Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8663 |
|---|---|
| ensemblid | ENSG00000184110.15 |
| hgncid | 3279 |
| symbol | EIF3C |
| name | eukaryotic translation initiation factor 3 subunit C |
| refseq_nuc | NM_003752.5 |
| refseq_prot | NP_003743.1 |
| ensembl_nuc | ENST00000331666.11 |
| ensembl_prot | ENSP00000332604.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 28711464 |
| end | 28735596 |
| strand | + |
| ver | v1.2 |
| region | chr16:28711464-28735596 |
| region5000 | chr16:28706464-28740596 |
| regionname0 | EIF3C_chr16_28711464_28735596 |
| regionname5000 | EIF3C_chr16_28706464_28740596 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 913 | 98 | 17 | 2 | 57 | 0 | 22 | 49 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0002 | 0/0 | 457 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0003 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2742 | 73 | 16 | 2 | 40 | 0 | 15 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0002 | 0/0 | 2742 | 16 | 0 | 0 | 10 | 0 | 6 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0003 | 0/0 | 2742 | 7 | 0 | 0 | 7 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0004 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0005 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0006 | 0/0 | 2742 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| c0007 | 0/0 | 2742 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 169 | 100 | 18 | 2 | 58 | 0 | 22 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2742 | 73 | 16 | 2 | 40 | 0 | 15 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0002 | 0/0 | 2742 | 16 | 0 | 0 | 10 | 0 | 6 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0003 | 0/0 | 2742 | 7 | 0 | 0 | 7 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0005 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0006 | 0/0 | 2742 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0002c0007 | 0/0 | 2742 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0003c0004 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2910 | 73 | 16 | 2 | 40 | 0 | 15 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0002t0001 | 0/0 | 2910 | 16 | 0 | 0 | 10 | 0 | 6 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0003t0001 | 0/0 | 2910 | 7 | 0 | 0 | 7 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0005t0001 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0001c0006t0001 | 0/0 | 2910 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0002c0007t0001 | 0/0 | 2910 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| a0003c0004t0001 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | copy fasta | chr16 | 28706464 | 28740596 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0001c0006t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0002c0007t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | CHS | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02572 | hp2 | a0003 | c0004 | t0001 | g0082 | AFR | GWD | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0055 | AFR | MSL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG04204 | hp2 | a0001 | c0006 | t0001 | g0014 | SAS | STU | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CHB | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18993 | hp1 | a0002 | c0007 | t0001 | g0031 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | GIH | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | EIF3C_chr16_28706464_28740596 | EIF3C | chr16 | 28706464 | 28740596 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28724982
|
A | T | 1 | a0002 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1372A>T | p.Ile458Leu | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/21 | 1457/2910 | 1372/2742 | 458/913 | chr16 | 28724982 | ||
| chr16:28724983
|
T | A | 1 | a0002 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1373T>A | p.Ile458Lys | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/21 | 1458/2910 | 1373/2742 | 458/913 | chr16 | 28724983 | ||
| chr16:28727173
|
G | A | 1 | a0003 | 1 | HG02572.hp2 | stop_gained | HIGH | c.1746G>A | p.Trp582* | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/21 | 1831/2910 | 1746/2742 | 582/913 | chr16 | 28727173 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28724996
|
T | G | 2 | a0001c0002a0002c0007 | 17 | HG03017.hp2 HG03688.hp2 HG04115.hp2 others(14): Show |
synonymous_variant | LOW | c.1386T>G | p.Thr462Thr | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/21 | 1471/2910 | 1386/2742 | 462/913 | chr16 | 28724996 | ||
| chr16:28727059
|
G | A | 1 | a0001c0003 | 7 | HG00408.hp2 NA18747.hp2 NA18955.hp1 others(4): Show |
synonymous_variant | LOW | c.1632G>A | p.Ser544Ser | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/21 | 1717/2910 | 1632/2742 | 544/913 | chr16 | 28727059 | ||
| chr16:28727125
|
A | G | 1 | a0001c0006 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1698A>G | p.Thr566Thr | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/21 | 1783/2910 | 1698/2742 | 566/913 | chr16 | 28727125 | ||
| chr16:28727167
|
G | C | 1 | a0003c0004 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1740G>C | p.Ser580Ser | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/21 | 1825/2910 | 1740/2742 | 580/913 | chr16 | 28727167 | ||
| chr16:28735456
|
C | T | 1 | a0001c0005 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2685C>T | p.Asn895Asn | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 21/21 | 2770/2910 | 2685/2742 | 895/913 | chr16 | 28735456 |
| 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 |
|---|
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28711874
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18947.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.101+87A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28711874 | ||||||
| chr16:28711907
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.101+120A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28711907 | ||||||
| chr16:28712220
|
C | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 54 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.101+433C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712220 | ||||||
| chr16:28712223
|
T | G | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.101+436T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712223 | ||||||
| chr16:28712234
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | NA18993.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.101+447T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712234 | ||||||
| chr16:28712475
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.101+688C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712475 | ||||||
| chr16:28712789
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | NA18993.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.102-912A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712789 | ||||||
| chr16:28712966
|
C | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 13 | HG02572.hp2 HG02602.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.102-735C>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28712966 | ||||||
| chr16:28713047
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(42): Show | 49 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.102-654G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28713047 | ||||||
| chr16:28713112
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.102-589A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 2/20 | chr16 | 28713112 | ||||||
| chr16:28714746
