Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8891 |
|---|---|
| ensemblid | ENSG00000070785.17 |
| hgncid | 3259 |
| symbol | EIF2B3 |
| name | eukaryotic translation initiation factor 2B subunit gamma |
| refseq_nuc | NM_020365.5 |
| refseq_prot | NP_065098.1 |
| ensembl_nuc | ENST00000360403.7 |
| ensembl_prot | ENSP00000353575.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 44850522 |
| end | 44986595 |
| strand | - |
| ver | v1.2 |
| region | chr1:44850522-44986595 |
| region5000 | chr1:44845522-44991595 |
| regionname0 | EIF2B3_chr1_44850522_44986595 |
| regionname5000 | EIF2B3_chr1_44845522_44991595 |
| 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 | 452 | 317 | 77 | 54 | 132 | 15 | 37 | 104 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0002 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0003 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0004 | 0/0 | 452 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0005 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0006 | 0/0 | 452 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| 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 | 1/0 | 1359 | 204 | 45 | 30 | 92 | 11 | 25 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0002 | 0/1 | 1359 | 113 | 32 | 24 | 40 | 4 | 12 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0003 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0004 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0005 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0006 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| c0007 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| 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 | 542 | 194 | 54 | 35 | 80 | 10 | 14 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| t0002 | 1/0 | 542 | 125 | 23 | 19 | 53 | 6 | 23 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| t0003 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| t0004 | 0/0 | 542 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| t0005 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| 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 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| 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 | 1/0 | 1359 | 204 | 45 | 30 | 92 | 11 | 25 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0002 | 0/1 | 1359 | 113 | 32 | 24 | 40 | 4 | 12 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0002c0007 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0003c0005 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0004c0006 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0005c0004 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0006c0003 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1900 | 80 | 22 | 11 | 39 | 5 | 3 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0001t0002 | 1/0 | 1900 | 123 | 23 | 19 | 52 | 6 | 22 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0001t0003 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0002t0001 | 0/1 | 1900 | 111 | 31 | 24 | 40 | 4 | 11 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0002t0004 | 0/0 | 1900 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0001c0002t0005 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0002c0007t0001 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0003c0005t0001 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0004c0006t0001 | 0/0 | 1900 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0005c0004t0002 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| a0006c0003t0002 | 0/0 | 1900 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | copy fasta | chr1 | 44845522 | 44991595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0001c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0002c0007t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0003c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0004c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0005c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| a0006c0003t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0209 | EUR | FIN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00323 | hp1 | a0004 | c0006 | t0001 | g0228 | EUR | FIN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0222 | EUR | IBS | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | KHV | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02698 | hp1 | a0006 | c0003 | t0002 | g0010 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0231 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03225 | hp1 | a0003 | c0005 | t0001 | g0314 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | BEB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04204 | hp1 | a0001 | c0002 | t0004 | g0184 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | CHB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | YRI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18975 | hp1 | a0005 | c0004 | t0002 | g0058 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18988 | hp2 | a0002 | c0007 | t0001 | g0166 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | LWK | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | LWK | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | YRI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | ASW | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0227 | EUR | TSI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | TSI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | GIH | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | GIH | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | ACB | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | MSL | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | USA | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | USA | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0226 | REF | REF | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0019 | REF | REF | EIF2B3_chr1_44845522_44991595 | EIF2B3 | chr1 | 44845522 | 44991595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44875688
|
T | C | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.983A>G | p.Lys328Arg | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 9/12 | 1095/1900 | 983/1359 | 328/452 | chr1 | 44875688 | ||
| chr1:44879929
|
G | C | 1 | a0005 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.864C>G | p.Asp288Glu | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/12 | 976/1900 | 864/1359 | 288/452 | chr1 | 44879929 | ||
| chr1:44881709
|
A | C | 1 | a0006 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.687T>G | p.Ile229Met | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/12 | 799/1900 | 687/1359 | 229/452 | chr1 | 44881709 | ||
| chr1:44941518
|
T | C | 1 | a0003 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.442A>G | p.Lys148Glu | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/12 | 554/1900 | 442/1359 | 148/452 | chr1 | 44941518 | ||
| chr1:44981036
|
G | A | 1 | a0002 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.133C>T | p.Arg45Cys | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/12 | 245/1900 | 133/1359 | 45/452 | chr1 | 44981036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44978366
|
G | A | 3 | a0001c0002a0002c0007a0004c0006 | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
synonymous_variant | LOW | c.243C>T | p.Asp81Asp | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/12 | 355/1900 | 243/1359 | 81/452 | chr1 | 44978366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44850549
|
G | C | 1 | a0001c0002t0005 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 12/12 | 402 | chr1 | 44850549 | |||||
| chr1:44850631
|
C | G | 1 | a0001c0001t0003 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 12/12 | 320 | chr1 | 44850631 | |||||
| chr1:44850698
|
A | G | 1 | a0001c0002t0004 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*253T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 12/12 | 253 | chr1 | 44850698 | |||||
| chr1:44986555
|
G | C | 7 | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(4): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-72C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/12 | 5387 | chr1 | 44986555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:44851133
|
C | T | 4 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-130G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851133 | ||||||
| chr1:44851213
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1307-210G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851213 | ||||||
| chr1:44851232
|
C | T | 291 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(288): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1307-229G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851232 | ||||||
| chr1:44851555
|
A | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1307-552T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851555 | ||||||
| chr1:44851720
|
G | A | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1307-717C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851720 | ||||||
| chr1:44851872
|
C | T | 2 | a0001c0002t0001g0178a0001c0002t0001g0182 | 2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1307-869G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851872 | ||||||
| chr1:44851953
|
C | CT | 24 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(21): Show | 24 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1307-951dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851953 | ||||||
| chr1:44851953
|
CT | C | 91 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(88): Show | 91 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1307-951delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44851953 | ||||||
| chr1:44852034
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1307-1031G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852034 | ||||||
| chr1:44852061
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1307-1058C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852061 | ||||||
| chr1:44852069
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0126 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1307-1066G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852069 | ||||||
| chr1:44852114
|
A | AT | 47 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(44): Show | 47 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1307-1112_1307-111 others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852114 | ||||||
| chr1:44852114
|
A | ATT | 14 | a0001c0001t0002g0012a0001c0001t0002g0026a0001c0001t0002g0032others(11): Show | 14 | HG00621.hp1 HG02738.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.1307-1112_1307-111 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852114 | ||||||
| chr1:44852115
|
A | AT | 14 | a0001c0001t0001g0258a0001c0001t0001g0279a0001c0001t0001g0280others(11): Show | 14 | HG01081.hp2 HG01943.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1307-1113dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852115 | ||||||
| chr1:44852115
|
A | ATT | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02145.hp2 NA18944.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-1114_1307-111 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852115 | ||||||
| chr1:44852115
|
A | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1307-1112T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852115 | ||||||
| chr1:44852115
|
AT | A | 10 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0001g0268others(7): Show | 10 | HG00280.hp1 HG00738.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-1113delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852115 | ||||||
| chr1:44852239
|
C | T | 4 | a0001c0001t0001g0278a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-1236G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852239 | ||||||
| chr1:44852243
|
C | T | 7 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0144others(4): Show | 7 | HG00639.hp2 HG01255.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307-1240G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852243 | ||||||
| chr1:44852244
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0105 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1307-1241C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852244 | ||||||
| chr1:44852398
|
T | G | 85 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1307-1395A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852398 | ||||||
| chr1:44852408
|
C | T | 63 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1307-1405G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852408 | ||||||
| chr1:44852449
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1307-1446G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852449 | ||||||
| chr1:44852507
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1307-1504G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852507 | ||||||
| chr1:44852669
|
C | T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-1666G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852669 | ||||||
| chr1:44852671
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1307-1668G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852671 | ||||||
| chr1:44852733
|
C | G | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-1730G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852733 | ||||||
| chr1:44852734
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-1731C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852734 | ||||||
| chr1:44852779
|
C | CA | 29 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(26): Show | 29 | HG00642.hp1 HG01167.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1307-1777dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852779 | ||||||
| chr1:44852779
|
CA | C | 149 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1307-1777delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44852779 | ||||||
| chr1:44853046
|
C | G | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1307-2043G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853046 | ||||||
| chr1:44853080
|
C | T | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1307-2077G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853080 | ||||||
| chr1:44853332
|
C | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02071.hp2 HG02074.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-2329G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853332 | ||||||
| chr1:44853333
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-2330C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853333 | ||||||
| chr1:44853449
|
A | T | 10 | a0001c0001t0002g0093a0001c0002t0001g0169a0001c0002t0001g0200others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1307-2446T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853449 | ||||||
| chr1:44853515
|
G | A | 1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1307-2512C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853515 | ||||||
| chr1:44853520
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1307-2517G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853520 | ||||||
| chr1:44853525
|
G | C | 85 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1307-2522C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853525 | ||||||
| chr1:44853593
|
T | C | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1307-2590A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853593 | ||||||
| chr1:44853994
|
G | GT | 19 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0030others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1307-2992dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853994 | ||||||
| chr1:44853994
|
GT | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1307-2992delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44853994 | ||||||
| chr1:44854003
|
T | G | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1307-3000A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854003 | ||||||
| chr1:44854004
|
T | G | 1 | a0001c0001t0002g0022 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1307-3001A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854004 | ||||||
| chr1:44854006
|
T | G | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1307-3003A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854006 | ||||||
| chr1:44854007
|
G | T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-3004C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854007 | ||||||
| chr1:44854053
|
A | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0089 | 2 | NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1307-3050T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854053 | ||||||
| chr1:44854145
|
G | A | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1307-3142C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854145 | ||||||
| chr1:44854291
|
C | T | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1307-3288G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854291 | ||||||
| chr1:44854292
|
A | C | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1307-3289T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854292 | ||||||
| chr1:44854409
|
G | A | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1306+3295C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854409 | ||||||
| chr1:44854472
|
G | A | 2 | a0001c0002t0001g0178a0001c0002t0001g0182 | 2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1306+3232C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854472 | ||||||
| chr1:44854589
|
C | CT | 169 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1306+3114dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854589 | ||||||
| chr1:44854679
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+3025G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854679 | ||||||
| chr1:44854763
|
A | C | 1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1306+2941T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44854763 | ||||||
| chr1:44855089
|
C | CA | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1306+2614dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855089 | ||||||
| chr1:44855089
|
CA | C | 10 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0288others(7): Show | 10 | HG01071.hp1 HG01081.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1306+2614delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855089 | ||||||
| chr1:44855286
|
A | G | 1 | a0001c0002t0001g0223 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1306+2418T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855286 | ||||||
| chr1:44855319
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1306+2385A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855319 | ||||||
| chr1:44855394
|
C | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0002t0001g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+2310G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855394 | ||||||
| chr1:44855519
|
C | G | 1 | a0001c0002t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1306+2185G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855519 | ||||||
| chr1:44855754
|
A | G | 51 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(48): Show | 51 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1306+1950T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855754 | ||||||
| chr1:44855808
|
C | T | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1306+1896G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855808 | ||||||
| chr1:44855891
|
C | T | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1306+1813G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44855891 | ||||||
| chr1:44856021
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1306+1683T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856021 | ||||||
| chr1:44856150
|
T | C | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1306+1554A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856150 | ||||||
| chr1:44856349
|
T | C | 2 | a0001c0002t0001g0194a0001c0002t0001g0198 | 2 | NA19009.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1306+1355A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856349 | ||||||
| chr1:44856412
|
G | C | 1 | a0001c0001t0002g0023 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1306+1292C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856412 | ||||||
| chr1:44856418
|
G | A | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1306+1286C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856418 | ||||||
| chr1:44856506
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1306+1198G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856506 | ||||||
| chr1:44856528
|
T | TA | 30 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(27): Show | 30 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1306+1175dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856528 | ||||||
| chr1:44856528
|
TAA | T | 47 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(44): Show | 47 | HG00621.hp2 HG00639.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.1306+1174_1306+117 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856528 | ||||||
| chr1:44856528
|
TAAA | T | 42 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1306+1173_1306+117 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856528 | ||||||
| chr1:44856619
|
A | G | 68 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1306+1085T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44856619 | ||||||
| chr1:44857024
|
G | A | 85 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1306+680C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857024 | ||||||
| chr1:44857138
|
A | G | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1306+566T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857138 | ||||||
| chr1:44857268
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02129.hp2 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306+436C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857268 | ||||||
| chr1:44857314
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1306+390C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857314 | ||||||
| chr1:44857462
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1306+242G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857462 | ||||||
| chr1:44857526
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1306+178G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857526 | ||||||
| chr1:44857527
|
G | GA | 28 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(25): Show | 28 | HG00544.hp1 HG02071.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1306+176dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 11/11 | chr1 | 44857527 | ||||||
| chr1:44857874
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1203-67C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44857874 | ||||||
| chr1:44857930
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1203-123G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44857930 | ||||||
| chr1:44857931
|
G | A | 8 | a0001c0001t0001g0263a0001c0001t0001g0291a0001c0001t0001g0292others(5): Show | 8 | HG00544.hp1 NA18950.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.1203-124C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44857931 | ||||||
| chr1:44858057
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1203-250A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858057 | ||||||
| chr1:44858070
|
C | CT | 7 | a0001c0001t0001g0260a0001c0001t0001g0286a0001c0001t0001g0298others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203-264dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858070 | ||||||
| chr1:44858070
|
C | CTT | 140 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(137): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1203-265_1203-264d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858070 | ||||||
| chr1:44858070
|
C | CTTT | 6 | a0001c0001t0001g0303a0001c0001t0001g0309a0001c0001t0001g0310others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1203-266_1203-264d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858070 | ||||||
| chr1:44858215
|
A | C | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1203-408T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858215 | ||||||
| chr1:44858315
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1203-508T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858315 | ||||||
| chr1:44858324
|
C | T | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1203-517G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858324 | ||||||
| chr1:44858341
|
A | C | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-534T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858341 | ||||||
| chr1:44858633
|
T | A | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0219 | 3 | NA18939.hp1 NA18940.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1203-826A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858633 | ||||||
| chr1:44858640
|
T | A | 86 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0093others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1203-833A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858640 | ||||||
| chr1:44858892
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1203-1085G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858892 | ||||||
| chr1:44858902
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1203-1095A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44858902 | ||||||
| chr1:44859139
|
C | CAAAATA | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-1338_1203-133 others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859139 | ||||||
| chr1:44859166
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1203-1359A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859166 | ||||||
| chr1:44859263
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1203-1456G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859263 | ||||||
| chr1:44859469
|
C | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-1662G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859469 | ||||||
| chr1:44859524
|
G | A | 4 | a0001c0001t0001g0254a0001c0002t0001g0186a0001c0002t0001g0187others(1): Show | 4 | HG02258.hp1 NA18939.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-1717C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859524 | ||||||
| chr1:44859575
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-1768A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859575 | ||||||
| chr1:44859878
|
C | T | 65 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1203-2071G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859878 | ||||||
| chr1:44859988
|
C | A | 1 | a0001c0002t0001g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1203-2181G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44859988 | ||||||
| chr1:44860003
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-2196G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860003 | ||||||
| chr1:44860004
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-2197G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860004 | ||||||
| chr1:44860009
|
T | G | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-2202A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860009 | ||||||
| chr1:44860313
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-2506G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860313 | ||||||
| chr1:44860351
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1203-2544A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860351 | ||||||
| chr1:44860748
|
C | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0002t0001g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-2941G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44860748 | ||||||
| chr1:44861266
|
G | A | 24 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0142others(21): Show | 24 | HG00621.hp2 HG00639.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1203-3459C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861266 | ||||||
| chr1:44861272
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1203-3465T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861272 | ||||||
| chr1:44861491
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1203-3684G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861491 | ||||||
| chr1:44861558
|
G | A | 85 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1203-3751C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861558 | ||||||
| chr1:44861634
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0105 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1203-3827A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861634 | ||||||
| chr1:44861703
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203-3896A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44861703 | ||||||
| chr1:44862004
|
A | C | 1 | a0001c0002t0001g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1203-4197T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862004 | ||||||
| chr1:44862022
|
A | G | 68 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1203-4215T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862022 | ||||||
| chr1:44862044
|
C | T | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.1203-4237G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862044 | ||||||
| chr1:44862211
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1203-4404G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862211 | ||||||
| chr1:44862256
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-4449G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862256 | ||||||
| chr1:44862525
|
TAGGTAGG others(9): Show |
T | 1 | a0001c0002t0001g0208 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1203-4734_1203-471 others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862525 | ||||||
| chr1:44862669
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-4862C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862669 | ||||||
| chr1:44862903
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1203-5096G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862903 | ||||||
| chr1:44862967
|
G | A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-5160C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44862967 | ||||||
| chr1:44863031
|
C | G | 1 | a0001c0002t0001g0208 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1203-5224G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44863031 | ||||||
| chr1:44863255
|
G | A | 62 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(59): Show | 62 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1203-5448C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44863255 | ||||||
| chr1:44863288
|
T | C | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1203-5481A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44863288 | ||||||
| chr1:44863753
|
T | C | 5 | a0001c0002t0001g0170a0001c0002t0001g0188a0001c0002t0001g0189others(2): Show | 5 | NA18951.hp1 NA18953.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203-5946A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44863753 | ||||||
| chr1:44864198
|
G | T | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1203-6391C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864198 | ||||||
| chr1:44864335
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1203-6528G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864335 | ||||||
| chr1:44864336
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1203-6529C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864336 | ||||||
| chr1:44864341
|
G | T | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1203-6534C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864341 | ||||||
| chr1:44864390
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1203-6583G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864390 | ||||||
| chr1:44864414
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-6607A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864414 | ||||||
| chr1:44864462
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203-6655A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864462 | ||||||
| chr1:44864599
|
A | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1203-6792T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864599 | ||||||
| chr1:44864700
|
TAG | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0029a0001c0001t0002g0032others(5): Show | 8 | HG00609.hp2 HG02523.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203-6895_1203-689 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864700 | ||||||
| chr1:44864848
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1203-7041T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44864848 | ||||||
| chr1:44865208
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-7401G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865208 | ||||||
| chr1:44865216
|
T | TAAAAAAA others(3): Show |
7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG01243.hp2 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203-7419_1203-741 others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865216 | ||||||
| chr1:44865216
|
T | TAAAAAAA others(4): Show |
56 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(53): Show | 56 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1203-7420_1203-741 others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865216 | ||||||
| chr1:44865216
|
T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0267a0001c0001t0001g0277a0001c0001t0001g0279others(2): Show | 5 | HG00735.hp1 HG01358.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203-7421_1203-741 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865216 | ||||||
| chr1:44865216
|
TAA | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-7411_1203-741 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865216 | ||||||
| chr1:44865478
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1203-7671A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865478 | ||||||
| chr1:44865540
|
C | A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-7733G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44865540 | ||||||
| chr1:44866081
|
G | A | 85 | a0001c0001t0002g0028a0001c0001t0002g0093a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1203-8274C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866081 | ||||||
| chr1:44866145
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1203-8338G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866145 | ||||||
| chr1:44866274
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+8404G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866274 | ||||||
| chr1:44866304
|
T | A | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.1202+8374A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866304 | ||||||
| chr1:44866345
|
C | T | 1 | a0001c0002t0001g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1202+8333G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866345 | ||||||
| chr1:44866397
|
C | CA | 97 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0266others(94): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1202+8280dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866397 | ||||||
| chr1:44866410
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1202+8268T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866410 | ||||||
| chr1:44866411
|
C | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+8267G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866411 | ||||||
| chr1:44866504
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+8174C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866504 | ||||||
| chr1:44866558
|
ATT | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+8118_1202+811 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866558 | ||||||
| chr1:44866997
|
T | C | 1 | a0001c0002t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1202+7681A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44866997 | ||||||
| chr1:44867327
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1202+7351T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867327 | ||||||
| chr1:44867392
|
G | A | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0140 | 3 | HG02976.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1202+7286C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867392 | ||||||
| chr1:44867430
|
C | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+7248G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867430 | ||||||
| chr1:44867516
|
C | A | 1 | a0001c0002t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1202+7162G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867516 | ||||||
| chr1:44867584
|
A | G | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1202+7094T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867584 | ||||||
| chr1:44867722
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+6956G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867722 | ||||||
| chr1:44867822
|
T | A | 183 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1202+6856A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867822 | ||||||
| chr1:44867867
|
T | TA | 22 | a0001c0001t0001g0158a0001c0001t0001g0273a0001c0001t0001g0297others(19): Show | 22 | HG00639.hp2 HG00735.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1202+6810dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867867 | ||||||
| chr1:44867867
|
TA | T | 17 | a0001c0001t0001g0254a0001c0001t0001g0258a0001c0001t0001g0292others(14): Show | 17 | HG01069.hp1 HG01167.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1202+6810delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867867 | ||||||
| chr1:44867955
|
T | C | 5 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0155others(2): Show | 5 | HG00642.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+6723A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44867955 | ||||||
| chr1:44868047
|
G | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+6631C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868047 | ||||||
| chr1:44868068
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0046 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1202+6610G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868068 | ||||||
| chr1:44868069
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1202+6609A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868069 | ||||||
| chr1:44868397
|
C | CA | 19 | a0001c0001t0001g0284a0001c0001t0001g0318a0001c0001t0001g0320others(16): Show | 19 | HG00639.hp1 HG01081.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1202+6280dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868397 | ||||||
| chr1:44868397
|
CA | C | 112 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(109): Show | 112 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1202+6280delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868397 | ||||||
| chr1:44868397
|
CAA | C | 108 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0250others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1202+6279_1202+628 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868397 | ||||||
| chr1:44868496
|
A | AT | 68 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0254others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1202+6181dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868496 | ||||||
| chr1:44868531
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1202+6147C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868531 | ||||||
| chr1:44868725
|
G | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5953C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868725 | ||||||
| chr1:44868865
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+5813T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868865 | ||||||
| chr1:44868977
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1202+5701C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44868977 | ||||||
| chr1:44869188
|
C | T | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | NA18972.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1202+5490G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869188 | ||||||
| chr1:44869200
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+5478C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869200 | ||||||
| chr1:44869371
|
G | C | 1 | a0001c0001t0002g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1202+5307C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869371 | ||||||
| chr1:44869393
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1202+5285C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869393 | ||||||
| chr1:44869410
|
G | A | 6 | a0001c0002t0001g0143a0001c0002t0001g0165a0001c0002t0001g0192others(3): Show | 6 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202+5268C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869410 | ||||||
| chr1:44869438
|
A | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+5240T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869438 | ||||||
