr8:116730156
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.133-3984C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730156 | ||||||
| chr8:116730297
|
G | A | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0240others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-4125C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730297 | ||||||
| chr8:116730332
|
C | T | 2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.133-4160G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730332 | ||||||
| chr8:116730350
|
C | T | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-4178G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730350 | ||||||
| chr8:116730384
|
G | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-4212C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730384 | ||||||
| chr8:116730419
|
TCATCCAG others(4): Show |
T | 1 | a0001c0001t0002g0305 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.133-4258_133-4248d others(13): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730419 | ||||||
| chr8:116730500
|
GAAAGGTT others(8): Show |
G | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.133-4343_133-4329d others(17): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730500 | ||||||
| chr8:116730600
|
C | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-4428G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730600 | ||||||
| chr8:116730656
|
A | C | 4 | a0001c0001t0005g0220a0001c0001t0005g0233a0001c0001t0005g0234others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-4484T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730656 | ||||||
| chr8:116730694
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.133-4522G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730694 | ||||||
| chr8:116730826
|
T | C | 2 | a0001c0001t0008g0051a0001c0001t0008g0058 | 2 | NA18950.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.133-4654A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730826 | ||||||
| chr8:116730854
|
G | A | 2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.133-4682C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730854 | ||||||
| chr8:116730906
|
T | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.133-4734A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730906 | ||||||
| chr8:116730935
|
T | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02602.hp1 HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.133-4763A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730935 | ||||||
| chr8:116730962
|
A | T | 1 | a0001c0001t0010g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133-4790T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116730962 | ||||||
| chr8:116731014
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-4842C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731014 | ||||||
| chr8:116731251
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-5079A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731251 | ||||||
| chr8:116731337
|
C | T | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.133-5165G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731337 | ||||||
| chr8:116731659
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.133-5487A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731659 | ||||||
| chr8:116731707
|
T | C | 1 | a0001c0001t0008g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.133-5535A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731707 | ||||||
| chr8:116731775
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-5603C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731775 | ||||||
| chr8:116731779
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG03491.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.133-5607G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731779 | ||||||
| chr8:116731828
|
C | CCATGAAT others(7): Show |
1 | a0001c0001t0004g0181 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.133-5670_133-5657d others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731828 | ||||||
| chr8:116731947
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133-5775A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731947 | ||||||
| chr8:116731989
|
G | T | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.133-5817C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116731989 | ||||||
| chr8:116732000
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.133-5828A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732000 | ||||||
| chr8:116732276
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.133-6104A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732276 | ||||||
| chr8:116732321
|
A | G | 3 | a0001c0001t0014g0101a0001c0001t0014g0103a0001c0001t0014g0104 | 3 | HG01109.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.133-6149T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732321 | ||||||
| chr8:116732351
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133-6179T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732351 | ||||||
| chr8:116732379
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-6207T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732379 | ||||||
| chr8:116732425
|
G | T | 1 | a0001c0001t0007g0325 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.133-6253C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732425 | ||||||
| chr8:116732458
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.133-6286A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732458 | ||||||
| chr8:116732532
|
C | T | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.133-6360G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732532 | ||||||
| chr8:116732654
|
CTCAT | C | 14 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(11): Show | 15 | HG01261.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-6486_133-6483d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732654 | ||||||
| chr8:116732654
|
CTCATTCA others(1): Show |
C | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.133-6490_133-6483d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732654 | ||||||
| chr8:116732857
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG03491.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.133-6685C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116732857 | ||||||
| chr8:116733193
|
G | C | 114 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.133-7021C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116733193 | ||||||
| chr8:116733227
|
G | C | 2 | a0001c0001t0016g0040a0001c0001t0016g0041 | 2 | NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.133-7055C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116733227 | ||||||
| chr8:116733576
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133-7404T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116733576 | ||||||
| chr8:116733688
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.133-7516G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116733688 | ||||||
| chr8:116733992
|
G | A | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.133-7820C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116733992 | ||||||
| chr8:116734223
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.133-8051T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116734223 | ||||||
| chr8:116734717
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-8545C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116734717 | ||||||
| chr8:116734776
|
T | C | 1 | a0001c0001t0002g0257 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.133-8604A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116734776 | ||||||
| chr8:116734852
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133-8680A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116734852 | ||||||
| chr8:116734905
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.133-8733G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116734905 | ||||||
| chr8:116735285
|
G | A | 21 | a0001c0001t0006g0082a0001c0001t0006g0086a0001c0001t0006g0087others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.133-9113C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735285 | ||||||
| chr8:116735471
|
T | C | 2 | a0001c0001t0006g0088a0001c0001t0006g0093 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-9299A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735471 | ||||||
| chr8:116735497
|
C | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.133-9325G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735497 | ||||||
| chr8:116735702
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.133-9530G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735702 | ||||||
| chr8:116735763
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0141 | 2 | HG01256.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.133-9591G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735763 | ||||||
| chr8:116735800
|
G | GA | 11 | a0001c0001t0001g0112a0001c0001t0001g0225a0001c0001t0002g0279others(8): Show | 11 | HG01243.hp2 HG01361.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-9629dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735800 | ||||||
| chr8:116735862
|
C | A | 2 | a0001c0001t0004g0170a0001c0001t0004g0178 | 2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.133-9690G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735862 | ||||||
| chr8:116735983
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | NA18994.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.133-9811A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116735983 | ||||||
| chr8:116736021
|
T | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133-9849A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736021 | ||||||
| chr8:116736036
|
T | C | 1 | a0001c0001t0011g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133-9864A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736036 | ||||||