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.538+56G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 6/20 | chr16 | 28714746 | ||||||
| chr16:28715218
|
T | C | 2 | a0001c0001t0001g0011a0003c0004t0001g0082 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.649-89T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 7/20 | chr16 | 28715218 | ||||||
| chr16:28715228
|
T | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.649-79T>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 7/20 | chr16 | 28715228 | ||||||
| chr16:28715662
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.776+228C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28715662 | ||||||
| chr16:28715938
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG03516.hp1 HG03516.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.776+504C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28715938 | ||||||
| chr16:28716085
|
C | A | 2 | a0001c0001t0001g0008a0003c0004t0001g0082 | 2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.776+651C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28716085 | ||||||
| chr16:28716839
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.776+1405G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28716839 | ||||||
| chr16:28716894
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.776+1460A>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28716894 | ||||||
| chr16:28716930
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 82 | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(79): Show |
intron_variant | MODIFIER | c.776+1496C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28716930 | ||||||
| chr16:28716999
|
A | C | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.776+1565A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28716999 | ||||||
| chr16:28717166
|
T | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(46): Show | 54 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.776+1732T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28717166 | ||||||
| chr16:28717279
|
G | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(12): Show | 18 | HG00408.hp2 HG02074.hp2 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.776+1845G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28717279 | ||||||
| chr16:28717490
|
A | T | 1 | a0001c0005t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776+2056A>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28717490 | ||||||
| chr16:28717789
|
G | A | 1 | a0001c0005t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776+2355G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28717789 | ||||||
| chr16:28717798
|
C | CA | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.776+2365dupA | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28717798 | |||||
| chr16:28717960
|
G | A | 1 | a0001c0003t0001g0006 | 2 | NA18989.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.776+2526G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28717960 | ||||||
| chr16:28718066
|
G | GA | 17 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0025others(14): Show | 18 | HG02056.hp1 HG02056.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.776+2656dupA | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28718066 | |||||
| chr16:28718066
|
GA | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0044others(2): Show | 5 | HG03688.hp1 NA19009.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.776+2656delA | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28718066 | |||||
| chr16:28718614
|
G | GT | 7 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 7 | HG02074.hp2 HG02572.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.776+3204dupT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28718614 | |||||
| chr16:28718614
|
GT | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 50 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(47): Show |
intron_variant | MODIFIER | c.776+3204delT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28718614 | |||||
| chr16:28718614
|
GTT | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0002t0001g0001others(9): Show | 14 | HG02602.hp2 HG03017.hp2 HG04115.hp2 others(11): Show |
intron_variant | MODIFIER | c.776+3203_776+3204d others(4): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28718614 | |||||
| chr16:28718681
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01123.hp2 HG02056.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+3247C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28718681 | ||||||
| chr16:28719136
|
T | G | 1 | a0001c0001t0001g0009 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.776+3702T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28719136 | ||||||
| chr16:28719762
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.777-3402C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28719762 | ||||||
| chr16:28719959
|
A | ATTT | 16 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(13): Show | 18 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.777-3188_777-3186d others(5): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28719959 | |||||
| chr16:28719959
|
AT | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | NA18968.hp1 NA19010.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.777-3186delT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28719959 | |||||
| chr16:28719968
|
T | A | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.777-3196T>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28719968 | ||||||
| chr16:28720028
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.777-3136C>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28720028 | ||||||
| chr16:28720152
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.777-3012G>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28720152 | ||||||
| chr16:28720905
|
C | CTTTTTTT others(3): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 85 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(82): Show |
intron_variant | MODIFIER | c.777-2252_777-2251i others(12): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28720905 | |||||
| chr16:28720905
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0068 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.777-2252_777-2251i others(13): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28720905 | |||||
| chr16:28720905
|
C | T | 2 | a0001c0001t0001g0069a0003c0004t0001g0082 | 2 | HG02572.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.777-2259C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28720905 | ||||||
| chr16:28720976
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01123.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.777-2188C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28720976 | ||||||
| chr16:28721063
|
G | T | 1 | a0001c0002t0001g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.777-2101G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28721063 | ||||||
| chr16:28721091
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.777-2073G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28721091 | ||||||
| chr16:28721155
|
T | TG | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(3): Show | 6 | HG02615.hp2 HG03516.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.777-2006dupG | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28721155 | |||||
| chr16:28721443
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0033 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.777-1721G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28721443 | ||||||
| chr16:28721879
