Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 440275 |
|---|---|
| ensemblid | ENSG00000128829.12 |
| hgncid | 19687 |
| symbol | EIF2AK4 |
| name | eukaryotic translation initiation factor 2 alpha kinase 4 |
| refseq_nuc | NM_001013703.4 |
| refseq_prot | NP_001013725.2 |
| ensembl_nuc | ENST00000263791.10 |
| ensembl_prot | ENSP00000263791.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 39934115 |
| end | 40035591 |
| strand | + |
| ver | v1.2 |
| region | chr15:39934115-40035591 |
| region5000 | chr15:39929115-40040591 |
| regionname0 | EIF2AK4_chr15_39934115_40035591 |
| regionname5000 | EIF2AK4_chr15_39929115_40040591 |
| 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 | 0/0 | 1649 | 126 | 18 | 10 | 90 | 3 | 5 | 65 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002 | 0/1 | 1649 | 120 | 50 | 22 | 29 | 6 | 12 | 24 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003 | 1/0 | 1649 | 61 | 7 | 11 | 41 | 0 | 1 | 30 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004 | 0/0 | 1651 | 27 | 3 | 5 | 12 | 0 | 7 | 10 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005 | 0/0 | 1649 | 10 | 1 | 4 | 1 | 1 | 3 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006 | 0/0 | 732 | 5 | 1 | 0 | 2 | 0 | 2 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0007 | 0/0 | 1649 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0008 | 0/0 | 1649 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0009 | 0/0 | 1649 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0010 | 0/0 | 1649 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0011 | 0/0 | 732 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0012 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0013 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0014 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0015 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0016 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0017 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| 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 | 0/0 | 4950 | 104 | 11 | 7 | 81 | 1 | 4 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0002 | 0/0 | 4950 | 56 | 35 | 8 | 4 | 4 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0003 | 0/0 | 4950 | 54 | 3 | 11 | 39 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0004 | 0/0 | 4950 | 51 | 11 | 11 | 21 | 1 | 7 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0005 | 0/0 | 4950 | 18 | 7 | 3 | 6 | 2 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0006 | 0/0 | 4956 | 14 | 3 | 3 | 3 | 0 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0007 | 0/0 | 4956 | 12 | 0 | 1 | 9 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0008 | 0/0 | 4950 | 6 | 1 | 1 | 1 | 1 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0009 | 0/0 | 4950 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0010 | 0/0 | 4950 | 4 | 2 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0011 | 0/0 | 4950 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0012 | 0/0 | 4951 | 4 | 0 | 0 | 2 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0013 | 0/1 | 4950 | 4 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0014 | 0/0 | 4950 | 4 | 0 | 3 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0015 | 0/0 | 4950 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0016 | 0/0 | 4950 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0017 | 0/0 | 4951 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0018 | 0/0 | 4950 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0019 | 0/0 | 4950 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0020 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0021 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0022 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0023 | 0/0 | 4951 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0024 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0025 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0026 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0027 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0028 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0029 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0030 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0031 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0032 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0033 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0034 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0035 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0036 | 1/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| c0037 | 0/0 | 4956 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| 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 | 589 | 123 | 20 | 29 | 49 | 8 | 16 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0002 | 0/0 | 589 | 115 | 23 | 12 | 73 | 0 | 7 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0003 | 1/0 | 589 | 71 | 10 | 5 | 51 | 1 | 3 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0004 | 0/0 | 589 | 23 | 8 | 5 | 3 | 1 | 6 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0005 | 0/0 | 588 | 20 | 18 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0006 | 0/0 | 589 | 6 | 5 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0007 | 0/0 | 589 | 3 | 2 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0008 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0009 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0010 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0011 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0012 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0013 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| t0014 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0355 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| 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 | 0/0 | 4950 | 104 | 11 | 7 | 81 | 1 | 4 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0005 | 0/0 | 4950 | 18 | 7 | 3 | 6 | 2 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0020 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0021 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0022 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0033 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002 | 0/0 | 4950 | 56 | 35 | 8 | 4 | 4 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004 | 0/0 | 4950 | 51 | 11 | 11 | 21 | 1 | 7 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0011 | 0/0 | 4950 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0013 | 0/1 | 4950 | 4 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0019 | 0/0 | 4950 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0029 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0030 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0031 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003 | 0/0 | 4950 | 54 | 3 | 11 | 39 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0010 | 0/0 | 4950 | 4 | 2 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0025 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0026 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0036 | 1/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006 | 0/0 | 4956 | 14 | 3 | 3 | 3 | 0 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0007 | 0/0 | 4956 | 12 | 0 | 1 | 9 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0037 | 0/0 | 4956 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005c0008 | 0/0 | 4950 | 6 | 1 | 1 | 1 | 1 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005c0014 | 0/0 | 4950 | 4 | 0 | 3 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0012 | 0/0 | 4951 | 4 | 0 | 0 | 2 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0032 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0007c0009 | 0/0 | 4950 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0008c0015 | 0/0 | 4950 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0009c0016 | 0/0 | 4950 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0010c0018 | 0/0 | 4950 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0011c0017 | 0/0 | 4951 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0012c0024 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0013c0023 | 0/0 | 4951 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0014c0028 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0015c0027 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0016c0034 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0017c0035 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5538 | 21 | 1 | 3 | 16 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0002 | 0/0 | 5538 | 29 | 1 | 1 | 25 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0003 | 0/0 | 5538 | 43 | 1 | 3 | 37 | 1 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0004 | 0/0 | 5538 | 2 | 1 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0005 | 0/0 | 5537 | 7 | 7 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0011 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0001t0012 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0005t0001 | 0/0 | 5538 | 11 | 4 | 1 | 4 | 2 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0005t0002 | 0/0 | 5538 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0005t0004 | 0/0 | 5538 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0005t0005 | 0/0 | 5537 | 4 | 3 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0020t0001 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0021t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0022t0002 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0001c0033t0001 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0001 | 0/0 | 5538 | 23 | 7 | 7 | 0 | 4 | 5 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0002 | 0/0 | 5538 | 14 | 13 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0003 | 0/0 | 5538 | 8 | 5 | 1 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0004 | 0/0 | 5538 | 6 | 6 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0005 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0007 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0008 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0002t0010 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0001 | 0/0 | 5538 | 31 | 1 | 11 | 13 | 0 | 6 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0002 | 0/0 | 5538 | 9 | 4 | 0 | 5 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0003 | 0/0 | 5538 | 5 | 3 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0004 | 0/0 | 5538 | 2 | 0 | 0 | 0 | 1 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0005 | 0/0 | 5537 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0004t0014 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0011t0002 | 0/0 | 5538 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0013t0001 | 0/1 | 5538 | 4 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0019t0001 | 0/0 | 5538 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0029t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0030t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0002c0031t0009 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0001 | 0/0 | 5538 | 6 | 2 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0002 | 0/0 | 5538 | 42 | 1 | 10 | 30 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0003 | 0/0 | 5538 | 3 | 0 | 1 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0004 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0006 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0003t0013 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0010t0001 | 0/0 | 5538 | 4 | 2 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0025t0004 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0026t0001 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0003c0036t0003 | 1/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006t0001 | 0/0 | 5544 | 5 | 0 | 2 | 2 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006t0002 | 0/0 | 5544 | 2 | 0 | 0 | 1 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006t0003 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006t0004 | 0/0 | 5544 | 3 | 0 | 1 | 0 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0006t0006 | 0/0 | 5544 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0007t0001 | 0/0 | 5544 | 7 | 0 | 0 | 5 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0007t0002 | 0/0 | 5544 | 4 | 0 | 1 | 3 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0007t0003 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0004c0037t0001 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005c0008t0001 | 0/0 | 5538 | 3 | 1 | 1 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005c0008t0004 | 0/0 | 5538 | 3 | 0 | 0 | 1 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0005c0014t0004 | 0/0 | 5538 | 4 | 0 | 3 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0012t0001 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0012t0002 | 0/0 | 5539 | 2 | 0 | 0 | 1 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0012t0003 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0006c0032t0005 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0007c0009t0003 | 0/0 | 5538 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0008c0015t0005 | 0/0 | 5537 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0008c0015t0006 | 0/0 | 5538 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0009c0016t0007 | 0/0 | 5538 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0010c0018t0005 | 0/0 | 5537 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0011c0017t0002 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0011c0017t0003 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0012c0024t0002 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0013c0023t0003 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0014c0028t0002 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0015c0027t0002 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0016c0034t0001 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| a0017c0035t0003 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | copy fasta | chr15 | 39929115 | 40040591 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0005t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0020t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0021t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0022t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0001c0033t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0002t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0004g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0004t0014g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0011t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0011t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0011t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0011t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0013t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0013t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0013t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0013t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0019t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0019t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0029t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0030t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0002c0031t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0003t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0010t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0025t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0026t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0003c0036t0003g0355 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0006t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0007t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0004c0037t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0008t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0008t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0008t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0008t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0014t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0014t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0005c0014t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0006c0012t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0006c0012t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0006c0012t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0006c0012t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0006c0032t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0007c0009t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0007c0009t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0007c0009t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0007c0009t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0008c0015t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0008c0015t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0008c0015t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0009c0016t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0009c0016t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0010c0018t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0010c0018t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0011c0017t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0011c0017t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0012c0024t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0013c0023t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0014c0028t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0015c0027t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0016c0034t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| a0017c0035t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0290 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0226 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0271 | EUR | GBR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00280 | hp1 | a0001 | c0005 | t0001 | g0135 | EUR | FIN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0298 | EUR | FIN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00408 | hp1 | a0003 | c0003 | t0004 | g0074 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00544 | hp1 | a0002 | c0004 | t0001 | g0258 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00544 | hp2 | a0004 | c0007 | t0002 | g0215 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00609 | hp1 | a0004 | c0006 | t0001 | g0211 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00609 | hp2 | a0001 | c0005 | t0001 | g0153 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00621 | hp2 | a0003 | c0010 | t0001 | g0079 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00639 | hp2 | a0002 | c0013 | t0001 | g0281 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0359 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0277 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00673 | hp1 | a0003 | c0003 | t0006 | g0105 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00741 | hp1 | a0001 | c0005 | t0005 | g0154 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0327 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01069 | hp1 | a0002 | c0004 | t0001 | g0005 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01074 | hp1 | a0002 | c0004 | t0001 | g0275 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01074 | hp2 | a0004 | c0006 | t0004 | g0249 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01099 | hp1 | a0002 | c0019 | t0001 | g0282 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01099 | hp2 | a0003 | c0003 | t0002 | g0066 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01106 | hp1 | a0002 | c0004 | t0001 | g0326 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01106 | hp2 | a0004 | c0037 | t0001 | g0274 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0362 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01109 | hp2 | a0003 | c0003 | t0003 | g0063 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01168 | hp1 | a0004 | c0006 | t0001 | g0260 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01169 | hp1 | a0005 | c0008 | t0001 | g0357 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01175 | hp1 | a0002 | c0004 | t0001 | g0325 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01175 | hp2 | a0002 | c0019 | t0001 | g0285 | AMR | PUR | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01255 | hp1 | a0009 | c0016 | t0007 | g0042 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0284 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0323 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0210 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01257 | hp2 | a0005 | c0014 | t0004 | g0006 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01258 | hp1 | a0005 | c0014 | t0004 | g0006 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0330 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0102 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0329 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0064 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01496 | hp2 | a0010 | c0018 | t0005 | g0241 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01516 | hp1 | a0002 | c0013 | t0001 | g0279 | EUR | IBS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01516 | hp2 | a0005 | c0008 | t0001 | g0297 | EUR | IBS | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01884 | hp1 | a0002 | c0031 | t0009 | g0045 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01884 | hp2 | a0002 | c0004 | t0002 | g0273 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0018 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01891 | hp2 | a0002 | c0004 | t0003 | g0036 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0060 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0061 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01978 | hp2 | a0004 | c0007 | t0002 | g0263 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01981 | hp1 | a0004 | c0006 | t0001 | g0262 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0101 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02004 | hp2 | a0003 | c0003 | t0002 | g0062 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0231 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0104 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02040 | hp2 | a0001 | c0021 | t0003 | g0224 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02055 | hp2 | a0002 | c0030 | t0002 | g0306 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02056 | hp1 | a0001 | c0022 | t0002 | g0169 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02071 | hp1 | a0003 | c0003 | t0002 | g0089 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02074 | hp2 | a0005 | c0008 | t0004 | g0340 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02080 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02135 | hp1 | a0002 | c0004 | t0003 | g0264 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02145 | hp1 | a0011 | c0017 | t0002 | g0240 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02148 | hp1 | a0001 | c0005 | t0001 | g0134 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0065 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0316 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | CDX | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0247 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02258 | hp2 | a0002 | c0029 | t0002 | g0307 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02273 | hp2 | a0003 | c0003 | t0002 | g0098 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0125 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02300 | hp1 | a0005 | c0014 | t0004 | g0292 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02300 | hp2 | a0002 | c0004 | t0001 | g0322 | AMR | PEL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02451 | hp1 | a0001 | c0005 | t0005 | g0123 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02451 | hp2 | a0003 | c0010 | t0001 | g0047 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0091 | EAS | KHV | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02572 | hp1 | a0002 | c0002 | t0005 | g0293 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02572 | hp2 | a0002 | c0002 | t0010 | g0046 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0296 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02615 | hp1 | a0004 | c0006 | t0006 | g0253 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02615 | hp2 | a0002 | c0004 | t0005 | g0238 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0344 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02630 | hp2 | a0002 | c0004 | t0003 | g0038 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02698 | hp1 | a0004 | c0006 | t0001 | g0256 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02717 | hp1 | a0004 | c0006 | t0006 | g0252 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0041 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02738 | hp1 | a0014 | c0028 | t0002 | g0308 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02738 | hp2 | a0006 | c0012 | t0003 | g0270 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02809 | hp1 | a0002 | c0002 | t0005 | g0021 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0360 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02886 | hp1 | a0002 | c0004 | t0002 | g0354 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02886 | hp2 | a0003 | c0026 | t0001 | g0011 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0338 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02896 | hp2 | a0002 | c0004 | t0005 | g0037 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0337 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0339 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0335 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02976 | hp1 | a0008 | c0015 | t0006 | g0025 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0237 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03041 | hp2 | a0008 | c0015 | t0006 | g0027 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03098 | hp1 | a0011 | c0017 | t0003 | g0342 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03098 | hp2 | a0015 | c0027 | t0002 | g0024 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0034 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03139 | hp1 | a0010 | c0018 | t0005 | g0239 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0309 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0050 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03209 | hp1 | a0002 | c0004 | t0002 | g0315 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03225 | hp1 | a0004 | c0006 | t0006 | g0261 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0336 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03239 | hp1 | a0002 | c0004 | t0004 | g0331 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03239 | hp2 | a0004 | c0007 | t0001 | g0265 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0352 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03490 | hp1 | a0004 | c0006 | t0003 | g0345 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03490 | hp2 | a0005 | c0008 | t0004 | g0004 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03492 | hp1 | a0005 | c0008 | t0004 | g0004 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03492 | hp2 | a0002 | c0004 | t0001 | g0348 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03516 | hp1 | a0001 | c0005 | t0005 | g0108 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03540 | hp1 | a0002 | c0004 | t0002 | g0276 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03540 | hp2 | a0002 | c0004 | t0005 | g0114 | AFR | GWD | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0351 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0016 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03654 | hp2 | a0004 | c0006 | t0004 | g0250 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03669 | hp1 | a0001 | c0033 | t0001 | g0131 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03669 | hp2 | a0006 | c0012 | t0002 | g0177 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03704 | hp1 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03710 | hp1 | a0004 | c0007 | t0001 | g0251 