| chr8:116736150
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.133-9978A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736150 | ||||||
| chr8:116736287
|
T | G | 72 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.133-10115A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736287 | ||||||
| chr8:116736303
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-10131G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736303 | ||||||
| chr8:116736523
|
G | A | 1 | a0001c0001t0019g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.133-10351C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736523 | ||||||
| chr8:116736620
|
C | T | 3 | a0001c0001t0008g0035a0001c0001t0008g0042a0001c0001t0008g0061 | 3 | NA18985.hp1 NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.133-10448G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736620 | ||||||
| chr8:116736653
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-10481G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736653 | ||||||
| chr8:116736968
|
T | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.133-10796A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116736968 | ||||||
| chr8:116737088
|
C | G | 1 | a0001c0001t0013g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.133-10916G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737088 | ||||||
| chr8:116737119
|
T | A | 61 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(58): Show | 61 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.133-10947A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737119 | ||||||
| chr8:116737129
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-10957G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737129 | ||||||
| chr8:116737173
|
G | A | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133-11001C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737173 | ||||||
| chr8:116737296
|
GA | G | 99 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(96): Show | 99 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.133-11125delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737296 | ||||||
| chr8:116737318
|
T | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-11146A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737318 | ||||||
| chr8:116737381
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.133-11209G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737381 | ||||||
| chr8:116737548
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-11376G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737548 | ||||||
| chr8:116737595
|
T | G | 3 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0001g0229 | 3 | HG00280.hp2 HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.133-11423A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737595 | ||||||
| chr8:116737684
|
A | T | 20 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.133-11512T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737684 | ||||||
| chr8:116737711
|
A | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0279 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.133-11539T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737711 | ||||||
| chr8:116737754
|
C | T | 107 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(104): Show | 107 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.133-11582G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737754 | ||||||
| chr8:116737762
|
G | A | 1 | a0001c0001t0003g0066 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.133-11590C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737762 | ||||||
| chr8:116737813
|
T | C | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-11641A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737813 | ||||||
| chr8:116737833
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.133-11661C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737833 | ||||||
| chr8:116737966
|
C | T | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-11794G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116737966 | ||||||
| chr8:116738031
|
T | C | 4 | a0001c0001t0007g0317a0001c0001t0007g0318a0001c0001t0007g0321others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-11859A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738031 | ||||||
| chr8:116738034
|
C | CA | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(22): Show | 25 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.133-11863dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738034 | ||||||
| chr8:116738034
|
C | CAA | 64 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(61): Show | 64 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.133-11864_133-1186 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738034 | ||||||
| chr8:116738034
|
CA | C | 7 | a0001c0001t0001g0146a0001c0001t0003g0048a0001c0001t0003g0063others(4): Show | 7 | HG01070.hp1 HG01884.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-11863delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738034 | ||||||
| chr8:116738147
|
C | CA | 17 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(14): Show | 17 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.133-11976dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738147 | ||||||
| chr8:116738185
|
G | GT | 12 | a0001c0001t0007g0001a0001c0001t0007g0314a0001c0001t0007g0316others(9): Show | 13 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-12014dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738185 | ||||||
| chr8:116738557
|
C | CT | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.133-12386_133-1238 others(5): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738557 | ||||||
| chr8:116738566
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.133-12394C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738566 | ||||||
| chr8:116738649
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133-12477A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738649 | ||||||
| chr8:116738769
|
A | G | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.133-12597T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116738769 | ||||||
| chr8:116739389
|
G | A | 1 | a0001c0001t0004g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.133-13217C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739389 | ||||||
| chr8:116739435
|
G | A | 1 | a0001c0001t0002g0298 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.133-13263C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739435 | ||||||
| chr8:116739478
|
A | G | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.133-13306T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739478 | ||||||
| chr8:116739511
|
G | A | 1 | a0001c0001t0015g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.133-13339C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739511 | ||||||
| chr8:116739620
|
A | G | 1 | a0001c0001t0008g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.133-13448T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739620 | ||||||
| chr8:116739723
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.133-13551T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739723 | ||||||
| chr8:116739740
|
C | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-13568G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739740 | ||||||
| chr8:116739931
|
T | C | 82 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(79): Show | 83 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.133-13759A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739931 | ||||||
| chr8:116739947
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133-13775A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739947 | ||||||
| chr8:116739991
|
A | AAC | 185 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(182): Show | 186 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.133-13821_133-1382 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116739991 | ||||||
| chr8:116740263
|
C | T | 4 | a0001c0001t0005g0220a0001c0001t0005g0233a0001c0001t0005g0234others(1): Show | 4 | HG01099.hp1 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-14091G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740263 | ||||||
| chr8:116740264
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133-14092C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740264 | ||||||
| chr8:116740276
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.133-14104C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740276 | ||||||
| chr8:116740404
|
CAGG | C | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-14235_133-1423 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740404 | ||||||
| chr8:116740478
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.133-14306C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740478 | ||||||
| chr8:116740615
|
T | A | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.133-14443A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740615 | ||||||
| chr8:116740701
|
T | C | 15 | a0001c0001t0006g0086a0001c0001t0006g0087a0001c0001t0006g0088others(12): Show | 15 | HG00639.hp2 HG01167.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-14529A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740701 | ||||||
| chr8:116740757
|
C | G | 74 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(71): Show | 74 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.133-14585G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740757 | ||||||
| chr8:116740953
|
A | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+14713T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116740953 | ||||||
| chr8:116741012
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.132+14654A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741012 | ||||||
| chr8:116741236
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.132+14430C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741236 | ||||||