| chr1:44869475
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5203G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869475 | ||||||
| chr1:44869489
|
AGCTTT | A | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5184_1202+518 others(9): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869489 | ||||||
| chr1:44869495
|
A | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5183T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869495 | ||||||
| chr1:44869498
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1202+5180A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869498 | ||||||
| chr1:44869498
|
T | G | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5180A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869498 | ||||||
| chr1:44869509
|
ATTTAGTA others(40): Show |
A | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5122_1202+516 others(51): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869509 | ||||||
| chr1:44869593
|
C | CT | 22 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(19): Show | 22 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+5084dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869593 | ||||||
| chr1:44869593
|
CT | C | 80 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0269others(77): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1202+5084delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869593 | ||||||
| chr1:44869593
|
CTT | C | 81 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1202+5083_1202+508 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869593 | ||||||
| chr1:44869593
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0002t0001g0168a0001c0002t0001g0208a0001c0002t0001g0212others(2): Show | 5 | HG02129.hp2 HG03239.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+5071_1202+508 others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869593 | ||||||
| chr1:44869641
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1202+5037G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869641 | ||||||
| chr1:44869714
|
C | T | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1202+4964G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869714 | ||||||
| chr1:44869754
|
C | T | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1202+4924G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44869754 | ||||||
| chr1:44870017
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+4661G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870017 | ||||||
| chr1:44870081
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+4597G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870081 | ||||||
| chr1:44870107
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1202+4571C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870107 | ||||||
| chr1:44870176
|
A | AAG | 20 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(17): Show | 20 | HG00639.hp1 HG01891.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202+4500_1202+450 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870176 | ||||||
| chr1:44870176
|
AAG | A | 173 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(170): Show | 173 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.1202+4500_1202+450 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870176 | ||||||
| chr1:44870176
|
AAGAG | A | 90 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(87): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1202+4498_1202+450 others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870176 | ||||||
| chr1:44870387
|
C | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | NA18962.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1202+4291G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870387 | ||||||
| chr1:44870552
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+4126G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870552 | ||||||
| chr1:44870648
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+4030C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870648 | ||||||
| chr1:44870656
|
G | GT | 68 | a0001c0001t0001g0160a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1202+4021dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870656 | ||||||
| chr1:44870778
|
G | A | 2 | a0001c0002t0001g0183a0002c0007t0001g0166 | 2 | NA18988.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1202+3900C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870778 | ||||||
| chr1:44870809
|
C | T | 4 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0065others(1): Show | 4 | HG01175.hp2 HG01981.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+3869G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44870809 | ||||||
| chr1:44871224
|
CAT | C | 3 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0150 | 3 | HG00642.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1202+3452_1202+345 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871224 | ||||||
| chr1:44871296
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+3382C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871296 | ||||||
| chr1:44871355
|
G | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+3323C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871355 | ||||||
| chr1:44871461
|
G | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+3217C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871461 | ||||||
| chr1:44871490
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1202+3188A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871490 | ||||||
| chr1:44871677
|
A | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+3001T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871677 | ||||||
| chr1:44871807
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0057 | 2 | NA18942.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1202+2871G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871807 | ||||||
| chr1:44871874
|
C | CT | 94 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1202+2803dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871874 | ||||||
| chr1:44871874
|
C | CTT | 61 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(58): Show | 61 | HG00140.hp1 HG00544.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.1202+2802_1202+280 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871874 | ||||||
| chr1:44871874
|
CT | C | 6 | a0001c0001t0002g0018a0001c0001t0002g0062a0001c0001t0002g0084others(3): Show | 6 | HG01167.hp1 HG01167.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+2803delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44871874 | ||||||
| chr1:44872002
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1202+2676G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872002 | ||||||
| chr1:44872146
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+2532A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872146 | ||||||
| chr1:44872363
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+2315A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872363 | ||||||
| chr1:44872463
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+2215G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872463 | ||||||
| chr1:44872494
|
A | T | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0055others(4): Show | 7 | HG02723.hp1 HG03927.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+2184T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872494 | ||||||
| chr1:44872691
|
C | G | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1202+1987G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44872691 | ||||||
| chr1:44873078
|
C | G | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1202+1600G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873078 | ||||||
| chr1:44873097
|
C | T | 3 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0249 | 3 | HG02257.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1202+1581G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873097 | ||||||
| chr1:44873119
|
G | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+1559C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873119 | ||||||
| chr1:44873201
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1202+1477A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873201 | ||||||
| chr1:44873202
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0105 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1202+1476T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873202 | ||||||
| chr1:44873401
|
G | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1202+1277C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873401 | ||||||
| chr1:44873448
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+1230G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873448 | ||||||
| chr1:44873471
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+1207T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873471 | ||||||
| chr1:44873647
|
A | T | 1 | a0001c0002t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1202+1031T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873647 | ||||||
| chr1:44873651
|
T | A | 180 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(177): Show | 180 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1202+1027A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873651 | ||||||
| chr1:44873700
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1202+978C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873700 | ||||||
| chr1:44873719
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1202+959G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873719 | ||||||
| chr1:44873794
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+884G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873794 | ||||||
| chr1:44873807
|
A | AT | 68 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1202+870dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873807 | ||||||
| chr1:44873956
|
GTTTTAGA others(137): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1202+578_1202+721d others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873956 | ||||||
| chr1:44873976
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+702A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44873976 | ||||||
| chr1:44874010
|
G | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+668C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44874010 | ||||||
| chr1:44874039
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1202+639T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44874039 | ||||||
| chr1:44874128
|
GGATTAGG others(81): Show |
G | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1202+462_1202+549d others(90): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44874128 | ||||||
| chr1:44874610
|
C | T | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1202+68G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44874610 | ||||||
| chr1:44874670
|
A | C | 7 | a0001c0002t0001g0143a0001c0002t0001g0149a0001c0002t0001g0165others(4): Show | 7 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1202+8T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 10/11 | chr1 | 44874670 | ||||||
| chr1:44874976
|
G | C | 10 | a0001c0002t0001g0170a0001c0002t0001g0183a0001c0002t0001g0188others(7): Show | 10 | NA18951.hp1 NA18953.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.1054-150C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 9/11 | chr1 | 44874976 | ||||||
| chr1:44875031
|
T | C | 291 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(288): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1054-205A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 9/11 | chr1 | 44875031 | ||||||
| chr1:44875191
|
C | CA | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-366dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 9/11 | chr1 | 44875191 | ||||||
| chr1:44875607
|
C | T | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1053+11G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 9/11 | chr1 | 44875607 | ||||||
| chr1:44875874
|
C | G | 1 | a0001c0002t0001g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.976-179G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44875874 | ||||||
| chr1:44875936
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.976-241G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44875936 | ||||||
| chr1:44875937
|
G | A | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.976-242C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44875937 | ||||||
| chr1:44876031
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-336G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876031 | ||||||
| chr1:44876193
|
C | G | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-498G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876193 | ||||||
| chr1:44876309
|
T | C | 6 | a0001c0002t0001g0221a0001c0002t0001g0225a0001c0002t0001g0226others(3): Show | 6 | HG00323.hp1 HG00735.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-614A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876309 | ||||||
| chr1:44876313
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.976-618G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876313 | ||||||
| chr1:44876425
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-730A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876425 | ||||||
| chr1:44876430
|
G | C | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.976-735C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876430 | ||||||
| chr1:44876500
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.976-805A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876500 | ||||||
| chr1:44876558
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.976-863G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876558 | ||||||
| chr1:44876573
|
T | TGGGGGGG others(346): Show |
1 | a0001c0001t0002g0036 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(353): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(396): Show |
1 | a0001c0001t0002g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(403): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(561): Show |
1 | a0001c0001t0001g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(568): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
7 | a0001c0001t0002g0009a0001c0002t0001g0153a0001c0002t0001g0154others(4): Show | 7 | HG00642.hp1 HG01261.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(394): Show |
1 | a0001c0001t0002g0035 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(401): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
1 | a0001c0001t0002g0050 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(558): Show |
1 | a0001c0001t0001g0283 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(565): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(394): Show |
1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(401): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
2 | a0001c0002t0001g0150a0001c0002t0001g0232 | 2 | HG00642.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(394): Show |
1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(401): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
1 | a0001c0001t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
1 | a0001c0001t0002g0042 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(557): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0291 | 2 | HG02647.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.976-879_976-878ins others(564): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
7 | a0001c0001t0001g0255a0001c0001t0001g0277a0001c0001t0001g0304others(4): Show | 7 | HG01069.hp2 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
40 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(37): Show | 40 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0317 | 3 | HG01516.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(556): Show |
1 | a0001c0001t0001g0290 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(563): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
1 | a0001c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(395): Show |
1 | a0001c0001t0002g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(402): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
5 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0037others(2): Show | 5 | HG02015.hp1 NA18962.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
199 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(196): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(393): Show |
1 | a0001c0001t0002g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(400): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
1 | a0001c0001t0002g0045 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
10 | a0001c0001t0002g0006a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 10 | HG00639.hp1 HG01891.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(343): Show |
1 | a0001c0002t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(350): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(507): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(514): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(507): Show |
1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(514): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(470): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-879_976-878ins others(477): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
3 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102 | 3 | HG02723.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(343): Show |
2 | a0001c0001t0002g0118a0001c0001t0002g0126 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.976-879_976-878ins others(350): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(392): Show |
2 | a0001c0001t0002g0053a0001c0001t0002g0056 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.976-879_976-878ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(581): Show |
1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.976-879_976-878ins others(588): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876573
|
T | TGGGGGTC others(343): Show |
1 | a0001c0002t0001g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.976-879_976-878ins others(350): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876573 | ||||||
| chr1:44876574
|
G | GGGGGTCA others(392): Show |
1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.976-880_976-879ins others(399): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876574 | ||||||
| chr1:44876637
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0105 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.976-942G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876637 | ||||||
| chr1:44876671
|
G | A | 62 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(59): Show | 62 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.976-976C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876671 | ||||||
| chr1:44876672
|
G | C | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.976-977C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876672 | ||||||
| chr1:44876681
|
C | T | 3 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0150 | 3 | HG00642.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.976-986G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876681 | ||||||
| chr1:44876682
|
C | G | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.976-987G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876682 | ||||||
| chr1:44876683
|
C | G | 181 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(178): Show | 181 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.976-988G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876683 | ||||||
| chr1:44876709
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.976-1014A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876709 | ||||||
| chr1:44876723
|
T | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-1028A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876723 | ||||||
| chr1:44876749
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.976-1054T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876749 | ||||||
| chr1:44876785
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.976-1090G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876785 | ||||||
| chr1:44876839
|
T | G | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.976-1144A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876839 | ||||||
| chr1:44876887
|
C | T | 308 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(305): Show | 308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.976-1192G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876887 | ||||||
| chr1:44876946
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-1251A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876946 | ||||||
| chr1:44876959
|
G | A | 6 | a0001c0001t0002g0099a0001c0001t0002g0107a0001c0001t0002g0108others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-1264C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44876959 | ||||||
| chr1:44877053
|
C | T | 5 | a0001c0002t0001g0143a0001c0002t0001g0165a0001c0002t0001g0192others(2): Show | 5 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1358G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877053 | ||||||
| chr1:44877067
|
A | G | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.976-1372T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877067 | ||||||
| chr1:44877186
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.976-1491C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877186 | ||||||
| chr1:44877187
|
A | AT | 3 | a0001c0001t0001g0266a0001c0001t0001g0290a0001c0001t0001g0302 | 3 | NA18941.hp2 NA18988.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.976-1493dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877187 | ||||||
| chr1:44877188
|
T | A | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.976-1493A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877188 | ||||||
| chr1:44877189
|
C | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0290a0001c0001t0001g0302others(1): Show | 4 | NA18941.hp2 NA18988.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-1494G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877189 | ||||||
| chr1:44877189
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.976-1494G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877189 | ||||||
| chr1:44877192
|
T | A | 5 | a0001c0001t0001g0266a0001c0001t0001g0282a0001c0001t0001g0290others(2): Show | 5 | NA18941.hp2 NA18977.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1497A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TA | 9 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0011others(6): Show | 9 | HG01099.hp2 HG01346.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.976-1498dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAA | 41 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0025others(38): Show | 41 | HG00280.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.976-1501_976-1498d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAAA | 31 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0031others(28): Show | 31 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.976-1502_976-1498d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAAAA | 14 | a0001c0001t0001g0132a0001c0001t0002g0012a0001c0001t0002g0039others(11): Show | 14 | HG01175.hp1 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.976-1503_976-1498d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAAAAA others(2): Show |
13 | a0001c0001t0001g0278a0001c0002t0001g0233a0001c0002t0001g0234others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.976-1506_976-1498d others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAAAAA others(3): Show |
9 | a0001c0001t0001g0251a0001c0001t0001g0259a0001c0001t0001g0281others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.976-1507_976-1498d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0250a0001c0002t0001g0248 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.976-1509_976-1498d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TTAA | 8 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01516.hp1 HG01943.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.976-1498_976-1497i others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TTAAA | 24 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0263others(21): Show | 24 | HG00544.hp1 HG01346.hp1 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.976-1498_976-1497i others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TTAAAA | 22 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.976-1498_976-1497i others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
T | TTAAAAA | 6 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0300others(3): Show | 6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-1498_976-1497i others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
TA | T | 16 | a0001c0001t0001g0254a0001c0001t0002g0006a0001c0001t0002g0021others(13): Show | 16 | HG00323.hp2 HG00639.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.976-1498delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877192
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.976-1507_976-1498d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877192 | ||||||
| chr1:44877198
|
A | C | 83 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.976-1503T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877198 | ||||||
| chr1:44877201
|
A | C | 1 | a0001c0002t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.976-1506T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877201 | ||||||
| chr1:44877202
|
A | C | 83 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.976-1507T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877202 | ||||||
| chr1:44877205
|
A | C | 1 | a0001c0002t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.976-1510T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877205 | ||||||
| chr1:44877206
|
A | C | 83 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(80): Show | 83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.976-1511T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877206 | ||||||
| chr1:44877209
|
A | C | 13 | a0001c0002t0001g0162a0001c0002t0001g0169a0001c0002t0001g0200others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.976-1514T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877209 | ||||||
| chr1:44877210
|
A | C | 2 | a0001c0002t0001g0171a0001c0002t0001g0214 | 2 | HG02083.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.976-1515T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877210 | ||||||
| chr1:44877212
|
A | C | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.976-1517T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877212 | ||||||
| chr1:44877214
|
A | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-1519T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877214 | ||||||
| chr1:44877220
|
A | C | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.976-1525T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877220 | ||||||
| chr1:44877292
|
G | C | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.976-1597C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877292 | ||||||
| chr1:44877483
|
G | C | 5 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0037others(2): Show | 5 | HG02015.hp1 NA18962.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1788C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877483 | ||||||
| chr1:44877632
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.976-1937G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877632 | ||||||
| chr1:44877834
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.975+1984G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877834 | ||||||
| chr1:44877967
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.975+1851G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44877967 | ||||||
| chr1:44878276
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.975+1542A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878276 | ||||||
| chr1:44878375
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.975+1443C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878375 | ||||||
| chr1:44878483
|
G | A | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0140 | 3 | HG02976.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.975+1335C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878483 | ||||||
| chr1:44878500
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.975+1318G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878500 | ||||||
| chr1:44878542
|
C | G | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.975+1276G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878542 | ||||||
| chr1:44878543
|
G | A | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.975+1275C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878543 | ||||||
| chr1:44878602
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.975+1216G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878602 | ||||||
| chr1:44878695
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.975+1123G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44878695 | ||||||
| chr1:44879364
|
A | C | 2 | a0001c0001t0002g0093a0001c0001t0002g0120 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.975+454T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44879364 | ||||||
| chr1:44879575
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.975+243G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44879575 | ||||||
| chr1:44879683
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+135G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44879683 | ||||||
| chr1:44879774
|
T | A | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.975+44A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44879774 | ||||||
| chr1:44879809
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+9A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 8/11 | chr1 | 44879809 | ||||||
| chr1:44880122
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.785-114G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880122 | ||||||
| chr1:44880540
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.785-532C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880540 | ||||||
| chr1:44880628
|
A | T | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.785-620T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880628 | ||||||
| chr1:44880641
|
G | A | 2 | a0001c0002t0001g0163a0001c0002t0001g0181 | 2 | NA18956.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.785-633C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880641 | ||||||
| chr1:44880665
|
C | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-657G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880665 | ||||||
| chr1:44880734
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | NA18972.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.785-726C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880734 | ||||||
| chr1:44880885
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.784+727G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880885 | ||||||
| chr1:44880886
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.784+726C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880886 | ||||||
| chr1:44880918
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.784+694C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880918 | ||||||
| chr1:44880968
|
T | A | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.784+644A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880968 | ||||||
| chr1:44880969
|
A | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+643T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44880969 | ||||||
| chr1:44881236
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.784+376A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44881236 | ||||||
| chr1:44881387
|
T | C | 1 | a0001c0002t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+225A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44881387 | ||||||
| chr1:44881419
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.784+193C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44881419 | ||||||
| chr1:44881489
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.784+123G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44881489 | ||||||
| chr1:44881578
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.784+34A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 7/11 | chr1 | 44881578 | ||||||
| chr1:44882438
|
C | CT | 8 | a0001c0001t0002g0049a0001c0002t0001g0190a0001c0002t0001g0219others(5): Show | 8 | HG00323.hp1 HG01256.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-700dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882438 | ||||||
| chr1:44882618
|
A | AT | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(7): Show | 10 | HG00639.hp1 HG02258.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.657-880dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882618 | ||||||
| chr1:44882700
|
T | G | 1 | a0001c0001t0002g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.657-961A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882700 | ||||||
| chr1:44882928
|
C | CT | 18 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(15): Show | 18 | HG01069.hp2 HG01243.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.657-1190dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882928 | ||||||
| chr1:44882928
|
C | CTT | 45 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(42): Show | 45 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.657-1191_657-1190d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882928 | ||||||
| chr1:44882928
|
CT | C | 25 | a0001c0001t0001g0129a0001c0001t0001g0250a0001c0001t0001g0251others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.657-1190delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882928 | ||||||
| chr1:44882932
|
T | C | 2 | a0001c0001t0002g0050a0001c0002t0001g0168 | 2 | HG01981.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.657-1193A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882932 | ||||||
| chr1:44882983
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.657-1244C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44882983 | ||||||
| chr1:44883076
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.657-1337G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883076 | ||||||
| chr1:44883082
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1343G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883082 | ||||||
| chr1:44883126
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0112 | 2 | HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.657-1387C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883126 | ||||||
| chr1:44883203
|
G | C | 1 | a0002c0007t0001g0166 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.657-1464C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883203 | ||||||
| chr1:44883316
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-1577G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883316 | ||||||
| chr1:44883317
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0040 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.657-1578C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883317 | ||||||
| chr1:44883364
|
ATCATTTT others(8): Show |
A | 1 | a0001c0001t0002g0095 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.657-1640_657-1626d others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883364 | ||||||
| chr1:44883528
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0306 | 2 | HG01993.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.657-1789G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883528 | ||||||
| chr1:44883557
|
G | T | 94 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.657-1818C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883557 | ||||||
| chr1:44883701
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-1962C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883701 | ||||||
| chr1:44883771
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG00639.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.657-2032C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883771 | ||||||
| chr1:44883910
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.657-2171G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44883910 | ||||||
| chr1:44884129
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.657-2390C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884129 | ||||||
| chr1:44884290
|
T | A | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657-2551A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884290 | ||||||
| chr1:44884356
|
C | A | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.657-2617G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884356 | ||||||
| chr1:44884358
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657-2619G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884358 | ||||||
| chr1:44884517
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.657-2778A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884517 | ||||||
| chr1:44884661
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-2922A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884661 | ||||||
| chr1:44884713
|
A | C | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.657-2974T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884713 | ||||||
| chr1:44884966
|
G | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-3227C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884966 | ||||||
| chr1:44884999
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-3260G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44884999 | ||||||
| chr1:44885312
|
TA | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-3574delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885312 | ||||||
| chr1:44885456
|
G | A | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.657-3717C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885456 | ||||||
| chr1:44885461
|
A | G | 11 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-3722T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885461 | ||||||
| chr1:44885521
|
T | G | 1 | a0001c0001t0002g0031 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.657-3782A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885521 | ||||||
| chr1:44885651
|
C | T | 4 | a0001c0001t0001g0279a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-3912G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885651 | ||||||
| chr1:44885901
|
A | AT | 17 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00140.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.657-4163dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885901 | ||||||
| chr1:44885901
|
A | ATT | 82 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0002g0028others(79): Show | 82 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.657-4164_657-4163d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885901 | ||||||
| chr1:44885901
|
A | ATTT | 69 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(66): Show | 69 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.657-4165_657-4163d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885901 | ||||||
| chr1:44885901
|
A | ATTTT | 19 | a0001c0001t0001g0263a0001c0001t0001g0266a0001c0001t0001g0283others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.657-4166_657-4163d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44885901 | ||||||
| chr1:44886270
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-4531C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886270 | ||||||
| chr1:44886300
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-4561G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886300 | ||||||
| chr1:44886382
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.657-4643C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886382 | ||||||
| chr1:44886455
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.657-4716G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886455 | ||||||
| chr1:44886477
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.657-4738T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886477 | ||||||
| chr1:44886658
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657-4919G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886658 | ||||||
| chr1:44886723
|
G | A | 1 | a0001c0002t0005g0231 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.657-4984C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886723 | ||||||
| chr1:44886826
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-5087G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886826 | ||||||
| chr1:44886865
|
T | C | 23 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0269others(20): Show | 23 | HG00544.hp1 HG02071.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.657-5126A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886865 | ||||||