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.777-1285C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28721879 | ||||||
| chr16:28721900
|
TTTG | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(40): Show | 48 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.777-1234_777-1232d others(5): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28721900 | |||||
| chr16:28721900
|
TTTGTTG | T | 2 | a0001c0001t0001g0039a0001c0002t0001g0043 | 2 | HG02683.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.777-1237_777-1232d others(8): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr16 | 28721900 | |||||
| chr16:28721999
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.777-1165C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28721999 | ||||||
| chr16:28722067
|
C | G | 15 | a0001c0001t0001g0026a0001c0002t0001g0001a0001c0002t0001g0021others(12): Show | 17 | HG02602.hp2 HG03017.hp2 HG03688.hp2 others(14): Show |
intron_variant | MODIFIER | c.777-1097C>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28722067 | ||||||
| chr16:28722208
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.777-956T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28722208 | ||||||
| chr16:28722449
|
T | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(65): Show | 76 | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.777-715T>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28722449 | ||||||
| chr16:28722626
|
T | C | 2 | a0001c0002t0001g0021a0001c0002t0001g0033 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.777-538T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28722626 | ||||||
| chr16:28722921
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(52): Show | 60 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.777-243G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28722921 | ||||||
| chr16:28723058
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.777-106A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 8/20 | chr16 | 28723058 | ||||||
| chr16:28723438
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0057a0003c0004t0001g0082 | 3 | HG02572.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.937-10G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 9/20 | chr16 | 28723438 | ||||||
| chr16:28723773
|
C | CT | 45 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(42): Show | 50 | HG01123.hp1 HG01123.hp2 HG02074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1040+245dupT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr16 | 28723773 | |||||
| chr16:28723773
|
C | CTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(6): Show | 9 | HG00408.hp1 HG02056.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+244_1040+245d others(4): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr16 | 28723773 | |||||
| chr16:28723811
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0005t0001g0055 | 3 | HG02615.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1040+260C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 10/20 | chr16 | 28723811 | ||||||
| chr16:28724243
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1041-79C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 10/20 | chr16 | 28724243 | ||||||
| chr16:28724853
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1309-66G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 12/20 | chr16 | 28724853 | ||||||
| chr16:28725173
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1402+161C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725173 | ||||||
| chr16:28725483
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1402+471G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725483 | ||||||
| chr16:28725499
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1402+487G>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725499 | ||||||
| chr16:28725614
|
A | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(60): Show | 68 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.1402+602A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725614 | ||||||
| chr16:28725616
|
A | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(58): Show | 66 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.1402+604A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725616 | ||||||
| chr16:28725720
|
C | G | 1 | a0001c0002t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1402+708C>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725720 | ||||||
| chr16:28725790
|
G | A | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1402+778G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725790 | ||||||
| chr16:28725940
|
G | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02056.hp2 HG02735.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.1403-665G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28725940 | ||||||
| chr16:28726083
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-522A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28726083 | ||||||
| chr16:28726494
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1403-111C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 13/20 | chr16 | 28726494 | ||||||
| chr16:28726842
|
G | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 37 | HG00408.hp2 HG02074.hp2 HG02572.hp2 others(34): Show |
intron_variant | MODIFIER | c.1593+47G>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 14/20 | chr16 | 28726842 | ||||||
| chr16:28726894
|
C | T | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1593+99C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 14/20 | chr16 | 28726894 | ||||||
| chr16:28726907
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1593+112G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 14/20 | chr16 | 28726907 | ||||||
| chr16:28726989
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1594-32C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 14/20 | chr16 | 28726989 | ||||||
| chr16:28727337
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1818+92T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28727337 | ||||||
| chr16:28727662
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0006t0001g0014others(1): Show | 4 | HG02572.hp2 HG02683.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1818+417A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28727662 | ||||||
| chr16:28727796
|
G | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1818+551G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28727796 | ||||||
| chr16:28727811
|
A | T | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1818+566A>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28727811 | ||||||
| chr16:28727818
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0050a0003c0004t0001g0082 | 3 | HG02572.hp2 HG03579.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1818+573T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28727818 | ||||||
| chr16:28728141
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1818+896G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728141 | ||||||
| chr16:28728179
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1818+934G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728179 | ||||||
| chr16:28728180
|
T | G | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1818+935T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728180 | ||||||
| chr16:28728337
|
G | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG02738.hp2 HG03688.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1818+1092G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728337 | ||||||