| chr8:116741430
|
T | C | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+14236A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741430 | ||||||
| chr8:116741459
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.132+14207T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741459 | ||||||
| chr8:116741469
|
A | G | 15 | a0001c0001t0004g0160a0001c0001t0004g0161a0001c0001t0004g0162others(12): Show | 15 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+14197T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741469 | ||||||
| chr8:116741486
|
A | C | 61 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(58): Show | 61 | HG00609.hp2 HG00639.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.132+14180T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741486 | ||||||
| chr8:116741552
|
C | T | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.132+14114G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741552 | ||||||
| chr8:116741664
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+14002T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741664 | ||||||
| chr8:116741683
|
C | T | 3 | a0001c0001t0002g0277a0001c0001t0002g0290a0001c0001t0002g0292 | 3 | NA18943.hp2 NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.132+13983G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741683 | ||||||
| chr8:116741744
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.132+13922C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116741744 | ||||||
| chr8:116742226
|
A | G | 3 | a0001c0001t0014g0101a0001c0001t0014g0103a0001c0001t0014g0104 | 3 | HG01109.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.132+13440T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742226 | ||||||
| chr8:116742329
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+13337A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742329 | ||||||
| chr8:116742421
|
A | G | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+13245T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742421 | ||||||
| chr8:116742672
|
C | T | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+12994G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742672 | ||||||
| chr8:116742746
|
T | C | 2 | a0001c0001t0002g0284a0001c0001t0002g0288 | 2 | HG02155.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.132+12920A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742746 | ||||||
| chr8:116742876
|
G | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+12790C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742876 | ||||||
| chr8:116742898
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.132+12768A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742898 | ||||||
| chr8:116742940
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+12726C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116742940 | ||||||
| chr8:116743009
|
A | G | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.132+12657T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743009 | ||||||
| chr8:116743167
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.132+12499C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743167 | ||||||
| chr8:116743331
|
T | C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+12335A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743331 | ||||||
| chr8:116743496
|
T | C | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.132+12170A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743496 | ||||||
| chr8:116743698
|
C | T | 3 | a0001c0001t0003g0014a0001c0001t0003g0018a0001c0001t0003g0029 | 3 | NA18951.hp1 NA19055.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.132+11968G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743698 | ||||||
| chr8:116743702
|
G | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+11964C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743702 | ||||||
| chr8:116743736
|
C | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0285 | 3 | HG00609.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.132+11930G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743736 | ||||||
| chr8:116743769
|
C | CAT | 15 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0114others(12): Show | 15 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+11895_132+1189 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
C | CATAT | 5 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0135others(2): Show | 5 | HG01261.hp2 HG02683.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+11893_132+1189 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
C | CATATAT | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0132 | 3 | HG01169.hp1 NA19077.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.132+11891_132+1189 others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
C | CATATATA others(1): Show |
5 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG01175.hp2 HG02630.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+11889_132+1189 others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.132+11887_132+1189 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.132+11885_132+1189 others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
CAT | C | 4 | a0001c0001t0003g0038a0001c0001t0003g0048a0001c0001t0003g0067others(1): Show | 4 | HG01123.hp2 NA18959.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11895_132+1189 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743769
|
CATAT | C | 12 | a0001c0001t0002g0301a0001c0001t0003g0017a0001c0001t0003g0049others(9): Show | 13 | HG01934.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+11893_132+1189 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743769 | ||||||
| chr8:116743773
|
T | C | 4 | a0001c0001t0013g0102a0001c0001t0014g0101a0001c0001t0014g0103others(1): Show | 4 | HG01109.hp1 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+11893A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743773 | ||||||
| chr8:116743777
|
T | C | 3 | a0001c0001t0014g0101a0001c0001t0014g0103a0001c0001t0014g0104 | 3 | HG01109.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.132+11889A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743777 | ||||||
| chr8:116743785
|
T | C | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11881A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743785 | ||||||
| chr8:116743789
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+11861_132+1187 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743789 | ||||||
| chr8:116743789
|
TATATATA others(13): Show |
T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11857_132+1187 others(24): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743789 | ||||||
| chr8:116743791
|
T | C | 27 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.132+11875A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743791 | ||||||
| chr8:116743791
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.132+11863_132+1187 others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743791 | ||||||
| chr8:116743791
|
TATATATA others(7): Show |
T | 3 | a0001c0001t0009g0152a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02055.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+11861_132+1187 others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743791 | ||||||
| chr8:116743793
|
T | C | 53 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(50): Show | 53 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.132+11873A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
T | TAC | 8 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(5): Show | 8 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.132+11872_132+1187 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAA | T | 26 | a0001c0001t0003g0011a0001c0001t0003g0024a0001c0001t0003g0025others(23): Show | 26 | HG01496.hp2 HG02071.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.132+11867_132+1187 others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAAA others(1): Show |
T | 8 | a0001c0001t0002g0305a0001c0001t0003g0045a0001c0001t0003g0073others(5): Show | 8 | HG02132.hp1 HG02257.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+11865_132+1187 others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAAA others(3): Show |
T | 66 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253others(63): Show | 66 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.132+11863_132+1187 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAAA others(5): Show |
T | 7 | a0001c0001t0002g0275a0001c0001t0002g0278a0001c0001t0002g0280others(4): Show | 7 | HG00323.hp2 HG01243.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+11861_132+1187 others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAAA others(11): Show |
T | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.132+11855_132+1187 others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743793
|
TATATAAA others(15): Show |
T | 1 | a0001c0001t0003g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.132+11851_132+1187 others(26): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743793 | ||||||
| chr8:116743795
|
TATAAAC | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+11865_132+1187 others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743795 | ||||||
| chr8:116743795
|
TATAAACA others(1): Show |
T | 10 | a0001c0001t0001g0235a0001c0001t0002g0261a0001c0001t0002g0291others(7): Show | 10 | HG02004.hp2 HG02602.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+11863_132+1187 others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743795 | ||||||
| chr8:116743795
|
TATAAACA others(3): Show |
T | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0219others(4): Show | 7 | HG00280.hp2 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+11861_132+1187 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743795 | ||||||
| chr8:116743795
|
TATAAACA others(5): Show |