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0328 | SAS | PJL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0278 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03942 | hp2 | a0005 | c0014 | t0004 | g0295 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0358 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04115 | hp2 | a0004 | c0006 | t0004 | g0266 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0051 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04184 | hp2 | a0004 | c0006 | t0002 | g0254 | SAS | BEB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0294 | SAS | STU | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18522 | hp1 | a0003 | c0025 | t0004 | g0010 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0100 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18747 | hp1 | a0001 | c0005 | t0001 | g0137 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18747 | hp2 | a0001 | c0005 | t0002 | g0196 | EAS | CHB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18906 | hp1 | a0003 | c0010 | t0001 | g0048 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18906 | hp2 | a0008 | c0015 | t0005 | g0026 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18940 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18940 | hp2 | a0002 | c0004 | t0002 | g0312 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18941 | hp1 | a0002 | c0004 | t0003 | g0257 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18944 | hp1 | a0002 | c0004 | t0002 | g0317 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18946 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0321 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18948 | hp2 | a0001 | c0001 | t0011 | g0164 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0319 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18950 | hp1 | a0001 | c0005 | t0002 | g0221 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18950 | hp2 | a0002 | c0002 | t0008 | g0324 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18951 | hp2 | a0002 | c0004 | t0014 | g0303 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18952 | hp1 | a0002 | c0004 | t0002 | g0229 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18953 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18953 | hp2 | a0002 | c0011 | t0002 | g0332 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18956 | hp1 | a0003 | c0003 | t0002 | g0053 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18957 | hp2 | a0006 | c0012 | t0002 | g0151 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0083 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18964 | hp1 | a0007 | c0009 | t0003 | g0232 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0301 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18972 | hp1 | a0004 | c0007 | t0003 | g0259 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18972 | hp2 | a0017 | c0035 | t0003 | g0236 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18974 | hp1 | a0007 | c0009 | t0003 | g0234 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18974 | hp2 | a0001 | c0005 | t0001 | g0181 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18975 | hp1 | a0001 | c0020 | t0001 | g0174 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18977 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18979 | hp2 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18983 | hp1 | a0002 | c0004 | t0001 | g0313 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18984 | hp2 | a0002 | c0004 | t0001 | g0353 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18989 | hp1 | a0001 | c0001 | t0012 | g0156 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18990 | hp2 | a0002 | c0004 | t0001 | g0320 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18991 | hp2 | a0004 | c0007 | t0002 | g0267 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18992 | hp2 | a0004 | c0007 | t0001 | g0214 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18993 | hp1 | a0007 | c0009 | t0003 | g0230 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18993 | hp2 | a0004 | c0006 | t0002 | g0212 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18995 | hp1 | a0004 | c0007 | t0001 | g0213 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19001 | hp2 | a0002 | c0004 | t0001 | g0350 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19002 | hp1 | a0002 | c0004 | t0001 | g0343 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19006 | hp1 | a0002 | c0011 | t0002 | g0347 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19006 | hp2 | a0006 | c0012 | t0001 | g0268 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19010 | hp2 | a0002 | c0004 | t0002 | g0349 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0318 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19012 | hp1 | a0002 | c0004 | t0002 | g0333 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19030 | hp1 | a0003 | c0003 | t0002 | g0059 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19043 | hp1 | a0005 | c0008 | t0001 | g0299 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0311 | AFR | LWK | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19060 | hp1 | a0003 | c0010 | t0001 | g0077 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19064 | hp1 | a0004 | c0007 | t0001 | g0216 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19064 | hp2 | a0004 | c0006 | t0001 | g0255 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19066 | hp1 | a0002 | c0004 | t0001 | g0272 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19067 | hp2 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19068 | hp1 | a0002 | c0004 | t0001 | g0304 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19068 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19070 | hp1 | a0004 | c0007 | t0002 | g0248 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19072 | hp2 | a0003 | c0003 | t0013 | g0086 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19075 | hp2 | a0004 | c0007 | t0001 | g0217 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19077 | hp1 | a0002 | c0011 | t0002 | g0096 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0052 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19079 | hp2 | a0007 | c0009 | t0003 | g0235 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19080 | hp1 | a0002 | c0011 | t0002 | g0302 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19081 | hp2 | a0004 | c0007 | t0001 | g0228 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0097 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19085 | hp1 | a0001 | c0005 | t0001 | g0132 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19086 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0103 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19087 | hp2 | a0013 | c0023 | t0003 | g0233 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19088 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19090 | hp1 | a0002 | c0004 | t0001 | g0346 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19091 | hp1 | a0016 | c0034 | t0001 | g0150 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0019 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA19240 | hp2 | a0009 | c0016 | t0007 | g0044 | AFR | YRI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20752 | hp1 | a0002 | c0004 | t0004 | g0341 | EUR | TSI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0287 | EUR | TSI | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0005 | SAS | GIH | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20905 | hp2 | a0012 | c0024 | t0002 | g0068 | SAS | GIH | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0107 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG01123 | hp2 | a0001 | c0005 | t0004 | g0121 | AMR | CLM | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02486 | hp1 | a0002 | c0013 | t0001 | g0280 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02486 | hp2 | a0002 | c0002 | t0007 | g0043 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02559 | hp1 | a0001 | c0005 | t0005 | g0124 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0314 | AFR | ACB | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03471 | hp1 | a0006 | c0032 | t0005 | g0122 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0049 | AFR | MSL | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0162 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0310 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| NA20300 | hp2 | a0002 | c0004 | t0003 | g0039 | AFR | USA | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0013 | t0001 | g0283 | REF | REF | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| homoSapiens_grch38 | hp1 | a0003 | c0036 | t0003 | g0355 | REF | REF | EIF2AK4_chr15_39929115_40040591 | EIF2AK4 | chr15 | 39929115 | 40040591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:39967647
|
A | C | 5 | a0001a0006a0008others(2): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
missense_variant | MODERATE | c.1321A>C | p.Ile441Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/39 | 1402/5538 | 1321/4950 | 441/1649 | chr15 | 39967647 | ||
| chr15:39967801
|
G | A | 1 | a0009 | 2 | HG01255.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1475G>A | p.Ser492Asn | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/39 | 1556/5538 | 1475/4950 | 492/1649 | chr15 | 39967801 | ||
| chr15:39973598
|
A | G | 13 | a0001a0002a0004others(10): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
missense_variant | MODERATE | c.1667A>G | p.Glu556Gly | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/39 | 1748/5538 | 1667/4950 | 556/1649 | chr15 | 39973598 | ||
| chr15:39973625
|
T | C | 1 | a0015 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1694T>C | p.Ile565Thr | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/39 | 1775/5538 | 1694/4950 | 565/1649 | chr15 | 39973625 | ||
| chr15:39976615
|
C | T | 1 | a0008 | 3 | HG02976.hp1 HG03041.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2020C>T | p.Pro674Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2101/5538 | 2020/4950 | 674/1649 | chr15 | 39976615 | ||
| chr15:39976763
|
T | TC | 3 | a0006a0011a0013 | 8 | HG02145.hp1 HG02738.hp2 HG03098.hp1 others(5): Show |
frameshift_variant | HIGH | c.2172dupC | p.Ala725fs | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2254/5538 | 2173/4950 | 725/1649 | INFO_REALIGN_3_PRIME | chr15 | 39976763 | |
| chr15:39976797
|
G | GGACGAC | 1 | a0004 | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
disruptive_inframe_insertion | MODERATE | c.2208_2213dupCGACGA | p.Asp736_Asp737dup | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2295/5538 | 2214/4950 | 738/1649 | INFO_REALIGN_3_PRIME | chr15 | 39976797 | |
| chr15:39992205
|
G | C | 2 | a0007a0013 | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
missense_variant | MODERATE | c.2662G>C | p.Asp888His | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/39 | 2743/5538 | 2662/4950 | 888/1649 | chr15 | 39992205 | ||
| chr15:40002770
|
C | T | 1 | a0012 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3217C>T | p.Arg1073Cys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 22/39 | 3298/5538 | 3217/4950 | 1073/1649 | chr15 | 40002770 | ||
| chr15:40008148
|
A | G | 1 | a0017 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.3529A>G | p.Ile1177Val | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/39 | 3610/5538 | 3529/4950 | 1177/1649 | chr15 | 40008148 | ||
| chr15:40016509
|
G | A | 1 | a0014 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.3767G>A | p.Arg1256Gln | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/39 | 3848/5538 | 3767/4950 | 1256/1649 | chr15 | 40016509 | ||
| chr15:40016658
|
G | T | 1 | a0005 | 10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
missense_variant | MODERATE | c.3916G>T | p.Gly1306Cys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/39 | 3997/5538 | 3916/4950 | 1306/1649 | chr15 | 40016658 | ||
| chr15:40017184
|
A | G | 1 | a0010 | 2 | HG01496.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.4007A>G | p.Lys1336Arg | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/39 | 4088/5538 | 4007/4950 | 1336/1649 | chr15 | 40017184 | ||
| chr15:40020943
|
G | T | 1 | a0016 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.4218G>T | p.Gln1406His | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/39 | 4299/5538 | 4218/4950 | 1406/1649 | chr15 | 40020943 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:39934294
|
T | C | 32 | a0001c0001a0001c0005a0001c0020others(29): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
synonymous_variant | LOW | c.99T>C | p.Ile33Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 180/5538 | 99/4950 | 33/1649 | chr15 | 39934294 | ||
| chr15:39939570
|
T | C | 1 | a0001c0020 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.210T>C | p.Tyr70Tyr | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/39 | 291/5538 | 210/4950 | 70/1649 | chr15 | 39939570 | ||
| chr15:39943399
|
T | C | 1 | a0001c0021 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.274T>C | p.Leu92Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/39 | 355/5538 | 274/4950 | 92/1649 | chr15 | 39943399 | ||
| chr15:39955634
|
T | C | 1 | a0001c0022 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.609T>C | p.Ile203Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/39 | 690/5538 | 609/4950 | 203/1649 | chr15 | 39955634 | ||
| chr15:39976563
|
C | T | 1 | a0002c0031 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1968C>T | p.Ile656Ile | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/39 | 2049/5538 | 1968/4950 | 656/1649 | chr15 | 39976563 | ||
| chr15:39985879
|
A | G | 2 | a0003c0025a0003c0026 | 2 | HG02886.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.2394A>G | p.Leu798Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/39 | 2475/5538 | 2394/4950 | 798/1649 | chr15 | 39985879 | ||
| chr15:40001212
|
C | T | 1 | a0002c0030 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.3147C>T | p.Ser1049Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/39 | 3228/5538 | 3147/4950 | 1049/1649 | chr15 | 40001212 | ||
| chr15:40020940
|
C | T | 12 | a0001c0005a0001c0020a0002c0004others(9): Show | 100 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(97): Show |
synonymous_variant | LOW | c.4215C>T | p.Gly1405Gly | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/39 | 4296/5538 | 4215/4950 | 1405/1649 | chr15 | 40020940 | ||
| chr15:40026055
|
C | T | 1 | a0002c0011 | 4 | NA18953.hp2 NA19006.hp1 NA19077.hp1 others(1): Show |
synonymous_variant | LOW | c.4468C>T | p.Leu1490Leu | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/39 | 4549/5538 | 4468/4950 | 1490/1649 | chr15 | 40026055 | ||
| chr15:40029415
|
C | T | 1 | a0001c0033 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.4512C>T | p.Ser1504Ser | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/39 | 4593/5538 | 4512/4950 | 1504/1649 | chr15 | 40029415 | ||
| chr15:40034403
|
A | G | 1 | a0002c0029 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.4851A>G | p.Lys1617Lys | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/39 | 4932/5538 | 4851/4950 | 1617/1649 | chr15 | 40034403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:39934176
|
G | A | 1 | a0002c0002t0008 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 20 | chr15 | 39934176 | |||||
| chr15:39934184
|
C | A | 4 | a0002c0002t0007a0002c0002t0010a0002c0031t0009others(1): Show | 5 | HG01255.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-12C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/39 | 12 | chr15 | 39934184 | |||||
| chr15:40035089
|
A | G | 21 | a0001c0001t0002a0001c0001t0012a0001c0005t0002others(18): Show | 120 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 5 | chr15 | 40035089 | |||||
| chr15:40035100
|
G | A | 28 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(25): Show | 140 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 16 | chr15 | 40035100 | |||||
| chr15:40035179
|
C | T | 3 | a0003c0003t0006a0004c0006t0006a0008c0015t0006 | 6 | HG00673.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*95C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 95 | chr15 | 40035179 | |||||
| chr15:40035479
|
GA | G | 9 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(6): Show | 22 | HG00741.hp1 HG01496.hp2 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*405delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 405 | INFO_REALIGN_3_PRIME | chr15 | 40035479 | ||||
| chr15:40035488
|
A | T | 1 | a0003c0003t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 404 | chr15 | 40035488 | |||||
| chr15:40035489
|
A | T | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(41): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 405 | chr15 | 40035489 | |||||
| chr15:40035497
|
C | G | 9 | a0001c0001t0004a0001c0005t0004a0002c0002t0004others(6): Show | 23 | HG00408.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 39/39 | 413 | chr15 | 40035497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:39934359
|
G | C | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.144+20G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934359 | ||||||
| chr15:39934502
|
G | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.144+163G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934502 | ||||||
| chr15:39934676
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(262): Show | 267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.144+337T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934676 | ||||||
| chr15:39934791
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.144+452G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934791 | ||||||
| chr15:39934814
|
A | G | 1 | a0002c0002t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.144+475A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934814 | ||||||
| chr15:39934881
|
G | A | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.144+542G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934881 | ||||||
| chr15:39934888
|
C | G | 1 | a0002c0002t0001g0361 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.144+549C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934888 | ||||||
| chr15:39934956
|
C | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.144+617C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934956 | ||||||
| chr15:39934971
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.144+632G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39934971 | ||||||
| chr15:39935072
|
A | G | 1 | a0001c0001t0003g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.144+733A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935072 | ||||||
| chr15:39935337
|
C | CT | 21 | a0002c0004t0001g0258a0002c0004t0003g0257a0002c0004t0003g0264others(18): Show | 21 | HG00544.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.144+1011dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr15 | 39935337 | |||||
| chr15:39935412
|
C | G | 2 | a0001c0001t0003g0246a0001c0005t0001g0247 | 2 | HG01081.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.144+1073C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935412 | ||||||
| chr15:39935557
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0004g0245 | 2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.144+1218C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935557 | ||||||
| chr15:39935624
|
C | T | 1 | a0002c0002t0001g0360 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.144+1285C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935624 | ||||||
| chr15:39935977
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.144+1638G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39935977 | ||||||
| chr15:39936018
|
G | T | 7 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(4): Show | 7 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+1679G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936018 | ||||||
| chr15:39936376
|
A | G | 8 | a0002c0004t0002g0229a0003c0003t0002g0231a0007c0009t0003g0230others(5): Show | 8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+2037A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936376 | ||||||
| chr15:39936409
|
C | T | 1 | a0004c0007t0001g0228 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.144+2070C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936409 | ||||||
| chr15:39936455
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.144+2116C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936455 | ||||||
| chr15:39936699
|
G | A | 3 | a0001c0001t0003g0246a0001c0005t0001g0247a0001c0005t0005g0108 | 3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.144+2360G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936699 | ||||||
| chr15:39936996
|
T | C | 6 | a0001c0001t0001g0112a0001c0001t0002g0111a0001c0001t0003g0109others(3): Show | 6 | HG00621.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-2509T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39936996 | ||||||
| chr15:39937039
|
A | G | 2 | a0002c0004t0001g0358a0002c0004t0001g0359 | 2 | HG00642.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.145-2466A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937039 | ||||||
| chr15:39937046
|
A | C | 86 | a0001c0001t0002g0090a0002c0002t0002g0242a0002c0002t0002g0243others(83): Show | 86 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.145-2459A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937046 | ||||||
| chr15:39937200
|
A | G | 1 | a0005c0008t0001g0357 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.145-2305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937200 | ||||||
| chr15:39937281
|
G | A | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-2224G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937281 | ||||||
| chr15:39937502
|
A | G | 8 | a0002c0004t0002g0229a0003c0003t0002g0231a0007c0009t0003g0230others(5): Show | 8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-2003A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937502 | ||||||
| chr15:39937622
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(130): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.145-1883C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937622 | ||||||
| chr15:39937650
|
C | T | 71 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.145-1855C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937650 | ||||||
| chr15:39937720
|
T | G | 35 | a0001c0001t0005g0014a0001c0001t0005g0023a0001c0001t0005g0028others(32): Show | 35 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.145-1785T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937720 | ||||||
| chr15:39937742
|
T | G | 1 | a0001c0001t0005g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-1763T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937742 | ||||||
| chr15:39937808
|
A | C | 1 | a0001c0022t0002g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.145-1697A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39937808 | ||||||
| chr15:39938033
|
C | G | 8 | a0002c0004t0002g0229a0003c0003t0002g0231a0007c0009t0003g0230others(5): Show | 8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-1472C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938033 | ||||||
| chr15:39938071
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.145-1434T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938071 | ||||||
| chr15:39938200
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0227a0001c0005t0001g0226 | 4 | HG00099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-1305C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938200 | ||||||
| chr15:39938571
|
C | A | 2 | a0003c0003t0002g0052a0003c0003t0002g0053 | 2 | NA18956.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.145-934C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938571 | ||||||
| chr15:39938609
|
A | C | 6 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0004t0003g0036others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-896A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938609 | ||||||
| chr15:39938817
|
T | A | 2 | a0002c0002t0003g0049a0002c0002t0003g0050 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.145-688T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938817 | ||||||
| chr15:39938968
|
A | G | 1 | a0003c0003t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.145-537A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39938968 | ||||||
| chr15:39939299
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.145-206A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939299 | ||||||
| chr15:39939424
|
A | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.145-81A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939424 | ||||||
| chr15:39939473
|
GAA | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | NA18941.hp2 NA18948.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-26_145-25delAA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr15 | 39939473 | |||||
| chr15:39939480
|
A | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | NA18941.hp2 NA18948.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-25A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 1/38 | chr15 | 39939480 | ||||||
| chr15:39939800
|
C | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.257+183C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39939800 | ||||||
| chr15:39939914
|
G | GA | 263 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(260): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.257+301dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39939914 | |||||
| chr15:39940159
|
G | A | 28 | a0001c0001t0005g0014a0001c0001t0005g0023a0001c0001t0005g0028others(25): Show | 28 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.257+542G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940159 | ||||||
| chr15:39940221
|
T | C | 1 | a0002c0002t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.257+604T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940221 | ||||||
| chr15:39940281
|
A | G | 2 | a0003c0003t0001g0106a0003c0003t0006g0105 | 2 | HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.257+664A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940281 | ||||||
| chr15:39940409
|
A | T | 11 | a0001c0001t0005g0014a0001c0001t0005g0028a0001c0001t0005g0029others(8): Show | 11 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.257+792A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940409 | ||||||
| chr15:39940665
|
T | C | 1 | a0002c0004t0002g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.257+1048T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940665 | ||||||
| chr15:39940671
|
G | C | 359 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(356): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.257+1054G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940671 | ||||||
| chr15:39940814
|
C | T | 1 | a0001c0005t0001g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.257+1197C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940814 | ||||||
| chr15:39940851
|
C | T | 27 | a0001c0001t0005g0014a0001c0001t0005g0023a0001c0001t0005g0028others(24): Show | 27 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.257+1234C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39940851 | ||||||
| chr15:39941068
|
A | G | 8 | a0002c0004t0002g0229a0003c0003t0002g0231a0007c0009t0003g0230others(5): Show | 8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+1451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941068 | ||||||
| chr15:39941108
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.257+1491T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941108 | ||||||
| chr15:39941141
|
C | T | 1 | a0002c0004t0002g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.257+1524C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941141 | ||||||
| chr15:39941179
|
T | C | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+1562T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941179 | ||||||
| chr15:39941279
|
G | A | 73 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.257+1662G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941279 | ||||||
| chr15:39941414
|
C | T | 2 | a0001c0001t0003g0225a0001c0021t0003g0224 | 2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+1797C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941414 | ||||||