| chr1:44886886
|
T | C | 1 | a0001c0001t0002g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.657-5147A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886886 | ||||||
| chr1:44886919
|
C | CTTGT | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.657-5181_657-5180i others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44886919 | ||||||
| chr1:44887171
|
G | C | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.657-5432C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887171 | ||||||
| chr1:44887562
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.657-5823A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887562 | ||||||
| chr1:44887612
|
C | T | 63 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(60): Show | 63 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.657-5873G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887612 | ||||||
| chr1:44887684
|
A | G | 1 | a0001c0002t0001g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.657-5945T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887684 | ||||||
| chr1:44887710
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.657-5971C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887710 | ||||||
| chr1:44887901
|
C | G | 1 | a0001c0002t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657-6162G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887901 | ||||||
| chr1:44887903
|
A | C | 5 | a0001c0002t0001g0171a0001c0002t0001g0204a0001c0002t0001g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-6164T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887903 | ||||||
| chr1:44887958
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.657-6219A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44887958 | ||||||
| chr1:44888004
|
T | A | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.657-6265A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888004 | ||||||
| chr1:44888088
|
T | C | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.657-6349A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888088 | ||||||
| chr1:44888277
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01891.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-6538G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888277 | ||||||
| chr1:44888463
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-6724A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888463 | ||||||
| chr1:44888473
|
A | ATC | 6 | a0001c0001t0001g0284a0001c0001t0001g0322a0001c0001t0002g0003others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-6736_657-6735d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
A | ATCTC | 54 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(51): Show | 54 | HG00544.hp1 HG01069.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.657-6738_657-6735d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
A | ATCTCTC | 4 | a0001c0001t0001g0300a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG01243.hp2 HG02145.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-6740_657-6735d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
A | ATCTCTCT others(1): Show |
3 | a0001c0001t0001g0268a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG00140.hp1 HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.657-6742_657-6735d others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
A | ATCTCTCT others(3): Show |
1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.657-6744_657-6735d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
ATC | A | 81 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.657-6736_657-6735d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
ATCTC | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-6738_657-6735d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888473
|
ATCTCTCT others(7): Show |
A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.657-6748_657-6735d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888473 | ||||||
| chr1:44888501
|
C | G | 1 | a0001c0001t0002g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.657-6762G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888501 | ||||||
| chr1:44888544
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.657-6805A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888544 | ||||||
| chr1:44888626
|
AATTT | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-6891_657-6888d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888626 | ||||||
| chr1:44888730
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-6991A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888730 | ||||||
| chr1:44888781
|
G | T | 87 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.657-7042C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888781 | ||||||
| chr1:44888960
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0116a0001c0001t0002g0117 | 3 | HG01255.hp1 HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.657-7221C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44888960 | ||||||
| chr1:44889315
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.657-7576G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889315 | ||||||
| chr1:44889348
|
G | C | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.657-7609C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889348 | ||||||
| chr1:44889390
|
G | A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.657-7651C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889390 | ||||||
| chr1:44889396
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.657-7657C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889396 | ||||||
| chr1:44889536
|
T | TAAAACAA others(303): Show |
5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-7798_657-7797i others(312): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889536 | ||||||
| chr1:44889536
|
T | TAAAACAA others(304): Show |
1 | a0001c0001t0001g0130 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.657-7798_657-7797i others(313): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889536 | ||||||
| chr1:44889638
|
C | T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.656+7717G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889638 | ||||||
| chr1:44889678
|
G | A | 87 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+7677C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44889678 | ||||||
| chr1:44890020
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+7335A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890020 | ||||||
| chr1:44890032
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0288 | 2 | HG01081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.656+7323G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890032 | ||||||
| chr1:44890033
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.656+7322C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890033 | ||||||
| chr1:44890120
|
G | C | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.656+7235C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890120 | ||||||
| chr1:44890180
|
G | A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.656+7175C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890180 | ||||||
| chr1:44890436
|
TTAAA | T | 85 | a0001c0001t0002g0028a0001c0001t0002g0070a0001c0001t0002g0118others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.656+6915_656+6918d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890436 | ||||||
| chr1:44890651
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.656+6704A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890651 | ||||||
| chr1:44890814
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656+6541C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890814 | ||||||
| chr1:44890949
|
C | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+6406G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890949 | ||||||
| chr1:44890960
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0126 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.656+6395G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890960 | ||||||
| chr1:44890966
|
C | T | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.656+6389G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44890966 | ||||||
| chr1:44891068
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.656+6287C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891068 | ||||||
| chr1:44891077
|
G | GA | 62 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(59): Show | 62 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+6277dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891077 | ||||||
| chr1:44891096
|
T | C | 1 | a0001c0002t0001g0253 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.656+6259A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891096 | ||||||
| chr1:44891097
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656+6258A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891097 | ||||||
| chr1:44891240
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656+6115G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891240 | ||||||
| chr1:44891321
|
G | A | 15 | a0001c0001t0002g0028a0001c0002t0001g0147a0001c0002t0001g0163others(12): Show | 15 | HG00408.hp1 HG00609.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.656+6034C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891321 | ||||||
| chr1:44891500
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+5855C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891500 | ||||||
| chr1:44891642
|
A | G | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.656+5713T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891642 | ||||||
| chr1:44891682
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.656+5673T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891682 | ||||||
| chr1:44891813
|
A | G | 21 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0051others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.656+5542T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44891813 | ||||||
| chr1:44892185
|
C | T | 38 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0142others(35): Show | 38 | HG00621.hp2 HG00639.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.656+5170G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892185 | ||||||
| chr1:44892320
|
T | C | 311 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(308): Show | 311 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.656+5035A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892320 | ||||||
| chr1:44892436
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.656+4919G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892436 | ||||||
| chr1:44892459
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+4896T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892459 | ||||||
| chr1:44892503
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.656+4852G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892503 | ||||||
| chr1:44892562
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.656+4793G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892562 | ||||||
| chr1:44892816
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.656+4539G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892816 | ||||||
| chr1:44892855
|
T | C | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.656+4500A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892855 | ||||||
| chr1:44892883
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+4472A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44892883 | ||||||
| chr1:44893157
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.656+4198C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893157 | ||||||
| chr1:44893244
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+4111A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893244 | ||||||
| chr1:44893324
|
C | G | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.656+4031G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893324 | ||||||
| chr1:44893445
|
G | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.656+3910C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893445 | ||||||
| chr1:44893643
|
G | GCT | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.656+3711_656+3712i others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893643 | ||||||
| chr1:44893869
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+3486C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44893869 | ||||||
| chr1:44894179
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656+3176C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44894179 | ||||||
| chr1:44894335
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+3020A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44894335 | ||||||
| chr1:44894615
|
T | G | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.656+2740A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44894615 | ||||||
| chr1:44894986
|
A | C | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.656+2369T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44894986 | ||||||
| chr1:44895020
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.656+2335C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895020 | ||||||
| chr1:44895044
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0105 | 2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.656+2311A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895044 | ||||||
| chr1:44895229
|
G | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+2126C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895229 | ||||||
| chr1:44895240
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.656+2115G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895240 | ||||||
| chr1:44895406
|
C | T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.656+1949G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895406 | ||||||
| chr1:44895474
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.656+1881C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895474 | ||||||
| chr1:44895513
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.656+1842A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895513 | ||||||
| chr1:44895524
|
C | A | 5 | a0001c0001t0002g0052a0001c0001t0002g0072a0001c0001t0002g0076others(2): Show | 5 | HG01123.hp1 HG03492.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+1831G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895524 | ||||||
| chr1:44895526
|
C | A | 24 | a0001c0001t0001g0250a0001c0001t0002g0052a0001c0001t0002g0053others(21): Show | 24 | HG00408.hp2 HG00738.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+1829G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895526 | ||||||
| chr1:44895528
|
C | A | 211 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0250others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.656+1827G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895528 | ||||||
| chr1:44895530
|
A | C | 24 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(21): Show | 24 | HG01243.hp2 HG01891.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+1825T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895530 | ||||||
| chr1:44895532
|
A | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.656+1823T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895532 | ||||||
| chr1:44895784
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.656+1571A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895784 | ||||||
| chr1:44895928
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+1427A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44895928 | ||||||
| chr1:44896034
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.656+1321T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896034 | ||||||
| chr1:44896123
|
C | G | 1 | a0001c0002t0001g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.656+1232G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896123 | ||||||
| chr1:44896373
|
TG | T | 24 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(21): Show | 24 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+981delC | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896373 | ||||||
| chr1:44896375
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+980C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896375 | ||||||
| chr1:44896450
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.656+905C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896450 | ||||||
| chr1:44896529
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.656+826C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896529 | ||||||
| chr1:44896744
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG00639.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.656+611A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896744 | ||||||
| chr1:44896773
|
T | C | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.656+582A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896773 | ||||||
| chr1:44896910
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.656+445C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896910 | ||||||
| chr1:44896919
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.656+436A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44896919 | ||||||
| chr1:44897050
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+305C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44897050 | ||||||
| chr1:44897320
|
T | C | 291 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(288): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.656+35A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 6/11 | chr1 | 44897320 | ||||||
| chr1:44897578
|
G | A | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.567-134C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897578 | ||||||
| chr1:44897628
|
G | C | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.567-184C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897628 | ||||||
| chr1:44897737
|
C | CT | 31 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(28): Show | 31 | HG00323.hp1 HG01167.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.567-294dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897737 | ||||||
| chr1:44897737
|
C | CTT | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-295_567-294dup others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897737 | ||||||
| chr1:44897860
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.567-416G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897860 | ||||||
| chr1:44897862
|
G | A | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.567-418C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897862 | ||||||
| chr1:44897901
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-457A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897901 | ||||||
| chr1:44897934
|
C | A | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.567-490G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897934 | ||||||
| chr1:44897937
|
T | A | 1 | a0001c0001t0002g0087 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.567-493A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44897937 | ||||||
| chr1:44898215
|
T | C | 88 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.567-771A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898215 | ||||||
| chr1:44898362
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-918G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898362 | ||||||
| chr1:44898460
|
A | G | 87 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.567-1016T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898460 | ||||||
| chr1:44898487
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.567-1043T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898487 | ||||||
| chr1:44898596
|
TA | T | 6 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01099.hp2 HG01256.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-1153delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898596 | ||||||
| chr1:44898718
|
G | C | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.567-1274C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898718 | ||||||
| chr1:44898836
|
A | G | 5 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0155others(2): Show | 5 | HG00642.hp1 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-1392T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898836 | ||||||
| chr1:44898955
|
C | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-1511G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44898955 | ||||||
| chr1:44899114
|
T | C | 87 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.567-1670A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899114 | ||||||
| chr1:44899304
|
C | T | 4 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0157others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-1860G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899304 | ||||||
| chr1:44899433
|
A | C | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.567-1989T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899433 | ||||||
| chr1:44899627
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0235others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-2183G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899627 | ||||||
| chr1:44899697
|
G | A | 20 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0230others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.567-2253C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899697 | ||||||
| chr1:44899724
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-2280A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899724 | ||||||
| chr1:44899937
|
C | G | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.567-2493G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899937 | ||||||
| chr1:44899988
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567-2544T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899988 | ||||||
| chr1:44899995
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.567-2551A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44899995 | ||||||
| chr1:44900162
|
A | G | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.567-2718T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900162 | ||||||
| chr1:44900444
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567-3000A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900444 | ||||||
| chr1:44900445
|
C | CA | 96 | a0001c0001t0001g0158a0001c0001t0001g0250a0001c0001t0001g0255others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.567-3002dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900445 | ||||||
| chr1:44900445
|
C | CAA | 12 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0304others(9): Show | 12 | HG00639.hp2 HG01069.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-3003_567-3002d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900445 | ||||||
| chr1:44900575
|
C | T | 4 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-3131G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900575 | ||||||
| chr1:44900651
|
T | A | 290 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(287): Show | 290 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.567-3207A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900651 | ||||||
| chr1:44900715
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.567-3271A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900715 | ||||||
| chr1:44900781
|
A | G | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-3337T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900781 | ||||||
| chr1:44900817
|
C | T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.567-3373G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900817 | ||||||
| chr1:44900818
|
A | G | 93 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(90): Show | 93 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.567-3374T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900818 | ||||||
| chr1:44900893
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.567-3449A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900893 | ||||||
| chr1:44900953
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.567-3509A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44900953 | ||||||
| chr1:44901121
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-3677A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901121 | ||||||
| chr1:44901138
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-3694C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901138 | ||||||
| chr1:44901271
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0089 | 2 | NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.567-3827T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901271 | ||||||
| chr1:44901363
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.567-3919C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901363 | ||||||
| chr1:44901478
|
T | C | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-4034A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901478 | ||||||
| chr1:44901508
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011 | 3 | HG03688.hp2 HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.567-4064G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901508 | ||||||
| chr1:44901550
|
C | CT | 16 | a0001c0001t0002g0042a0001c0001t0002g0049a0001c0001t0002g0061others(13): Show | 16 | HG01243.hp1 HG01358.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.567-4107dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901550 | ||||||
| chr1:44901550
|
CT | C | 30 | a0001c0001t0001g0158a0001c0001t0001g0250a0001c0001t0001g0251others(27): Show | 30 | HG01167.hp2 HG01884.hp2 HG01993.hp2 others(27): Show |
intron_variant | MODIFIER | c.567-4107delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901550 | ||||||
| chr1:44901550
|
CTT | C | 67 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.567-4108_567-4107d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901550 | ||||||
| chr1:44901601
|
C | CA | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-4158dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901601 | ||||||
| chr1:44901619
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-4175G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901619 | ||||||
| chr1:44901637
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.567-4193G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901637 | ||||||
| chr1:44901751
|
G | A | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-4307C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901751 | ||||||
| chr1:44901802
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.567-4358G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901802 | ||||||
| chr1:44901858
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567-4414G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901858 | ||||||
| chr1:44901913
|
A | C | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.567-4469T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44901913 | ||||||
| chr1:44902079
|
C | G | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.567-4635G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902079 | ||||||
| chr1:44902405
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-4961C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902405 | ||||||
| chr1:44902460
|
C | A | 1 | a0001c0002t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.567-5016G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902460 | ||||||
| chr1:44902538
|
C | T | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-5094G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902538 | ||||||
| chr1:44902619
|
C | T | 11 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0038others(8): Show | 11 | HG00280.hp2 HG00544.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.567-5175G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902619 | ||||||
| chr1:44902771
|
C | T | 98 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(95): Show | 98 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.567-5327G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902771 | ||||||
| chr1:44902783
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.567-5339C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902783 | ||||||
| chr1:44902821
|
T | C | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-5377A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902821 | ||||||
| chr1:44902829
|
T | TA | 72 | a0001c0001t0002g0015a0001c0001t0002g0021a0001c0001t0002g0062others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.567-5386dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44902829
|
T | TAA | 117 | a0001c0001t0001g0284a0001c0001t0002g0001a0001c0001t0002g0002others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.567-5387_567-5386d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44902829
|
T | TAAA | 30 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0002g0025others(27): Show | 30 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.567-5388_567-5386d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44902829
|
TAAA | T | 59 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0261others(56): Show | 59 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.567-5388_567-5386d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44902829
|
TAAAA | T | 8 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(5): Show | 8 | HG01069.hp2 HG02922.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.567-5389_567-5386d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44902829
|
TAAAAAAA others(3): Show |
T | 23 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.567-5395_567-5386d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44902829 | ||||||
| chr1:44903129
|
C | G | 20 | a0001c0001t0002g0012a0001c0001t0002g0029a0001c0001t0002g0032others(17): Show | 20 | HG00609.hp2 HG02056.hp2 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.567-5685G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903129 | ||||||
| chr1:44903308
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.567-5864G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903308 | ||||||
| chr1:44903414
|
A | G | 97 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(94): Show | 97 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.567-5970T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903414 | ||||||
| chr1:44903434
|
A | G | 291 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(288): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.567-5990T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903434 | ||||||
| chr1:44903550
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0119 | 2 | NA18998.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.567-6106G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903550 | ||||||
| chr1:44903690
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.567-6246C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903690 | ||||||
| chr1:44903876
|
C | A | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-6432G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903876 | ||||||
| chr1:44903981
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-6537C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44903981 | ||||||
| chr1:44904070
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-6626G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44904070 | ||||||
| chr1:44904115
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-6671C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44904115 | ||||||
| chr1:44904262
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.567-6818T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44904262 | ||||||
| chr1:44904764
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.567-7320G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44904764 | ||||||
| chr1:44905048
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.567-7604G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44905048 | ||||||
| chr1:44905487
|
C | T | 3 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102 | 3 | HG02723.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.567-8043G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44905487 | ||||||
| chr1:44905488
|
G | A | 97 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(94): Show | 97 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.567-8044C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44905488 | ||||||
| chr1:44905636
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.567-8192A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44905636 | ||||||
| chr1:44905762
|
T | C | 11 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0001g0136others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.567-8318A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44905762 | ||||||
| chr1:44906272
|
A | C | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.567-8828T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906272 | ||||||
| chr1:44906340
|
G | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-8896C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906340 | ||||||
| chr1:44906576
|
A | G | 2 | a0001c0001t0002g0005a0001c0002t0001g0172 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.567-9132T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906576 | ||||||
| chr1:44906647
|
A | G | 320 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(317): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.567-9203T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906647 | ||||||
| chr1:44906696
|
G | A | 1 | a0001c0002t0001g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.567-9252C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906696 | ||||||
| chr1:44906839
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.567-9395T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906839 | ||||||
| chr1:44906854
|
C | T | 1 | a0001c0002t0001g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.567-9410G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44906854 | ||||||
| chr1:44907286
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01175.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-9842C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907286 | ||||||
| chr1:44907287
|
C | T | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.567-9843G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907287 | ||||||
| chr1:44907566
|
C | T | 63 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(60): Show | 63 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.567-10122G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907566 | ||||||
| chr1:44907567
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.567-10123T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907567 | ||||||
| chr1:44907784
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567-10340C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907784 | ||||||
| chr1:44907791
|
A | G | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-10347T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907791 | ||||||
| chr1:44907890
|
C | CA | 26 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(23): Show | 26 | HG00544.hp1 HG01175.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.567-10447dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907890 | ||||||
| chr1:44907890
|
CA | C | 28 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(25): Show | 28 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.567-10447delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907890 | ||||||
| chr1:44907890
|
CAA | C | 81 | a0001c0001t0001g0129a0001c0001t0001g0251a0001c0001t0001g0281others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.567-10448_567-1044 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907890 | ||||||
| chr1:44907890
|
CAAA | C | 9 | a0001c0001t0001g0250a0001c0001t0002g0126a0001c0002t0001g0169others(6): Show | 9 | HG00280.hp1 HG00738.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.567-10449_567-1044 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907890 | ||||||
| chr1:44907994
|
G | A | 84 | a0001c0001t0002g0028a0001c0001t0002g0118a0001c0001t0002g0126others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.567-10550C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44907994 | ||||||
| chr1:44908096
|
A | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-10652T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908096 | ||||||
| chr1:44908123
|
A | G | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0219 | 3 | NA18939.hp1 NA18940.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.567-10679T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908123 | ||||||
| chr1:44908224
|
T | C | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0219 | 3 | NA18939.hp1 NA18940.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.567-10780A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908224 | ||||||
| chr1:44908537
|
C | T | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-11093G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908537 | ||||||
| chr1:44908755
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-11311A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908755 | ||||||
| chr1:44908930
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.567-11486A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44908930 | ||||||
| chr1:44909242
|
T | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-11798A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909242 | ||||||
| chr1:44909267
|
C | T | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.567-11823G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909267 | ||||||
| chr1:44909319
|
AT | A | 20 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.567-11876delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909319 | ||||||
| chr1:44909464
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0002g0070 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.567-12020A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909464 | ||||||
| chr1:44909654
|
G | A | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-12210C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909654 | ||||||
| chr1:44909807
|
T | A | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.567-12363A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909807 | ||||||
| chr1:44909853
|
C | T | 182 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.567-12409G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909853 | ||||||
| chr1:44909859
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.567-12415G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909859 | ||||||
| chr1:44909878
|
G | A | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-12434C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909878 | ||||||
| chr1:44909944
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.567-12500A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44909944 | ||||||
| chr1:44910103
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.567-12659T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910103 | ||||||
| chr1:44910162
|
T | C | 64 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-12718A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910162 | ||||||
| chr1:44910236
|
TA | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-12793delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910236 | ||||||
| chr1:44910374
|
C | T | 74 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(71): Show | 74 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.567-12930G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910374 | ||||||
| chr1:44910560
|
C | A | 150 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0159others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.567-13116G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910560 | ||||||
| chr1:44910620
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.567-13176G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910620 | ||||||
| chr1:44910620
|
C | G | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.567-13176G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910620 | ||||||
| chr1:44910631
|
C | CT | 61 | a0001c0001t0001g0284a0001c0001t0002g0001a0001c0001t0002g0004others(58): Show | 61 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.567-13188dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910631 | ||||||
| chr1:44910631
|
CT | C | 13 | a0001c0001t0002g0018a0001c0001t0002g0030a0001c0001t0002g0037others(10): Show | 13 | HG01123.hp1 HG01167.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.567-13188delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910631 | ||||||
| chr1:44910655
|
TTTA | T | 61 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(58): Show | 61 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.567-13214_567-1321 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910655 | ||||||