T | 16 | a0001c0001t0001g0221a0001c0001t0005g0197a0001c0001t0005g0198others(13): Show | 16 | HG00323.hp1 HG01099.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+11859_132+1187 others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743795 | ||||||
| chr8:116743795
|
TATAAACA others(9): Show |
T | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11855_132+1187 others(20): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743795 | ||||||
| chr8:116743797
|
T | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0070 | 2 | NA18947.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.132+11869A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743797 | ||||||
| chr8:116743797
|
TAA | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0118others(9): Show | 12 | HG01069.hp1 HG01099.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+11867_132+1186 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743797 | ||||||
| chr8:116743797
|
TAAAC | T | 13 | a0001c0001t0001g0151a0001c0001t0001g0207a0001c0001t0006g0082others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+11865_132+1186 others(8): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743797 | ||||||
| chr8:116743797
|
TAAACACA others(3): Show |
T | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.132+11859_132+1186 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743797 | ||||||
| chr8:116743799
|
A | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0046a0001c0001t0003g0070others(1): Show | 4 | HG01261.hp1 NA18947.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+11867T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743799 | ||||||
| chr8:116743799
|
A | T | 42 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(39): Show | 42 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.132+11867T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743799 | ||||||
| chr8:116743799
|
AACACAC | A | 8 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0059others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+11861_132+1186 others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743799 | ||||||
| chr8:116743799
|
AACACACA others(3): Show |
A | 4 | a0001c0001t0005g0222a0001c0001t0005g0226a0001c0001t0005g0227others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11857_132+1186 others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743799 | ||||||
| chr8:116743799
|
AACACACA others(15): Show |
A | 55 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(52): Show | 55 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+11845_132+1186 others(26): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743799 | ||||||
| chr8:116743800
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.132+11866T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743800 | ||||||
| chr8:116743801
|
C | A | 27 | a0001c0001t0001g0135a0001c0001t0003g0011a0001c0001t0003g0024others(24): Show | 27 | HG01496.hp2 HG02071.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.132+11865G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743801 | ||||||
| chr8:116743801
|
C | T | 54 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(51): Show | 54 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.132+11865G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743801 | ||||||
| chr8:116743803
|
C | A | 13 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(10): Show | 13 | HG01074.hp2 HG02132.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+11863G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743803 | ||||||
| chr8:116743803
|
C | T | 56 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(53): Show | 56 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.132+11863G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743803 | ||||||
| chr8:116743805
|
C | A | 126 | a0001c0001t0001g0106a0001c0001t0001g0110a0001c0001t0001g0112others(123): Show | 126 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.132+11861G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743805 | ||||||
| chr8:116743805
|
C | T | 18 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(15): Show | 18 | HG01169.hp1 HG02257.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.132+11861G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743805 | ||||||
| chr8:116743807
|
C | A | 22 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.132+11859G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743807 | ||||||
| chr8:116743807
|
C | T | 14 | a0001c0001t0001g0151a0001c0001t0001g0204a0001c0001t0001g0205others(11): Show | 14 | HG02257.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+11859G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743807 | ||||||
| chr8:116743809
|
C | A | 28 | a0001c0001t0001g0151a0001c0001t0001g0204a0001c0001t0001g0205others(25): Show | 28 | HG00323.hp1 HG01099.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.132+11857G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743809 | ||||||
| chr8:116743809
|
C | T | 3 | a0001c0001t0014g0101a0001c0001t0017g0331a0001c0001t0017g0332 | 3 | HG01109.hp1 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+11857G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743809 | ||||||
| chr8:116743811
|
C | A | 6 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(3): Show | 6 | HG01891.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+11855G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743811 | ||||||
| chr8:116743811
|
C | T | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.132+11855G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743811 | ||||||
| chr8:116743813
|
C | A | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+11853G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743813 | ||||||
| chr8:116743813
|
C | T | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.132+11853G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743813 | ||||||
| chr8:116743815
|
C | A | 1 | a0001c0001t0014g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.132+11851G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743815 | ||||||
| chr8:116743815
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.132+11851G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743815 | ||||||
| chr8:116743817
|
C | A | 1 | a0001c0001t0003g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.132+11849G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743817 | ||||||
| chr8:116743817
|
C | G | 1 | a0001c0001t0003g0028 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.132+11849G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743817 | ||||||
| chr8:116743817
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.132+11849G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743817 | ||||||
| chr8:116743819
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.132+11847G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743819 | ||||||
| chr8:116743827
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0005g0218 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.132+11827_132+1183 others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116743827 | ||||||
| chr8:116744040
|
C | T | 74 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(71): Show | 74 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.132+11626G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744040 | ||||||
| chr8:116744059
|
T | C | 326 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(323): Show | 327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.132+11607A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744059 | ||||||
| chr8:116744112
|
C | T | 9 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0262others(6): Show | 9 | NA18969.hp1 NA18973.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+11554G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744112 | ||||||
| chr8:116744189
|
G | A | 3 | a0001c0001t0009g0154a0001c0001t0009g0155a0001c0001t0009g0156 | 3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+11477C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744189 | ||||||
| chr8:116744214
|
T | TA | 49 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0107others(46): Show | 49 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.132+11451dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744214 | ||||||
| chr8:116744214
|
T | TAA | 116 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0196others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.132+11450_132+1145 others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744214 | ||||||
| chr8:116744225
|
A | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+11441T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744225 | ||||||
| chr8:116744259
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.132+11407A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744259 | ||||||
| chr8:116744279
|
C | G | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.132+11387G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744279 | ||||||
| chr8:116744718
|
G | A | 248 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.132+10948C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744718 | ||||||
| chr8:116744747
|
T | C | 2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.132+10919A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744747 | ||||||
| chr8:116744761
|
A | G | 1 | a0001c0001t0017g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.132+10905T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744761 | ||||||
| chr8:116744917
|
C | T | 1 | a0001c0001t0002g0330 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.132+10749G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116744917 | ||||||
| chr8:116745069
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.132+10597G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745069 | ||||||
| chr8:116745082