| chr15:39941441
|
G | C | 2 | a0003c0003t0002g0054a0003c0003t0002g0055 | 2 | NA19057.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.257+1824G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941441 | ||||||
| chr15:39941489
|
A | AT | 8 | a0001c0001t0005g0014a0001c0001t0005g0028a0001c0001t0005g0029others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+1879dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39941489 | |||||
| chr15:39941491
|
T | A | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.257+1874T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941491 | ||||||
| chr15:39941548
|
TAAAG | T | 21 | a0001c0001t0005g0014a0001c0001t0005g0023a0001c0001t0005g0028others(18): Show | 21 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.258-1831_258-1828d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39941548 | |||||
| chr15:39941717
|
T | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-1666T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941717 | ||||||
| chr15:39941760
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(56): Show | 60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.258-1623C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941760 | ||||||
| chr15:39941916
|
A | G | 73 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.258-1467A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39941916 | ||||||
| chr15:39942029
|
A | G | 7 | a0003c0003t0001g0099a0003c0003t0002g0098a0003c0003t0002g0100others(4): Show | 7 | HG01346.hp2 HG01981.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-1354A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942029 | ||||||
| chr15:39942047
|
T | C | 8 | a0002c0004t0002g0229a0003c0003t0002g0231a0007c0009t0003g0230others(5): Show | 8 | HG02015.hp2 NA18952.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-1336T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942047 | ||||||
| chr15:39942398
|
TC | T | 6 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0004t0003g0036others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-984delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942398 | ||||||
| chr15:39942545
|
T | C | 7 | a0002c0002t0007g0043a0002c0002t0010g0046a0002c0031t0009g0045others(4): Show | 7 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-838T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942545 | ||||||
| chr15:39942612
|
T | C | 189 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(186): Show | 190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.258-771T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942612 | ||||||
| chr15:39942614
|
G | C | 73 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.258-769G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942614 | ||||||
| chr15:39942653
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.258-730G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942653 | ||||||
| chr15:39942671
|
G | T | 1 | a0003c0003t0002g0097 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.258-712G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942671 | ||||||
| chr15:39942715
|
G | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-668G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942715 | ||||||
| chr15:39942801
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(70): Show | 74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-582G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942801 | ||||||
| chr15:39942957
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258-426G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942957 | ||||||
| chr15:39942994
|
G | A | 1 | a0002c0004t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.258-389G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39942994 | ||||||
| chr15:39943000
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.258-383G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943000 | ||||||
| chr15:39943029
|
A | AT | 80 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(77): Show | 81 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.258-339dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943029 | |||||
| chr15:39943033
|
T | C | 21 | a0001c0001t0001g0356a0002c0004t0001g0258a0002c0004t0003g0257others(18): Show | 21 | HG00544.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.258-350T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943033 | ||||||
| chr15:39943097
|
G | A | 1 | a0003c0003t0006g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258-286G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943097 | ||||||
| chr15:39943177
|
C | T | 1 | a0002c0004t0001g0353 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.258-206C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943177 | ||||||
| chr15:39943188
|
C | G | 1 | a0001c0001t0003g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.258-195C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | chr15 | 39943188 | ||||||
| chr15:39943351
|
C | CT | 100 | a0001c0001t0001g0356a0001c0001t0002g0090a0001c0001t0005g0014others(97): Show | 101 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.258-12dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | |||||
| chr15:39943351
|
C | CTT | 15 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(12): Show | 15 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-13_258-12dupTT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | |||||
| chr15:39943351
|
CT | C | 84 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(81): Show | 85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.258-12delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 39943351 | |||||
| chr15:39943785
|
G | A | 73 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.360+300G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943785 | ||||||
| chr15:39943793
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.360+308A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943793 | ||||||
| chr15:39943933
|
C | G | 1 | a0002c0004t0001g0343 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.360+448C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943933 | ||||||
| chr15:39943971
|
A | AAAG | 95 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(92): Show | 96 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.360+495_360+497dup others(3): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39943971 | |||||
| chr15:39943984
|
T | G | 1 | a0002c0004t0001g0353 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.360+499T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39943984 | ||||||
| chr15:39944008
|
C | T | 1 | a0003c0003t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.360+523C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944008 | ||||||
| chr15:39944171
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(260): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.360+686G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944171 | ||||||
| chr15:39944175
|
C | G | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.360+690C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944175 | ||||||
| chr15:39944364
|
G | A | 63 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.360+879G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944364 | ||||||
| chr15:39944426
|
C | T | 1 | a0002c0002t0002g0242 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.360+941C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944426 | ||||||
| chr15:39944432
|
C | CTTTTTT | 87 | a0001c0001t0001g0356a0002c0002t0002g0242a0002c0002t0002g0243others(84): Show | 87 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.360+959_360+964dup others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | |||||
| chr15:39944432
|
C | CTTTTTTT | 29 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0005g0023others(26): Show | 29 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.360+958_360+964dup others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | |||||
| chr15:39944432
|
C | CTTTTTTT others(1): Show |
114 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(111): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.360+957_360+964dup others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | |||||
| chr15:39944432
|
C | CTTTTTTT others(2): Show |
22 | a0001c0001t0001g0112a0001c0001t0001g0155a0001c0001t0002g0157others(19): Show | 22 | HG00609.hp2 HG00741.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.360+956_360+964dup others(9): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | |||||
| chr15:39944432
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0009a0007c0009t0003g0234a0007c0009t0003g0235others(1): Show | 4 | NA18972.hp2 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+955_360+964dup others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39944432 | |||||
| chr15:39944455
|
G | A | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360+970G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944455 | ||||||
| chr15:39944462
|
T | C | 1 | a0002c0004t0001g0275 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+977T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944462 | ||||||
| chr15:39944480
|
A | G | 1 | a0002c0004t0004g0341 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+995A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944480 | ||||||
| chr15:39944488
|
A | G | 20 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(17): Show | 20 | HG00408.hp2 HG00438.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.360+1003A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944488 | ||||||
| chr15:39944493
|
G | C | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.360+1008G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944493 | ||||||
| chr15:39944577
|
A | G | 1 | a0001c0001t0003g0225 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.360+1092A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944577 | ||||||
| chr15:39944634
|
C | T | 5 | a0002c0002t0003g0049a0002c0002t0003g0050a0003c0003t0001g0344others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+1149C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944634 | ||||||
| chr15:39944684
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.360+1199C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944684 | ||||||
| chr15:39944958
|
T | C | 1 | a0001c0005t0004g0121 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.360+1473T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39944958 | ||||||
| chr15:39945014
|
A | G | 347 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(344): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.360+1529A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945014 | ||||||
| chr15:39945017
|
T | A | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1532T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945017 | ||||||
| chr15:39945040
|
C | G | 8 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+1555C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945040 | ||||||
| chr15:39945121
|
G | A | 58 | a0002c0011t0002g0096a0003c0003t0001g0058a0003c0003t0001g0067others(55): Show | 58 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.360+1636G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945121 | ||||||
| chr15:39945513
|
A | G | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360+2028A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945513 | ||||||
| chr15:39945600
|
CCTAAGAT others(15): Show |
C | 1 | a0005c0008t0004g0340 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.360+2119_360+2140d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39945600 | |||||
| chr15:39945643
|
T | C | 1 | a0002c0004t0001g0275 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+2158T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945643 | ||||||
| chr15:39945789
|
G | A | 7 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(4): Show | 7 | HG02015.hp2 NA18964.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+2304G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945789 | ||||||
| chr15:39945815
|
A | C | 8 | a0004c0006t0001g0211a0004c0006t0002g0212a0004c0007t0001g0213others(5): Show | 8 | HG00544.hp2 HG00609.hp1 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+2330A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945815 | ||||||
| chr15:39945826
|
C | T | 58 | a0002c0011t0002g0096a0003c0003t0001g0058a0003c0003t0001g0067others(55): Show | 58 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.360+2341C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945826 | ||||||
| chr15:39945944
|
C | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.360+2459C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39945944 | ||||||
| chr15:39946174
|
A | T | 1 | a0001c0001t0002g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.360+2689A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946174 | ||||||
| chr15:39946218
|
G | A | 2 | a0002c0002t0001g0271a0002c0002t0001g0361 | 2 | HG00140.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.360+2733G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946218 | ||||||
| chr15:39946480
|
T | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-2636T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946480 | ||||||
| chr15:39946661
|
T | C | 10 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.361-2455T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946661 | ||||||
| chr15:39946752
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.361-2364C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946752 | ||||||
| chr15:39946833
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0140 | 3 | NA18962.hp1 NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.361-2283C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946833 | ||||||
| chr15:39946834
|
G | A | 1 | a0002c0004t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361-2282G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946834 | ||||||
| chr15:39946891
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0004g0245 | 2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.361-2225A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946891 | ||||||
| chr15:39946974
|
C | T | 1 | a0002c0002t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.361-2142C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39946974 | ||||||
| chr15:39947096
|
C | T | 30 | a0002c0004t0001g0258a0002c0004t0003g0257a0002c0004t0003g0264others(27): Show | 30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-2020C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947096 | ||||||
| chr15:39947155
|
T | C | 1 | a0001c0005t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.361-1961T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947155 | ||||||
| chr15:39947258
|
A | G | 52 | a0002c0011t0002g0096a0003c0003t0001g0067a0003c0003t0001g0073others(49): Show | 52 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.361-1858A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947258 | ||||||
| chr15:39947259
|
T | G | 30 | a0002c0004t0001g0258a0002c0004t0003g0257a0002c0004t0003g0264others(27): Show | 30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-1857T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947259 | ||||||
| chr15:39947276
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(316): Show | 322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.361-1840A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947276 | ||||||
| chr15:39947484
|
G | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.361-1632G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947484 | ||||||
| chr15:39947528
|
G | A | 4 | a0002c0002t0003g0277a0002c0004t0002g0273a0002c0004t0002g0276others(1): Show | 4 | HG00642.hp2 HG01884.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1588G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947528 | ||||||
| chr15:39947575
|
A | G | 65 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.361-1541A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947575 | ||||||
| chr15:39947684
|
G | A | 1 | a0001c0001t0003g0110 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.361-1432G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947684 | ||||||
| chr15:39947711
|
G | A | 75 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(72): Show | 76 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.361-1405G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947711 | ||||||
| chr15:39947727
|
A | G | 30 | a0002c0004t0001g0258a0002c0004t0003g0257a0002c0004t0003g0264others(27): Show | 30 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-1389A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947727 | ||||||
| chr15:39947827
|
G | C | 1 | a0001c0001t0003g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.361-1289G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947827 | ||||||
| chr15:39947848
|
TAGA | T | 3 | a0002c0002t0002g0337a0002c0002t0002g0338a0002c0002t0002g0339 | 3 | HG02895.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.361-1265_361-1263d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 39947848 | |||||
| chr15:39947915
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.361-1201C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39947915 | ||||||
| chr15:39948343
|
C | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(308): Show | 314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.361-773C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948343 | ||||||
| chr15:39948358
|
C | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361-758C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948358 | ||||||
| chr15:39948687
|
G | C | 9 | a0001c0001t0005g0014a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.361-429G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948687 | ||||||
| chr15:39948861
|
A | G | 1 | a0004c0007t0001g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.361-255A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948861 | ||||||
| chr15:39948936
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(63): Show | 67 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.361-180A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 3/38 | chr15 | 39948936 | ||||||
| chr15:39949401
|
CAT | C | 4 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0235others(1): Show | 4 | NA18964.hp1 NA18993.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+134_513+135del others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949401 | ||||||
| chr15:39949644
|
T | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(313): Show | 319 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.513+376T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949644 | ||||||
| chr15:39949652
|
T | C | 1 | a0002c0004t0001g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.513+384T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39949652 | ||||||
| chr15:39949772
|
T | TCAAAGAT others(5543): Show |
1 | a0001c0001t0003g0110 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.513+520_513+521ins others(5550): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39949772 | |||||
| chr15:39950048
|
T | G | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.513+780T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950048 | ||||||
| chr15:39950082
|
T | C | 2 | a0002c0004t0001g0301a0002c0004t0001g0346 | 2 | NA18969.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513+814T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950082 | ||||||
| chr15:39950190
|
A | G | 1 | a0002c0004t0001g0275 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.513+922A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950190 | ||||||
| chr15:39950370
|
A | C | 66 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.513+1102A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950370 | ||||||
| chr15:39950510
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1242G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950510 | ||||||
| chr15:39950647
|
G | A | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.513+1379G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950647 | ||||||
| chr15:39950750
|
CAT | C | 75 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(72): Show | 76 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.513+1483_513+1484d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950750 | ||||||
| chr15:39950949
|
A | G | 5 | a0002c0002t0002g0337a0002c0002t0002g0338a0002c0002t0002g0339others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1681A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950949 | ||||||
| chr15:39950979
|
T | C | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.513+1711T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39950979 | ||||||
| chr15:39951014
|
A | G | 1 | a0002c0004t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.513+1746A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951014 | ||||||
| chr15:39951027
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0004g0245 | 2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513+1759G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951027 | ||||||
| chr15:39951127
|
T | C | 66 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.513+1859T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951127 | ||||||
| chr15:39951207
|
G | C | 8 | a0004c0006t0001g0211a0004c0006t0002g0212a0004c0007t0001g0213others(5): Show | 8 | HG00544.hp2 HG00609.hp1 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1939G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951207 | ||||||
| chr15:39951212
|
A | C | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513+1944A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951212 | ||||||
| chr15:39951358
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(319): Show | 325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.513+2090C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951358 | ||||||
| chr15:39951375
|
C | T | 1 | a0002c0002t0003g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513+2107C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951375 | ||||||
| chr15:39951459
|
G | C | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.513+2191G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951459 | ||||||
| chr15:39951623
|
A | G | 1 | a0004c0007t0003g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.514-2281A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951623 | ||||||
| chr15:39951641
|
A | G | 8 | a0001c0001t0005g0014a0001c0001t0005g0028a0001c0001t0005g0029others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-2263A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951641 | ||||||
| chr15:39951714
|
G | C | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2190G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951714 | ||||||
| chr15:39951770
|
T | G | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2134T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951770 | ||||||
| chr15:39951822
|
C | G | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.514-2082C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951822 | ||||||
| chr15:39951832
|
AC | A | 65 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.514-2067delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39951832 | |||||
| chr15:39951857
|
A | G | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.514-2047A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951857 | ||||||
| chr15:39951892
|
C | G | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.514-2012C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39951892 | ||||||
| chr15:39952039
|
C | T | 8 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-1865C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952039 | ||||||
| chr15:39952294
|
CT | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.514-1596delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr15 | 39952294 | |||||
| chr15:39952319
|
C | T | 76 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(73): Show | 77 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.514-1585C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952319 | ||||||
| chr15:39952321
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.514-1583T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952321 | ||||||
| chr15:39952528
|
A | G | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1376A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952528 | ||||||
| chr15:39952580
|
T | C | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1324T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952580 | ||||||
| chr15:39952873
|
A | C | 1 | a0002c0004t0002g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.514-1031A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952873 | ||||||
| chr15:39952897
|
G | T | 77 | a0001c0001t0003g0219a0002c0002t0001g0020a0002c0002t0001g0022others(74): Show | 78 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.514-1007G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952897 | ||||||
| chr15:39952913
|
T | C | 69 | a0001c0001t0003g0219a0002c0002t0001g0360a0002c0002t0001g0362others(66): Show | 70 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.514-991T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39952913 | ||||||
| chr15:39953055
|
C | T | 6 | a0002c0002t0003g0049a0002c0002t0003g0050a0002c0002t0010g0046others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-849C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953055 | ||||||
| chr15:39953128
|
G | A | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.514-776G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953128 | ||||||
| chr15:39953253
|
C | G | 3 | a0003c0003t0002g0083a0003c0003t0002g0084a0003c0003t0002g0085 | 3 | NA18962.hp2 NA19004.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.514-651C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953253 | ||||||
| chr15:39953517
|
A | C | 1 | a0004c0007t0001g0217 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.514-387A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953517 | ||||||
| chr15:39953553
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.514-351T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953553 | ||||||
| chr15:39953578
|
G | A | 34 | a0002c0002t0001g0003a0002c0002t0001g0160a0002c0002t0001g0161others(31): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.514-326G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953578 | ||||||
| chr15:39953599
|
G | A | 55 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(52): Show | 55 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.514-305G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953599 | ||||||
| chr15:39953635
|
A | C | 66 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.514-269A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953635 | ||||||
| chr15:39953648
|
A | G | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.514-256A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953648 | ||||||
| chr15:39953725
|
G | A | 35 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(32): Show | 35 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-179G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 4/38 | chr15 | 39953725 | ||||||
| chr15:39954101
|
A | T | 1 | a0004c0007t0001g0217 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.594+117A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954101 | ||||||
| chr15:39954172
|
G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.594+188G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954172 | ||||||
| chr15:39954188
|
A | G | 8 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+204A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954188 | ||||||
| chr15:39954236
|
A | G | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.594+252A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954236 | ||||||
| chr15:39954398
|
G | A | 66 | a0001c0001t0001g0112a0001c0001t0001g0170a0001c0001t0001g0205others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.594+414G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954398 | ||||||
| chr15:39954523
|