| chr1:44910656
|
TTA | T | 34 | a0001c0001t0001g0130a0001c0001t0001g0250a0001c0001t0001g0251others(31): Show | 34 | HG01167.hp2 HG01261.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.567-13214_567-1321 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910656 | ||||||
| chr1:44910657
|
TA | T | 64 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0142others(61): Show | 64 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.567-13214delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910657 | ||||||
| chr1:44910658
|
A | T | 18 | a0001c0001t0002g0053a0001c0001t0002g0056a0001c0002t0001g0154others(15): Show | 18 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.567-13214T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910658 | ||||||
| chr1:44910659
|
A | T | 1 | a0001c0002t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.567-13215T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910659 | ||||||
| chr1:44910675
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.567-13231G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910675 | ||||||
| chr1:44910852
|
T | C | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.567-13408A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910852 | ||||||
| chr1:44910938
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.567-13494G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44910938 | ||||||
| chr1:44911065
|
G | A | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.567-13621C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911065 | ||||||
| chr1:44911095
|
T | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG03098.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.567-13651A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911095 | ||||||
| chr1:44911490
|
T | G | 6 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0143others(3): Show | 6 | HG00639.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-14046A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911490 | ||||||
| chr1:44911564
|
C | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0080 | 2 | HG03492.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.567-14120G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911564 | ||||||
| chr1:44911611
|
A | G | 22 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0230others(19): Show | 22 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.567-14167T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911611 | ||||||
| chr1:44911796
|
C | T | 5 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(2): Show | 5 | NA18950.hp2 NA18956.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-14352G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911796 | ||||||
| chr1:44911841
|
A | T | 1 | a0001c0001t0002g0007 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.567-14397T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911841 | ||||||
| chr1:44911869
|
A | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-14425T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911869 | ||||||
| chr1:44911920
|
T | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.567-14476A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44911920 | ||||||
| chr1:44912362
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.566+14266A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912362 | ||||||
| chr1:44912430
|
C | A | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566+14198G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912430 | ||||||
| chr1:44912435
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+14193G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912435 | ||||||
| chr1:44912689
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+13939G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912689 | ||||||
| chr1:44912800
|
G | C | 1 | a0001c0001t0002g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.566+13828C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912800 | ||||||
| chr1:44912953
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+13675A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44912953 | ||||||
| chr1:44913079
|
C | T | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566+13549G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913079 | ||||||
| chr1:44913080
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+13548T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913080 | ||||||
| chr1:44913095
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+13533T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913095 | ||||||
| chr1:44913109
|
T | TA | 14 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0290others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.566+13518dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
T | TAA | 58 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(55): Show | 58 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.566+13517_566+1351 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
T | TAAA | 12 | a0001c0002t0001g0138a0001c0002t0001g0144a0001c0002t0001g0147others(9): Show | 12 | HG01255.hp2 HG01978.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.566+13516_566+1351 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
TA | T | 87 | a0001c0001t0001g0265a0001c0001t0001g0269a0001c0001t0001g0286others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.566+13518delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
TAA | T | 7 | a0001c0001t0001g0319a0001c0001t0001g0321a0001c0001t0002g0039others(4): Show | 7 | HG00323.hp1 HG01891.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.566+13517_566+1351 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
TAAA | T | 35 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(32): Show | 35 | HG01069.hp2 HG01167.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.566+13516_566+1351 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913109
|
TAAAA | T | 13 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01943.hp1 HG02922.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.566+13515_566+1351 others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913109 | ||||||
| chr1:44913261
|
C | G | 1 | a0001c0002t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.566+13367G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913261 | ||||||
| chr1:44913312
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.566+13316G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913312 | ||||||
| chr1:44913501
|
G | GA | 88 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0256others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.566+13126dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913501 | ||||||
| chr1:44913530
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566+13098C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913530 | ||||||
| chr1:44913595
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.566+13033G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913595 | ||||||
| chr1:44913761
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+12867G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913761 | ||||||
| chr1:44913888
|
A | G | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+12740T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44913888 | ||||||
| chr1:44914160
|
A | AT | 73 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(70): Show | 73 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.566+12467dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914160 | ||||||
| chr1:44914405
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+12223A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914405 | ||||||
| chr1:44914468
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+12160A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914468 | ||||||
| chr1:44914498
|
A | T | 2 | a0001c0002t0001g0175a0001c0002t0001g0177 | 2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.566+12130T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914498 | ||||||
| chr1:44914782
|
T | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+11846A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914782 | ||||||
| chr1:44914790
|
G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.566+11838C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914790 | ||||||
| chr1:44914799
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+11829G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914799 | ||||||
| chr1:44914940
|
C | T | 9 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(6): Show | 9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.566+11688G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44914940 | ||||||
| chr1:44915024
|
C | T | 80 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.566+11604G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915024 | ||||||
| chr1:44915027
|
G | T | 2 | a0001c0002t0001g0194a0001c0002t0001g0198 | 2 | NA19009.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.566+11601C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915027 | ||||||
| chr1:44915056
|
T | C | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.566+11572A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915056 | ||||||
| chr1:44915062
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.566+11566C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915062 | ||||||
| chr1:44915093
|
G | A | 8 | a0001c0001t0001g0267a0001c0001t0001g0285a0001c0001t0001g0289others(5): Show | 8 | HG00140.hp1 HG00735.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.566+11535C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915093 | ||||||
| chr1:44915117
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.566+11511C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915117 | ||||||
| chr1:44915231
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.566+11397G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915231 | ||||||
| chr1:44915243
|
C | T | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+11385G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915243 | ||||||
| chr1:44915299
|
CA | C | 66 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.566+11328delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915299 | ||||||
| chr1:44915351
|
A | G | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+11277T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915351 | ||||||
| chr1:44915441
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566+11187T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915441 | ||||||
| chr1:44915505
|
A | G | 321 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(318): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.566+11123T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915505 | ||||||
| chr1:44915525
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.566+11103G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915525 | ||||||
| chr1:44915538
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+11090T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915538 | ||||||
| chr1:44915540
|
T | A | 73 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(70): Show | 73 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.566+11088A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915540 | ||||||
| chr1:44915579
|
C | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+11049G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915579 | ||||||
| chr1:44915693
|
A | G | 1 | a0001c0002t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.566+10935T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915693 | ||||||
| chr1:44915743
|
A | G | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.566+10885T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915743 | ||||||
| chr1:44915759
|
T | A | 1 | a0001c0001t0002g0085 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.566+10869A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915759 | ||||||
| chr1:44915991
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.566+10637A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44915991 | ||||||
| chr1:44916022
|
T | C | 75 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(72): Show | 75 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.566+10606A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916022 | ||||||
| chr1:44916191
|
T | G | 2 | a0001c0001t0002g0114a0001c0001t0002g0125 | 2 | HG02056.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.566+10437A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916191 | ||||||
| chr1:44916561
|
C | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.566+10067G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916561 | ||||||
| chr1:44916650
|
C | A | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+9978G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916650 | ||||||
| chr1:44916652
|
C | T | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.566+9976G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916652 | ||||||
| chr1:44916767
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.566+9861C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916767 | ||||||
| chr1:44916810
|
C | CA | 21 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(18): Show | 21 | HG01243.hp2 HG01981.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.566+9817dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916810 | ||||||
| chr1:44916810
|
C | CAA | 60 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.566+9816_566+9817d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916810 | ||||||
| chr1:44916853
|
A | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+9775T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44916853 | ||||||
| chr1:44917237
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.566+9391A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917237 | ||||||
| chr1:44917300
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+9328G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917300 | ||||||
| chr1:44917535
|
G | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.566+9093C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917535 | ||||||
| chr1:44917704
|
G | T | 100 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(97): Show | 100 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.566+8924C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917704 | ||||||
| chr1:44917710
|
CT | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+8917delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917710 | ||||||
| chr1:44917755
|
C | CT | 25 | a0001c0001t0001g0263a0001c0001t0001g0279a0001c0001t0001g0282others(22): Show | 25 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+8872dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
C | CTT | 17 | a0001c0001t0001g0313a0001c0001t0002g0003a0001c0001t0002g0004others(14): Show | 17 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.566+8871_566+8872d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
C | CTTT | 7 | a0001c0001t0002g0055a0001c0001t0002g0092a0001c0001t0002g0112others(4): Show | 7 | HG02109.hp2 HG02895.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.566+8870_566+8872d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0132 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.566+8861_566+8872d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.566+8857_566+8872d others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CT | C | 58 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(55): Show | 58 | HG00544.hp2 HG01346.hp2 HG01358.hp2 others(55): Show |
intron_variant | MODIFIER | c.566+8872delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTT | C | 37 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0275others(34): Show | 37 | HG00621.hp2 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.566+8871_566+8872d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTT | C | 39 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0002g0007others(36): Show | 39 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.566+8870_566+8872d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTT | C | 36 | a0001c0001t0001g0255a0001c0001t0001g0320a0001c0001t0002g0013others(33): Show | 36 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.566+8869_566+8872d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTT | C | 9 | a0001c0002t0001g0169a0001c0002t0001g0201a0001c0002t0001g0209others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+8868_566+8872d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130 | 3 | NA18971.hp2 NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.566+8863_566+8872d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.566+8861_566+8872d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0131a0001c0001t0001g0302 | 2 | NA18944.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.566+8860_566+8872d others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG00639.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.566+8859_566+8872d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(9): Show |
C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.566+8857_566+8872d others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(10): Show |
C | 24 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(21): Show | 24 | HG01167.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.566+8856_566+8872d others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917755
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0281a0001c0002t0001g0240 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.566+8855_566+8872d others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917755 | ||||||
| chr1:44917796
|
C | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.566+8832G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917796 | ||||||
| chr1:44917858
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0317 | 3 | HG01516.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.566+8770G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917858 | ||||||
| chr1:44917922
|
T | C | 321 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(318): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.566+8706A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44917922 | ||||||
| chr1:44918049
|
A | G | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+8579T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918049 | ||||||
| chr1:44918057
|
G | A | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566+8571C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918057 | ||||||
| chr1:44918072
|
C | CT | 49 | a0001c0001t0001g0259a0001c0001t0002g0001a0001c0001t0002g0002others(46): Show | 49 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.566+8555dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918072 | ||||||
| chr1:44918072
|
CT | C | 7 | a0001c0001t0001g0254a0001c0001t0002g0006a0001c0001t0002g0055others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.566+8555delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918072 | ||||||
| chr1:44918072
|
CTTTT | C | 16 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(13): Show | 16 | HG03098.hp1 HG03130.hp1 HG03225.hp1 others(13): Show |
intron_variant | MODIFIER | c.566+8552_566+8555d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918072 | ||||||
| chr1:44918072
|
CTTTTT | C | 58 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(55): Show | 58 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.566+8551_566+8555d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918072 | ||||||
| chr1:44918109
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566+8519C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918109 | ||||||
| chr1:44918209
|
G | C | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.566+8419C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918209 | ||||||
| chr1:44918357
|
T | C | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566+8271A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918357 | ||||||
| chr1:44918660
|
G | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.566+7968C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918660 | ||||||
| chr1:44918671
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566+7957C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918671 | ||||||
| chr1:44918788
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.566+7840T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918788 | ||||||
| chr1:44918826
|
G | C | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.566+7802C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918826 | ||||||
| chr1:44918959
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+7669G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44918959 | ||||||
| chr1:44919028
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+7600C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919028 | ||||||
| chr1:44919071
|
G | C | 1 | a0001c0002t0001g0211 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.566+7557C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919071 | ||||||
| chr1:44919145
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+7483G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919145 | ||||||
| chr1:44919147
|
A | G | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.566+7481T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919147 | ||||||
| chr1:44919349
|
C | CA | 10 | a0001c0001t0002g0001a0001c0001t0002g0099a0001c0001t0002g0107others(7): Show | 10 | HG01884.hp1 HG02559.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.566+7278dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919349 | ||||||
| chr1:44919349
|
CA | C | 66 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.566+7278delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919349 | ||||||
| chr1:44919715
|
C | CT | 39 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(36): Show | 39 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.566+6912dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919715 | ||||||
| chr1:44919715
|
C | CTT | 66 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.566+6911_566+6912d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919715 | ||||||
| chr1:44919740
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.566+6888G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919740 | ||||||
| chr1:44919785
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+6843G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919785 | ||||||
| chr1:44919793
|
C | T | 1 | a0001c0002t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.566+6835G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919793 | ||||||
| chr1:44919865
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.566+6763G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919865 | ||||||
| chr1:44919866
|
G | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+6762C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919866 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(8): Show | 11 | HG01069.hp2 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.566+6733_566+6744d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0277a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+6732_566+6744d others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(7): Show |
25 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0270others(22): Show | 25 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+6731_566+6744d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(12): Show | 15 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.566+6730_566+6744d others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0266a0001c0001t0001g0282a0001c0001t0001g0290others(4): Show | 7 | NA18941.hp2 NA18962.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.566+6729_566+6744d others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0300 | 2 | NA18969.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.566+6728_566+6744d others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44919883
|
CT | C | 8 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0055others(5): Show | 8 | HG02895.hp1 HG03927.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.566+6744delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44919883 | ||||||
| chr1:44920016
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566+6612C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920016 | ||||||
| chr1:44920038
|
CT | C | 72 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(69): Show | 72 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.566+6589delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920038 | ||||||
| chr1:44920042
|
T | C | 1 | a0001c0002t0001g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.566+6586A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920042 | ||||||
| chr1:44920369
|
T | C | 319 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(316): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.566+6259A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920369 | ||||||
| chr1:44920415
|
A | G | 1 | a0001c0002t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.566+6213T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920415 | ||||||
| chr1:44920520
|
C | T | 3 | a0001c0002t0001g0167a0001c0002t0001g0214a0001c0002t0001g0215 | 3 | HG02083.hp1 HG02132.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.566+6108G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920520 | ||||||
| chr1:44920602
|
A | AT | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0317 | 3 | HG01516.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.566+6025dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920602 | ||||||
| chr1:44920610
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.566+6018G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44920610 | ||||||
| chr1:44921034
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+5594A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921034 | ||||||
| chr1:44921087
|
C | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.566+5541G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921087 | ||||||
| chr1:44921189
|
T | C | 1 | a0001c0002t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.566+5439A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921189 | ||||||
| chr1:44921322
|
T | C | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566+5306A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921322 | ||||||
| chr1:44921513
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+5115A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921513 | ||||||
| chr1:44921893
|
TA | T | 4 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0318others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+4734delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921893 | ||||||
| chr1:44921895
|
TA | T | 79 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(76): Show | 79 | HG00544.hp1 HG01069.hp2 HG01081.hp2 others(76): Show |
intron_variant | MODIFIER | c.566+4732delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921895 | ||||||
| chr1:44921896
|
A | T | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0318others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.566+4732T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921896 | ||||||
| chr1:44921896
|
AT | A | 18 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG01943.hp1 HG02258.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.566+4731delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921896 | ||||||
| chr1:44921898
|
T | A | 157 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(154): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.566+4730A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921898 | ||||||
| chr1:44921899
|
T | A | 13 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.566+4729A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921899 | ||||||
| chr1:44921927
|
T | A | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+4701A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44921927 | ||||||
| chr1:44922160
|
C | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.566+4468G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922160 | ||||||
| chr1:44922183
|
GA | G | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.566+4444delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922183 | ||||||
| chr1:44922211
|
G | T | 2 | a0001c0002t0001g0174a0001c0002t0001g0210 | 2 | HG00408.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.566+4417C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922211 | ||||||
| chr1:44922352
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4276G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922352 | ||||||
| chr1:44922358
|
G | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+4270C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922358 | ||||||
| chr1:44922404
|
T | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4224A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922404 | ||||||
| chr1:44922460
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.566+4168C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922460 | ||||||
| chr1:44922512
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4116C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922512 | ||||||
| chr1:44922568
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.566+4060A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922568 | ||||||
| chr1:44922591
|
C | CA | 119 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(116): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.566+4036dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922591 | ||||||
| chr1:44922591
|
C | CAA | 67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.566+4035_566+4036d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922591 | ||||||
| chr1:44922591
|
C | CAAA | 12 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG01891.hp2 HG02129.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.566+4034_566+4036d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922591 | ||||||
| chr1:44922678
|
A | G | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+3950T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922678 | ||||||
| chr1:44922691
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.566+3937A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922691 | ||||||
| chr1:44922836
|
A | AT | 79 | a0001c0001t0001g0259a0001c0001t0002g0001a0001c0001t0002g0003others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.566+3791dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATT | 75 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0038others(72): Show | 75 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566+3790_566+3791d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTT | 33 | a0001c0001t0002g0035a0001c0001t0002g0069a0001c0002t0001g0134others(30): Show | 33 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.566+3789_566+3791d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(2): Show |
20 | a0001c0001t0001g0266a0001c0001t0001g0269a0001c0001t0001g0270others(17): Show | 20 | HG00140.hp1 HG01081.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.566+3783_566+3791d others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(3): Show |
24 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(21): Show | 24 | HG00544.hp1 HG00735.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.566+3782_566+3791d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(4): Show |
10 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0267others(7): Show | 10 | HG01243.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.566+3781_566+3791d others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0255a0001c0001t0001g0276 | 3 | HG02071.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.566+3780_566+3791d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.566+3778_566+3791d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG01943.hp1 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+3777_566+3791d others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566+3776_566+3791d others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.566+3774_566+3791d others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.566+3770_566+3791d others(24): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0001g0319 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566+3791_566+3792i others(32): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922836
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.566+3780_566+3791d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922836 | ||||||
| chr1:44922848
|
T | A | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.566+3780A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922848 | ||||||
| chr1:44922849
|
T | A | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.566+3779A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922849 | ||||||
| chr1:44922871
|
A | G | 1 | a0001c0002t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.566+3757T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922871 | ||||||
| chr1:44922892
|
C | A | 1 | a0001c0001t0001g0315 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.566+3736G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922892 | ||||||
| chr1:44922903
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566+3725G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922903 | ||||||
| chr1:44922960
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566+3668C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44922960 | ||||||
| chr1:44923218
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+3410G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923218 | ||||||
| chr1:44923314
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.566+3314A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923314 | ||||||
| chr1:44923484
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.566+3144G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923484 | ||||||
| chr1:44923654
|
C | CTT | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+2973_566+2974i others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923654 | ||||||
| chr1:44923940
|
C | CT | 38 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0159others(35): Show | 38 | HG01167.hp2 HG01175.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.566+2687dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923940 | ||||||
| chr1:44923940
|
CT | C | 12 | a0001c0001t0001g0287a0001c0001t0002g0071a0001c0001t0002g0073others(9): Show | 12 | HG00639.hp1 HG02056.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.566+2687delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923940 | ||||||
| chr1:44923976
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+2652A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44923976 | ||||||
| chr1:44924379
|
A | C | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.566+2249T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924379 | ||||||
| chr1:44924385
|
A | T | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.566+2243T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924385 | ||||||
| chr1:44924432
|
T | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0056 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.566+2196A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924432 | ||||||
| chr1:44924678
|
G | A | 1 | a0002c0007t0001g0166 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.566+1950C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924678 | ||||||
| chr1:44924777
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566+1851A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924777 | ||||||
| chr1:44924863
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566+1765G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924863 | ||||||
| chr1:44924904
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.566+1724A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44924904 | ||||||
| chr1:44925156
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566+1472G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925156 | ||||||
| chr1:44925238
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.566+1390G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925238 | ||||||
| chr1:44925275
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+1353C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925275 | ||||||
| chr1:44925297
|
G | A | 4 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0150others(1): Show | 4 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+1331C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925297 | ||||||
| chr1:44925372
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.566+1256C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925372 | ||||||
| chr1:44925376
|
T | A | 1 | a0001c0001t0002g0077 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.566+1252A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925376 | ||||||
| chr1:44925658
|
G | A | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.566+970C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925658 | ||||||
| chr1:44925794
|
C | A | 50 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(47): Show | 50 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.566+834G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925794 | ||||||
| chr1:44925854
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566+774C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925854 | ||||||
| chr1:44925952
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.566+676C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925952 | ||||||
| chr1:44925989
|
G | A | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.566+639C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925989 | ||||||
| chr1:44925993
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.566+635G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44925993 | ||||||
| chr1:44926056
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.566+572G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44926056 | ||||||
| chr1:44926190
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566+438A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44926190 | ||||||
| chr1:44926268
|
C | A | 188 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(185): Show | 188 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.566+360G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44926268 | ||||||
| chr1:44926491
|
T | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.566+137A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 5/11 | chr1 | 44926491 | ||||||
| chr1:44926980
|
C | CAAAAAAT others(158): Show |
1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-242_455-241ins others(165): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44926980 | ||||||
| chr1:44927088
|
C | G | 2 | a0001c0001t0002g0034a0001c0001t0002g0040 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.455-349G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927088 | ||||||
| chr1:44927101
|
T | G | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.455-362A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927101 | ||||||
| chr1:44927283
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-544G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927283 | ||||||
| chr1:44927416
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.455-677A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927416 | ||||||
| chr1:44927605
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-866T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927605 | ||||||
| chr1:44927668
|
G | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-929C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927668 | ||||||
| chr1:44927747
|
T | A | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-1008A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927747 | ||||||
| chr1:44927841
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-1102G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927841 | ||||||
| chr1:44927904
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.455-1165C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927904 | ||||||
| chr1:44927957
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-1218A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44927957 | ||||||
| chr1:44928060
|
G | C | 1 | a0001c0001t0002g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.455-1321C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928060 | ||||||
| chr1:44928346
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.455-1607G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928346 | ||||||
| chr1:44928499
|
CGT | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(2): Show | 5 | NA18944.hp2 NA18971.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-1762_455-1761d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928499 | ||||||