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.132+10584C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745082 | ||||||
| chr8:116745180
|
G | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+10486C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745180 | ||||||
| chr8:116745270
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA19077.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.132+10396A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745270 | ||||||
| chr8:116745298
|
TATC | T | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+10365_132+1036 others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745298 | ||||||
| chr8:116745376
|
T | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+10290A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745376 | ||||||
| chr8:116745512
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+10154C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745512 | ||||||
| chr8:116745628
|
A | T | 5 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(2): Show | 5 | HG02132.hp2 NA18952.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+10038T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745628 | ||||||
| chr8:116745721
|
G | A | 1 | a0001c0001t0003g0029 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.132+9945C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745721 | ||||||
| chr8:116745805
|
G | A | 74 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(71): Show | 74 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.132+9861C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745805 | ||||||
| chr8:116745812
|
G | A | 4 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0010g0333others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+9854C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745812 | ||||||
| chr8:116745888
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0009g0152a0001c0001t0009g0153others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+9778G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745888 | ||||||
| chr8:116745905
|
A | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.132+9761T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116745905 | ||||||
| chr8:116746024
|
C | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0012 | 2 | HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.132+9642G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116746024 | ||||||
| chr8:116746139
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.132+9527C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116746139 | ||||||
| chr8:116746339
|
C | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.132+9327G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116746339 | ||||||
| chr8:116746605
|
C | T | 180 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.132+9061G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116746605 | ||||||
| chr8:116746818
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0286a0001c0001t0019g0303 | 3 | HG00323.hp2 HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.132+8848G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116746818 | ||||||
| chr8:116747072
|
G | GT | 82 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(79): Show | 83 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.132+8593dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747072 | ||||||
| chr8:116747276
|
G | C | 5 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+8390C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747276 | ||||||
| chr8:116747308
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0123 | 2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.132+8358G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747308 | ||||||
| chr8:116747315
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.132+8351G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747315 | ||||||
| chr8:116747345
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0123 | 2 | NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.132+8321G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747345 | ||||||
| chr8:116747405
|
G | C | 1 | a0001c0001t0010g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.132+8261C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747405 | ||||||
| chr8:116747444
|
T | A | 2 | a0001c0001t0015g0258a0001c0001t0015g0315 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.132+8222A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747444 | ||||||
| chr8:116747599
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.132+8067C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747599 | ||||||
| chr8:116747838
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | NA18947.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.132+7828C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747838 | ||||||
| chr8:116747865
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.132+7801A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116747865 | ||||||
| chr8:116748025
|
C | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+7641G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748025 | ||||||
| chr8:116748068
|
C | T | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.132+7598G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748068 | ||||||
| chr8:116748084
|
A | G | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.132+7582T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748084 | ||||||
| chr8:116748113
|
T | C | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+7553A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748113 | ||||||
| chr8:116748158
|
C | CA | 31 | a0001c0001t0001g0080a0001c0001t0002g0275a0001c0001t0002g0328others(28): Show | 32 | HG00639.hp2 HG01167.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+7507dupT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748158 | ||||||
| chr8:116748162
|
A | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+7504T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748162 | ||||||
| chr8:116748170
|
C | A | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+7496G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748170 | ||||||
| chr8:116748271
|
T | TCCCCAAA others(19): Show |
1 | a0001c0001t0002g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.132+7369_132+7394d others(28): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748271 | ||||||
| chr8:116748491
|
T | A | 3 | a0001c0001t0004g0188a0001c0001t0004g0190a0001c0001t0004g0195 | 3 | NA19003.hp2 NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.132+7175A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748491 | ||||||
| chr8:116748706
|
C | T | 104 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.132+6960G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748706 | ||||||
| chr8:116748968
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+6698A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116748968 | ||||||
| chr8:116749098
|
A | G | 1 | a0001c0001t0002g0297 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.132+6568T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749098 | ||||||
| chr8:116749251
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.132+6415T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749251 | ||||||
| chr8:116749407
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0153a0001c0001t0009g0154others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+6259G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749407 | ||||||
| chr8:116749657
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132+6009G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749657 | ||||||
| chr8:116749661
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.132+6005A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749661 | ||||||
| chr8:116749750
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0279 | 2 | HG02071.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.132+5916G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749750 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0004g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0002g0279 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1497): Show |
1 | a0001c0001t0002g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1506): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0001g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0004g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
44 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(41): Show | 44 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
163 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(160): Show | 164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
1 | a0001c0001t0004g0179 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
2 | a0001c0001t0004g0160a0001c0001t0004g0162 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749854
|
G | GGAGGGAC others(1498): Show |
2 | a0001c0001t0013g0102a0001c0001t0013g0105 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.132+5811_132+5812i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749854 | ||||||
| chr8:116749863
|
G | GCTACATT others(1498): Show |
2 | a0001c0001t0002g0307a0001c0001t0002g0308 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.132+5802_132+5803i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749863 | ||||||
| chr8:116749934
|
G | GAAAAATT others(1498): Show |
1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.132+5731_132+5732i others(1507): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116749934 | ||||||
| chr8:116750037
|
TATATATG others(13): Show |
T | 1 | a0001c0001t0003g0334 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.132+5609_132+5628d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750037 | ||||||
| chr8:116750403
|