G | A | 1 | a0002c0004t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.594+539G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954523 | ||||||
| chr15:39954533
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(66): Show | 70 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.594+549C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954533 | ||||||
| chr15:39954534
|
G | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+550G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954534 | ||||||
| chr15:39954867
|
G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.595-753G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954867 | ||||||
| chr15:39954996
|
A | G | 3 | a0002c0002t0002g0242a0002c0002t0002g0243a0011c0017t0002g0240 | 3 | HG02145.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.595-624A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39954996 | ||||||
| chr15:39955077
|
C | A | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-543C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955077 | ||||||
| chr15:39955166
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.595-454T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955166 | ||||||
| chr15:39955262
|
C | T | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-358C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955262 | ||||||
| chr15:39955449
|
C | G | 1 | a0003c0003t0002g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.595-171C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955449 | ||||||
| chr15:39955488
|
A | G | 338 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(335): Show | 341 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.595-132A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 5/38 | chr15 | 39955488 | ||||||
| chr15:39955824
|
A | G | 2 | a0003c0003t0001g0058a0003c0003t0002g0059 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.743+56A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955824 | ||||||
| chr15:39955887
|
A | G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.743+119A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955887 | ||||||
| chr15:39955896
|
ATCTT | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(66): Show | 70 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.743+129_743+132del others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955896 | ||||||
| chr15:39955921
|
G | A | 79 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(76): Show | 80 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.743+153G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39955921 | ||||||
| chr15:39956004
|
CT | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(303): Show | 309 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.743+255delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39956004 | |||||
| chr15:39956004
|
CTT | C | 16 | a0001c0001t0003g0173a0001c0001t0005g0028a0001c0005t0001g0125others(13): Show | 16 | HG00609.hp2 HG00741.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+254_743+255del others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39956004 | |||||
| chr15:39956131
|
A | C | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+363A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956131 | ||||||
| chr15:39956384
|
A | G | 1 | a0002c0011t0002g0332 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.743+616A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956384 | ||||||
| chr15:39956515
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(324): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.743+747T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956515 | ||||||
| chr15:39956558
|
A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.743+790A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956558 | ||||||
| chr15:39956819
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(245): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.743+1051A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956819 | ||||||
| chr15:39956846
|
C | G | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+1078C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956846 | ||||||
| chr15:39956882
|
T | G | 1 | a0001c0001t0003g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.743+1114T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956882 | ||||||
| chr15:39956991
|
A | T | 1 | a0002c0004t0004g0331 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.743+1223A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39956991 | ||||||
| chr15:39957021
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(324): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.743+1253T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957021 | ||||||
| chr15:39957178
|
C | T | 8 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.743+1410C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957178 | ||||||
| chr15:39957325
|
C | G | 4 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+1557C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957325 | ||||||
| chr15:39957464
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(262): Show | 267 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.743+1696C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957464 | ||||||
| chr15:39957511
|
T | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(334): Show | 340 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.743+1743T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957511 | ||||||
| chr15:39957565
|
A | G | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.743+1797A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957565 | ||||||
| chr15:39957646
|
TG | T | 24 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(21): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.743+1879delG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957646 | ||||||
| chr15:39957710
|
A | T | 1 | a0015c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+1942A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957710 | ||||||
| chr15:39957730
|
A | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.743+1962A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957730 | ||||||
| chr15:39957807
|
A | G | 27 | a0004c0006t0001g0211a0004c0006t0001g0255a0004c0006t0001g0256others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.743+2039A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957807 | ||||||
| chr15:39957849
|
G | C | 11 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0286others(8): Show | 12 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2081G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39957849 | ||||||
| chr15:39958305
|
T | C | 80 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(77): Show | 81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.743+2537T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958305 | ||||||
| chr15:39958331
|
G | A | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+2563G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958331 | ||||||
| chr15:39958476
|
T | A | 80 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(77): Show | 81 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.743+2708T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958476 | ||||||
| chr15:39958531
|
G | C | 1 | a0005c0008t0001g0357 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.743+2763G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958531 | ||||||
| chr15:39958550
|
C | T | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.743+2782C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958550 | ||||||
| chr15:39958587
|
G | A | 1 | a0001c0001t0003g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.743+2819G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958587 | ||||||
| chr15:39958695
|
C | T | 1 | a0002c0002t0002g0339 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.743+2927C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958695 | ||||||
| chr15:39958736
|
A | G | 3 | a0001c0001t0002g0220a0001c0001t0002g0223a0001c0005t0002g0221 | 3 | NA18950.hp1 NA19082.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.743+2968A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958736 | ||||||
| chr15:39958800
|
A | G | 1 | a0001c0001t0002g0158 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.744-2984A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958800 | ||||||
| chr15:39958982
|
G | A | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744-2802G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958982 | ||||||
| chr15:39958996
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(258): Show | 263 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.744-2788T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958996 | ||||||
| chr15:39958997
|
G | A | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.744-2787G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39958997 | ||||||
| chr15:39959004
|
T | G | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-2780T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959004 | ||||||
| chr15:39959077
|
A | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.744-2707A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959077 | ||||||
| chr15:39959154
|
C | T | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-2630C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959154 | ||||||
| chr15:39959296
|
G | C | 1 | a0002c0002t0010g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.744-2488G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959296 | ||||||
| chr15:39959307
|
A | C | 1 | a0001c0001t0004g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.744-2477A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959307 | ||||||
| chr15:39959316
|
G | A | 8 | a0003c0003t0002g0060a0003c0003t0002g0061a0003c0003t0002g0062others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-2468G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959316 | ||||||
| chr15:39959394
|
T | C | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-2390T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959394 | ||||||
| chr15:39959540
|
A | G | 190 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0035others(187): Show | 191 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.744-2244A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959540 | ||||||
| chr15:39959714
|
G | C | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.744-2070G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959714 | ||||||
| chr15:39959731
|
A | G | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-2053A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959731 | ||||||
| chr15:39959850
|
C | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.744-1934C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959850 | ||||||
| chr15:39959901
|
T | C | 4 | a0002c0002t0001g0286a0002c0019t0001g0285a0004c0006t0004g0249others(1): Show | 4 | HG01074.hp2 HG01175.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-1883T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959901 | ||||||
| chr15:39959930
|
A | G | 10 | a0002c0004t0001g0005a0002c0004t0001g0325a0002c0004t0001g0326others(7): Show | 11 | HG00642.hp1 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-1854A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959930 | ||||||
| chr15:39959936
|
G | C | 2 | a0003c0003t0002g0054a0003c0003t0002g0055 | 2 | NA19057.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.744-1848G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959936 | ||||||
| chr15:39959959
|
C | T | 8 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-1825C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959959 | ||||||
| chr15:39959961
|
A | C | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-1823A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959961 | ||||||
| chr15:39959967
|
G | T | 9 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(6): Show | 9 | HG01106.hp2 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.744-1817G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39959967 | ||||||
| chr15:39960011
|
A | C | 115 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0002g0009others(112): Show | 116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.744-1773A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960011 | ||||||
| chr15:39960129
|
A | C | 79 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(76): Show | 80 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.744-1655A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960129 | ||||||
| chr15:39960150
|
C | T | 1 | a0004c0007t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.744-1634C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960150 | ||||||
| chr15:39960163
|
C | CAA | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-1602_744-1601d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 39960163 | |||||
| chr15:39960273
|
A | T | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-1511A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960273 | ||||||
| chr15:39960308
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.744-1476A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960308 | ||||||
| chr15:39960364
|
A | G | 61 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.744-1420A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960364 | ||||||
| chr15:39960470
|
C | T | 191 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0035others(188): Show | 192 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.744-1314C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960470 | ||||||
| chr15:39960556
|
G | C | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.744-1228G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960556 | ||||||
| chr15:39960584
|
A | G | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.744-1200A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960584 | ||||||
| chr15:39960766
|
T | G | 1 | a0008c0015t0006g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.744-1018T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960766 | ||||||
| chr15:39960923
|
T | A | 76 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(73): Show | 77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.744-861T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39960923 | ||||||
| chr15:39961045
|
C | A | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.744-739C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961045 | ||||||
| chr15:39961139
|
C | T | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-645C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961139 | ||||||
| chr15:39961162
|
A | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744-622A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961162 | ||||||
| chr15:39961166
|
A | G | 38 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0003g0162others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.744-618A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961166 | ||||||
| chr15:39961229
|
C | T | 9 | a0002c0002t0003g0318a0002c0002t0003g0319a0002c0004t0001g0301others(6): Show | 9 | NA18947.hp2 NA18949.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-555C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961229 | ||||||
| chr15:39961262
|
C | T | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-522C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961262 | ||||||
| chr15:39961473
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.744-311G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961473 | ||||||
| chr15:39961522
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.744-262C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961522 | ||||||
| chr15:39961542
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.744-242G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961542 | ||||||
| chr15:39961618
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.744-166C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961618 | ||||||
| chr15:39961685
|
G | A | 27 | a0004c0006t0001g0211a0004c0006t0001g0255a0004c0006t0001g0256others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.744-99G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961685 | ||||||
| chr15:39961758
|
A | T | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.744-26A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961758 | ||||||
| chr15:39961773
|
T | G | 1 | a0004c0006t0004g0250 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.744-11T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 6/38 | chr15 | 39961773 | ||||||
| chr15:39961954
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+55A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39961954 | ||||||
| chr15:39961983
|
C | G | 2 | a0004c0006t0001g0255a0004c0006t0001g0256 | 2 | HG02698.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.859+84C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39961983 | ||||||
| chr15:39962008
|
A | G | 4 | a0002c0002t0007g0043a0002c0004t0003g0039a0009c0016t0007g0042others(1): Show | 4 | HG01255.hp1 HG02486.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+109A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962008 | ||||||
| chr15:39962131
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+232T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962131 | ||||||
| chr15:39962350
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(67): Show | 71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.859+451G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962350 | ||||||
| chr15:39962412
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+513G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962412 | ||||||
| chr15:39962745
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.859+846G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962745 | ||||||
| chr15:39962852
|
C | T | 24 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(21): Show | 27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.859+953C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962852 | ||||||
| chr15:39962955
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+1056A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962955 | ||||||
| chr15:39962964
|
T | G | 2 | a0003c0025t0004g0010a0003c0026t0001g0011 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859+1065T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39962964 | ||||||
| chr15:39963061
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+1162C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963061 | ||||||
| chr15:39963199
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.859+1300T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963199 | ||||||
| chr15:39963229
|
G | A | 27 | a0004c0006t0001g0211a0004c0006t0001g0255a0004c0006t0001g0256others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.859+1330G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963229 | ||||||
| chr15:39963544
|
T | G | 1 | a0002c0002t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.859+1645T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963544 | ||||||
| chr15:39963568
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.859+1669A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963568 | ||||||
| chr15:39963659
|
A | G | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.859+1760A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963659 | ||||||
| chr15:39963763
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.859+1864T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963763 | ||||||
| chr15:39963843
|
C | T | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1843C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963843 | ||||||
| chr15:39963869
|
A | T | 27 | a0004c0006t0001g0211a0004c0006t0001g0255a0004c0006t0001g0256others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.860-1817A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39963869 | ||||||
| chr15:39964033
|
T | C | 1 | a0002c0004t0001g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.860-1653T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964033 | ||||||
| chr15:39964123
|
T | C | 34 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(31): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.860-1563T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964123 | ||||||
| chr15:39964205
|
A | G | 1 | a0002c0011t0002g0096 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.860-1481A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964205 | ||||||
| chr15:39964235
|
G | A | 76 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(73): Show | 77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.860-1451G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964235 | ||||||
| chr15:39964268
|
A | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.860-1418A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964268 | ||||||
| chr15:39964298
|
A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.860-1388A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964298 | ||||||
| chr15:39964400
|
G | A | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1286G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964400 | ||||||
| chr15:39964454
|
TAA | T | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.860-1231_860-1230d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964454 | ||||||
| chr15:39964470
|
G | A | 76 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(73): Show | 77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.860-1216G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964470 | ||||||
| chr15:39964502
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0003g0201a0001c0001t0003g0202others(2): Show | 5 | NA18970.hp2 NA18989.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.860-1184A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964502 | ||||||
| chr15:39964541
|
A | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0227a0001c0005t0001g0226 | 4 | HG00099.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1145A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964541 | ||||||
| chr15:39964584
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.860-1102T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964584 | ||||||
| chr15:39964774
|
A | G | 75 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0002g0305others(72): Show | 76 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.860-912A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964774 | ||||||
| chr15:39964902
|
T | C | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.860-784T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964902 | ||||||
| chr15:39964978
|
G | T | 1 | a0002c0013t0001g0283 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.860-708G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964978 | ||||||
| chr15:39964993
|
A | G | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.860-693A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39964993 | ||||||
| chr15:39965040
|
T | C | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.860-646T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965040 | ||||||
| chr15:39965156
|
T | C | 1 | a0001c0005t0001g0153 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.860-530T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965156 | ||||||
| chr15:39965161
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.860-525G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965161 | ||||||
| chr15:39965312
|
C | CG | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.860-370dupG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 39965312 | |||||
| chr15:39965316
|
G | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.860-370G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965316 | ||||||
| chr15:39965402
|
G | A | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.860-284G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965402 | ||||||
| chr15:39965404
|
G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.860-282G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965404 | ||||||
| chr15:39965413
|
C | T | 3 | a0002c0002t0003g0049a0002c0002t0003g0050a0002c0002t0010g0046 | 3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.860-273C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965413 | ||||||
| chr15:39965414
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.860-272A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965414 | ||||||
| chr15:39965544
|
A | G | 1 | a0002c0004t0001g0321 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.860-142A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965544 | ||||||
| chr15:39965559
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | NA18941.hp2 NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.860-127C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 7/38 | chr15 | 39965559 | ||||||
| chr15:39966127
|
T | C | 2 | a0004c0007t0002g0267a0004c0007t0003g0259 | 2 | NA18972.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1017+284T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966127 | ||||||
| chr15:39966128
|
A | C | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+285A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966128 | ||||||
| chr15:39966349
|
G | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(178): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1017+506G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966349 | ||||||
| chr15:39966430
|
G | C | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+587G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966430 | ||||||
| chr15:39966501
|
C | CA | 221 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(218): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1017+671dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966501 | |||||
| chr15:39966501
|
C | CAA | 73 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(70): Show | 74 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1017+670_1017+671d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966501 | |||||
| chr15:39966765
|
A | G | 1 | a0001c0001t0005g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1018-579A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966765 | ||||||
| chr15:39966793
|
A | G | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018-551A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966793 | ||||||
| chr15:39966828
|
A | G | 7 | a0003c0003t0002g0078a0003c0003t0002g0080a0003c0003t0002g0081others(4): Show | 7 | HG00621.hp2 NA18612.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018-516A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966828 | ||||||
| chr15:39966840
|
AT | A | 63 | a0001c0001t0001g0170a0001c0001t0001g0207a0001c0001t0001g0244others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1018-494delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39966840 | |||||
| chr15:39966853
|
G | A | 76 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(73): Show | 77 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1018-491G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39966853 | ||||||
| chr15:39967303
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1018-41G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | chr15 | 39967303 | ||||||
| chr15:39967318
|
C | CT | 275 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(272): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1018-11dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39967318 | |||||
| chr15:39967318
|
C | CTT | 40 | a0002c0002t0001g0003a0002c0002t0001g0035a0002c0002t0001g0271others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1018-12_1018-11dup others(2): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 39967318 | |||||
| chr15:39968007
|
C | T | 53 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(50): Show | 53 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1553+128C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968007 | ||||||
| chr15:39968015
|
G | A | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1553+136G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968015 | ||||||
| chr15:39968122
|