| chr16:28728339
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1818+1094C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728339 | ||||||
| chr16:28728453
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0002t0001g0028a0001c0002t0001g0083 | 2 | NA19058.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1818+1230_1818+125 others(26): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28728453 | |||||
| chr16:28728492
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18947.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1818+1247A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728492 | ||||||
| chr16:28728496
|
G | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1818+1251G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28728496 | ||||||
| chr16:28728521
|
G | GGT | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(10): Show | 13 | HG01123.hp1 HG02056.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+1303_1818+130 others(6): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28728521 | |||||
| chr16:28728917
|
CTACTTTT others(1): Show |
C | 2 | a0001c0001t0001g0013a0003c0004t0001g0082 | 2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1818+1683_1818+169 others(12): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28728917 | |||||
| chr16:28729071
|
A | AT | 5 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0052others(2): Show | 5 | HG00408.hp2 HG02056.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1818+1848dupT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28729071 | |||||
| chr16:28729071
|
AT | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(43): Show | 51 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.1818+1848delT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28729071 | |||||
| chr16:28729110
|
T | G | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1818+1865T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729110 | ||||||
| chr16:28729147
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1818+1902C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729147 | ||||||
| chr16:28729356
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1818+2111G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729356 | ||||||
| chr16:28729362
|
G | A | 1 | a0001c0003t0001g0006 | 2 | NA18989.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1818+2117G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729362 | ||||||
| chr16:28729754
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1819-2075A>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729754 | ||||||
| chr16:28729915
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0020others(1): Show | 4 | HG01123.hp2 HG02056.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-1914C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28729915 | ||||||
| chr16:28730015
|
A | G | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1819-1814A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730015 | ||||||
| chr16:28730091
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1819-1738C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730091 | ||||||
| chr16:28730114
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1819-1715T>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730114 | ||||||
| chr16:28730142
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1819-1687C>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730142 | ||||||
| chr16:28730159
|
G | T | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1819-1670G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730159 | ||||||
| chr16:28730319
|
C | T | 1 | a0001c0005t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1819-1510C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730319 | ||||||
| chr16:28730497
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1819-1332A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730497 | ||||||
| chr16:28730909
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1819-920G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730909 | ||||||
| chr16:28730970
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1819-859T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28730970 | ||||||
| chr16:28731138
|
C | CA | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0020others(16): Show | 19 | HG01123.hp2 HG02056.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1819-669dupA | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | 28731138 | |||||
| chr16:28731319
|
G | T | 1 | a0003c0004t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1819-510G>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28731319 | ||||||
| chr16:28731373
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(23): Show | 29 | HG00408.hp1 HG02056.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1819-456A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28731373 | ||||||
| chr16:28731475
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1819-354C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 15/20 | chr16 | 28731475 | ||||||
| chr16:28732374
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2182+182C>T | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28732374 | ||||||
| chr16:28732551
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(42): Show | 50 | HG00408.hp1 HG01123.hp1 HG02056.hp1 others(47): Show |
intron_variant | MODIFIER | c.2182+359G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28732551 | ||||||
| chr16:28732770
|
A | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0020others(3): Show | 6 | HG01123.hp2 HG02056.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2182+578A>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28732770 | ||||||
| chr16:28733071
|
TTTTC | T | 2 | a0001c0001t0001g0013a0001c0002t0001g0043 | 2 | NA18946.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2182+895_2182+898d others(6): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | 28733071 | |||||
| chr16:28733084
|
TTTC | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(45): Show | 53 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2182+895_2182+897d others(5): Show |
EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | 28733084 | |||||
| chr16:28733087
|
CT | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(10): Show | 13 | HG02056.hp2 HG02572.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.2182+911delT | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | 28733087 | |||||
| chr16:28733091
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2182+899T>C | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28733091 | ||||||
| chr16:28733886
|
T | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(13): Show | 16 | HG01123.hp2 HG02056.hp2 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.2183-634T>G | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28733886 | ||||||
| chr16:28733984
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2183-536G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 16/20 | chr16 | 28733984 | ||||||
| chr16:28734861
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2408+18G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 18/20 | chr16 | 28734861 | ||||||
| chr16:28735080
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2496+61G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 19/20 | chr16 | 28735080 | ||||||
| chr16:28735112
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2497-61G>A | EIF3C | ENSG00000184110.15 | transcript | ENST00000331666.11 | protein_coding | 19/20 | chr16 | 28735112 |