C | CT | 36 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0112others(33): Show | 36 | HG00423.hp2 HG01175.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.132+5262dupA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750403 | ||||||
| chr8:116750403
|
CT | C | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0289others(12): Show | 15 | HG01975.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+5262delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750403 | ||||||
| chr8:116750406
|
T | TC | 4 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0242others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+5259_132+5260i others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750406 | ||||||
| chr8:116750407
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+5259A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750407 | ||||||
| chr8:116750459
|
G | A | 2 | a0001c0001t0009g0152a0001c0001t0009g0153 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.132+5207C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750459 | ||||||
| chr8:116750556
|
C | T | 68 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.132+5110G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750556 | ||||||
| chr8:116750570
|
C | A | 1 | a0001c0001t0007g0316 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.132+5096G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750570 | ||||||
| chr8:116750671
|
A | T | 1 | a0001c0001t0012g0203 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.132+4995T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750671 | ||||||
| chr8:116750751
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.132+4915C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750751 | ||||||
| chr8:116750751
|
G | T | 260 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(257): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.132+4915C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750751 | ||||||
| chr8:116750759
|
A | T | 14 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 14 | HG01109.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+4907T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750759 | ||||||
| chr8:116750902
|
G | A | 4 | a0001c0001t0012g0203a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+4764C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750902 | ||||||
| chr8:116750939
|
A | G | 180 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.132+4727T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750939 | ||||||
| chr8:116750941
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.132+4725C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750941 | ||||||
| chr8:116750970
|
T | G | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+4696A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750970 | ||||||
| chr8:116750978
|
C | T | 3 | a0001c0001t0004g0170a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01358.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.132+4688G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116750978 | ||||||
| chr8:116751000
|
C | T | 1 | a0001c0001t0004g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.132+4666G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751000 | ||||||
| chr8:116751020
|
G | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+4646C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751020 | ||||||
| chr8:116751217
|
A | AAAAAT | 41 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(38): Show | 41 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.132+4444_132+4448d others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751217 | ||||||
| chr8:116751217
|
A | AAAAATAA others(3): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0139a0001c0001t0001g0144 | 3 | HG01256.hp2 NA18947.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.132+4439_132+4448d others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751217 | ||||||
| chr8:116751217
|
A | T | 1 | a0001c0001t0006g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.132+4449T>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751217 | ||||||
| chr8:116751260
|
G | T | 1 | a0001c0001t0003g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.132+4406C>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751260 | ||||||
| chr8:116751315
|
A | G | 1 | a0001c0001t0022g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.132+4351T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751315 | ||||||
| chr8:116751551
|
T | G | 1 | a0001c0001t0010g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.132+4115A>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751551 | ||||||
| chr8:116751634
|
A | G | 180 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.132+4032T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751634 | ||||||
| chr8:116751910
|
C | G | 1 | a0001c0001t0004g0191 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.132+3756G>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751910 | ||||||
| chr8:116751936
|
C | T | 8 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0305others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+3730G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116751936 | ||||||
| chr8:116752134
|
G | C | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+3532C>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752134 | ||||||
| chr8:116752135
|
G | A | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+3531C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752135 | ||||||
| chr8:116752665
|
G | GAAGA | 18 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 19 | HG01175.hp2 HG01261.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.132+2997_132+3000d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAAGAAAG others(1): Show |
6 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0006g0096others(3): Show | 6 | HG01074.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+2993_132+3000d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAAGAAAG others(7): Show |
1 | a0001c0001t0002g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.132+3000_132+3001i others(16): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAAGAAAG others(5): Show |
3 | a0001c0001t0001g0143a0001c0001t0002g0250a0001c0001t0006g0100 | 3 | HG01099.hp2 HG02965.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.132+2989_132+3000d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAAGAAAG others(9): Show |
1 | a0001c0001t0001g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.132+2985_132+3000d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAAGAAGA others(6): Show |
1 | a0001c0001t0004g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.132+3000_132+3001i others(15): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
G | GAGAAGAA others(3): Show |
1 | a0001c0001t0011g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.132+3000_132+3001i others(12): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGA | G | 59 | a0001c0001t0001g0108a0001c0001t0001g0135a0001c0001t0001g0136others(56): Show | 59 | HG00423.hp1 HG00639.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.132+2997_132+3000d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(1): Show |
G | 59 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.132+2993_132+3000d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(5): Show |
G | 29 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(26): Show | 29 | HG00558.hp1 HG01069.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.132+2989_132+3000d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(9): Show |
G | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0128others(13): Show | 16 | HG01192.hp1 HG02129.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+2985_132+3000d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(13): Show |
G | 2 | a0001c0001t0001g0127a0001c0001t0001g0246 | 2 | HG01081.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.132+2981_132+3000d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(17): Show |
G | 3 | a0001c0001t0001g0158a0001c0001t0003g0013a0001c0001t0003g0029 | 3 | HG01978.hp1 HG03471.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.132+2977_132+3000d others(26): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(21): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.132+2973_132+3000d others(30): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752665
|
GAAGAAAG others(25): Show |
G | 2 | a0001c0001t0001g0149a0001c0001t0005g0213 | 2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.132+2969_132+3000d others(34): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752665 | ||||||
| chr8:116752716
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0003g0028 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.132+2937_132+2949d others(15): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752716 | ||||||
| chr8:116752717
|
AAAGAAAG others(4): Show |
A | 3 | a0001c0001t0012g0210a0001c0001t0012g0211a0001c0001t0012g0212 | 3 | HG01891.hp2 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.132+2938_132+2948d others(13): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752717 | ||||||
| chr8:116752722
|
A | AAGAG | 13 | a0001c0001t0004g0084a0001c0001t0004g0160a0001c0001t0004g0161others(10): Show | 13 | HG01070.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+2943_132+2944i others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752722 | ||||||
| chr8:116752722
|
A | G | 14 | a0001c0001t0004g0163a0001c0001t0004g0165a0001c0001t0004g0166others(11): Show | 14 | HG01074.hp1 HG01192.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+2944T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752722 | ||||||
| chr8:116752729
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132+2937T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752729 | ||||||
| chr8:116752730
|