G | A | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+243G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968122 | ||||||
| chr15:39968210
|
G | C | 1 | a0015c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1553+331G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968210 | ||||||
| chr15:39968230
|
G | C | 1 | a0005c0014t0004g0292 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+351G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968230 | ||||||
| chr15:39968287
|
A | G | 5 | a0001c0005t0001g0125a0001c0005t0005g0123a0001c0005t0005g0124others(2): Show | 5 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553+408A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968287 | ||||||
| chr15:39968313
|
A | G | 1 | a0007c0009t0003g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1553+434A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968313 | ||||||
| chr15:39968341
|
C | T | 1 | a0005c0014t0004g0292 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+462C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968341 | ||||||
| chr15:39968369
|
C | A | 38 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0003g0162others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1553+490C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968369 | ||||||
| chr15:39968451
|
C | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1553+572C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968451 | ||||||
| chr15:39968507
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1553+628T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968507 | ||||||
| chr15:39968545
|
C | A | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+666C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968545 | ||||||
| chr15:39968745
|
A | G | 38 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0003g0162others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1553+866A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968745 | ||||||
| chr15:39968824
|
G | A | 1 | a0002c0011t0002g0302 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1553+945G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39968824 | ||||||
| chr15:39968873
|
G | GAT | 6 | a0002c0004t0001g0041a0003c0003t0001g0106a0003c0003t0002g0054others(3): Show | 6 | HG00673.hp1 HG02165.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1553+1012_1553+101 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATAT | 15 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(12): Show | 15 | HG01255.hp1 HG01891.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1553+1010_1553+101 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATATAT | 64 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(61): Show | 65 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1553+1008_1553+101 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATATATA others(1): Show |
9 | a0001c0001t0002g0118a0001c0001t0002g0149a0001c0001t0002g0152others(6): Show | 9 | HG02129.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+1006_1553+101 others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATATATA others(3): Show |
19 | a0002c0002t0003g0162a0002c0002t0003g0335a0004c0006t0001g0255others(16): Show | 19 | HG01074.hp2 HG01106.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1553+1004_1553+101 others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATATATA others(5): Show |
9 | a0002c0002t0003g0336a0004c0006t0001g0260a0004c0006t0002g0212others(6): Show | 9 | HG00544.hp2 HG01168.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+1002_1553+101 others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968873
|
G | GATATATA others(7): Show |
1 | a0004c0007t0001g0216 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1553+1000_1553+101 others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968873 | |||||
| chr15:39968891
|
T | TATAC | 93 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | |||||
| chr15:39968891
|
T | TATATAC | 4 | a0001c0001t0003g0176a0002c0002t0001g0291a0005c0008t0004g0004others(1): Show | 5 | HG00140.hp1 HG01361.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | |||||
| chr15:39968891
|
T | TATATATA others(3): Show |
6 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0004g0237others(3): Show | 6 | HG02145.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | |||||
| chr15:39968891
|
T | TATATATA others(5): Show |
3 | a0004c0006t0001g0211a0010c0018t0005g0239a0010c0018t0005g0241 | 3 | HG00609.hp1 HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1553+1013_1553+101 others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39968891 | |||||
| chr15:39969065
|
C | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1553+1186C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969065 | ||||||
| chr15:39969078
|
T | C | 55 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(52): Show | 55 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1553+1199T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969078 | ||||||
| chr15:39969097
|
A | G | 3 | a0002c0002t0001g0035a0002c0004t0003g0038a0002c0004t0003g0039 | 3 | HG02630.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1553+1218A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969097 | ||||||
| chr15:39969227
|
A | G | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1348A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969227 | ||||||
| chr15:39969345
|
A | T | 2 | a0003c0003t0002g0076a0003c0010t0001g0077 | 2 | NA19056.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1553+1466A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969345 | ||||||
| chr15:39969356
|
C | CT | 78 | a0001c0001t0003g0199a0002c0002t0001g0020a0002c0002t0001g0022others(75): Show | 79 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1553+1499dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | |||||
| chr15:39969356
|
CT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(80): Show | 84 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1553+1499delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | |||||
| chr15:39969356
|
CTT | C | 41 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1553+1498_1553+149 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | |||||
| chr15:39969356
|
CTTTTTT | C | 54 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(51): Show | 54 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1553+1494_1553+149 others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39969356 | |||||
| chr15:39969423
|
C | T | 1 | a0003c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1553+1544C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969423 | ||||||
| chr15:39969477
|
C | G | 1 | a0004c0006t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1553+1598C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969477 | ||||||
| chr15:39969522
|
G | A | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1553+1643G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969522 | ||||||
| chr15:39969529
|
G | T | 1 | a0003c0003t0002g0095 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1553+1650G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969529 | ||||||
| chr15:39969554
|
G | A | 14 | a0003c0003t0001g0099a0003c0003t0002g0052a0003c0003t0002g0053others(11): Show | 14 | HG01346.hp2 HG01981.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1553+1675G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969554 | ||||||
| chr15:39969651
|
C | T | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1553+1772C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969651 | ||||||
| chr15:39969701
|
A | G | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553+1822A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969701 | ||||||
| chr15:39969811
|
T | C | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1553+1932T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39969811 | ||||||
| chr15:39970074
|
G | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(297): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1553+2195G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970074 | ||||||
| chr15:39970123
|
A | G | 1 | a0004c0006t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1553+2244A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970123 | ||||||
| chr15:39970128
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1553+2249C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970128 | ||||||
| chr15:39970215
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1553+2336C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970215 | ||||||
| chr15:39970263
|
A | G | 27 | a0004c0006t0001g0211a0004c0006t0001g0255a0004c0006t0001g0256others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1553+2384A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970263 | ||||||
| chr15:39970300
|
T | G | 3 | a0002c0002t0003g0049a0002c0002t0003g0050a0002c0002t0010g0046 | 3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1553+2421T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970300 | ||||||
| chr15:39970358
|
A | G | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1553+2479A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970358 | ||||||
| chr15:39970482
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1554-2426G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970482 | ||||||
| chr15:39970490
|
G | C | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1554-2418G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970490 | ||||||
| chr15:39970530
|
A | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1554-2378A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970530 | ||||||
| chr15:39970617
|
A | C | 4 | a0002c0002t0001g0271a0002c0002t0001g0286a0002c0002t0001g0361others(1): Show | 4 | HG00140.hp2 HG01081.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-2291A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970617 | ||||||
| chr15:39970647
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1554-2261T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970647 | ||||||
| chr15:39970789
|
G | A | 53 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(50): Show | 53 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1554-2119G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970789 | ||||||
| chr15:39970790
|
C | T | 2 | a0002c0002t0004g0018a0002c0002t0004g0019 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1554-2118C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970790 | ||||||
| chr15:39970881
|
A | G | 2 | a0002c0004t0002g0273a0002c0004t0002g0354 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1554-2027A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970881 | ||||||
| chr15:39970915
|
G | A | 70 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0002g0305others(67): Show | 71 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1554-1993G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39970915 | ||||||
| chr15:39971161
|
T | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1554-1747T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971161 | ||||||
| chr15:39971172
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1554-1736T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971172 | ||||||
| chr15:39971250
|
G | A | 2 | a0001c0005t0005g0154a0006c0032t0005g0122 | 2 | HG00741.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1554-1658G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971250 | ||||||
| chr15:39971262
|
A | C | 3 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0005g0021 | 3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1554-1646A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971262 | ||||||
| chr15:39971357
|
C | G | 1 | a0004c0006t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1554-1551C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971357 | ||||||
| chr15:39971402
|
T | C | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1554-1506T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971402 | ||||||
| chr15:39971498
|
T | G | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1554-1410T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971498 | ||||||
| chr15:39971506
|
G | C | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1554-1402G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971506 | ||||||
| chr15:39971564
|
C | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1554-1344C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971564 | ||||||
| chr15:39971628
|
G | T | 1 | a0005c0008t0004g0340 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1554-1280G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971628 | ||||||
| chr15:39971716
|
C | CA | 38 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0003g0162others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1554-1181dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39971716 | |||||
| chr15:39971720
|
A | C | 1 | a0003c0003t0002g0081 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1554-1188A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39971720 | ||||||
| chr15:39972036
|
T | A | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1554-872T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972036 | ||||||
| chr15:39972180
|
G | A | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1554-728G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972180 | ||||||
| chr15:39972290
|
G | A | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1554-618G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972290 | ||||||
| chr15:39972328
|
C | T | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1554-580C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972328 | ||||||
| chr15:39972349
|
C | CA | 39 | a0001c0001t0002g0206a0001c0021t0003g0224a0002c0002t0001g0003others(36): Show | 42 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1554-544dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 39972349 | |||||
| chr15:39972381
|
A | T | 1 | a0002c0002t0001g0286 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1554-527A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972381 | ||||||
| chr15:39972544
|
T | C | 4 | a0002c0002t0004g0237a0002c0004t0005g0238a0010c0018t0005g0239others(1): Show | 4 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-364T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972544 | ||||||
| chr15:39972649
|
G | A | 1 | a0002c0004t0002g0317 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1554-259G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972649 | ||||||
| chr15:39972804
|
A | G | 1 | a0001c0005t0005g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1554-104A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 9/38 | chr15 | 39972804 | ||||||
| chr15:39973023
|
G | A | 1 | a0002c0002t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1660+9G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973023 | ||||||
| chr15:39973026
|
A | T | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1660+12A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973026 | ||||||
| chr15:39973109
|
T | G | 56 | a0002c0004t0014g0303a0003c0003t0001g0058a0003c0003t0001g0067others(53): Show | 56 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1660+95T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973109 | ||||||
| chr15:39973203
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(291): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1660+189T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973203 | ||||||
| chr15:39973238
|
T | C | 2 | a0002c0004t0002g0273a0002c0004t0002g0354 | 2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1660+224T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973238 | ||||||
| chr15:39973255
|
T | C | 1 | a0002c0002t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1660+241T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973255 | ||||||
| chr15:39973302
|
C | A | 74 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(71): Show | 75 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+288C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973302 | ||||||
| chr15:39973387
|
C | T | 74 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(71): Show | 75 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-205C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973387 | ||||||
| chr15:39973535
|
T | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1661-57T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973535 | ||||||
| chr15:39973543
|
C | T | 1 | a0002c0011t0002g0347 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1661-49C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 10/38 | chr15 | 39973543 | ||||||
| chr15:39974042
|
T | G | 1 | a0002c0004t0001g0322 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1818+293T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974042 | ||||||
| chr15:39974075
|
T | C | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1818+326T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974075 | ||||||
| chr15:39974334
|
T | C | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1818+585T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974334 | ||||||
| chr15:39974625
|
C | T | 1 | a0002c0002t0001g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1818+876C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974625 | ||||||
| chr15:39974635
|
C | T | 38 | a0002c0002t0002g0242a0002c0002t0002g0243a0002c0002t0003g0162others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1818+886C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974635 | ||||||
| chr15:39974761
|
T | C | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1818+1012T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974761 | ||||||
| chr15:39974909
|
G | A | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1818+1160G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39974909 | ||||||
| chr15:39975046
|
C | G | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1818+1297C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975046 | ||||||
| chr15:39975174
|
C | T | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1819-1240C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975174 | ||||||
| chr15:39975246
|
A | ATGACACA others(7): Show |
297 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(294): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1819-1167_1819-116 others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr15 | 39975246 | |||||
| chr15:39975328
|
AAGAT | A | 78 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(75): Show | 79 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1819-1084_1819-108 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr15 | 39975328 | |||||
| chr15:39975342
|
C | G | 34 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(31): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1819-1072C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975342 | ||||||
| chr15:39975526
|
A | C | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1819-888A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975526 | ||||||
| chr15:39975736
|
A | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | NA18941.hp2 NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1819-678A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39975736 | ||||||
| chr15:39976013
|
G | A | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1819-401G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976013 | ||||||
| chr15:39976058
|
C | G | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1819-356C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976058 | ||||||
| chr15:39976148
|
A | G | 1 | a0002c0004t0002g0349 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1819-266A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976148 | ||||||
| chr15:39976225
|
G | C | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1819-189G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976225 | ||||||
| chr15:39976343
|
G | A | 57 | a0003c0003t0001g0058a0003c0003t0001g0067a0003c0003t0001g0073others(54): Show | 57 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1819-71G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 11/38 | chr15 | 39976343 | ||||||
| chr15:39976851
|
G | A | 81 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(78): Show | 82 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(79): Show |
splice_region_variant&intron_variant | LOW | c.2249+7G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976851 | ||||||
| chr15:39976878
|
G | T | 64 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2249+34G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976878 | ||||||
| chr15:39976901
|
A | AT | 82 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0001g0360others(79): Show | 83 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2249+66dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39976901 | |||||
| chr15:39976925
|
T | TTTCC | 214 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2249+93_2249+96dup others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39976925 | |||||
| chr15:39976946
|
T | C | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+102T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39976946 | ||||||
| chr15:39977131
|
T | TCAAAAA | 174 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(171): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2249+287_2249+288i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977131 | ||||||
| chr15:39977132
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2249+288T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977132 | ||||||
| chr15:39977132
|
T | TAAAAAC | 33 | a0002c0002t0002g0242a0002c0002t0002g0243a0004c0006t0001g0211others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.2249+305_2249+310d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977132 | |||||
| chr15:39977132
|
T | TAAAAACA others(5): Show |
2 | a0002c0002t0004g0237a0002c0004t0005g0238 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2249+299_2249+310d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977132 | |||||
| chr15:39977149
|
A | G | 2 | a0003c0003t0001g0058a0003c0003t0002g0059 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2249+305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977149 | ||||||
| chr15:39977151
|
A | AAAAACG | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+310_2249+311i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977151 | |||||
| chr15:39977161
|
C | T | 1 | a0002c0002t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2249+317C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977161 | ||||||
| chr15:39977300
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2249+456C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977300 | ||||||
| chr15:39977397
|
A | G | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2249+553A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977397 | ||||||
| chr15:39977410
|
G | A | 9 | a0002c0002t0001g0035a0002c0002t0002g0040a0002c0002t0007g0043others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2249+566G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977410 | ||||||
| chr15:39977482
|
AGGCAGTG others(5): Show |
A | 214 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2250-594_2250-583d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 39977482 | |||||
| chr15:39977599
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(291): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2250-479T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977599 | ||||||
| chr15:39977612
|
T | G | 1 | a0003c0003t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2250-466T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977612 | ||||||
| chr15:39977642
|
A | G | 159 | a0002c0002t0001g0003a0002c0002t0001g0020a0002c0002t0001g0022others(156): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2250-436A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977642 | ||||||
| chr15:39977715
|
T | C | 2 | a0002c0004t0001g0322a0002c0004t0001g0323 | 2 | HG01256.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2250-363T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977715 | ||||||
| chr15:39977722
|
C | T | 1 | a0004c0006t0001g0256 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2250-356C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977722 | ||||||
| chr15:39977845
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2250-233C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977845 | ||||||
| chr15:39977846
|
A | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2250-232A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977846 | ||||||
| chr15:39977950
|
C | T | 6 | a0003c0003t0002g0231a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02015.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-128C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39977950 | ||||||
| chr15:39978013
|
A | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2250-65A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 12/38 | chr15 | 39978013 | ||||||
| chr15:39978220
|
A | G | 3 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0005g0021 | 3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2319+73A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978220 | ||||||
| chr15:39978437
|
A | G | 54 | a0002c0004t0014g0303a0003c0003t0001g0058a0003c0003t0001g0067others(51): Show | 54 | HG00408.hp1 HG00621.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2319+290A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978437 | ||||||
| chr15:39978454
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(67): Show | 71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2319+307T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978454 | ||||||
| chr15:39978505
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(67): Show | 71 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2319+358G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978505 | ||||||
| chr15:39978505
|
G | T | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2319+358G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978505 | ||||||
| chr15:39978595
|
G | A | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2319+448G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978595 | ||||||
| chr15:39978743
|
T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2319+596T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978743 | ||||||
| chr15:39978801
|
T | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2319+654T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978801 | ||||||
| chr15:39978923
|
A | G | 3 | a0003c0003t0002g0083a0003c0003t0002g0084a0003c0003t0002g0085 | 3 | NA18962.hp2 NA19004.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2319+776A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39978923 | ||||||
| chr15:39979001
|
A | G | 29 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(26): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.2319+854A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979001 | ||||||
| chr15:39979003
|
C | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2319+856C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979003 | ||||||
| chr15:39979053
|
T | G | 1 | a0002c0002t0004g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2319+906T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979053 | ||||||
| chr15:39979070
|
A | G | 34 | a0001c0001t0001g0356a0002c0002t0003g0162a0002c0002t0003g0335others(31): Show | 34 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.2319+923A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979070 | ||||||
| chr15:39979080
|
G | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(63): Show | 67 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2319+933G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979080 | ||||||
| chr15:39979102
|
C | T | 70 | a0001c0005t0001g0032a0001c0005t0001g0034a0002c0002t0001g0360others(67): Show | 71 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.2319+955C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979102 | ||||||
| chr15:39979256
|
G | A | 84 | a0001c0005t0001g0032a0001c0005t0001g0034a0002c0002t0001g0020others(81): Show | 85 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.2319+1109G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979256 | ||||||