| chr1:44928500
|
G | GT | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG03098.hp1 HG03130.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-1762dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928500 | ||||||
| chr1:44928500
|
GT | G | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.455-1762delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928500 | ||||||
| chr1:44928584
|
A | G | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.455-1845T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928584 | ||||||
| chr1:44928638
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.455-1899A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928638 | ||||||
| chr1:44928638
|
T | G | 3 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0249 | 3 | HG02257.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.455-1899A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928638 | ||||||
| chr1:44928697
|
A | G | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.455-1958T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928697 | ||||||
| chr1:44928950
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-2211T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44928950 | ||||||
| chr1:44929001
|
T | A | 1 | a0001c0002t0001g0252 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.455-2262A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44929001 | ||||||
| chr1:44929014
|
G | T | 1 | a0001c0002t0001g0211 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.455-2275C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44929014 | ||||||
| chr1:44929051
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.455-2312C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44929051 | ||||||
| chr1:44929060
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.455-2321T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44929060 | ||||||
| chr1:44929462
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-2723A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44929462 | ||||||
| chr1:44930061
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0107a0001c0001t0002g0109 | 3 | HG02647.hp2 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.455-3322C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930061 | ||||||
| chr1:44930082
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.455-3343A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930082 | ||||||
| chr1:44930459
|
G | A | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-3720C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930459 | ||||||
| chr1:44930516
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-3777G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930516 | ||||||
| chr1:44930666
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-3927T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930666 | ||||||
| chr1:44930704
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-3965T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930704 | ||||||
| chr1:44930724
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-3985A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44930724 | ||||||
| chr1:44931119
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4380A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931119 | ||||||
| chr1:44931247
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.455-4508C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931247 | ||||||
| chr1:44931367
|
A | G | 1 | a0001c0002t0001g0171 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.455-4628T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931367 | ||||||
| chr1:44931428
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.455-4689A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931428 | ||||||
| chr1:44931776
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-5037G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931776 | ||||||
| chr1:44931779
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.455-5040C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931779 | ||||||
| chr1:44931835
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-5096G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931835 | ||||||
| chr1:44931891
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-5152A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44931891 | ||||||
| chr1:44932016
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.455-5277C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932016 | ||||||
| chr1:44932116
|
A | AAC | 4 | a0001c0001t0002g0029a0001c0001t0002g0101a0001c0002t0001g0169others(1): Show | 4 | HG00609.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-5379_455-5378d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932116 | ||||||
| chr1:44932116
|
A | AACACACA others(1): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-5385_455-5378d others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932116 | ||||||
| chr1:44932116
|
AACAC | A | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.455-5381_455-5378d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932116 | ||||||
| chr1:44932367
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-5628A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932367 | ||||||
| chr1:44932398
|
T | C | 1 | a0001c0002t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.455-5659A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932398 | ||||||
| chr1:44932610
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.455-5871A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932610 | ||||||
| chr1:44932611
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.455-5872G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932611 | ||||||
| chr1:44932735
|
TAAAAC | T | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.455-6001_455-5997d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932735 | ||||||
| chr1:44932793
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-6054A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932793 | ||||||
| chr1:44932854
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.455-6115G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44932854 | ||||||
| chr1:44933146
|
A | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0073 | 2 | NA18943.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.455-6407T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933146 | ||||||
| chr1:44933214
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.455-6475T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933214 | ||||||
| chr1:44933434
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-6695G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933434 | ||||||
| chr1:44933484
|
G | A | 10 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0285others(7): Show | 10 | HG00140.hp1 HG00735.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.455-6745C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933484 | ||||||
| chr1:44933567
|
G | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0291a0001c0001t0001g0292others(5): Show | 8 | HG00544.hp1 NA18950.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-6828C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933567 | ||||||
| chr1:44933712
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-6973A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933712 | ||||||
| chr1:44933820
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.455-7081G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933820 | ||||||
| chr1:44933893
|
C | T | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455-7154G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933893 | ||||||
| chr1:44933956
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-7217G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933956 | ||||||
| chr1:44933997
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.455-7258G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44933997 | ||||||
| chr1:44934032
|
G | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.455-7293C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934032 | ||||||
| chr1:44934074
|
A | T | 71 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(68): Show | 71 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.455-7335T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934074 | ||||||
| chr1:44934077
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.455-7338C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934077 | ||||||
| chr1:44934139
|
T | C | 5 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0055others(2): Show | 5 | HG03927.hp2 NA18942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+7367A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934139 | ||||||
| chr1:44934221
|
C | T | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+7285G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934221 | ||||||
| chr1:44934225
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+7281C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934225 | ||||||
| chr1:44934242
|
C | CA | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+7263dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934242 | ||||||
| chr1:44934270
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.454+7236G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934270 | ||||||
| chr1:44934271
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.454+7235C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934271 | ||||||
| chr1:44934307
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.454+7199T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934307 | ||||||
| chr1:44934308
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.454+7198C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934308 | ||||||
| chr1:44934309
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.454+7197T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934309 | ||||||
| chr1:44934399
|
A | AAAAAC | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+7102_454+7106d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934399 | ||||||
| chr1:44934399
|
AAAAAC | A | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+7102_454+7106d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934399 | ||||||
| chr1:44934591
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+6915T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934591 | ||||||
| chr1:44934600
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+6906C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934600 | ||||||
| chr1:44934746
|
C | T | 4 | a0001c0002t0001g0221a0001c0002t0001g0225a0001c0002t0001g0226others(1): Show | 4 | HG00323.hp1 HG01256.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+6760G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934746 | ||||||
| chr1:44934981
|
G | A | 9 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0051others(6): Show | 9 | HG01071.hp2 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+6525C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44934981 | ||||||
| chr1:44935083
|
C | G | 1 | a0001c0002t0001g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.454+6423G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935083 | ||||||
| chr1:44935112
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.454+6394A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935112 | ||||||
| chr1:44935155
|
T | C | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+6351A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935155 | ||||||
| chr1:44935326
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0120 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.454+6180T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935326 | ||||||
| chr1:44935387
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454+6119A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935387 | ||||||
| chr1:44935454
|
T | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+6052A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935454 | ||||||
| chr1:44935748
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+5758T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935748 | ||||||
| chr1:44935860
|
C | T | 1 | a0001c0002t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.454+5646G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935860 | ||||||
| chr1:44935941
|
G | GT | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG03098.hp1 HG03130.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+5564dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935941 | ||||||
| chr1:44935941
|
GT | G | 70 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.454+5564delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44935941 | ||||||
| chr1:44936024
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+5482T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936024 | ||||||
| chr1:44936072
|
A | C | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+5434T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936072 | ||||||
| chr1:44936149
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.454+5357C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936149 | ||||||
| chr1:44936198
|
C | A | 1 | a0001c0002t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.454+5308G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936198 | ||||||
| chr1:44936235
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+5271A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936235 | ||||||
| chr1:44936288
|
G | C | 1 | a0001c0001t0001g0266 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.454+5218C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936288 | ||||||
| chr1:44936298
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0317 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.454+5208C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936298 | ||||||
| chr1:44936425
|
C | CA | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+5080dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936425 | ||||||
| chr1:44936425
|
CA | C | 161 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.454+5080delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936425 | ||||||
| chr1:44936515
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.454+4991G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936515 | ||||||
| chr1:44936856
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.454+4650G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44936856 | ||||||
| chr1:44937235
|
G | A | 14 | a0001c0002t0001g0147a0001c0002t0001g0163a0001c0002t0001g0173others(11): Show | 14 | HG00408.hp1 HG00609.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.454+4271C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937235 | ||||||
| chr1:44937424
|
T | C | 1 | a0001c0002t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454+4082A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937424 | ||||||
| chr1:44937459
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.454+4047C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937459 | ||||||
| chr1:44937606
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.454+3900C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937606 | ||||||
| chr1:44937641
|
T | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+3865A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937641 | ||||||
| chr1:44937649
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.454+3857G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937649 | ||||||
| chr1:44937654
|
C | A | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.454+3852G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937654 | ||||||
| chr1:44937840
|
C | T | 13 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(10): Show | 13 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.454+3666G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937840 | ||||||
| chr1:44937880
|
T | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.454+3626A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937880 | ||||||
| chr1:44937883
|
C | CA | 24 | a0001c0001t0001g0159a0001c0001t0002g0002a0001c0001t0002g0005others(21): Show | 24 | HG01071.hp2 HG01123.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.454+3622dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
C | CAA | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0132others(8): Show | 11 | HG00140.hp2 HG01175.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.454+3621_454+3622d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
C | CAAA | 6 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG01099.hp2 HG02129.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+3620_454+3622d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.454+3613_454+3622d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CA | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0012others(48): Show | 51 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.454+3622delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAA | C | 9 | a0001c0001t0001g0319a0001c0001t0002g0053a0001c0001t0002g0056others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+3621_454+3622d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAA | C | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(3): Show | 6 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+3617_454+3622d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(2): Show |
C | 20 | a0001c0001t0001g0291a0001c0002t0001g0138a0001c0002t0001g0140others(17): Show | 20 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.454+3614_454+3622d others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(3): Show |
C | 78 | a0001c0001t0001g0263a0001c0001t0001g0268a0001c0001t0001g0279others(75): Show | 78 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.454+3613_454+3622d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(4): Show |
C | 45 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(42): Show | 45 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.454+3612_454+3622d others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0317 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.454+3611_454+3622d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(6): Show |
C | 21 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0230others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.454+3610_454+3622d others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG01167.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+3609_454+3622d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937883
|
CAAAAAAA others(13): Show |
C | 1 | a0006c0003t0002g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.454+3603_454+3622d others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937883 | ||||||
| chr1:44937980
|
C | CT | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.454+3525dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937980 | ||||||
| chr1:44937989
|
A | T | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.454+3517T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44937989 | ||||||
| chr1:44938057
|
G | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.454+3449C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938057 | ||||||
| chr1:44938109
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+3397G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938109 | ||||||
| chr1:44938235
|
C | A | 1 | a0001c0002t0001g0249 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.454+3271G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938235 | ||||||
| chr1:44938367
|
A | AGC | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+3138_454+3139i others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938367 | ||||||
| chr1:44938393
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.454+3113A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938393 | ||||||
| chr1:44938416
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.454+3090C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938416 | ||||||
| chr1:44938478
|
T | TTC | 4 | a0001c0001t0002g0066a0001c0001t0002g0114a0001c0001t0002g0125others(1): Show | 4 | HG01175.hp1 HG02056.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+3026_454+3027d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938478 | ||||||
| chr1:44938502
|
G | C | 61 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(58): Show | 61 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.454+3004C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938502 | ||||||
| chr1:44938502
|
GT | G | 14 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+3003delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938502 | ||||||
| chr1:44938503
|
T | TCTG | 58 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(55): Show | 58 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.454+3002_454+3003i others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938503 | ||||||
| chr1:44938552
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.454+2954C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938552 | ||||||
| chr1:44938566
|
C | T | 50 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(47): Show | 50 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.454+2940G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938566 | ||||||
| chr1:44938641
|
G | A | 11 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0001g0136others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.454+2865C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938641 | ||||||
| chr1:44938673
|
G | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+2833C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938673 | ||||||
| chr1:44938698
|
A | G | 295 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(292): Show | 295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.454+2808T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938698 | ||||||
| chr1:44938908
|
T | G | 2 | a0001c0002t0001g0149a0001c0002t0001g0199 | 2 | HG01975.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.454+2598A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938908 | ||||||
| chr1:44938943
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+2563A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44938943 | ||||||
| chr1:44939030
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2476T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939030 | ||||||
| chr1:44939035
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2471T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939035 | ||||||
| chr1:44939036
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2470C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939036 | ||||||
| chr1:44939046
|
G | GAGCCAAT others(9): Show |
1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2459_454+2460i others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939046 | ||||||
| chr1:44939060
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2446G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939060 | ||||||
| chr1:44939090
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2416T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939090 | ||||||
| chr1:44939091
|
G | T | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2415C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939091 | ||||||
| chr1:44939098
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2408A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939098 | ||||||
| chr1:44939100
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.454+2406A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939100 | ||||||
| chr1:44939101
|
C | CA | 32 | a0001c0001t0001g0259a0001c0001t0002g0006a0001c0001t0002g0012others(29): Show | 32 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.454+2404dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939101 | ||||||
| chr1:44939101
|
CA | C | 9 | a0001c0001t0001g0254a0001c0001t0002g0034a0001c0001t0002g0057others(6): Show | 9 | HG01943.hp2 HG02258.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+2404delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939101 | ||||||
| chr1:44939101
|
CAA | C | 17 | a0001c0001t0001g0130a0001c0001t0001g0255a0001c0001t0001g0263others(14): Show | 17 | HG02071.hp2 HG02922.hp1 NA18943.hp2 others(14): Show |
intron_variant | MODIFIER | c.454+2403_454+2404d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939101 | ||||||
| chr1:44939101
|
CAAA | C | 53 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(50): Show | 53 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.454+2402_454+2404d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939101 | ||||||
| chr1:44939290
|
T | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+2216A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939290 | ||||||
| chr1:44939355
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+2151G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939355 | ||||||
| chr1:44939385
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.454+2121T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939385 | ||||||
| chr1:44939593
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+1913A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939593 | ||||||
| chr1:44939594
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.454+1912C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939594 | ||||||
| chr1:44939614
|
C | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0002t0001g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+1892G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939614 | ||||||
| chr1:44939693
|
A | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+1813T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939693 | ||||||
| chr1:44939724
|
T | C | 18 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(15): Show | 18 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.454+1782A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939724 | ||||||
| chr1:44939728
|
TAA | T | 16 | a0001c0001t0002g0006a0001c0001t0002g0098a0001c0001t0002g0099others(13): Show | 16 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.454+1776_454+1777d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939728 | ||||||
| chr1:44939796
|
CAA | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.454+1708_454+1709d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939796 | ||||||
| chr1:44939971
|
G | A | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.454+1535C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44939971 | ||||||
| chr1:44940059
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.454+1447C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940059 | ||||||
| chr1:44940174
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454+1332C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940174 | ||||||
| chr1:44940385
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454+1121C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940385 | ||||||
| chr1:44940419
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.454+1087T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940419 | ||||||
| chr1:44940451
|
T | TA | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.454+1054dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940451 | ||||||
| chr1:44940532
|
C | A | 1 | a0001c0002t0001g0216 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.454+974G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940532 | ||||||
| chr1:44940549
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.454+957G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940549 | ||||||
| chr1:44940720
|
G | A | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.454+786C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940720 | ||||||
| chr1:44940774
|
AAAAG | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+728_454+731del others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940774 | ||||||
| chr1:44940888
|
C | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.454+618G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940888 | ||||||
| chr1:44940905
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.454+601C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44940905 | ||||||
| chr1:44941035
|
C | T | 3 | a0001c0002t0001g0167a0001c0002t0001g0214a0001c0002t0001g0215 | 3 | HG02083.hp1 HG02132.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.454+471G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44941035 | ||||||
| chr1:44941240
|
C | A | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.454+266G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44941240 | ||||||
| chr1:44941241
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+265C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44941241 | ||||||
| chr1:44941267
|
C | T | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+239G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44941267 | ||||||
| chr1:44941429
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+77C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 4/11 | chr1 | 44941429 | ||||||
| chr1:44941751
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.295-86T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44941751 | ||||||
| chr1:44942108
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.295-443A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942108 | ||||||
| chr1:44942121
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.295-456T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942121 | ||||||
| chr1:44942356
|
T | A | 100 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(97): Show | 100 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.295-691A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942356 | ||||||
| chr1:44942377
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0002g0105a0001c0002t0001g0170 | 2 | HG02970.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.295-722_295-713dup others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(5): Show |
3 | a0001c0001t0002g0006a0001c0002t0001g0179a0001c0002t0001g0180 | 3 | HG02622.hp1 NA19074.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.295-724_295-713dup others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295-726_295-713dup others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.295-730_295-713dup others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(15): Show |
1 | a0001c0002t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-734_295-713dup others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(97): Show |
1 | a0001c0001t0001g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.295-713_295-712ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(103): Show |
1 | a0001c0001t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.295-713_295-712ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(99): Show |
1 | a0001c0001t0001g0276 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.295-713_295-712ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(103): Show |
1 | a0001c0001t0001g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.295-713_295-712ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(101): Show |
6 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0293others(3): Show | 6 | HG02132.hp1 NA18956.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-713_295-712ins others(108): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(103): Show |
4 | a0001c0001t0001g0271a0001c0001t0001g0274a0001c0001t0001g0288others(1): Show | 4 | HG01081.hp2 NA18983.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-713_295-712ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(131): Show |
1 | a0001c0001t0001g0292 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.295-713_295-712ins others(138): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(107): Show |
1 | a0001c0001t0001g0319 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295-713_295-712ins others(114): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
T | TTATATAT others(101): Show |
1 | a0001c0001t0001g0290 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.295-713_295-712ins others(108): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
TTA | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0062others(5): Show | 8 | HG00323.hp2 HG01346.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-714_295-713del others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0065others(2): Show | 5 | HG01071.hp2 HG01175.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-722_295-713del others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
TTATATAT others(7): Show |
T | 1 | a0001c0002t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.295-726_295-713del others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942377
|
TTATATAT others(9): Show |
T | 1 | a0001c0002t0001g0151 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.295-728_295-713del others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942377 | ||||||
| chr1:44942378
|
T | TATATATA others(99): Show |
1 | a0001c0001t0001g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.295-714_295-713ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(97): Show |
2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | NA18962.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.295-714_295-713ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(99): Show |
1 | a0001c0001t0001g0310 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.295-714_295-713ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(101): Show |
2 | a0001c0001t0001g0309a0001c0001t0001g0317 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.295-714_295-713ins others(108): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(101): Show |
1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.295-714_295-713ins others(108): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(97): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0275 | 2 | HG02083.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.295-714_295-713ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(99): Show |
1 | a0001c0001t0001g0289 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.295-714_295-713ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942378
|
T | TATATATA others(99): Show |
8 | a0001c0001t0001g0263a0001c0001t0001g0279a0001c0001t0001g0291others(5): Show | 8 | HG01993.hp1 HG02148.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-714_295-713ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942378 | ||||||
| chr1:44942379
|
A | T | 4 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(1): Show | 4 | HG02723.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-714T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942379 | ||||||
| chr1:44942380
|
T | TATATATA others(97): Show |
1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295-716_295-715ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(97): Show |
1 | a0001c0001t0001g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.295-716_295-715ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(99): Show |
3 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0280 | 3 | HG01943.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.295-716_295-715ins others(106): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(101): Show |
1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295-716_295-715ins others(108): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(95): Show |
1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295-716_295-715ins others(102): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(97): Show |
3 | a0001c0001t0001g0285a0001c0001t0001g0311a0001c0001t0001g0313 | 3 | HG00544.hp1 HG01346.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.295-716_295-715ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942380
|
T | TATATATA others(105): Show |
1 | a0001c0001t0001g0318 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-716_295-715ins others(112): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942380 | ||||||
| chr1:44942382
|
T | TATATATA others(97): Show |
1 | a0001c0001t0001g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.295-718_295-717ins others(104): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942382 | ||||||
| chr1:44942382
|
T | TATATATA others(95): Show |
2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.295-718_295-717ins others(102): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942382 | ||||||
| chr1:44942382
|
T | TATATATA others(103): Show |
1 | a0001c0001t0001g0320 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-718_295-717ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942382 | ||||||
| chr1:44942384
|
T | TATATATA others(95): Show |
1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.295-720_295-719ins others(102): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942384 | ||||||
| chr1:44942386
|
T | TATATATG others(91): Show |
1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.295-722_295-721ins others(98): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942386 | ||||||
| chr1:44942388
|
T | TATATGTG others(65): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-724_295-723ins others(72): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942388 | ||||||
| chr1:44942390
|
T | TATATGTG others(57): Show |
1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.295-726_295-725ins others(64): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942390 | ||||||
| chr1:44942390
|
T | TATGTGTG others(103): Show |
1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-726_295-725ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942390 | ||||||
| chr1:44942391
|
A | ATGTGTGT others(103): Show |
1 | a0001c0001t0001g0296 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.295-727_295-726ins others(110): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942391 | ||||||
| chr1:44942391
|
A | ATGTGTGT others(105): Show |
1 | a0001c0001t0001g0294 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.295-727_295-726ins others(112): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942391 | ||||||
| chr1:44942391
|
A | ATGTGTGT others(105): Show |
5 | a0001c0001t0001g0265a0001c0001t0001g0269a0001c0001t0001g0283others(2): Show | 5 | NA18943.hp2 NA18985.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-727_295-726ins others(112): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942391 | ||||||
| chr1:44942391
|
A | ATGTGTGT others(107): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0316 | 2 | NA18954.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.295-727_295-726ins others(114): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942391 | ||||||
| chr1:44942393
|
A | ATGTATAT others(67): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | NA18944.hp2 NA18989.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.295-729_295-728ins others(74): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942393 | ||||||
| chr1:44942393
|
A | ATGTATAT others(69): Show |
1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.295-729_295-728ins others(76): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942393 | ||||||
| chr1:44942393
|
A | G | 11 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0269others(8): Show | 11 | NA18943.hp2 NA18983.hp1 NA18985.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-728T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942393 | ||||||
| chr1:44942395
|
A | G | 21 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01081.hp2 HG01261.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.295-730T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942395 | ||||||
| chr1:44942397
|
A | ATACATAC others(79): Show |
1 | a0001c0001t0001g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.295-733_295-732ins others(86): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942397 | ||||||
| chr1:44942397
|
A | G | 39 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(36): Show | 39 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.295-732T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942397 | ||||||
| chr1:44942399
|
A | ACATACAT others(77): Show |
1 | a0001c0001t0001g0297 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.295-735_295-734ins others(84): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942399 | ||||||
| chr1:44942399
|
A | G | 31 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(28): Show | 31 | HG00544.hp1 HG01346.hp1 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.295-734T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942399 | ||||||
| chr1:44942399
|
ATATATAT others(25): Show |
A | 1 | a0001c0002t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.295-766_295-735del others(32): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942399 | ||||||
| chr1:44942400
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.295-735A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942400 | ||||||