A | G | 13 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0003g0075others(10): Show | 13 | HG00609.hp2 HG01071.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+2936T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752730 | ||||||
| chr8:116752731
|
AGAAGAGA others(22): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.132+2906_132+2934d others(31): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752731 | ||||||
| chr8:116752731
|
AGAAGAGA others(30): Show |
A | 1 | a0001c0001t0007g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.132+2898_132+2934d others(39): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752731 | ||||||
| chr8:116752732
|
G | A | 2 | a0001c0001t0002g0298a0001c0001t0002g0324 | 2 | NA18952.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.132+2934C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752732 | ||||||
| chr8:116752732
|
GA | G | 3 | a0001c0001t0004g0085a0001c0001t0004g0191a0001c0001t0004g0192 | 3 | HG02129.hp1 NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.132+2933delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752732 | ||||||
| chr8:116752733
|
A | AAAG | 10 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0244others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+2932_132+2933i others(5): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752733 | ||||||
| chr8:116752733
|
A | AAAGAAAG | 8 | a0001c0001t0001g0081a0001c0001t0001g0245a0001c0001t0002g0293others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2932_132+2933i others(9): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752733 | ||||||
| chr8:116752733
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0003g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.132+2932_132+2933i others(13): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752733 | ||||||
| chr8:116752734
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.132+2932T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752734 | ||||||
| chr8:116752734
|
AG | A | 41 | a0001c0001t0001g0080a0001c0001t0001g0113a0001c0001t0001g0240others(38): Show | 41 | HG00609.hp2 HG00639.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.132+2931delC | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752734 | ||||||
| chr8:116752734
|
AGAGAAAG others(26): Show |
A | 1 | a0001c0001t0013g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.132+2899_132+2931d others(35): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752734 | ||||||
| chr8:116752735
|
G | A | 20 | a0001c0001t0001g0081a0001c0001t0001g0112a0001c0001t0001g0231others(17): Show | 20 | HG02083.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.132+2931C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752735 | ||||||
| chr8:116752736
|
A | G | 50 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(47): Show | 50 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.132+2930T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752736 | ||||||
| chr8:116752739
|
A | AG | 19 | a0001c0001t0001g0081a0001c0001t0001g0243a0001c0001t0001g0244others(16): Show | 19 | HG02071.hp1 HG02083.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.132+2926_132+2927i others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752739 | ||||||
| chr8:116752739
|
A | G | 2 | a0001c0001t0004g0193a0001c0001t0021g0194 | 2 | HG02080.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.132+2927T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752739 | ||||||
| chr8:116752740
|
A | AGAAGG | 11 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(8): Show | 11 | HG00639.hp1 NA18939.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+2925_132+2926i others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752740 | ||||||
| chr8:116752740
|
A | G | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02155.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.132+2926T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752740 | ||||||
| chr8:116752740
|
AGAAAGAA others(25): Show |
A | 1 | a0001c0001t0005g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.132+2894_132+2925d others(34): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752740 | ||||||
| chr8:116752743
|
A | AG | 12 | a0001c0001t0001g0080a0001c0001t0001g0239a0001c0001t0001g0240others(9): Show | 12 | HG00609.hp2 HG01891.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+2922_132+2923i others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752743 | ||||||
| chr8:116752744
|
A | AGAAGG | 3 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0311 | 3 | HG01175.hp1 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.132+2921_132+2922i others(7): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752744 | ||||||
| chr8:116752747
|
A | AG | 5 | a0001c0001t0001g0231a0001c0001t0004g0085a0001c0001t0004g0191others(2): Show | 5 | HG02129.hp1 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+2918_132+2919i others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752747 | ||||||
| chr8:116752748
|
AGAAAGAG others(5): Show |
A | 1 | a0001c0001t0009g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.132+2906_132+2917d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752748 | ||||||
| chr8:116752751
|
A | AG | 3 | a0001c0001t0003g0027a0001c0001t0004g0193a0001c0001t0021g0194 | 3 | HG02080.hp2 NA18943.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.132+2914_132+2915i others(3): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752751 | ||||||
| chr8:116752751
|
A | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0003g0075others(4): Show | 7 | HG01071.hp2 HG01891.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+2915T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752751 | ||||||
| chr8:116752752
|
A | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0003g0075others(4): Show | 7 | HG01071.hp2 HG01891.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+2914T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752752
|
AGAGG | A | 47 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0232others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.132+2910_132+2913d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752752
|
AGAGGGAG others(1): Show |
A | 27 | a0001c0001t0001g0079a0001c0001t0001g0146a0001c0001t0001g0147others(24): Show | 27 | HG01123.hp2 HG02027.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.132+2906_132+2913d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752752
|
AGAGGGAG others(5): Show |
A | 9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.132+2902_132+2913d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752752
|
AGAGGGAG others(9): Show |
A | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2898_132+2913d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752752
|
AGAGGGAG others(13): Show |
A | 4 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(1): Show | 4 | HG02717.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2894_132+2913d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752752 | ||||||
| chr8:116752755
|
G | A | 57 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0231others(54): Show | 57 | HG00609.hp2 HG00639.hp1 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.132+2911C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752755 | ||||||
| chr8:116752756
|
G | A | 52 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0231others(49): Show | 52 | HG00609.hp2 HG00639.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.132+2910C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752756 | ||||||
| chr8:116752756
|
G | GGGAAAGA others(10): Show |
2 | a0001c0001t0002g0296a0001c0001t0002g0297 | 2 | NA18999.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.132+2909_132+2910i others(19): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752756 | ||||||
| chr8:116752759
|
G | A | 24 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0231others(21): Show | 24 | HG00609.hp2 HG01175.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+2907C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752759 | ||||||
| chr8:116752760
|
G | A | 24 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0231others(21): Show | 24 | HG00609.hp2 HG01175.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+2906C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752760 | ||||||
| chr8:116752763
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0209others(9): Show | 12 | HG02080.hp2 HG02129.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+2903C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752763 | ||||||
| chr8:116752764
|
G | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0209others(9): Show | 12 | HG02080.hp2 HG02129.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+2902C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752764 | ||||||
| chr8:116752767
|
G | A | 3 | a0001c0001t0004g0083a0001c0001t0004g0193a0001c0001t0021g0194 | 3 | HG02080.hp2 NA18978.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.132+2899C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752767 | ||||||
| chr8:116752768
|
G | A | 4 | a0001c0001t0004g0083a0001c0001t0004g0193a0001c0001t0013g0102others(1): Show | 4 | HG02080.hp2 NA18906.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+2898C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752768 | ||||||
| chr8:116752775
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+2891C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752775 | ||||||
| chr8:116752779
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0246 | 3 | HG03471.hp1 HG03490.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.132+2887C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752779 | ||||||
| chr8:116752779
|
GGGAGGGA others(13): Show |
G | 2 | a0001c0001t0005g0197a0001c0001t0014g0101 | 2 | HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.132+2867_132+2886d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752779 | ||||||
| chr8:116752783
|