| chr15:39979536
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(166): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2319+1389G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979536 | ||||||
| chr15:39979560
|
T | C | 2 | a0001c0001t0003g0246a0001c0005t0001g0247 | 2 | HG01081.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2319+1413T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979560 | ||||||
| chr15:39979661
|
C | T | 2 | a0002c0004t0001g0301a0002c0004t0001g0346 | 2 | NA18969.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2319+1514C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979661 | ||||||
| chr15:39979734
|
A | G | 63 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2319+1587A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979734 | ||||||
| chr15:39979760
|
C | G | 5 | a0001c0001t0002g0090a0001c0001t0002g0120a0001c0001t0002g0146others(2): Show | 5 | HG00438.hp2 HG02129.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+1613C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979760 | ||||||
| chr15:39979773
|
C | T | 1 | a0001c0022t0002g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2319+1626C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979773 | ||||||
| chr15:39979831
|
C | T | 75 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2319+1684C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979831 | ||||||
| chr15:39979947
|
C | T | 114 | a0001c0001t0001g0356a0001c0005t0001g0032a0001c0005t0001g0034others(111): Show | 115 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.2319+1800C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979947 | ||||||
| chr15:39979948
|
G | A | 1 | a0003c0003t0002g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2319+1801G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979948 | ||||||
| chr15:39979978
|
A | G | 1 | a0004c0006t0003g0345 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2319+1831A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39979978 | ||||||
| chr15:39980056
|
A | C | 3 | a0002c0002t0003g0049a0002c0002t0003g0050a0002c0002t0010g0046 | 3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2319+1909A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980056 | ||||||
| chr15:39980153
|
A | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2319+2006A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980153 | ||||||
| chr15:39980154
|
A | G | 1 | a0002c0019t0001g0282 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2319+2007A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980154 | ||||||
| chr15:39980190
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(222): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2319+2043G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980190 | ||||||
| chr15:39980217
|
A | G | 1 | a0003c0003t0002g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2319+2070A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980217 | ||||||
| chr15:39980219
|
G | A | 5 | a0001c0005t0001g0125a0001c0005t0005g0123a0001c0005t0005g0124others(2): Show | 5 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+2072G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980219 | ||||||
| chr15:39980222
|
C | T | 2 | a0003c0003t0002g0098a0003c0003t0002g0102 | 2 | HG01346.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2319+2075C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980222 | ||||||
| chr15:39980348
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0155 | 2 | HG02027.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2319+2201C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980348 | ||||||
| chr15:39980515
|
A | G | 3 | a0001c0001t0002g0138a0003c0003t0001g0058a0003c0003t0002g0059 | 3 | HG02647.hp2 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2319+2368A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980515 | ||||||
| chr15:39980634
|
C | T | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+2487C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980634 | ||||||
| chr15:39980657
|
T | G | 1 | a0002c0029t0002g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2319+2510T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980657 | ||||||
| chr15:39980829
|
T | C | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2319+2682T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39980829 | ||||||
| chr15:39981185
|
C | G | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+3038C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981185 | ||||||
| chr15:39981273
|
G | T | 3 | a0002c0002t0002g0242a0002c0002t0002g0243a0011c0017t0002g0240 | 3 | HG02145.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2319+3126G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981273 | ||||||
| chr15:39981327
|
G | A | 10 | a0001c0005t0001g0137a0001c0005t0001g0153a0004c0006t0001g0211others(7): Show | 10 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2319+3180G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981327 | ||||||
| chr15:39981436
|
G | A | 20 | a0001c0001t0001g0356a0002c0002t0001g0020a0002c0002t0001g0022others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2319+3289G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981436 | ||||||
| chr15:39981573
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(173): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2319+3426T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981573 | ||||||
| chr15:39981587
|
C | T | 72 | a0001c0001t0002g0138a0001c0001t0002g0148a0001c0005t0005g0108others(69): Show | 72 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2319+3440C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981587 | ||||||
| chr15:39981608
|
CT | C | 84 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(81): Show | 85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2319+3473delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981608 | |||||
| chr15:39981613
|
T | C | 62 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2319+3466T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981613 | ||||||
| chr15:39981624
|
T | C | 1 | a0001c0001t0005g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2319+3477T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981624 | ||||||
| chr15:39981649
|
T | C | 9 | a0001c0005t0005g0108a0002c0002t0002g0242a0002c0002t0002g0243others(6): Show | 9 | HG01496.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2319+3502T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981649 | ||||||
| chr15:39981699
|
T | C | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2319+3552T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981699 | ||||||
| chr15:39981742
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(168): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2319+3595T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981742 | ||||||
| chr15:39981813
|
A | C | 1 | a0002c0002t0001g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2319+3666A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981813 | ||||||
| chr15:39981842
|
T | G | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2319+3695T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981842 | ||||||
| chr15:39981924
|
C | CT | 12 | a0001c0005t0005g0108a0002c0002t0002g0242a0002c0002t0002g0243others(9): Show | 12 | HG00544.hp2 HG01175.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.2319+3796dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | |||||
| chr15:39981924
|
C | CTT | 76 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2319+3795_2319+379 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | |||||
| chr15:39981924
|
C | CTTT | 89 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(86): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2319+3794_2319+379 others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | |||||
| chr15:39981924
|
C | CTTTT | 7 | a0001c0001t0001g0133a0001c0001t0001g0155a0001c0001t0002g0119others(4): Show | 7 | HG02055.hp2 HG02074.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.2319+3793_2319+379 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | |||||
| chr15:39981924
|
CT | C | 62 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2319+3796delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39981924 | |||||
| chr15:39981988
|
G | A | 1 | a0014c0028t0002g0308 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2320-3817G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39981988 | ||||||
| chr15:39982049
|
C | T | 1 | a0002c0004t0003g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2320-3756C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982049 | ||||||
| chr15:39982115
|
A | G | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3690A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982115 | ||||||
| chr15:39982125
|
C | T | 2 | a0003c0003t0001g0058a0003c0003t0002g0059 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2320-3680C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982125 | ||||||
| chr15:39982172
|
C | A | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-3633C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982172 | ||||||
| chr15:39982188
|
T | G | 1 | a0002c0002t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2320-3617T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982188 | ||||||
| chr15:39982399
|
A | C | 1 | a0003c0003t0004g0074 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2320-3406A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982399 | ||||||
| chr15:39982526
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2320-3279T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982526 | ||||||
| chr15:39982538
|
TTTTTC | T | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-3252_2320-324 others(9): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39982538 | |||||
| chr15:39982605
|
T | C | 11 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2320-3200T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982605 | ||||||
| chr15:39982616
|
A | G | 62 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(59): Show | 63 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2320-3189A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982616 | ||||||
| chr15:39982617
|
C | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3188C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982617 | ||||||
| chr15:39982618
|
A | C | 1 | a0002c0004t0001g0320 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2320-3187A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982618 | ||||||
| chr15:39982633
|
G | GT | 265 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(262): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2320-3170dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39982633 | |||||
| chr15:39982693
|
C | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3112C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982693 | ||||||
| chr15:39982708
|
C | A | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3097C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982708 | ||||||
| chr15:39982709
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(171): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2320-3096T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982709 | ||||||
| chr15:39982780
|
A | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-3025A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982780 | ||||||
| chr15:39982840
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(259): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2320-2965T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982840 | ||||||
| chr15:39982956
|
T | G | 2 | a0001c0001t0001g0244a0001c0001t0004g0245 | 2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2320-2849T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39982956 | ||||||
| chr15:39983088
|
A | G | 2 | a0002c0004t0001g0322a0002c0004t0001g0323 | 2 | HG01256.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2320-2717A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983088 | ||||||
| chr15:39983115
|
T | C | 8 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048others(5): Show | 8 | HG02451.hp2 HG02622.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-2690T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983115 | ||||||
| chr15:39983163
|
T | A | 83 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2320-2642T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983163 | ||||||
| chr15:39983201
|
G | A | 3 | a0002c0004t0001g0005a0002c0004t0001g0326a0002c0004t0001g0327 | 4 | HG00741.hp2 HG01069.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.2320-2604G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983201 | ||||||
| chr15:39983447
|
CT | C | 162 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2320-2346delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39983447 | |||||
| chr15:39983592
|
G | A | 1 | a0002c0002t0005g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2320-2213G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983592 | ||||||
| chr15:39983652
|
G | A | 14 | a0001c0001t0001g0356a0004c0006t0001g0255a0004c0006t0001g0256others(11): Show | 14 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.2320-2153G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983652 | ||||||
| chr15:39983693
|
C | T | 23 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(20): Show | 26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.2320-2112C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983693 | ||||||
| chr15:39983694
|
G | A | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-2111G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983694 | ||||||
| chr15:39983732
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(60): Show | 64 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2320-2073G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983732 | ||||||
| chr15:39983733
|
C | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2320-2072C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39983733 | ||||||
| chr15:39984033
|
G | A | 1 | a0003c0003t0002g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2320-1772G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984033 | ||||||
| chr15:39984226
|
C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2320-1579C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984226 | ||||||
| chr15:39984371
|
TTTCCTAA | T | 3 | a0002c0004t0001g0258a0002c0004t0003g0257a0002c0004t0003g0264 | 3 | HG00544.hp1 HG02135.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2320-1430_2320-142 others(11): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 39984371 | |||||
| chr15:39984685
|
T | C | 28 | a0002c0002t0001g0003a0002c0002t0001g0271a0002c0002t0001g0284others(25): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.2320-1120T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984685 | ||||||
| chr15:39984770
|
C | T | 83 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2320-1035C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984770 | ||||||
| chr15:39984871
|
A | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(258): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2320-934A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39984871 | ||||||
| chr15:39985017
|
A | C | 105 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2320-788A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985017 | ||||||
| chr15:39985255
|
A | G | 62 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2320-550A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985255 | ||||||
| chr15:39985383
|
C | T | 105 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2320-422C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985383 | ||||||
| chr15:39985402
|
G | A | 60 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(57): Show | 60 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2320-403G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985402 | ||||||
| chr15:39985508
|
C | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2320-297C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985508 | ||||||
| chr15:39985651
|
T | G | 1 | a0002c0004t0004g0331 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2320-154T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985651 | ||||||
| chr15:39985703
|
G | A | 11 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2320-102G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985703 | ||||||
| chr15:39985801
|
T | G | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2320-4T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 13/38 | chr15 | 39985801 | ||||||
| chr15:39985900
|
G | A | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39985900 | ||||||
| chr15:39985991
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2403+103T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39985991 | ||||||
| chr15:39986011
|
T | C | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+123T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986011 | ||||||
| chr15:39986017
|
G | A | 3 | a0002c0002t0002g0309a0002c0002t0002g0310a0002c0002t0002g0311 | 3 | HG03139.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2403+129G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986017 | ||||||
| chr15:39986025
|
T | A | 1 | a0001c0001t0001g0127 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2403+137T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986025 | ||||||
| chr15:39986201
|
CTATA | C | 6 | a0001c0005t0005g0108a0002c0002t0004g0237a0002c0004t0005g0238others(3): Show | 6 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+314_2403+317d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986201 | ||||||
| chr15:39986205
|
A | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2403+317A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986205 | ||||||
| chr15:39986208
|
T | G | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+320T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986208 | ||||||
| chr15:39986283
|
A | G | 1 | a0002c0004t0002g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2403+395A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986283 | ||||||
| chr15:39986367
|
G | T | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2403+479G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986367 | ||||||
| chr15:39986821
|
CT | C | 7 | a0001c0005t0001g0134a0001c0005t0001g0135a0001c0005t0004g0121others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+934delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986821 | ||||||
| chr15:39986877
|
C | CAAA | 62 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2403+991_2403+992i others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr15 | 39986877 | |||||
| chr15:39986880
|
C | A | 67 | a0001c0001t0002g0138a0001c0001t0002g0148a0002c0004t0014g0303others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.2403+992C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39986880 | ||||||
| chr15:39986880
|
C | CAACA | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+994_2403+995i others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr15 | 39986880 | |||||
| chr15:39987086
|
G | A | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-897G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987086 | ||||||
| chr15:39987117
|
A | G | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-866A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987117 | ||||||
| chr15:39987244
|
T | C | 2 | a0002c0002t0002g0351a0002c0002t0002g0352 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2404-739T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987244 | ||||||
| chr15:39987261
|
G | A | 63 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2404-722G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987261 | ||||||
| chr15:39987274
|
C | T | 1 | a0002c0002t0002g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-709C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987274 | ||||||
| chr15:39987317
|
T | C | 8 | a0002c0002t0002g0040a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404-666T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987317 | ||||||
| chr15:39987380
|
A | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(92): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2404-603A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987380 | ||||||
| chr15:39987579
|
T | C | 10 | a0001c0005t0001g0137a0001c0005t0001g0153a0004c0006t0001g0211others(7): Show | 10 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2404-404T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987579 | ||||||
| chr15:39987775
|
A | G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2404-208A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 14/38 | chr15 | 39987775 | ||||||
| chr15:39988296
|
T | G | 1 | a0003c0003t0002g0056 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2526+191T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988296 | ||||||
| chr15:39988338
|
G | A | 20 | a0001c0001t0001g0356a0002c0002t0001g0020a0002c0002t0001g0022others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2526+233G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988338 | ||||||
| chr15:39988415
|
C | T | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2526+310C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988415 | ||||||
| chr15:39988492
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2526+387G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988492 | ||||||
| chr15:39988527
|
T | C | 2 | a0001c0001t0003g0179a0001c0001t0003g0180 | 2 | NA18965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2526+422T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988527 | ||||||
| chr15:39988536
|
A | G | 2 | a0001c0001t0003g0203a0001c0001t0003g0204 | 2 | NA19001.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2526+431A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988536 | ||||||
| chr15:39988565
|
C | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(230): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2526+460C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988565 | ||||||
| chr15:39988592
|
G | T | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2526+487G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988592 | ||||||
| chr15:39988636
|
A | G | 1 | a0001c0001t0011g0164 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2526+531A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988636 | ||||||
| chr15:39988642
|
G | A | 3 | a0002c0002t0003g0049a0002c0002t0003g0050a0002c0002t0010g0046 | 3 | HG02572.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2526+537G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988642 | ||||||
| chr15:39988817
|
A | G | 20 | a0001c0001t0001g0356a0002c0002t0001g0020a0002c0002t0001g0022others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2526+712A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988817 | ||||||
| chr15:39988852
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0002g0128 | 2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2526+747T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988852 | ||||||
| chr15:39988895
|
G | A | 3 | a0001c0001t0002g0117a0001c0001t0002g0141a0001c0001t0002g0178 | 3 | HG00673.hp2 HG02071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2526+790G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39988895 | ||||||
| chr15:39989058
|
A | T | 61 | a0001c0001t0002g0138a0001c0001t0002g0148a0003c0003t0001g0058others(58): Show | 61 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2526+953A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989058 | ||||||
| chr15:39989275
|
A | C | 3 | a0003c0003t0001g0344a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02451.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2527-998A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989275 | ||||||
| chr15:39989276
|
A | G | 10 | a0001c0005t0005g0108a0002c0002t0002g0242a0002c0002t0002g0243others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2527-997A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989276 | ||||||
| chr15:39989337
|
T | C | 91 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0001g0207others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2527-936T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989337 | ||||||
| chr15:39989466
|
G | A | 5 | a0001c0005t0005g0108a0002c0002t0004g0237a0002c0004t0005g0238others(2): Show | 5 | HG01496.hp2 HG02615.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2527-807G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989466 | ||||||
| chr15:39989483
|
T | C | 20 | a0001c0001t0001g0356a0002c0002t0001g0020a0002c0002t0001g0022others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2527-790T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989483 | ||||||
| chr15:39989571
|
A | G | 59 | a0001c0001t0002g0138a0001c0001t0002g0148a0003c0003t0001g0058others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.2527-702A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989571 | ||||||
| chr15:39989650
|
C | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2527-623C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39989650 | ||||||
| chr15:39990122
|
A | G | 3 | a0002c0002t0001g0020a0002c0002t0001g0022a0002c0002t0005g0021 | 3 | HG02055.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2527-151A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39990122 | ||||||
| chr15:39990180
|
A | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2527-93A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 15/38 | chr15 | 39990180 | ||||||
| chr15:39990404
|
C | T | 2 | a0001c0001t0003g0197a0001c0001t0003g0198 | 2 | NA18943.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2631+27C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990404 | ||||||
| chr15:39990424
|
T | C | 346 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(343): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2631+47T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990424 | ||||||
| chr15:39990500
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(93): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2631+123T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990500 | ||||||
| chr15:39990530
|
T | C | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2631+153T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990530 | ||||||
| chr15:39990739
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(266): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2631+362G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990739 | ||||||
| chr15:39990862
|
G | A | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2631+485G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990862 | ||||||
| chr15:39990898
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(79): Show | 85 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2631+521A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990898 | ||||||
| chr15:39990998
|
G | A | 1 | a0002c0004t0001g0275 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2631+621G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39990998 | ||||||
| chr15:39991049
|
T | C | 155 | a0001c0001t0001g0205a0001c0001t0002g0013a0001c0001t0002g0111others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2631+672T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991049 | ||||||
| chr15:39991053
|
A | G | 68 | a0001c0001t0001g0205a0001c0001t0002g0013a0001c0001t0002g0111others(65): Show | 69 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2631+676A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991053 | ||||||
| chr15:39991073
|
G | A | 188 | a0001c0001t0001g0205a0001c0001t0001g0356a0001c0001t0002g0013others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2631+696G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991073 | ||||||
| chr15:39991248
|
C | A | 340 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.2631+871C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991248 | ||||||
| chr15:39991258
|