| chr1:44942401
|
A | G | 6 | a0001c0001t0001g0277a0001c0001t0001g0304a0001c0001t0001g0311others(3): Show | 6 | HG00544.hp1 HG01069.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-736T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942401 | ||||||
| chr1:44942403
|
A | G | 4 | a0001c0001t0001g0264a0001c0001t0001g0277a0001c0001t0001g0304others(1): Show | 4 | HG01069.hp2 HG01243.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-738T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942403 | ||||||
| chr1:44942404
|
TATATATA others(4): Show |
T | 1 | a0001c0002t0001g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.295-750_295-740del others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942404 | ||||||
| chr1:44942405
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG03098.hp1 HG03130.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-740T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942405 | ||||||
| chr1:44942407
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.295-742T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942407 | ||||||
| chr1:44942409
|
A | T | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.295-744T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942409 | ||||||
| chr1:44942409
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0002g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.295-757_295-745del others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942409 | ||||||
| chr1:44942410
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA18969.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.295-745A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942410 | ||||||
| chr1:44942410
|
TA | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0114 | 3 | HG02056.hp1 HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.295-746delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942410 | ||||||
| chr1:44942411
|
A | ATTTT | 5 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0002t0001g0236others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-747_295-746ins others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942411 | ||||||
| chr1:44942411
|
A | T | 3 | a0001c0002t0001g0232a0001c0002t0001g0243a0001c0002t0001g0248 | 3 | HG02559.hp2 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.295-746T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942411 | ||||||
| chr1:44942412
|
TA | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0018 | 3 | HG01167.hp1 HG01258.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.295-748delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942412 | ||||||
| chr1:44942413
|
A | AT | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0215 | 3 | HG02132.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.295-749dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942413 | ||||||
| chr1:44942413
|
A | ATTTT | 6 | a0001c0001t0002g0031a0001c0001t0002g0078a0001c0002t0001g0242others(3): Show | 6 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-749_295-748ins others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942413 | ||||||
| chr1:44942413
|
A | T | 20 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(17): Show | 20 | HG00639.hp2 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-748T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942413 | ||||||
| chr1:44942415
|
A | ATTTT | 4 | a0001c0001t0002g0025a0001c0001t0002g0037a0001c0001t0002g0070others(1): Show | 4 | HG02015.hp1 HG04228.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-751_295-750ins others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942415 | ||||||
| chr1:44942415
|
A | ATTTTT | 12 | a0001c0001t0002g0029a0001c0001t0002g0034a0001c0001t0002g0054others(9): Show | 12 | HG00280.hp1 HG00609.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-751_295-750ins others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942415 | ||||||
| chr1:44942415
|
A | ATTTTTT | 5 | a0001c0001t0002g0096a0001c0002t0001g0233a0001c0002t0001g0239others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-751_295-750ins others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942415 | ||||||
| chr1:44942415
|
A | T | 44 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0001others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.295-750T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942415 | ||||||
| chr1:44942416
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.295-751A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942416 | ||||||
| chr1:44942417
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0061 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(21): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(23): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(33): Show |
1 | a0001c0002t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(40): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0045 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(24): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(19): Show |
1 | a0001c0002t0001g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(26): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(22): Show |
1 | a0001c0002t0001g0191 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(29): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(17): Show |
2 | a0001c0002t0001g0140a0002c0007t0001g0166 | 2 | HG03516.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(24): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0186 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(27): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(13): Show |
3 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0175 | 3 | HG00609.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(16): Show |
2 | a0001c0002t0001g0134a0001c0002t0001g0135 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(23): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0002g0095a0001c0001t0002g0100 | 2 | HG00408.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(21): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(23): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(27): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0056a0001c0001t0002g0104 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(10): Show |
2 | a0001c0002t0001g0154a0001c0002t0001g0211 | 2 | HG03209.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(11): Show |
2 | a0001c0002t0001g0148a0001c0002t0001g0182 | 2 | HG01123.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(21): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0002g0046a0001c0002t0001g0196 | 2 | HG02273.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(8): Show |
3 | a0001c0002t0001g0163a0001c0002t0001g0177a0001c0002t0001g0181 | 3 | NA18956.hp2 NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0001g0188 | 3 | HG01069.hp1 HG01071.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(12): Show |
2 | a0001c0002t0001g0174a0001c0002t0001g0201 | 2 | HG00408.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(13): Show |
1 | a0001c0002t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(21): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(6): Show |
3 | a0001c0002t0001g0153a0001c0002t0001g0208a0001c0002t0001g0252 | 3 | HG01975.hp1 HG02970.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0124 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(8): Show |
3 | a0001c0002t0001g0150a0001c0002t0001g0176a0001c0002t0001g0210 | 3 | HG00642.hp2 NA18966.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0098a0001c0002t0001g0156 | 2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.295-753_295-752ins others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0002g0091a0001c0002t0001g0138a0001c0002t0001g0139 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(11): Show |
4 | a0001c0002t0001g0133a0001c0002t0001g0146a0001c0002t0001g0195others(1): Show | 4 | HG01975.hp2 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-753_295-752ins others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(4): Show |
2 | a0001c0002t0001g0165a0001c0002t0001g0178 | 2 | HG01261.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0001g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(3): Show |
1 | a0001c0002t0001g0147 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.295-753_295-752ins others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0002g0075a0001c0001t0002g0092 | 2 | HG03486.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0281 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0164 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0001g0144 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATTT others(4): Show |
2 | a0001c0001t0001g0278a0001c0001t0002g0040 | 2 | HG03486.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.295-753_295-752ins others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATATTTTT others(4): Show |
1 | a0001c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.295-753_295-752ins others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATTTTTTT others(3): Show |
1 | a0001c0002t0001g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.295-762_295-753dup others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0207 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.295-766_295-753dup others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942417
|
A | T | 80 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0001others(77): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.295-752T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942417 | ||||||
| chr1:44942418
|
T | TA | 5 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0001g0303others(2): Show | 5 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-754_295-753ins others(1): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATATATA others(4): Show |
1 | a0001c0002t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.295-754_295-753ins others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATATATA others(6): Show |
4 | a0001c0001t0002g0080a0001c0001t0002g0118a0001c0001t0002g0126others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-754_295-753ins others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATATATA others(8): Show |
1 | a0001c0001t0002g0072 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.295-754_295-753ins others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATATATA others(10): Show |
1 | a0001c0002t0001g0173 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.295-754_295-753ins others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATATATA others(12): Show |
1 | a0001c0001t0002g0052 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.295-754_295-753ins others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942418
|
T | TATGTGTA others(66): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA18969.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.295-754_295-753ins others(73): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942418 | ||||||
| chr1:44942419
|
T | A | 72 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(69): Show | 72 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.295-754A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942419 | ||||||
| chr1:44942420
|
T | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(11): Show | 14 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-755A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942420 | ||||||
| chr1:44942421
|
T | A | 70 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.295-756A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942421 | ||||||
| chr1:44942422
|
T | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(11): Show | 14 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-757A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942422 | ||||||
| chr1:44942423
|
T | A | 68 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0132others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.295-758A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942423 | ||||||
| chr1:44942424
|
T | A | 12 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-759A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942424 | ||||||
| chr1:44942425
|
T | A | 66 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0158others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.295-760A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942425 | ||||||
| chr1:44942426
|
T | A | 10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-761A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942426 | ||||||
| chr1:44942427
|
T | A | 60 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0255others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.295-762A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942427 | ||||||
| chr1:44942428
|
T | A | 7 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0001g0294others(4): Show | 7 | HG01069.hp2 HG01243.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-763A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942428 | ||||||
| chr1:44942429
|
T | A | 55 | a0001c0001t0001g0159a0001c0001t0001g0256a0001c0001t0001g0257others(52): Show | 55 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.295-764A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942429 | ||||||
| chr1:44942430
|
T | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | HG01069.hp2 HG02109.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-765A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942430 | ||||||
| chr1:44942431
|
T | A | 25 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(22): Show | 25 | HG01081.hp2 HG01346.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-766A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942431 | ||||||
| chr1:44942432
|
T | A | 1 | a0001c0001t0001g0303 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.295-767A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942432 | ||||||
| chr1:44942433
|
T | A | 8 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-768A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942433 | ||||||
| chr1:44942443
|
T | C | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.295-778A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942443 | ||||||
| chr1:44942444
|
T | C | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.295-779A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942444 | ||||||
| chr1:44942485
|
C | T | 4 | a0001c0002t0001g0169a0001c0002t0001g0200a0001c0002t0001g0202others(1): Show | 4 | HG00738.hp2 HG03704.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-820G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942485 | ||||||
| chr1:44942491
|
G | A | 5 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0055others(2): Show | 5 | HG03927.hp2 NA18942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-826C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942491 | ||||||
| chr1:44942558
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-893C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942558 | ||||||
| chr1:44942596
|
T | A | 1 | a0001c0001t0002g0025 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.295-931A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942596 | ||||||
| chr1:44942597
|
T | C | 50 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(47): Show | 50 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.295-932A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942597 | ||||||
| chr1:44942617
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-952C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942617 | ||||||
| chr1:44942768
|
A | G | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-1103T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942768 | ||||||
| chr1:44942769
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.295-1104T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942769 | ||||||
| chr1:44942835
|
ATTTAT | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG01981.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-1175_295-1171d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942835 | ||||||
| chr1:44942886
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1221G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942886 | ||||||
| chr1:44942887
|
C | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.295-1222G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44942887 | ||||||
| chr1:44943016
|
C | T | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG03098.hp1 HG03130.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-1351G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943016 | ||||||
| chr1:44943047
|
C | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1382G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943047 | ||||||
| chr1:44943101
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1436G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943101 | ||||||
| chr1:44943152
|
C | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.295-1487G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943152 | ||||||
| chr1:44943153
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.295-1488C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943153 | ||||||
| chr1:44943196
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.295-1531T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943196 | ||||||
| chr1:44943235
|
C | T | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-1570G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943235 | ||||||
| chr1:44943368
|
C | CTATCTA | 28 | a0001c0001t0001g0256a0001c0001t0002g0005a0001c0001t0002g0012others(25): Show | 28 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-1709_295-1704d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943368 | ||||||
| chr1:44943368
|
C | CTATCTAT others(5): Show |
3 | a0001c0001t0002g0042a0001c0001t0002g0115a0001c0002t0001g0196 | 3 | HG01081.hp1 HG02738.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.295-1715_295-1704d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943368 | ||||||
| chr1:44943368
|
CTATCTA | C | 100 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.295-1709_295-1704d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943368 | ||||||
| chr1:44943368
|
CTATCTAT others(5): Show |
C | 51 | a0001c0001t0001g0159a0001c0001t0001g0255a0001c0001t0001g0263others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.295-1715_295-1704d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943368 | ||||||
| chr1:44943368
|
CTATCTAT others(11): Show |
C | 3 | a0001c0001t0001g0254a0001c0001t0001g0309a0001c0001t0001g0317 | 3 | HG01516.hp1 HG01517.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.295-1721_295-1704d others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943368 | ||||||
| chr1:44943399
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1734A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943399 | ||||||
| chr1:44943503
|
T | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.295-1838A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943503 | ||||||
| chr1:44943564
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-1899G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943564 | ||||||
| chr1:44943753
|
C | T | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-2088G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943753 | ||||||
| chr1:44943754
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG03471.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-2089C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943754 | ||||||
| chr1:44943871
|
C | T | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-2206G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943871 | ||||||
| chr1:44943872
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.295-2207C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943872 | ||||||
| chr1:44943962
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.295-2297G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44943962 | ||||||
| chr1:44944212
|
T | A | 24 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0269others(21): Show | 24 | HG00544.hp1 HG02071.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.295-2547A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944212 | ||||||
| chr1:44944246
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-2581G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944246 | ||||||
| chr1:44944494
|
C | CA | 18 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(15): Show | 18 | HG01346.hp1 HG02129.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-2830dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944494 | ||||||
| chr1:44944494
|
CA | C | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG02145.hp2 HG02976.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-2830delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944494 | ||||||
| chr1:44944619
|
C | G | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.295-2954G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944619 | ||||||
| chr1:44944900
|
A | AT | 11 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0046others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-3236dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944900 | ||||||
| chr1:44944900
|
AT | A | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-3236delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44944900 | ||||||
| chr1:44945251
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-3586C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945251 | ||||||
| chr1:44945254
|
TA | T | 68 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.295-3590delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945254 | ||||||
| chr1:44945553
|
CA | C | 72 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(69): Show | 72 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.295-3889delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945553 | ||||||
| chr1:44945591
|
G | GA | 10 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0051others(7): Show | 10 | HG01071.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-3927dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945591 | ||||||
| chr1:44945591
|
GA | G | 195 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.295-3927delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945591 | ||||||
| chr1:44945598
|
A | G | 1 | a0001c0002t0001g0164 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.295-3933T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945598 | ||||||
| chr1:44945641
|
G | A | 60 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(57): Show | 60 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.295-3976C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945641 | ||||||
| chr1:44945725
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-4060T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945725 | ||||||
| chr1:44945802
|
T | C | 1 | a0001c0002t0001g0173 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.295-4137A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945802 | ||||||
| chr1:44945880
|
T | G | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.295-4215A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44945880 | ||||||
| chr1:44946014
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.295-4349C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946014 | ||||||
| chr1:44946028
|
G | C | 1 | a0001c0002t0001g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.295-4363C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946028 | ||||||
| chr1:44946110
|
G | A | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0259others(22): Show | 25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-4445C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946110 | ||||||
| chr1:44946217
|
A | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.295-4552T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946217 | ||||||
| chr1:44946312
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-4647T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946312 | ||||||
| chr1:44946399
|
GAAGA | G | 23 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0001g0269others(20): Show | 23 | HG00544.hp1 HG02071.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.295-4738_295-4735d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946399 | ||||||
| chr1:44946444
|
C | CTTTTTTT others(3): Show |
80 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(77): Show | 80 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.295-4789_295-4780d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946444 | ||||||
| chr1:44946444
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-4790_295-4780d others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946444 | ||||||
| chr1:44946604
|
A | C | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.295-4939T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946604 | ||||||
| chr1:44946627
|
C | CT | 155 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.295-4963dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946627 | ||||||
| chr1:44946630
|
T | C | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0130others(2): Show | 5 | NA18944.hp2 NA18971.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-4965A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946630 | ||||||
| chr1:44946631
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.295-4966A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946631 | ||||||
| chr1:44946666
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-5001A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946666 | ||||||
| chr1:44946738
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-5073G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946738 | ||||||
| chr1:44946779
|
G | C | 1 | a0001c0001t0002g0030 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.295-5114C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44946779 | ||||||
| chr1:44947276
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-5611A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44947276 | ||||||
| chr1:44947476
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.295-5811C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44947476 | ||||||
| chr1:44947750
|
C | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-6085G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44947750 | ||||||
| chr1:44947961
|
C | T | 65 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(62): Show | 65 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.295-6296G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44947961 | ||||||
| chr1:44948174
|
A | G | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.295-6509T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948174 | ||||||
| chr1:44948375
|
T | A | 1 | a0001c0002t0001g0164 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.295-6710A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948375 | ||||||
| chr1:44948435
|
C | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.295-6770G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948435 | ||||||
| chr1:44948552
|
A | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01099.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-6887T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948552 | ||||||
| chr1:44948611
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.295-6946C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948611 | ||||||
| chr1:44948761
|
T | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.295-7096A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948761 | ||||||
| chr1:44948864
|
CT | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(72): Show | 75 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.295-7200delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948864 | ||||||
| chr1:44948959
|
C | A | 1 | a0001c0002t0001g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.295-7294G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948959 | ||||||
| chr1:44948959
|
C | G | 94 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.295-7294G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44948959 | ||||||
| chr1:44949423
|
T | C | 100 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(97): Show | 100 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.295-7758A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44949423 | ||||||
| chr1:44949762
|
C | G | 1 | a0001c0002t0001g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.295-8097G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44949762 | ||||||
| chr1:44949796
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.295-8131A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44949796 | ||||||
| chr1:44950433
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.295-8768G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950433 | ||||||
| chr1:44950703
|
T | A | 1 | a0001c0002t0001g0249 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.295-9038A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950703 | ||||||
| chr1:44950772
|
T | C | 6 | a0001c0001t0002g0098a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-9107A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950772 | ||||||
| chr1:44950856
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.295-9191A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950856 | ||||||
| chr1:44950929
|
TCCA | T | 67 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.295-9267_295-9265d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950929 | ||||||
| chr1:44950949
|
G | A | 50 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(47): Show | 50 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.295-9284C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950949 | ||||||
| chr1:44950969
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.295-9304C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44950969 | ||||||
| chr1:44951157
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0040 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.295-9492G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951157 | ||||||
| chr1:44951228
|
G | A | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-9563C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951228 | ||||||
| chr1:44951469
|
C | CT | 4 | a0001c0002t0001g0137a0001c0002t0001g0150a0001c0002t0001g0151others(1): Show | 4 | HG00642.hp2 HG01258.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-9805dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951469 | ||||||
| chr1:44951473
|
T | TG | 295 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(292): Show | 295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.295-9809dupC | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951473 | ||||||
| chr1:44951512
|
T | C | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.295-9847A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951512 | ||||||
| chr1:44951529
|
T | G | 2 | a0001c0002t0001g0162a0001c0002t0001g0201 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.295-9864A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951529 | ||||||
| chr1:44951791
|
C | CT | 177 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.295-10127dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951791 | ||||||
| chr1:44951791
|
C | CTT | 13 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(10): Show | 13 | HG01891.hp2 HG01943.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-10128_295-1012 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951791 | ||||||
| chr1:44951811
|
G | A | 5 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0192others(2): Show | 5 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-10146C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951811 | ||||||
| chr1:44951812
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.295-10147C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951812 | ||||||
| chr1:44951871
|
T | A | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.295-10206A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951871 | ||||||
| chr1:44951912
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-10247G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951912 | ||||||
| chr1:44951950
|
GCTAATTT others(305): Show |
G | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-10597_295-1028 others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951950 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(1): Show |
7 | a0001c0001t0002g0012a0001c0001t0002g0032a0001c0001t0002g0033others(4): Show | 7 | NA18939.hp2 NA18950.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-10297_295-1029 others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0060a0001c0002t0001g0155a0001c0002t0001g0162 | 3 | HG00642.hp1 HG02055.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.295-10299_295-1029 others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(4): Show |
7 | a0001c0001t0002g0111a0001c0002t0001g0201a0001c0002t0001g0203others(4): Show | 7 | HG02258.hp2 HG02922.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-10300_295-1029 others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(5): Show |
13 | a0001c0001t0002g0110a0001c0002t0001g0170a0001c0002t0001g0174others(10): Show | 13 | HG00408.hp1 HG00609.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-10301_295-1029 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(6): Show |
24 | a0001c0001t0002g0075a0001c0001t0002g0099a0001c0001t0002g0100others(21): Show | 24 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.295-10302_295-1029 others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(7): Show |
24 | a0001c0001t0002g0098a0001c0001t0002g0105a0001c0001t0002g0107others(21): Show | 24 | HG00621.hp2 HG00639.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.295-10303_295-1029 others(18): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(8): Show |
11 | a0001c0001t0002g0006a0001c0001t0002g0056a0001c0002t0001g0133others(8): Show | 11 | HG01123.hp2 HG01255.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-10304_295-1029 others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0002g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295-10305_295-1029 others(20): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0064a0001c0002t0001g0168a0001c0002t0001g0194 | 3 | HG00621.hp1 HG03239.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.295-10306_295-1029 others(21): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(11): Show |
11 | a0001c0001t0002g0026a0001c0001t0002g0029a0001c0001t0002g0037others(8): Show | 11 | HG00609.hp2 HG02015.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-10307_295-1029 others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(12): Show |
15 | a0001c0001t0002g0030a0001c0001t0002g0038a0001c0001t0002g0043others(12): Show | 15 | HG00544.hp2 HG01175.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.295-10308_295-1029 others(23): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(13): Show |
7 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0027others(4): Show | 7 | HG02602.hp1 HG03471.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-10309_295-1029 others(24): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(14): Show |
8 | a0001c0001t0002g0053a0001c0001t0002g0070a0001c0002t0001g0134others(5): Show | 8 | HG00280.hp1 HG00738.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-10310_295-1029 others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(15): Show |
5 | a0001c0001t0002g0071a0001c0001t0002g0083a0001c0002t0001g0138others(2): Show | 5 | HG00738.hp1 HG03516.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-10311_295-1029 others(26): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(16): Show |
8 | a0001c0001t0002g0031a0001c0001t0002g0035a0001c0001t0002g0048others(5): Show | 8 | HG00408.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-10312_295-1029 others(27): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(17): Show |
5 | a0001c0001t0002g0041a0001c0001t0002g0045a0001c0001t0002g0051others(2): Show | 5 | HG00280.hp2 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-10313_295-1029 others(28): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(18): Show |
12 | a0001c0001t0002g0034a0001c0001t0002g0040a0001c0001t0002g0044others(9): Show | 12 | HG00735.hp2 HG01243.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-10314_295-1029 others(29): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0002g0039 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.295-10315_295-1029 others(30): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(21): Show |
2 | a0001c0001t0002g0054a0001c0001t0002g0062 | 2 | HG03704.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.295-10290_295-1028 others(32): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(22): Show |
1 | a0001c0001t0002g0036 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.295-10290_295-1028 others(33): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(23): Show |
3 | a0001c0001t0002g0003a0001c0001t0002g0063a0004c0006t0001g0228 | 3 | HG00323.hp1 HG01071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.295-10290_295-1028 others(34): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(24): Show |
1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.295-10290_295-1028 others(35): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(26): Show |
2 | a0001c0002t0001g0136a0001c0002t0001g0221 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.295-10290_295-1028 others(37): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(28): Show |
1 | a0001c0002t0001g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.295-10290_295-1028 others(39): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
A | ATTTTTTT others(30): Show |
1 | a0001c0001t0002g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.295-10290_295-1028 others(41): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
AT | A | 9 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0002g0022others(6): Show | 9 | HG01346.hp2 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-10290delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951954
|
ATTTTTTT others(1): Show |
A | 11 | a0001c0002t0001g0230a0001c0002t0001g0233a0001c0002t0001g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-10297_295-1029 others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951954 | ||||||
| chr1:44951986
|
G | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0115a0001c0001t0002g0116others(2): Show | 5 | HG01081.hp1 HG01515.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-10321C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44951986 | ||||||
| chr1:44952028
|
A | T | 24 | a0001c0001t0001g0254a0001c0001t0001g0259a0001c0001t0001g0278others(21): Show | 24 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.295-10363T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952028 | ||||||
| chr1:44952111
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0046 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.295-10446G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952111 | ||||||
| chr1:44952143
|
T | A | 1 | a0001c0002t0001g0153 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.295-10478A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952143 | ||||||
| chr1:44952215
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.295-10550C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952215 | ||||||
| chr1:44952297
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-10632C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952297 | ||||||
| chr1:44952498
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.295-10833A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952498 | ||||||
| chr1:44952556
|
A | ATT | 90 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(87): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.295-10893_295-1089 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952556 | ||||||
| chr1:44952556
|
AT | A | 91 | a0001c0001t0001g0129a0001c0001t0001g0250a0001c0001t0001g0251others(88): Show | 91 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.295-10892delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952556 | ||||||
| chr1:44952690
|
C | T | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.295-11025G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952690 | ||||||
| chr1:44952751
|
A | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01099.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.295-11086T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952751 | ||||||
| chr1:44952842
|
A | G | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-11177T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952842 | ||||||
| chr1:44952900
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-11235G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952900 | ||||||
| chr1:44952919