G | A | 17 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(14): Show | 17 | HG01243.hp1 HG02258.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.132+2883C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752783 | ||||||
| chr8:116752783
|
GGGAGGGA others(9): Show |
G | 40 | a0001c0001t0003g0012a0001c0001t0004g0084a0001c0001t0004g0163others(37): Show | 40 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.132+2867_132+2882d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752783 | ||||||
| chr8:116752783
|
GGGAGGGA others(13): Show |
G | 5 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0007g0325others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2863_132+2882d others(22): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752783 | ||||||
| chr8:116752787
|
G | A | 31 | a0001c0001t0001g0081a0001c0001t0001g0113a0001c0001t0001g0145others(28): Show | 31 | HG01071.hp2 HG01099.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.132+2879C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752787
|
G | GGGAA | 12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG01069.hp1 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+2878_132+2879i others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752787
|
G | GGGAAGGA others(1): Show |
18 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(15): Show | 18 | HG00280.hp1 HG00558.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.132+2878_132+2879i others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752787
|
G | GGGAAGGA others(5): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.132+2878_132+2879i others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752787
|
GGGAGGGA others(5): Show |
G | 3 | a0001c0001t0004g0160a0001c0001t0004g0161a0001c0001t0004g0162 | 3 | HG01070.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.132+2867_132+2878d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752787
|
GGGAGGGA others(9): Show |
G | 6 | a0001c0001t0007g0001a0001c0001t0007g0317a0001c0001t0007g0318others(3): Show | 7 | HG02109.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+2863_132+2878d others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752787 | ||||||
| chr8:116752791
|
G | A | 91 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(88): Show | 91 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.132+2875C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752791
|
G | GGGAAGGA others(1): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG02602.hp2 NA19078.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.132+2874_132+2875i others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752791
|
G | GGGAAGGA others(5): Show |
1 | a0001c0001t0001g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.132+2874_132+2875i others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752791
|
G | GGGAAGGA others(9): Show |
1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.132+2874_132+2875i others(18): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752791
|
GGGAGGGA others(1): Show |
G | 7 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0004g0186others(4): Show | 7 | HG00609.hp2 HG01361.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+2867_132+2874d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752791
|
GGGAGGGA others(5): Show |
G | 3 | a0001c0001t0002g0313a0001c0001t0007g0314a0001c0001t0015g0315 | 3 | HG01261.hp1 NA19030.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.132+2863_132+2874d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752791 | ||||||
| chr8:116752795
|
G | A | 116 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.132+2871C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752795 | ||||||
| chr8:116752795
|
G | GGGAAGGA others(5): Show |
3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | NA18950.hp1 NA19077.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.132+2859_132+2870d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752795 | ||||||
| chr8:116752795
|
GGGAA | G | 30 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0262others(27): Show | 30 | HG00323.hp2 HG01109.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.132+2867_132+2870d others(6): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752795 | ||||||
| chr8:116752795
|
GGGAAGGA others(1): Show |
G | 10 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+2863_132+2870d others(10): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752795 | ||||||
| chr8:116752795
|
GGGAAGGA others(5): Show |
G | 1 | a0001c0001t0002g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.132+2859_132+2870d others(14): Show |
EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752795 | ||||||
| chr8:116752799
|
A | G | 35 | a0001c0001t0002g0250a0001c0001t0002g0252a0001c0001t0002g0253others(32): Show | 35 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.132+2867T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752799 | ||||||
| chr8:116752803
|
A | G | 55 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+2863T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752803 | ||||||
| chr8:116752815
|
A | G | 1 | a0001c0001t0002g0250 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.132+2851T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752815 | ||||||
| chr8:116752833
|
G | A | 4 | a0001c0001t0010g0247a0001c0001t0010g0248a0001c0001t0010g0249others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+2833C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752833 | ||||||
| chr8:116752851
|
GA | G | 63 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.132+2814delT | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116752851 | ||||||
| chr8:116753092
|
G | A | 1 | a0001c0001t0008g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.132+2574C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753092 | ||||||
| chr8:116753210
|
A | G | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.132+2456T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753210 | ||||||
| chr8:116753356
|
C | T | 107 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(104): Show | 107 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.132+2310G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753356 | ||||||
| chr8:116753593
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132+2073C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753593 | ||||||
| chr8:116753647
|
A | C | 2 | a0001c0001t0006g0086a0001c0001t0006g0087 | 2 | HG00639.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2019T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753647 | ||||||
| chr8:116753711
|
C | T | 40 | a0001c0001t0004g0083a0001c0001t0004g0084a0001c0001t0004g0085others(37): Show | 40 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.132+1955G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753711 | ||||||
| chr8:116753751
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.132+1915G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753751 | ||||||
| chr8:116753828
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.132+1838G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753828 | ||||||
| chr8:116753831
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.132+1835T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116753831 | ||||||
| chr8:116754106
|
T | A | 37 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0161others(34): Show | 37 | HG00609.hp2 HG01070.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.132+1560A>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116754106 | ||||||
| chr8:116754217
|
G | A | 1 | a0001c0001t0002g0330 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.132+1449C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116754217 | ||||||
| chr8:116754383
|
T | C | 2 | a0001c0001t0017g0331a0001c0001t0017g0332 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.132+1283A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116754383 | ||||||
| chr8:116754666
|
CT | C | 261 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(258): Show | 262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.132+999delA | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116754666 | ||||||
| chr8:116754754
|
C | A | 1 | a0001c0001t0010g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.132+912G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116754754 | ||||||
| chr8:116755268
|
A | G | 114 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.132+398T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755268 | ||||||
| chr8:116755322
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG02809.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.132+344T>C | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755322 | ||||||
| chr8:116755382
|
T | C | 262 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(259): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.132+284A>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755382 | ||||||
| chr8:116755394
|
A | C | 1 | a0001c0001t0003g0334 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.132+272T>G | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755394 | ||||||
| chr8:116755395
|
C | A | 1 | a0001c0001t0003g0334 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.132+271G>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755395 | ||||||
| chr8:116755437
|
C | T | 5 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+229G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755437 | ||||||
| chr8:116755453
|
C | T | 2 | a0001c0001t0003g0002a0001c0001t0003g0003 | 2 | NA19007.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.132+213G>A | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755453 | ||||||
| chr8:116755627
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.132+39C>T | EIF3H | ENSG00000147677.12 | transcript | ENST00000521861.6 | protein_coding | 1/7 | chr8 | 116755627 |