C | T | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2631+881C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991258 | ||||||
| chr15:39991500
|
G | A | 2 | a0002c0002t0001g0360a0002c0031t0009g0045 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2632-675G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991500 | ||||||
| chr15:39991573
|
A | G | 1 | a0004c0007t0003g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2632-602A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991573 | ||||||
| chr15:39991596
|
T | G | 92 | a0001c0001t0001g0244a0001c0001t0002g0178a0001c0005t0001g0125others(89): Show | 93 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2632-579T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991596 | ||||||
| chr15:39991918
|
C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2632-257C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39991918 | ||||||
| chr15:39992007
|
T | A | 8 | a0005c0008t0001g0297a0005c0008t0001g0299a0005c0008t0001g0357others(5): Show | 10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2632-168T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 16/38 | chr15 | 39992007 | ||||||
| chr15:39992322
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2686+93C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992322 | ||||||
| chr15:39992601
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2687-168C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992601 | ||||||
| chr15:39992648
|
T | C | 3 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0005g0037 | 3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2687-121T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 17/38 | chr15 | 39992648 | ||||||
| chr15:39992919
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2766+71A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39992919 | ||||||
| chr15:39993030
|
G | GTCCA | 38 | a0001c0001t0001g0244a0001c0001t0002g0119a0001c0001t0002g0141others(35): Show | 38 | HG00280.hp1 HG01123.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2766+224_2766+227d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993030 | |||||
| chr15:39993030
|
GTCCA | G | 14 | a0001c0001t0002g0178a0001c0001t0003g0197a0001c0001t0003g0198others(11): Show | 14 | HG00673.hp2 HG01346.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2766+224_2766+227d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993030 | |||||
| chr15:39993048
|
CCATCCAT others(21): Show |
C | 8 | a0001c0001t0001g0356a0002c0002t0001g0287a0002c0002t0001g0291others(5): Show | 8 | HG01074.hp2 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.2766+228_2766+255d others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993048 | |||||
| chr15:39993052
|
CCATCCAT others(17): Show |
C | 10 | a0002c0002t0001g0003a0002c0002t0001g0020a0002c0002t0001g0022others(7): Show | 11 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.2766+228_2766+251d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993052 | |||||
| chr15:39993056
|
CCATCCAT others(13): Show |
C | 10 | a0002c0002t0001g0290a0002c0002t0001g0294a0002c0002t0001g0298others(7): Show | 10 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2766+228_2766+247d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993056 | |||||
| chr15:39993064
|
CCATCCAT others(5): Show |
C | 1 | a0002c0004t0001g0320 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2766+228_2766+239d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993064 | |||||
| chr15:39993091
|
TCCATCCA others(9): Show |
T | 3 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0005g0037 | 3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2766+247_2766+262d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993091 | |||||
| chr15:39993103
|
T | C | 60 | a0001c0001t0001g0205a0001c0001t0002g0013a0001c0001t0002g0111others(57): Show | 61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2766+255T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993103 | ||||||
| chr15:39993138
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2766+290A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993138 | ||||||
| chr15:39993149
|
T | C | 1 | a0003c0003t0002g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2766+301T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993149 | ||||||
| chr15:39993193
|
C | T | 8 | a0002c0004t0001g0322a0002c0004t0001g0323a0007c0009t0003g0230others(5): Show | 8 | HG01256.hp2 HG02300.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2766+345C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993193 | ||||||
| chr15:39993194
|
G | GTCCGTCC others(9): Show |
1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2766+350_2766+365d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39993194 | |||||
| chr15:39993208
|
C | T | 2 | a0003c0010t0001g0047a0003c0010t0001g0048 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2766+360C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993208 | ||||||
| chr15:39993227
|
T | G | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0005g0037others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766+379T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993227 | ||||||
| chr15:39993309
|
T | A | 60 | a0001c0001t0001g0205a0001c0001t0002g0013a0001c0001t0002g0111others(57): Show | 61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2766+461T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993309 | ||||||
| chr15:39993555
|
C | T | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2766+707C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993555 | ||||||
| chr15:39993916
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2766+1068T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993916 | ||||||
| chr15:39993967
|
C | T | 1 | a0001c0005t0001g0132 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2766+1119C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39993967 | ||||||
| chr15:39994075
|
C | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2766+1227C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994075 | ||||||
| chr15:39994250
|
T | G | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2766+1402T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994250 | ||||||
| chr15:39994335
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(60): Show | 64 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.2766+1487T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994335 | ||||||
| chr15:39994425
|
T | A | 7 | a0003c0010t0001g0047a0003c0010t0001g0048a0007c0009t0003g0230others(4): Show | 7 | HG02451.hp2 NA18906.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.2766+1577T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994425 | ||||||
| chr15:39994429
|
G | A | 11 | a0002c0013t0001g0279a0002c0013t0001g0280a0002c0013t0001g0281others(8): Show | 12 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2766+1581G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994429 | ||||||
| chr15:39994482
|
G | A | 2 | a0006c0012t0002g0177a0012c0024t0002g0068 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2766+1634G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994482 | ||||||
| chr15:39994540
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2766+1692T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994540 | ||||||
| chr15:39994672
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2766+1824C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994672 | ||||||
| chr15:39994731
|
A | C | 1 | a0002c0002t0001g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2766+1883A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994731 | ||||||
| chr15:39994778
|
T | G | 2 | a0001c0005t0001g0137a0001c0005t0001g0153 | 2 | HG00609.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2766+1930T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994778 | ||||||
| chr15:39994794
|
G | A | 2 | a0002c0004t0001g0041a0002c0004t0005g0114 | 2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2766+1946G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994794 | ||||||
| chr15:39994923
|
C | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2767-2041C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39994923 | ||||||
| chr15:39995033
|
G | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(200): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2767-1931G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995033 | ||||||
| chr15:39995166
|
C | A | 1 | a0001c0005t0005g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2767-1798C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995166 | ||||||
| chr15:39995308
|
A | G | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2767-1656A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995308 | ||||||
| chr15:39995321
|
C | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2767-1643C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995321 | ||||||
| chr15:39995436
|
G | GC | 17 | a0002c0002t0007g0043a0002c0004t0003g0039a0002c0013t0001g0279others(14): Show | 19 | HG00639.hp2 HG01169.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.2767-1524dupC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr15 | 39995436 | |||||
| chr15:39995589
|
G | A | 172 | a0001c0001t0001g0170a0001c0001t0002g0009a0001c0001t0002g0129others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.2767-1375G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995589 | ||||||
| chr15:39995781
|
T | C | 28 | a0001c0001t0001g0356a0002c0002t0001g0003a0002c0002t0001g0020others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.2767-1183T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995781 | ||||||
| chr15:39995810
|
G | A | 19 | a0001c0001t0001g0244a0001c0001t0003g0246a0001c0005t0001g0247others(16): Show | 19 | HG01081.hp1 HG01255.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2767-1154G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995810 | ||||||
| chr15:39995821
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2767-1143C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995821 | ||||||
| chr15:39995830
|
C | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2767-1134C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995830 | ||||||
| chr15:39995872
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2767-1092G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995872 | ||||||
| chr15:39995985
|
C | T | 1 | a0002c0004t0002g0317 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2767-979C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39995985 | ||||||
| chr15:39996020
|
G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2767-944G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996020 | ||||||
| chr15:39996429
|
G | A | 2 | a0002c0002t0002g0337a0002c0002t0002g0338 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2767-535G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996429 | ||||||
| chr15:39996508
|
C | A | 2 | a0003c0010t0001g0047a0003c0010t0001g0048 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2767-456C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996508 | ||||||
| chr15:39996601
|
C | A | 1 | a0007c0009t0003g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2767-363C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 18/38 | chr15 | 39996601 | ||||||
| chr15:39997105
|
C | T | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2868+40C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997105 | ||||||
| chr15:39997362
|
A | G | 1 | a0017c0035t0003g0236 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2868+297A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997362 | ||||||
| chr15:39997381
|
T | C | 1 | a0003c0003t0002g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2868+316T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997381 | ||||||
| chr15:39997386
|
C | A | 1 | a0002c0002t0001g0294 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2868+321C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997386 | ||||||
| chr15:39997387
|
T | C | 5 | a0007c0009t0003g0230a0007c0009t0003g0232a0007c0009t0003g0234others(2): Show | 5 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2868+322T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997387 | ||||||
| chr15:39997407
|
C | G | 3 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0005g0037 | 3 | HG01891.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2868+342C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997407 | ||||||
| chr15:39997434
|
C | A | 1 | a0003c0003t0001g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2868+369C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997434 | ||||||
| chr15:39997629
|
G | A | 3 | a0004c0006t0006g0252a0004c0006t0006g0253a0004c0006t0006g0261 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2868+564G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997629 | ||||||
| chr15:39997670
|
G | A | 5 | a0002c0002t0007g0043a0002c0004t0003g0039a0003c0026t0001g0011others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2868+605G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997670 | ||||||
| chr15:39997670
|
G | C | 1 | a0002c0002t0001g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2868+605G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997670 | ||||||
| chr15:39997763
|
A | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2868+698A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997763 | ||||||
| chr15:39997826
|
A | T | 27 | a0001c0001t0001g0356a0002c0002t0001g0003a0002c0002t0001g0020others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2868+761A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997826 | ||||||
| chr15:39997962
|
T | A | 1 | a0002c0004t0002g0354 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2869-769T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39997962 | ||||||
| chr15:39998084
|
G | C | 1 | a0001c0001t0003g0209 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2869-647G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998084 | ||||||
| chr15:39998135
|
T | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2869-596T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998135 | ||||||
| chr15:39998215
|
A | AT | 12 | a0002c0013t0001g0279a0002c0013t0001g0280a0002c0013t0001g0281others(9): Show | 14 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2869-508dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998215 | |||||
| chr15:39998257
|
GT | G | 6 | a0002c0002t0002g0242a0002c0002t0002g0243a0003c0003t0001g0058others(3): Show | 6 | HG02145.hp1 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2869-462delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998257 | |||||
| chr15:39998265
|
T | G | 5 | a0001c0001t0003g0218a0002c0011t0002g0096a0002c0011t0002g0302others(2): Show | 5 | NA18953.hp2 NA18995.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.2869-466T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998265 | ||||||
| chr15:39998266
|
T | G | 3 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0004g0237 | 3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2869-465T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998266 | ||||||
| chr15:39998269
|
T | G | 5 | a0001c0005t0001g0125a0001c0005t0005g0123a0001c0005t0005g0124others(2): Show | 5 | HG01169.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2869-462T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998269 | ||||||
| chr15:39998269
|
T | TTG | 7 | a0002c0004t0001g0041a0002c0004t0001g0358a0002c0004t0001g0359others(4): Show | 7 | HG00642.hp1 HG02723.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.2869-462_2869-461i others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998269 | ||||||
| chr15:39998270
|
G | GT | 84 | a0001c0001t0002g0009a0001c0005t0001g0134a0001c0005t0001g0135others(81): Show | 87 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2869-457dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998270 | |||||
| chr15:39998270
|
G | T | 16 | a0001c0001t0002g0159a0001c0005t0001g0125a0001c0005t0005g0123others(13): Show | 16 | HG00597.hp1 HG00642.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.2869-461G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998270 | ||||||
| chr15:39998275
|
G | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(266): Show | 273 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2869-456G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998275 | ||||||
| chr15:39998280
|
T | G | 32 | a0001c0001t0001g0356a0001c0001t0003g0186a0001c0001t0003g0187others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.2869-451T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998280 | ||||||
| chr15:39998299
|
G | T | 1 | a0002c0004t0001g0350 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2869-432G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998299 | ||||||
| chr15:39998460
|
CA | C | 9 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0175others(6): Show | 9 | HG02015.hp1 HG02040.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2869-269delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 39998460 | |||||
| chr15:39998505
|
G | A | 84 | a0001c0005t0001g0125a0001c0005t0001g0134a0001c0005t0001g0135others(81): Show | 85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2869-226G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998505 | ||||||
| chr15:39998519
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2869-212A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 19/38 | chr15 | 39998519 | ||||||
| chr15:39998929
|
C | G | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2922+145C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39998929 | ||||||
| chr15:39998939
|
C | T | 361 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(358): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.2922+155C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39998939 | ||||||
| chr15:39999020
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2922+236G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999020 | ||||||
| chr15:39999024
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2922+240T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999024 | ||||||
| chr15:39999047
|
C | G | 3 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0004g0237 | 3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2922+263C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999047 | ||||||
| chr15:39999078
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(76): Show | 80 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2922+294T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999078 | ||||||
| chr15:39999242
|
A | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(355): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2922+458A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999242 | ||||||
| chr15:39999602
|
A | G | 1 | a0004c0006t0001g0256 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2922+818A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999602 | ||||||
| chr15:39999666
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(63): Show | 67 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.2922+882T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999666 | ||||||
| chr15:39999889
|
A | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(76): Show | 80 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2923-1099A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999889 | ||||||
| chr15:39999916
|
C | T | 1 | a0017c0035t0003g0236 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2923-1072C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 39999916 | ||||||
| chr15:40000057
|
A | G | 84 | a0001c0005t0001g0125a0001c0005t0001g0134a0001c0005t0001g0135others(81): Show | 85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2923-931A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000057 | ||||||
| chr15:40000185
|
A | G | 4 | a0001c0005t0005g0108a0002c0004t0005g0238a0010c0018t0005g0239others(1): Show | 4 | HG01496.hp2 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2923-803A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000185 | ||||||
| chr15:40000364
|
C | G | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2923-624C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000364 | ||||||
| chr15:40000755
|
G | C | 1 | a0005c0008t0004g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2923-233G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000755 | ||||||
| chr15:40000821
|
T | C | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923-167T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000821 | ||||||
| chr15:40000835
|
AAAT | A | 83 | a0001c0005t0001g0125a0001c0005t0001g0134a0001c0005t0001g0135others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2923-149_2923-147d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 40000835 | |||||
| chr15:40000926
|
C | T | 2 | a0001c0001t0002g0120a0003c0003t0002g0066 | 2 | HG01099.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2923-62C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000926 | ||||||
| chr15:40000954
|
A | T | 1 | a0006c0012t0003g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2923-34A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000954 | ||||||
| chr15:40000975
|
G | C | 3 | a0001c0001t0001g0168a0001c0001t0011g0164a0006c0012t0001g0268 | 3 | NA18948.hp2 NA18956.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.2923-13G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 20/38 | chr15 | 40000975 | ||||||
| chr15:40001236
|
C | A | 8 | a0003c0003t0002g0056a0003c0003t0002g0078a0003c0003t0002g0080others(5): Show | 8 | NA18612.hp2 NA18962.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.3159+12C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001236 | ||||||
| chr15:40001329
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(53): Show | 57 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3159+105T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001329 | ||||||
| chr15:40001486
|
C | T | 2 | a0002c0002t0003g0050a0002c0002t0003g0277 | 2 | HG00642.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3159+262C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001486 | ||||||
| chr15:40001523
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3159+299G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001523 | ||||||
| chr15:40001552
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3159+328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001552 | ||||||
| chr15:40001633
|
C | CA | 244 | a0001c0001t0001g0170a0001c0001t0001g0356a0001c0001t0002g0009others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.3159+427dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr15 | 40001633 | |||||
| chr15:40001633
|
C | CAA | 28 | a0001c0001t0001g0244a0001c0001t0002g0159a0001c0001t0003g0246others(25): Show | 30 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.3159+426_3159+427d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr15 | 40001633 | |||||
| chr15:40001685
|
A | T | 1 | a0001c0001t0004g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3159+461A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001685 | ||||||
| chr15:40001688
|
C | T | 2 | a0003c0003t0002g0098a0003c0003t0002g0102 | 2 | HG01346.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.3159+464C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001688 | ||||||
| chr15:40001807
|
C | G | 1 | a0008c0015t0006g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3159+583C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001807 | ||||||
| chr15:40001864
|
A | C | 1 | a0002c0004t0005g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3159+640A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001864 | ||||||
| chr15:40001983
|
T | C | 1 | a0004c0007t0003g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3160-730T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001983 | ||||||
| chr15:40001992
|
G | A | 76 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.3160-721G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40001992 | ||||||
| chr15:40002253
|
C | G | 1 | a0002c0002t0002g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3160-460C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002253 | ||||||
| chr15:40002385
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(8): Show | 11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3160-328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002385 | ||||||
| chr15:40002387
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3160-326C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002387 | ||||||
| chr15:40002577
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3160-136G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002577 | ||||||
| chr15:40002590
|
C | G | 1 | a0002c0004t0001g0320 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3160-123C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002590 | ||||||
| chr15:40002705
|
T | C | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.3160-8T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 21/38 | chr15 | 40002705 | ||||||
| chr15:40003551
|
T | C | 2 | a0005c0008t0001g0297a0005c0008t0001g0357 | 2 | HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3357+237T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003551 | ||||||
| chr15:40003663
|
G | A | 1 | a0002c0030t0002g0306 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3357+349G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003663 | ||||||
| chr15:40003758
|
C | T | 236 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3357+444C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003758 | ||||||
| chr15:40003794
|
G | A | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3357+480G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40003794 | ||||||
| chr15:40004046
|
T | C | 12 | a0001c0001t0002g0111a0001c0001t0002g0206a0001c0001t0003g0109others(9): Show | 12 | HG00621.hp1 HG02015.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.3357+732T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004046 | ||||||
| chr15:40004128
|
G | A | 275 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(272): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.3357+814G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004128 | ||||||
| chr15:40004140
|
A | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3357+826A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004140 | ||||||
| chr15:40004226
|
C | T | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3357+912C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004226 | ||||||
| chr15:40004249
|
A | C | 24 | a0001c0001t0001g0244a0001c0001t0003g0246a0001c0001t0004g0245others(21): Show | 26 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.3357+935A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004249 | ||||||
| chr15:40004354
|
CTGTT | C | 3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1042_3357+104 others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40004354 | |||||
| chr15:40004487
|
G | A | 1 | a0002c0002t0002g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3357+1173G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004487 | ||||||
| chr15:40004497
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(8): Show | 11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3357+1183C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004497 | ||||||
| chr15:40004498
|
C | T | 138 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(135): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.3357+1184C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004498 | ||||||
| chr15:40004721
|
T | A | 24 | a0001c0001t0001g0244a0001c0001t0003g0246a0001c0001t0004g0245others(21): Show | 26 | HG00639.hp2 HG01081.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.3357+1407T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004721 | ||||||
| chr15:40004727
|
T | A | 28 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3357+1413T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004727 | ||||||
| chr15:40004727
|
T | C | 3 | a0002c0002t0001g0020a0002c0002t0001g0022a0003c0003t0001g0344 | 3 | HG02055.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3357+1413T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004727 | ||||||