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.295-11254A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44952919 | ||||||
| chr1:44953042
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.295-11377A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953042 | ||||||
| chr1:44953090
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-11425C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953090 | ||||||
| chr1:44953131
|
C | A | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-11466G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953131 | ||||||
| chr1:44953151
|
T | TA | 169 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.295-11487dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953151 | ||||||
| chr1:44953151
|
T | TAA | 34 | a0001c0001t0001g0130a0001c0001t0001g0250a0001c0001t0001g0251others(31): Show | 34 | HG01167.hp2 HG01358.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.295-11488_295-1148 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953151 | ||||||
| chr1:44953263
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.295-11598T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953263 | ||||||
| chr1:44953264
|
G | GA | 9 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0051others(6): Show | 9 | HG01071.hp2 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-11600dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953264 | ||||||
| chr1:44953264
|
GA | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-11600delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953264 | ||||||
| chr1:44953343
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.295-11678A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953343 | ||||||
| chr1:44953493
|
C | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-11828G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953493 | ||||||
| chr1:44953553
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.295-11888A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953553 | ||||||
| chr1:44953585
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-11920A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953585 | ||||||
| chr1:44953598
|
G | A | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-11933C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953598 | ||||||
| chr1:44953645
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-11980A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953645 | ||||||
| chr1:44953706
|
C | T | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.295-12041G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953706 | ||||||
| chr1:44953941
|
C | T | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-12276G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953941 | ||||||
| chr1:44953966
|
C | G | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-12301G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953966 | ||||||
| chr1:44953966
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.295-12301G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44953966 | ||||||
| chr1:44954181
|
CAGG | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-12519_295-1251 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44954181 | ||||||
| chr1:44954195
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-12530G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44954195 | ||||||
| chr1:44954395
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.295-12730C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44954395 | ||||||
| chr1:44954691
|
C | G | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.295-13026G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44954691 | ||||||
| chr1:44954763
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.295-13098C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44954763 | ||||||
| chr1:44955388
|
G | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-13723C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44955388 | ||||||
| chr1:44955520
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.295-13855G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44955520 | ||||||
| chr1:44955582
|
T | C | 1 | a0001c0002t0001g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.295-13917A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44955582 | ||||||
| chr1:44955601
|
T | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-13936A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44955601 | ||||||
| chr1:44955765
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-14100G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44955765 | ||||||
| chr1:44956078
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.295-14413C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956078 | ||||||
| chr1:44956140
|
T | A | 16 | a0001c0002t0001g0162a0001c0002t0001g0169a0001c0002t0001g0200others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.295-14475A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956140 | ||||||
| chr1:44956153
|
G | C | 11 | a0001c0001t0002g0071a0001c0001t0002g0073a0001c0001t0002g0077others(8): Show | 11 | HG02056.hp2 NA18943.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-14488C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956153 | ||||||
| chr1:44956157
|
T | A | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-14492A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956157 | ||||||
| chr1:44956207
|
C | A | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0219 | 3 | NA18939.hp1 NA18940.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.295-14542G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956207 | ||||||
| chr1:44956301
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(2): Show | 5 | HG02698.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-14636C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956301 | ||||||
| chr1:44956430
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295-14765C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956430 | ||||||
| chr1:44956476
|
C | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-14811G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956476 | ||||||
| chr1:44956488
|
T | TA | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.295-14824dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956488 | ||||||
| chr1:44956675
|
T | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-15010A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956675 | ||||||
| chr1:44956858
|
T | G | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295-15193A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44956858 | ||||||
| chr1:44957025
|
G | C | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-15360C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957025 | ||||||
| chr1:44957049
|
A | G | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.295-15384T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957049 | ||||||
| chr1:44957123
|
G | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.295-15458C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957123 | ||||||
| chr1:44957244
|
C | T | 3 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102 | 3 | HG02723.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.295-15579G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957244 | ||||||
| chr1:44957257
|
C | CCCTGTAT others(11): Show |
81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-15593_295-1559 others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957257 | ||||||
| chr1:44957259
|
T | A | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-15594A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957259 | ||||||
| chr1:44957588
|
T | C | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-15923A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957588 | ||||||
| chr1:44957718
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.295-16053C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44957718 | ||||||
| chr1:44958048
|
A | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.295-16383T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958048 | ||||||
| chr1:44958114
|
G | A | 50 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(47): Show | 50 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.295-16449C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958114 | ||||||
| chr1:44958116
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.295-16451G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958116 | ||||||
| chr1:44958147
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-16482C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958147 | ||||||
| chr1:44958271
|
A | G | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-16606T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958271 | ||||||
| chr1:44958684
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-17019C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958684 | ||||||
| chr1:44958709
|
A | G | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-17044T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958709 | ||||||
| chr1:44958773
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295-17108T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958773 | ||||||
| chr1:44958833
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.295-17168C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958833 | ||||||
| chr1:44958837
|
G | C | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.295-17172C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958837 | ||||||
| chr1:44958847
|
A | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-17182T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958847 | ||||||
| chr1:44958883
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-17218G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958883 | ||||||
| chr1:44958986
|
A | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-17321T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44958986 | ||||||
| chr1:44959584
|
T | C | 3 | a0001c0001t0001g0259a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG03041.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-17919A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44959584 | ||||||
| chr1:44959633
|
C | G | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.295-17968G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44959633 | ||||||
| chr1:44959967
|
T | C | 1 | a0001c0002t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.295-18302A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44959967 | ||||||
| chr1:44960267
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+18048A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960267 | ||||||
| chr1:44960325
|
C | T | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.294+17990G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960325 | ||||||
| chr1:44960366
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+17949C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960366 | ||||||
| chr1:44960415
|
G | A | 4 | a0001c0002t0001g0221a0001c0002t0001g0225a0001c0002t0001g0226others(1): Show | 4 | HG00323.hp1 HG01256.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+17900C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960415 | ||||||
| chr1:44960494
|
C | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+17821G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960494 | ||||||
| chr1:44960521
|
C | T | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+17794G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960521 | ||||||
| chr1:44960528
|
A | G | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.294+17787T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960528 | ||||||
| chr1:44960532
|
C | T | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.294+17783G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960532 | ||||||
| chr1:44960544
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+17771G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960544 | ||||||
| chr1:44960592
|
C | T | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+17723G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960592 | ||||||
| chr1:44960629
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+17686G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960629 | ||||||
| chr1:44960807
|
G | C | 1 | a0001c0002t0005g0231 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.294+17508C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960807 | ||||||
| chr1:44960854
|
C | T | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.294+17461G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960854 | ||||||
| chr1:44960918
|
AC | A | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+17396delG | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44960918 | ||||||
| chr1:44961040
|
TA | T | 23 | a0001c0001t0002g0025a0001c0002t0001g0147a0001c0002t0001g0164others(20): Show | 23 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+17274delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961040 | ||||||
| chr1:44961085
|
T | C | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+17230A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961085 | ||||||
| chr1:44961252
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+17063C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961252 | ||||||
| chr1:44961286
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.294+17029G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961286 | ||||||
| chr1:44961316
|
C | CA | 41 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.294+16998dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961316 | ||||||
| chr1:44961316
|
C | CAA | 55 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(52): Show | 55 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.294+16997_294+1699 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961316 | ||||||
| chr1:44961316
|
CA | C | 18 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(15): Show | 18 | HG01256.hp1 HG01515.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.294+16998delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961316 | ||||||
| chr1:44961396
|
C | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+16919G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961396 | ||||||
| chr1:44961402
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+16913G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961402 | ||||||
| chr1:44961472
|
A | G | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.294+16843T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961472 | ||||||
| chr1:44961480
|
C | T | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.294+16835G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961480 | ||||||
| chr1:44961702
|
T | A | 1 | a0001c0002t0001g0208 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.294+16613A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961702 | ||||||
| chr1:44961876
|
T | A | 1 | a0001c0002t0001g0211 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.294+16439A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961876 | ||||||
| chr1:44961898
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+16417T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961898 | ||||||
| chr1:44961974
|
T | C | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+16341A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44961974 | ||||||
| chr1:44962188
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+16127C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962188 | ||||||
| chr1:44962204
|
A | ACAT | 20 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(17): Show | 20 | HG01346.hp1 HG01943.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.294+16108_294+1611 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCAAC others(5): Show |
2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.294+16110_294+1611 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCAT | 231 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0263others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.294+16105_294+1611 others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCATC others(2): Show |
25 | a0001c0001t0001g0132a0001c0001t0001g0251a0001c0001t0001g0291others(22): Show | 25 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.294+16102_294+1611 others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCATC others(5): Show |
7 | a0001c0001t0001g0131a0001c0001t0001g0250a0001c0002t0001g0170others(4): Show | 7 | HG02976.hp1 NA18944.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+16099_294+1611 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCATC others(8): Show |
5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG00639.hp1 NA18969.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+16096_294+1611 others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | ACATCATC others(11): Show |
1 | a0001c0001t0002g0104 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.294+16093_294+1611 others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
A | T | 19 | a0001c0002t0001g0230a0001c0002t0001g0233a0001c0002t0001g0234others(16): Show | 19 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.294+16111T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962204
|
ACATCATC others(5): Show |
A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+16099_294+1611 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962204 | ||||||
| chr1:44962255
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0001g0199 | 2 | HG01975.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.294+16060C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962255 | ||||||
| chr1:44962467
|
C | G | 64 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(61): Show | 64 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.294+15848G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962467 | ||||||
| chr1:44962471
|
G | A | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+15844C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962471 | ||||||
| chr1:44962569
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+15746G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962569 | ||||||
| chr1:44962837
|
T | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01099.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.294+15478A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962837 | ||||||
| chr1:44962928
|
G | A | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(7): Show | 10 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+15387C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962928 | ||||||
| chr1:44962970
|
A | C | 1 | a0001c0001t0001g0311 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.294+15345T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44962970 | ||||||
| chr1:44963014
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.294+15301C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963014 | ||||||
| chr1:44963123
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.294+15192C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963123 | ||||||
| chr1:44963231
|
C | CA | 6 | a0001c0001t0001g0313a0001c0001t0001g0318a0001c0001t0001g0319others(3): Show | 6 | HG00544.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+15083dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963231 | ||||||
| chr1:44963235
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+15080T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963235 | ||||||
| chr1:44963240
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.294+15075G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963240 | ||||||
| chr1:44963254
|
A | C | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.294+15061T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963254 | ||||||
| chr1:44963271
|
G | A | 295 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(292): Show | 295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.294+15044C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963271 | ||||||
| chr1:44963599
|
TGCCTAAG others(6): Show |
T | 2 | a0001c0001t0001g0277a0001c0001t0001g0304 | 2 | HG01069.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.294+14703_294+1471 others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963599 | ||||||
| chr1:44963620
|
T | G | 1 | a0001c0002t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.294+14695A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963620 | ||||||
| chr1:44963658
|
T | C | 1 | a0001c0002t0004g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.294+14657A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963658 | ||||||
| chr1:44963666
|
T | C | 1 | a0001c0002t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.294+14649A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963666 | ||||||
| chr1:44963693
|
T | C | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.294+14622A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963693 | ||||||
| chr1:44963785
|
C | A | 67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.294+14530G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963785 | ||||||
| chr1:44963928
|
C | T | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+14387G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963928 | ||||||
| chr1:44963942
|
G | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01099.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.294+14373C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44963942 | ||||||
| chr1:44964010
|
T | A | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+14305A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964010 | ||||||
| chr1:44964067
|
A | G | 77 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.294+14248T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964067 | ||||||
| chr1:44964131
|
C | CA | 116 | a0001c0001t0001g0131a0001c0001t0001g0158a0001c0001t0001g0159others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.294+14183dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964131 | ||||||
| chr1:44964131
|
C | CAA | 26 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(23): Show | 26 | HG01243.hp2 HG01517.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.294+14182_294+1418 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964131 | ||||||
| chr1:44964131
|
C | CAAA | 51 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(48): Show | 51 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.294+14181_294+1418 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964131 | ||||||
| chr1:44964173
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+14142G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964173 | ||||||
| chr1:44964215
|
A | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.294+14100T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964215 | ||||||
| chr1:44964315
|
T | C | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.294+14000A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964315 | ||||||
| chr1:44964456
|
T | C | 3 | a0001c0002t0001g0242a0001c0002t0001g0243a0001c0002t0001g0244 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294+13859A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964456 | ||||||
| chr1:44964511
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.294+13804A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964511 | ||||||
| chr1:44964546
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+13769G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964546 | ||||||
| chr1:44964557
|
A | G | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(7): Show | 10 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+13758T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44964557 | ||||||
| chr1:44965009
|
G | T | 1 | a0001c0002t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.294+13306C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965009 | ||||||
| chr1:44965275
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01099.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.294+13040T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965275 | ||||||
| chr1:44965491
|
T | TA | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+12823_294+1282 others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965491 | ||||||
| chr1:44965608
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.294+12707A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965608 | ||||||
| chr1:44965634
|
C | CT | 31 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(28): Show | 31 | HG01069.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.294+12680dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
C | CTT | 51 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0254others(48): Show | 51 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.294+12679_294+1268 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
C | CTTT | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG01358.hp2 HG02273.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.294+12678_294+1268 others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.294+12669_294+1268 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
CT | C | 48 | a0001c0001t0002g0085a0001c0002t0001g0133a0001c0002t0001g0134others(45): Show | 48 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.294+12680delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
CTT | C | 21 | a0001c0002t0001g0144a0001c0002t0001g0187a0001c0002t0001g0219others(18): Show | 21 | HG01167.hp2 HG01255.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.294+12679_294+1268 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965634
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.294+12669_294+1268 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965634 | ||||||
| chr1:44965742
|
C | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+12573G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965742 | ||||||
| chr1:44965771
|
C | G | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG01943.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+12544G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965771 | ||||||
| chr1:44965919
|
T | C | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+12396A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965919 | ||||||
| chr1:44965945
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+12370A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965945 | ||||||
| chr1:44965972
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.294+12343T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965972 | ||||||
| chr1:44965992
|
A | G | 101 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 101 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.294+12323T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44965992 | ||||||
| chr1:44966211
|
A | G | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+12104T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966211 | ||||||
| chr1:44966255
|
T | C | 294 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(291): Show | 294 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.294+12060A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966255 | ||||||
| chr1:44966262
|
A | AC | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+12052dupG | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966262 | ||||||
| chr1:44966330
|
T | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+11985A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966330 | ||||||
| chr1:44966387
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+11928G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966387 | ||||||
| chr1:44966438
|
C | CAA | 66 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0256others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.294+11875_294+1187 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966438 | ||||||
| chr1:44966438
|
C | CAAAA | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+11873_294+1187 others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966438 | ||||||
| chr1:44966438
|
CAA | C | 74 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(71): Show | 74 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.294+11875_294+1187 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966438 | ||||||
| chr1:44966472
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG00639.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.294+11843A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966472 | ||||||
| chr1:44966556
|
G | T | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.294+11759C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966556 | ||||||
| chr1:44966666
|
A | G | 6 | a0001c0001t0002g0052a0001c0001t0002g0072a0001c0001t0002g0076others(3): Show | 6 | HG01123.hp1 HG03017.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+11649T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966666 | ||||||
| chr1:44966720
|
T | C | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+11595A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966720 | ||||||
| chr1:44966862
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294+11453C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966862 | ||||||
| chr1:44966964
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+11351G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44966964 | ||||||
| chr1:44967049
|
C | T | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+11266G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967049 | ||||||
| chr1:44967147
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.294+11168A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967147 | ||||||
| chr1:44967172
|
C | T | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+11143G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967172 | ||||||
| chr1:44967189
|
G | C | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.294+11126C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967189 | ||||||
| chr1:44967419
|
C | T | 4 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0155others(1): Show | 4 | HG00642.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+10896G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967419 | ||||||
| chr1:44967466
|
C | T | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+10849G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967466 | ||||||
| chr1:44967467
|
G | A | 1 | a0001c0002t0001g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.294+10848C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967467 | ||||||
| chr1:44967739
|
C | CA | 25 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0265others(22): Show | 25 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.294+10575dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967739 | ||||||
| chr1:44967739
|
CA | C | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(7): Show | 10 | HG02273.hp1 HG03098.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+10575delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967739 | ||||||
| chr1:44967739
|
CAA | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+10574_294+1057 others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967739 | ||||||
| chr1:44967843
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+10472C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44967843 | ||||||
| chr1:44968014
|
G | A | 1 | a0001c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.294+10301C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968014 | ||||||
| chr1:44968016
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.294+10299G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968016 | ||||||
| chr1:44968017
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+10298C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968017 | ||||||
| chr1:44968047
|
T | TAAATAA | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02630.hp1 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.294+10262_294+1026 others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968047 | ||||||
| chr1:44968047
|
T | TAAATAAA others(5): Show |
67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.294+10256_294+1026 others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968047 | ||||||
| chr1:44968317
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+9998C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968317 | ||||||
| chr1:44968372
|
G | GA | 15 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 15 | HG01978.hp2 HG02148.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.294+9942dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968372 | ||||||
| chr1:44968372
|
G | GAA | 70 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255others(67): Show | 70 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.294+9941_294+9942d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968372 | ||||||
| chr1:44968759
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG00639.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.294+9556A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968759 | ||||||
| chr1:44968767
|
T | C | 81 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 81 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.294+9548A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968767 | ||||||
| chr1:44968830
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+9485C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968830 | ||||||
| chr1:44968896
|
CA | C | 287 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(284): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.294+9418delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968896 | ||||||
| chr1:44968987
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0288 | 2 | HG01081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.294+9328G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44968987 | ||||||
| chr1:44969049
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+9266G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969049 | ||||||
| chr1:44969169
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+9146G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969169 | ||||||
| chr1:44969183
|
C | T | 2 | a0001c0002t0001g0153a0001c0002t0001g0154 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.294+9132G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969183 | ||||||
| chr1:44969516
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+8799A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969516 | ||||||
| chr1:44969532
|
T | C | 2 | a0001c0002t0001g0162a0001c0002t0001g0201 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.294+8783A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969532 | ||||||
| chr1:44969686
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.294+8629C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969686 | ||||||
| chr1:44969708
|
A | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0280 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.294+8607T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969708 | ||||||
| chr1:44969736
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0057 | 3 | NA18942.hp2 NA18947.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.294+8579C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969736 | ||||||
| chr1:44969820
|
C | A | 195 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.294+8495G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44969820 | ||||||
| chr1:44970141
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.294+8174A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970141 | ||||||
| chr1:44970283
|
C | G | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.294+8032G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970283 | ||||||
| chr1:44970342
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024 | 3 | HG01099.hp2 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.294+7973A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970342 | ||||||
| chr1:44970372
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+7943G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970372 | ||||||
| chr1:44970542
|
A | G | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.294+7773T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970542 | ||||||
| chr1:44970649
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+7666A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970649 | ||||||
| chr1:44970807
|
A | G | 1 | a0001c0001t0002g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.294+7508T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970807 | ||||||
| chr1:44970894
|
C | A | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+7421G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970894 | ||||||
| chr1:44970897
|
A | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+7418T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970897 | ||||||
| chr1:44970997
|
C | T | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+7318G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44970997 | ||||||
| chr1:44971004
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.294+7311G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971004 | ||||||
| chr1:44971371
|
AG | A | 5 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0150others(2): Show | 5 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+6943delC | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971371 | ||||||
| chr1:44971372
|
GA | G | 184 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.294+6942delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971372 | ||||||
| chr1:44971389
|
A | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+6926T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971389 | ||||||
| chr1:44971530
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+6785G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971530 | ||||||
| chr1:44971654
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+6661C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971654 | ||||||
| chr1:44971732
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+6583A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971732 | ||||||
| chr1:44971968
|
G | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0200 | 2 | HG00738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.294+6347C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44971968 | ||||||
| chr1:44972005
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.294+6310G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972005 | ||||||
| chr1:44972114
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+6201G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972114 | ||||||
| chr1:44972141
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.294+6174G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972141 | ||||||
| chr1:44972248
|
C | A | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+6067G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972248 | ||||||
| chr1:44972250
|
A | C | 128 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+6065T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972250 | ||||||
| chr1:44972260
|
CACACACA others(23): Show |
C | 77 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0001g0136others(74): Show | 77 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.294+6025_294+6054d others(32): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972260 | ||||||
| chr1:44972262
|
C | CACACACA others(3): Show |
67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.294+6052_294+6053i others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972262 | ||||||
| chr1:44972262
|
C | CACATAT | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+6052_294+6053i others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972262 | ||||||
| chr1:44972262
|
C | CATAT | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+6052_294+6053i others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972262 | ||||||
| chr1:44972262
|
CACACATA others(21): Show |
C | 17 | a0001c0002t0001g0133a0001c0002t0001g0147a0001c0002t0001g0163others(14): Show | 17 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.294+6025_294+6052d others(30): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972262 | ||||||
| chr1:44972264
|
CACATATA others(19): Show |
C | 21 | a0001c0002t0001g0182a0001c0002t0001g0230a0001c0002t0001g0232others(18): Show | 21 | HG01167.hp2 HG01884.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.294+6025_294+6050d others(28): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972264 | ||||||
| chr1:44972268
|
T | C | 80 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(77): Show | 80 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.294+6047A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972268 | ||||||
| chr1:44972278
|
CAA | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+6035_294+6036d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972278 | ||||||
| chr1:44972296
|
T | C | 1 | a0001c0002t0001g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.294+6019A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972296 | ||||||
| chr1:44972308
|
C | CAT | 9 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0155others(6): Show | 9 | HG00642.hp1 HG02723.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+6005_294+6006d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972308 | ||||||
| chr1:44972499
|
A | C | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+5816T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972499 | ||||||
| chr1:44972621
|
A | AAT | 41 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264others(38): Show | 41 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.294+5692_294+5693d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972621 | ||||||
| chr1:44972623
|
T | TAC | 7 | a0001c0001t0001g0255a0001c0001t0002g0117a0001c0001t0002g0121others(4): Show | 7 | HG00323.hp1 HG00738.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+5690_294+5691d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TACAC | 79 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0068others(76): Show | 79 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.294+5688_294+5691d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TACACAC | 64 | a0001c0001t0001g0254a0001c0001t0002g0001a0001c0001t0002g0003others(61): Show | 64 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.294+5686_294+5691d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TACACACA others(1): Show |
34 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(31): Show | 34 | HG00280.hp2 HG00642.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.294+5684_294+5691d others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TACACACA others(3): Show |
7 | a0001c0001t0002g0042a0001c0001t0002g0051a0001c0001t0002g0065others(4): Show | 7 | HG01071.hp2 HG01175.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+5682_294+5691d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0050others(1): Show | 4 | HG01175.hp1 HG01981.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+5680_294+5691d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TATAC | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0257others(12): Show | 15 | HG00544.hp1 HG01943.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.294+5691_294+5692i others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TATACAC | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0307 | 3 | HG02148.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.294+5691_294+5692i others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
T | TATACACA others(3): Show |
1 | a0001c0001t0001g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294+5691_294+5692i others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
TAC | T | 8 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | NA18939.hp2 NA18944.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+5690_294+5691d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972623
|
TACACAC | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+5686_294+5691d others(8): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972623 | ||||||
| chr1:44972625
|
C | T | 10 | a0001c0001t0001g0265a0001c0001t0001g0269a0001c0001t0001g0283others(7): Show | 10 | HG01243.hp2 HG02145.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+5690G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972625 | ||||||
| chr1:44972627
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.294+5688G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972627 | ||||||
| chr1:44972679
|
T | TA | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+5635_294+5636i others(3): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972679 | ||||||
| chr1:44972809
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+5506C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972809 | ||||||
| chr1:44972826
|
G | A | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+5489C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972826 | ||||||
| chr1:44972998
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.294+5317C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44972998 | ||||||
| chr1:44973035
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.294+5280A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973035 | ||||||
| chr1:44973036
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.294+5279C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973036 | ||||||
| chr1:44973205
|
T | C | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.294+5110A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973205 | ||||||
| chr1:44973373
|
C | G | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+4942G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973373 | ||||||
| chr1:44973464
|
AAGGTGGG others(16): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.294+4828_294+4850d others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973464 | ||||||
| chr1:44973492
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0014 | 2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.294+4823C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973492 | ||||||
| chr1:44973819
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.294+4496T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973819 | ||||||
| chr1:44973902
|
T | C | 1 | a0001c0001t0001g0308 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.294+4413A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44973902 | ||||||
| chr1:44974152
|
C | G | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+4163G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974152 | ||||||
| chr1:44974173
|
AT | A | 23 | a0001c0001t0002g0018a0001c0001t0002g0125a0001c0002t0001g0167others(20): Show | 23 | HG01167.hp1 HG01167.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.294+4141delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974173 | ||||||
| chr1:44974202
|
A | G | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+4113T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974202 | ||||||
| chr1:44974223
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+4092G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974223 | ||||||
| chr1:44974250
|
G | T | 4 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0065others(1): Show | 4 | HG01175.hp2 HG01981.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+4065C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974250 | ||||||
| chr1:44974260
|
T | C | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+4055A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974260 | ||||||
| chr1:44974313
|
A | C | 123 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.294+4002T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974313 | ||||||
| chr1:44974345
|
T | A | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+3970A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974345 | ||||||
| chr1:44974422
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+3893G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974422 | ||||||
| chr1:44974423
|
G | A | 8 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+3892C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974423 | ||||||
| chr1:44974473
|
T | TA | 6 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0001g0138others(3): Show | 6 | HG00738.hp1 HG02976.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+3841dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974473 | ||||||
| chr1:44974555
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.294+3760T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974555 | ||||||
| chr1:44974645
|
T | A | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+3670A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974645 | ||||||
| chr1:44974768
|
A | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+3547T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974768 | ||||||
| chr1:44974818
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+3497T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974818 | ||||||
| chr1:44974850
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.294+3465A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44974850 | ||||||
| chr1:44975153
|
C | G | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.294+3162G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975153 | ||||||
| chr1:44975268
|
C | T | 50 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(47): Show | 50 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.294+3047G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975268 | ||||||
| chr1:44975300
|
G | A | 67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.294+3015C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975300 | ||||||
| chr1:44975346
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+2969T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975346 | ||||||
| chr1:44975369
|
C | T | 52 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(49): Show | 52 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.294+2946G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975369 | ||||||
| chr1:44975376
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294+2939G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975376 | ||||||
| chr1:44975394
|
CT | C | 4 | a0001c0001t0001g0279a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+2920delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975394 | ||||||
| chr1:44975455
|
T | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+2860A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975455 | ||||||
| chr1:44975498
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+2817G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975498 | ||||||
| chr1:44975511
|
G | C | 1 | a0001c0001t0002g0106 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.294+2804C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975511 | ||||||
| chr1:44975599
|
C | A | 1 | a0001c0002t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.294+2716G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975599 | ||||||
| chr1:44975622
|
A | G | 67 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.294+2693T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975622 | ||||||
| chr1:44975645
|
G | C | 196 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.294+2670C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975645 | ||||||
| chr1:44975798
|
C | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+2517G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975798 | ||||||
| chr1:44975930
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.294+2385T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975930 | ||||||
| chr1:44975992
|
T | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+2323A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44975992 | ||||||
| chr1:44976244
|
T | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+2071A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44976244 | ||||||
| chr1:44976318
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.294+1997A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44976318 | ||||||
| chr1:44976445
|
C | A | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.294+1870G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44976445 | ||||||
| chr1:44976713
|
A | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+1602T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44976713 | ||||||
| chr1:44976963
|
G | C | 4 | a0001c0002t0001g0204a0001c0002t0001g0205a0001c0002t0001g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1352C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44976963 | ||||||
| chr1:44977018
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294+1297C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977018 | ||||||
| chr1:44977164
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1151A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977164 | ||||||
| chr1:44977220
|
G | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.294+1095C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977220 | ||||||
| chr1:44977307
|
A | T | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.294+1008T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977307 | ||||||
| chr1:44977351
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+964G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977351 | ||||||
| chr1:44977393
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+922G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977393 | ||||||
| chr1:44977430
|
A | C | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.294+885T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977430 | ||||||
| chr1:44977468
|
C | CT | 62 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(59): Show | 62 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.294+846dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977468 | ||||||
| chr1:44977472
|
T | A | 1 | a0001c0002t0001g0167 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.294+843A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977472 | ||||||
| chr1:44977567
|
C | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.294+748G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977567 | ||||||
| chr1:44977665
|
A | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.294+650T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977665 | ||||||
| chr1:44977948
|
ATGCACTG others(18): Show |
A | 1 | a0001c0002t0001g0167 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.294+342_294+366del others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977948 | ||||||
| chr1:44977977
|
C | T | 20 | a0001c0002t0001g0147a0001c0002t0001g0163a0001c0002t0001g0168others(17): Show | 20 | HG00408.hp1 HG00609.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.294+338G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977977 | ||||||
| chr1:44977990
|
A | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0028 | 2 | NA18968.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.294+325T>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44977990 | ||||||
| chr1:44978094
|
G | A | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.294+221C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44978094 | ||||||
| chr1:44978094
|
G | C | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.294+221C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44978094 | ||||||
| chr1:44978100
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+215C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44978100 | ||||||
| chr1:44978189
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294+126G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44978189 | ||||||
| chr1:44978222
|
T | C | 128 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+93A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 3/11 | chr1 | 44978222 | ||||||
| chr1:44978464
|
T | C | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
splice_region_variant&intron_variant | LOW | c.149-4A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978464 | ||||||
| chr1:44978604
|
C | CATTCCCC others(4): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.149-155_149-145dup others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978604 | ||||||
| chr1:44978621
|
C | CT | 48 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(45): Show | 48 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.149-162dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTT | 28 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0014others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.149-163_149-162dup others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTTT | 15 | a0001c0001t0002g0042a0001c0001t0002g0049a0001c0001t0002g0050others(12): Show | 15 | HG00639.hp1 HG01175.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.149-164_149-162dup others(3): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTTTT | 6 | a0001c0001t0002g0048a0001c0001t0002g0068a0001c0001t0002g0083others(3): Show | 6 | HG02071.hp1 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-165_149-162dup others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.149-171_149-162dup others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.149-173_149-162dup others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.149-177_149-162dup others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CT | C | 16 | a0001c0001t0001g0127a0001c0002t0001g0235a0001c0002t0001g0236others(13): Show | 16 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.149-162delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTT | C | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02897.hp1 NA18944.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-163_149-162del others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0002t0001g0162a0001c0002t0001g0170a0001c0002t0001g0171others(3): Show | 6 | HG00323.hp1 HG02055.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-170_149-162del others(9): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(3): Show |
C | 86 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(83): Show | 86 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.149-171_149-162del others(10): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | HG00280.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.149-172_149-162del others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0002g0006a0001c0001t0002g0105a0001c0001t0002g0118others(1): Show | 4 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-173_149-162del others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.149-176_149-162del others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978621
|
CTTTTTTT others(9): Show |
C | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.149-177_149-162del others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978621 | ||||||
| chr1:44978700
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.149-240A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44978700 | ||||||
| chr1:44979011
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.149-551G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979011 | ||||||
| chr1:44979324
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.149-864G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979324 | ||||||
| chr1:44979474
|
C | CA | 121 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(118): Show | 121 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.149-1015dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979474 | ||||||
| chr1:44979474
|
C | CAA | 19 | a0001c0001t0001g0259a0001c0001t0001g0265a0001c0001t0001g0312others(16): Show | 19 | HG00544.hp1 HG02015.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.149-1016_149-1015d others(4): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979474 | ||||||
| chr1:44979474
|
CA | C | 11 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(8): Show | 11 | HG00140.hp2 HG00323.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-1015delT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979474 | ||||||
| chr1:44979496
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-1036T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979496 | ||||||
| chr1:44979518
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.149-1058C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979518 | ||||||
| chr1:44979579
|
T | G | 128 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.149-1119A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979579 | ||||||
| chr1:44979580
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149-1120G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979580 | ||||||
| chr1:44979638
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.149-1178C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979638 | ||||||
| chr1:44979689
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.149-1229G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979689 | ||||||
| chr1:44979716
|
C | A | 115 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.149-1256G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979716 | ||||||
| chr1:44979767
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148+1254G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979767 | ||||||
| chr1:44979784
|
C | T | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.148+1237G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979784 | ||||||
| chr1:44979924
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.148+1097G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44979924 | ||||||
| chr1:44980192
|
C | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+829G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980192 | ||||||
| chr1:44980320
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.148+701G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980320 | ||||||
| chr1:44980325
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.148+696T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980325 | ||||||
| chr1:44980461
|
C | A | 128 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.148+560G>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980461 | ||||||
| chr1:44980649
|
G | A | 3 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0249 | 3 | HG02257.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.148+372C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980649 | ||||||
| chr1:44980787
|
T | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.148+234A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980787 | ||||||
| chr1:44980899
|
G | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+122C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980899 | ||||||
| chr1:44980979
|
T | C | 1 | a0004c0006t0001g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.148+42A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 2/11 | chr1 | 44980979 | ||||||
| chr1:44981238
|
C | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0124 | 3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9-61G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981238 | ||||||
| chr1:44981298
|
C | T | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9-121G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981298 | ||||||
| chr1:44981542
|
T | C | 1 | a0001c0002t0001g0248 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9-365A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981542 | ||||||
| chr1:44981676
|
C | CT | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01243.hp2 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-9-500dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981676 | ||||||
| chr1:44981797
|
G | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-9-620C>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981797 | ||||||
| chr1:44981867
|
G | A | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9-690C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981867 | ||||||
| chr1:44981885
|
C | T | 1 | a0003c0005t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-9-708G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981885 | ||||||
| chr1:44981886
|
G | A | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-709C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981886 | ||||||
| chr1:44981942
|
C | CA | 32 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(29): Show | 32 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-9-766dupT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981942 | ||||||
| chr1:44981942
|
C | CAA | 86 | a0001c0001t0001g0266a0001c0001t0001g0282a0001c0001t0001g0316others(83): Show | 86 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-9-767_-9-766dupTT | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981942 | ||||||
| chr1:44981942
|
C | CAAA | 69 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0258others(66): Show | 69 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.-9-768_-9-766dupTT others(1): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981942 | ||||||
| chr1:44981960
|
A | G | 7 | a0001c0002t0001g0133a0001c0002t0001g0141a0001c0002t0001g0142others(4): Show | 7 | HG00639.hp2 HG01255.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-783T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44981960 | ||||||
| chr1:44982127
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-9-950G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982127 | ||||||
| chr1:44982607
|
T | C | 6 | a0001c0001t0002g0099a0001c0001t0002g0107a0001c0001t0002g0108others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1430A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982607 | ||||||
| chr1:44982608
|
T | G | 6 | a0001c0001t0002g0099a0001c0001t0002g0107a0001c0001t0002g0108others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1431A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982608 | ||||||
| chr1:44982622
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-9-1445G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982622 | ||||||
| chr1:44982687
|
A | G | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0140 | 3 | HG02976.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9-1510T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982687 | ||||||
| chr1:44982718
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9-1541T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982718 | ||||||
| chr1:44982764
|
C | CT | 69 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(66): Show | 69 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.-9-1588dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982764 | ||||||
| chr1:44982816
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9-1639C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982816 | ||||||
| chr1:44982928
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-1751C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44982928 | ||||||
| chr1:44983042
|
T | C | 1 | a0001c0002t0001g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-9-1865A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983042 | ||||||
| chr1:44983131
|
T | C | 4 | a0001c0002t0001g0167a0001c0002t0001g0214a0001c0002t0001g0215others(1): Show | 4 | HG02083.hp1 HG02132.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-1954A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983131 | ||||||
| chr1:44983186
|
T | G | 1 | a0001c0001t0002g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9-2009A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983186 | ||||||
| chr1:44983214
|
G | A | 8 | a0001c0001t0002g0042a0001c0001t0002g0050a0001c0001t0002g0051others(5): Show | 8 | HG01071.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-2037C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983214 | ||||||
| chr1:44983249
|
T | A | 1 | a0001c0002t0001g0167 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-9-2072A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983249 | ||||||
| chr1:44983251
|
C | T | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-2074G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983251 | ||||||
| chr1:44983376
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-9-2199G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983376 | ||||||
| chr1:44983403
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG02258.hp1 NA18944.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-2226G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983403 | ||||||
| chr1:44983433
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-9-2256C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983433 | ||||||
| chr1:44983465
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9-2288C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983465 | ||||||
| chr1:44983472
|
T | A | 1 | a0001c0002t0001g0167 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-9-2295A>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983472 | ||||||
| chr1:44983696
|
ACT | A | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-9-2521_-9-2520del others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983696 | ||||||
| chr1:44983702
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-2525A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983702 | ||||||
| chr1:44983799
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-9-2622G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983799 | ||||||
| chr1:44983910
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-10+2583C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44983910 | ||||||
| chr1:44984005
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-10+2488C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984005 | ||||||
| chr1:44984055
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10+2438G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984055 | ||||||
| chr1:44984114
|
A | G | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10+2379T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984114 | ||||||
| chr1:44984183
|
A | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2310T>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984183 | ||||||
| chr1:44984217
|
C | T | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-10+2276G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984217 | ||||||
| chr1:44984252
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-10+2241C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984252 | ||||||
| chr1:44984270
|
A | G | 68 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(65): Show | 68 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-10+2223T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984270 | ||||||
| chr1:44984537
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1956A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984537 | ||||||
| chr1:44984740
|
AGTT | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1750_-10+1752d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984740 | ||||||
| chr1:44984754
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+1739A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984754 | ||||||
| chr1:44984797
|
C | CTTT | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG02056.hp1 HG03704.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10+1693_-10+1695d others(5): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTT | 84 | a0001c0001t0001g0254a0001c0001t0002g0113a0001c0002t0001g0136others(81): Show | 84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-10+1692_-10+1695d others(6): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTT | 30 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0133others(27): Show | 30 | HG01167.hp2 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-10+1691_-10+1695d others(7): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0002g0006others(13): Show | 16 | HG00639.hp1 HG01516.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10+1687_-10+1695d others(11): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(3): Show |
40 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(37): Show | 40 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10+1686_-10+1695d others(12): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(4): Show |
21 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(18): Show | 21 | HG01243.hp2 HG01261.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10+1685_-10+1695d others(13): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG01943.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1684_-10+1695d others(14): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-10+1683_-10+1695d others(15): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0002g0097 | 3 | HG03225.hp2 HG06807.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-10+1682_-10+1695d others(16): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0095a0001c0001t0002g0096 | 2 | HG00408.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-10+1681_-10+1695d others(17): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0003g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-10+1679_-10+1695d others(19): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-10+1676_-10+1695d others(22): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG02145.hp1 HG03017.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(23): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(16): Show |
10 | a0001c0001t0002g0005a0001c0001t0002g0081a0001c0001t0002g0082others(7): Show | 10 | HG02056.hp2 HG03239.hp2 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(25): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(17): Show |
6 | a0001c0001t0002g0001a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 6 | HG01123.hp1 HG02602.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(26): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(18): Show |
5 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(2): Show | 5 | HG02895.hp2 HG03492.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(27): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(19): Show |
2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG04228.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(28): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(20): Show |
3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG01175.hp2 NA18906.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(29): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(21): Show |
6 | a0001c0001t0002g0004a0001c0001t0002g0062a0001c0001t0002g0063others(3): Show | 6 | HG00621.hp1 HG01069.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(30): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(22): Show |
11 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0053others(8): Show | 11 | HG01071.hp1 HG02257.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(31): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(23): Show |
8 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(5): Show | 8 | HG01071.hp2 HG01981.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(32): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(24): Show |
8 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(5): Show | 8 | HG00280.hp2 HG00544.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(33): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(25): Show |
5 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(2): Show | 5 | HG03831.hp2 NA18941.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(34): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0002g0030 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-10+1695_-10+1696i others(35): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0029 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-10+1695_-10+1696i others(36): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(28): Show |
3 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028 | 3 | NA18968.hp1 NA18968.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-10+1695_-10+1696i others(37): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984797
|
C | CTTTTTTT others(33): Show |
1 | a0001c0001t0002g0025 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-10+1695_-10+1696i others(42): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984797 | ||||||
| chr1:44984847
|
C | T | 63 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(60): Show | 63 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10+1646G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984847 | ||||||
| chr1:44984900
|
G | T | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10+1593C>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984900 | ||||||
| chr1:44984911
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1582T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984911 | ||||||
| chr1:44984962
|
G | A | 20 | a0001c0002t0001g0230a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 20 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+1531C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984962 | ||||||
| chr1:44984964
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+1529C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984964 | ||||||
| chr1:44984968
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-10+1525C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44984968 | ||||||
| chr1:44985033
|
C | T | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-10+1460G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985033 | ||||||
| chr1:44985086
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+1407C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985086 | ||||||
| chr1:44985096
|
G | A | 95 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-10+1397C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985096 | ||||||
| chr1:44985101
|
C | T | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10+1392G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985101 | ||||||
| chr1:44985103
|
G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1390C>T | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985103 | ||||||
| chr1:44985163
|
T | C | 124 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10+1330A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985163 | ||||||
| chr1:44985406
|
C | CA | 308 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(305): Show | 308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.-10+1086_-10+1087i others(3): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985406 | ||||||
| chr1:44985416
|
T | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+1077A>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985416 | ||||||
| chr1:44985583
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-10+910T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985583 | ||||||
| chr1:44985756
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-10+737G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985756 | ||||||
| chr1:44985805
|
C | T | 115 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-10+688G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985805 | ||||||
| chr1:44985955
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(2): Show | 5 | HG02698.hp1 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+538G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44985955 | ||||||
| chr1:44986080
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-10+413G>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986080 | ||||||
| chr1:44986103
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+390T>C | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986103 | ||||||
| chr1:44986133
|
CT | C | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0002t0001g0252others(1): Show | 4 | HG01975.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+359delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986133 | ||||||
| chr1:44986135
|
T | TTC | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | NA18944.hp2 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+357_-10+358ins others(2): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986135 | ||||||
| chr1:44986136
|
T | TC | 26 | a0001c0001t0001g0254a0001c0002t0001g0133a0001c0002t0001g0134others(23): Show | 26 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-10+356_-10+357ins others(1): Show |
EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986136 | ||||||
| chr1:44986137
|
T | C | 68 | a0001c0002t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-10+356A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986137 | ||||||
| chr1:44986138
|
C | CT | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+354dupA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986138 | ||||||
| chr1:44986138
|
C | T | 100 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(97): Show | 100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-10+355G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986138 | ||||||
| chr1:44986138
|
CT | C | 72 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(69): Show | 72 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10+354delA | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986138 | ||||||
| chr1:44986140
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+353A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986140 | ||||||
| chr1:44986144
|
T | C | 67 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(64): Show | 67 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.-10+349A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986144 | ||||||
| chr1:44986145
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-10+348A>G | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986145 | ||||||
| chr1:44986271
|
C | T | 1 | a0001c0001t0002g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10+222G>A | EIF2B3 | ENSG00000070785.17 | transcript | ENST00000360403.7 | protein_coding | 1/11 | chr1 | 44986271 |