| chr15:40004814
|
C | G | 3 | a0002c0002t0007g0043a0009c0016t0007g0042a0009c0016t0007g0044 | 3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3357+1500C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004814 | ||||||
| chr15:40004845
|
C | T | 8 | a0002c0002t0007g0043a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3357+1531C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004845 | ||||||
| chr15:40004851
|
C | T | 3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1537C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004851 | ||||||
| chr15:40004852
|
A | G | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.3357+1538A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004852 | ||||||
| chr15:40004873
|
A | G | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3357+1559A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004873 | ||||||
| chr15:40004898
|
T | A | 8 | a0002c0002t0007g0043a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3357+1584T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40004898 | ||||||
| chr15:40005018
|
T | A | 31 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.3357+1704T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005018 | ||||||
| chr15:40005046
|
T | A | 1 | a0001c0001t0003g0199 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3357+1732T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005046 | ||||||
| chr15:40005067
|
A | G | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3357+1753A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005067 | ||||||
| chr15:40005093
|
T | G | 13 | a0001c0001t0004g0245a0002c0013t0001g0279a0002c0013t0001g0280others(10): Show | 15 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3357+1779T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005093 | ||||||
| chr15:40005140
|
A | G | 3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3357+1826A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005140 | ||||||
| chr15:40005193
|
T | C | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1823T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005193 | ||||||
| chr15:40005261
|
A | G | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3358-1755A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005261 | ||||||
| chr15:40005306
|
T | A | 84 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0125others(81): Show | 85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.3358-1710T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005306 | ||||||
| chr15:40005456
|
C | T | 1 | a0015c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3358-1560C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005456 | ||||||
| chr15:40005516
|
C | CA | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1493dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40005516 | |||||
| chr15:40005531
|
C | T | 4 | a0002c0002t0007g0043a0003c0026t0001g0011a0009c0016t0007g0042others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1485C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005531 | ||||||
| chr15:40005551
|
G | A | 4 | a0002c0002t0007g0043a0003c0026t0001g0011a0009c0016t0007g0042others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3358-1465G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005551 | ||||||
| chr15:40005565
|
A | G | 8 | a0002c0002t0007g0043a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3358-1451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005565 | ||||||
| chr15:40005707
|
G | A | 1 | a0004c0007t0002g0267 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3358-1309G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005707 | ||||||
| chr15:40005759
|
G | A | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.3358-1257G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005759 | ||||||
| chr15:40005867
|
G | A | 12 | a0002c0013t0001g0279a0002c0013t0001g0280a0002c0013t0001g0281others(9): Show | 14 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3358-1149G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005867 | ||||||
| chr15:40005939
|
C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3358-1077C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40005939 | ||||||
| chr15:40006157
|
C | T | 85 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0125others(82): Show | 86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3358-859C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006157 | ||||||
| chr15:40006492
|
G | A | 8 | a0002c0002t0007g0043a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3358-524G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006492 | ||||||
| chr15:40006669
|
T | A | 139 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(136): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3358-347T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006669 | ||||||
| chr15:40006670
|
T | A | 239 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.3358-346T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006670 | ||||||
| chr15:40006711
|
A | T | 1 | a0002c0011t0002g0332 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3358-305A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006711 | ||||||
| chr15:40006815
|
C | T | 77 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(74): Show | 77 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.3358-201C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | chr15 | 40006815 | ||||||
| chr15:40006999
|
TTTTG | T | 8 | a0005c0008t0001g0297a0005c0008t0001g0299a0005c0008t0001g0357others(5): Show | 10 | HG01169.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3358-13_3358-10del others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr15 | 40006999 | |||||
| chr15:40007299
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3407+234A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007299 | ||||||
| chr15:40007427
|
G | A | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3407+362G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007427 | ||||||
| chr15:40007486
|
A | G | 1 | a0002c0002t0001g0360 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3407+421A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007486 | ||||||
| chr15:40007713
|
T | C | 8 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0004g0015others(5): Show | 8 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3408-314T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007713 | ||||||
| chr15:40007802
|
A | T | 4 | a0003c0003t0002g0008a0003c0003t0002g0055a0003c0003t0002g0072others(1): Show | 4 | NA18940.hp1 NA18969.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3408-225A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007802 | ||||||
| chr15:40007854
|
A | G | 8 | a0002c0002t0007g0043a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3408-173A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007854 | ||||||
| chr15:40007891
|
T | C | 238 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.3408-136T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007891 | ||||||
| chr15:40007920
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(8): Show | 11 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3408-107C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007920 | ||||||
| chr15:40007973
|
A | T | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3408-54A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40007973 | ||||||
| chr15:40008013
|
G | C | 111 | a0001c0001t0001g0170a0001c0001t0001g0356a0001c0001t0002g0009others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.3408-14G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 24/38 | chr15 | 40008013 | ||||||
| chr15:40008242
|
T | G | 90 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0125others(87): Show | 91 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3576+47T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008242 | ||||||
| chr15:40008346
|
T | C | 12 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3576+151T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008346 | ||||||
| chr15:40008443
|
T | C | 1 | a0002c0004t0002g0349 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3576+248T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008443 | ||||||
| chr15:40008490
|
G | T | 21 | a0001c0001t0003g0246a0001c0001t0004g0245a0002c0002t0001g0360others(18): Show | 23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.3576+295G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008490 | ||||||
| chr15:40008617
|
A | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0130others(62): Show | 67 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3576+422A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008617 | ||||||
| chr15:40008857
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0003g0113 | 2 | HG02074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.3576+662A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008857 | ||||||
| chr15:40008862
|
G | A | 12 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3576+667G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008862 | ||||||
| chr15:40008899
|
A | G | 4 | a0001c0005t0001g0247a0002c0031t0009g0045a0003c0010t0001g0047others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3576+704A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008899 | ||||||
| chr15:40008969
|
G | A | 274 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.3577-645G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008969 | ||||||
| chr15:40008996
|
T | C | 5 | a0002c0002t0004g0015a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3577-618T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40008996 | ||||||
| chr15:40009069
|
T | TTTTTG | 94 | a0001c0001t0002g0223a0001c0005t0001g0032a0001c0005t0001g0034others(91): Show | 95 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.3577-509_3577-505d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009069
|
T | TTTTTGTT others(3): Show |
47 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.3577-514_3577-505d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009069
|
T | TTTTTGTT others(8): Show |
5 | a0001c0005t0005g0154a0002c0004t0004g0331a0004c0007t0001g0251others(2): Show | 5 | HG00741.hp1 HG01978.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3577-519_3577-505d others(17): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009069
|
TTTTTG | T | 53 | a0001c0001t0001g0207a0001c0001t0001g0244a0001c0001t0001g0356others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.3577-509_3577-505d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009069
|
TTTTTGTT others(3): Show |
T | 4 | a0001c0005t0001g0247a0002c0004t0001g0328a0003c0010t0001g0047others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3577-514_3577-505d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009069
|
TTTTTGTT others(8): Show |
T | 1 | a0005c0014t0004g0295 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3577-519_3577-505d others(17): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr15 | 40009069 | |||||
| chr15:40009170
|
G | A | 12 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.3577-444G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40009170 | ||||||
| chr15:40009301
|
C | A | 79 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.3577-313C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 25/38 | chr15 | 40009301 | ||||||
| chr15:40010042
|
C | T | 205 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(202): Show | 208 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.3693+312C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010042 | ||||||
| chr15:40010224
|
G | A | 19 | a0001c0001t0003g0246a0001c0001t0004g0245a0002c0002t0001g0360others(16): Show | 21 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3693+494G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010224 | ||||||
| chr15:40010240
|
G | A | 205 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(202): Show | 208 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.3693+510G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010240 | ||||||
| chr15:40010346
|
C | T | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3693+616C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010346 | ||||||
| chr15:40010461
|
T | C | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3693+731T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010461 | ||||||
| chr15:40010486
|
G | A | 18 | a0001c0001t0002g0138a0002c0002t0001g0035a0002c0002t0002g0040others(15): Show | 18 | HG02145.hp1 HG02258.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.3693+756G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010486 | ||||||
| chr15:40010572
|
G | C | 2 | a0002c0002t0002g0314a0002c0002t0010g0046 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3694-709G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010572 | ||||||
| chr15:40010629
|
G | GA | 274 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.3694-650dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40010629 | |||||
| chr15:40010646
|
CAG | C | 7 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0220others(4): Show | 7 | HG00597.hp1 HG03669.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.3694-632_3694-631d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40010646 | |||||
| chr15:40010769
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3694-512G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010769 | ||||||
| chr15:40010772
|
C | G | 85 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0125others(82): Show | 86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3694-509C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010772 | ||||||
| chr15:40010799
|
G | C | 1 | a0002c0004t0001g0348 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3694-482G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010799 | ||||||
| chr15:40010830
|
A | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3694-451A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40010830 | ||||||
| chr15:40011092
|
ATAAGT | A | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0005g0037others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3694-185_3694-181d others(7): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 40011092 | |||||
| chr15:40011105
|
G | A | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3694-176G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 26/38 | chr15 | 40011105 | ||||||
| chr15:40011382
|
C | G | 1 | a0005c0014t0004g0292 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3759+36C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011382 | ||||||
| chr15:40011641
|
G | A | 191 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(188): Show | 194 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.3759+295G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011641 | ||||||
| chr15:40011969
|
T | G | 238 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.3759+623T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40011969 | ||||||
| chr15:40012047
|
C | A | 2 | a0001c0001t0002g0009a0002c0002t0002g0334 | 2 | HG00597.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.3759+701C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012047 | ||||||
| chr15:40012093
|
T | G | 1 | a0002c0004t0002g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3759+747T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012093 | ||||||
| chr15:40012206
|
A | C | 103 | a0001c0001t0001g0244a0001c0005t0001g0032a0001c0005t0001g0034others(100): Show | 104 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.3759+860A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012206 | ||||||
| chr15:40012512
|
T | C | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.3759+1166T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012512 | ||||||
| chr15:40012639
|
A | G | 1 | a0003c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3759+1293A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012639 | ||||||
| chr15:40012662
|
CT | C | 9 | a0001c0001t0001g0244a0001c0001t0002g0119a0001c0001t0003g0190others(6): Show | 9 | HG01168.hp1 HG02015.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3759+1329delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr15 | 40012662 | |||||
| chr15:40012701
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3759+1355G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012701 | ||||||
| chr15:40012849
|
G | A | 1 | a0002c0004t0001g0301 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3759+1503G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012849 | ||||||
| chr15:40012875
|
T | C | 1 | a0005c0014t0004g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3759+1529T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012875 | ||||||
| chr15:40012929
|
G | T | 3 | a0002c0004t0001g0304a0002c0004t0001g0313a0002c0004t0014g0303 | 3 | NA18951.hp2 NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3759+1583G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012929 | ||||||
| chr15:40012961
|
C | T | 80 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3759+1615C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40012961 | ||||||
| chr15:40013264
|
G | A | 1 | a0004c0007t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3759+1918G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013264 | ||||||
| chr15:40013322
|
G | A | 1 | a0011c0017t0003g0342 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3759+1976G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013322 | ||||||
| chr15:40013414
|
C | T | 80 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3759+2068C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013414 | ||||||
| chr15:40013422
|
G | A | 1 | a0002c0004t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3759+2076G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013422 | ||||||
| chr15:40013517
|
C | T | 6 | a0001c0001t0003g0246a0002c0002t0001g0360a0002c0002t0001g0362others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3759+2171C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013517 | ||||||
| chr15:40013985
|
A | C | 1 | a0002c0004t0001g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3760-2517A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40013985 | ||||||
| chr15:40014063
|
T | A | 80 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.3760-2439T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014063 | ||||||
| chr15:40014117
|
C | T | 1 | a0005c0008t0001g0299 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3760-2385C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014117 | ||||||
| chr15:40014123
|
C | T | 5 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3760-2379C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014123 | ||||||
| chr15:40014133
|
C | A | 95 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0129others(92): Show | 97 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.3760-2369C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014133 | ||||||
| chr15:40014308
|
G | T | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3760-2194G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014308 | ||||||
| chr15:40014347
|
C | T | 3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3760-2155C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014347 | ||||||
| chr15:40014420
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3760-2082G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014420 | ||||||
| chr15:40014737
|
C | T | 1 | a0002c0013t0001g0279 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3760-1765C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014737 | ||||||
| chr15:40014894
|
A | C | 260 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.3760-1608A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014894 | ||||||
| chr15:40014979
|
T | C | 1 | a0001c0001t0003g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3760-1523T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40014979 | ||||||
| chr15:40015273
|
G | A | 2 | a0004c0006t0001g0260a0004c0037t0001g0274 | 2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3760-1229G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015273 | ||||||
| chr15:40015518
|
G | A | 3 | a0001c0001t0001g0170a0004c0006t0001g0255a0004c0006t0001g0256 | 3 | HG02129.hp1 HG02698.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3760-984G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015518 | ||||||
| chr15:40015574
|
A | G | 207 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(204): Show | 210 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.3760-928A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015574 | ||||||
| chr15:40015612
|
A | G | 5 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3760-890A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015612 | ||||||
| chr15:40015706
|
T | C | 1 | a0002c0002t0005g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3760-796T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015706 | ||||||
| chr15:40015960
|
A | C | 12 | a0002c0013t0001g0279a0002c0013t0001g0280a0002c0013t0001g0281others(9): Show | 14 | HG00639.hp2 HG01169.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3760-542A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40015960 | ||||||
| chr15:40016100
|
G | A | 7 | a0001c0001t0001g0205a0001c0001t0003g0201a0001c0001t0003g0202others(4): Show | 7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.3760-402G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016100 | ||||||
| chr15:40016159
|
A | T | 1 | a0001c0001t0003g0201 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3760-343A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016159 | ||||||
| chr15:40016397
|
C | T | 2 | a0001c0005t0001g0032a0001c0005t0001g0034 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3760-105C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016397 | ||||||
| chr15:40016447
|
A | C | 8 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0004g0015others(5): Show | 8 | HG01081.hp1 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3760-55A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 27/38 | chr15 | 40016447 | ||||||
| chr15:40016836
|
A | G | 2 | a0001c0001t0003g0246a0003c0003t0001g0058 | 2 | HG01081.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3930+164A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/38 | chr15 | 40016836 | ||||||
| chr15:40017001
|
A | G | 1 | a0002c0004t0001g0275 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3931-107A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 28/38 | chr15 | 40017001 | ||||||
| chr15:40017281
|
T | A | 1 | a0003c0003t0013g0086 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4065+39T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017281 | ||||||
| chr15:40017363
|
T | C | 1 | a0001c0005t0005g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4065+121T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017363 | ||||||
| chr15:40017370
|
A | G | 1 | a0015c0027t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4065+128A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017370 | ||||||
| chr15:40017495
|
C | G | 1 | a0001c0001t0002g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4065+253C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017495 | ||||||
| chr15:40017501
|
C | CATATATA others(4): Show |
1 | a0004c0006t0004g0250 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4065+259_4065+260i others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017501 | ||||||
| chr15:40017501
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(1): Show | 4 | NA18972.hp2 NA19074.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+305_4065+312d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(3): Show |
4 | a0001c0001t0003g0191a0001c0001t0003g0198a0001c0001t0003g0225others(1): Show | 4 | HG02738.hp2 NA19007.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+303_4065+312d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0005g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4065+301_4065+312d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(7): Show |
6 | a0001c0001t0003g0012a0001c0001t0003g0172a0001c0001t0003g0189others(3): Show | 6 | HG00438.hp1 HG01168.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+299_4065+312d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(9): Show |
6 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0197others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+297_4065+312d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(11): Show |
3 | a0001c0001t0003g0110a0001c0001t0003g0222a0002c0002t0003g0049 | 3 | HG03471.hp2 NA19054.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4065+295_4065+312d others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(13): Show |
6 | a0001c0001t0003g0109a0001c0001t0003g0180a0001c0001t0003g0188others(3): Show | 6 | HG02132.hp2 HG03486.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+293_4065+312d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(15): Show |
4 | a0001c0001t0001g0136a0001c0001t0001g0155a0001c0001t0003g0179others(1): Show | 4 | HG02027.hp1 HG02145.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+291_4065+312d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0003g0183 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4065+289_4065+312d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(19): Show |
2 | a0001c0001t0003g0173a0001c0001t0003g0202 | 2 | HG02155.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.4065+287_4065+312d others(28): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(23): Show |
1 | a0002c0002t0003g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4065+283_4065+312d others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTATATAT others(27): Show |
3 | a0001c0001t0002g0126a0001c0001t0003g0171a0001c0001t0003g0182 | 3 | HG02165.hp1 HG02602.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.4065+279_4065+312d others(36): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTATATA others(6): Show |
1 | a0003c0003t0013g0086 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(15): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTTATAT others(3): Show |
2 | a0002c0002t0001g0362a0002c0002t0004g0237 | 2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4065+260_4065+261i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTTATAT others(7): Show |
1 | a0002c0002t0001g0360 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4065+260_4065+261i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTTATAT others(9): Show |
2 | a0003c0003t0002g0061a0003c0025t0004g0010 | 2 | HG01978.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4065+260_4065+261i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTTTTAT others(3): Show |
1 | a0009c0016t0007g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
C | CTTTTTAT others(5): Show |
1 | a0002c0002t0007g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4065+260_4065+261i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATA | C | 12 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0002g0013others(9): Show | 12 | HG00597.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4065+307_4065+312d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(1): Show |
C | 5 | a0001c0001t0002g0009a0002c0002t0002g0243a0004c0006t0003g0345others(2): Show | 5 | HG02965.hp1 HG03490.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+305_4065+312d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(3): Show |
C | 5 | a0001c0001t0001g0244a0001c0001t0003g0208a0001c0001t0003g0227others(2): Show | 5 | HG02818.hp2 HG02895.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+303_4065+312d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(5): Show |
C | 2 | a0003c0003t0002g0055a0003c0003t0002g0076 | 2 | NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4065+301_4065+312d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(7): Show |
C | 5 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0005t0001g0181others(2): Show | 5 | HG02602.hp1 NA18948.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+299_4065+312d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(9): Show |
C | 6 | a0001c0001t0005g0023a0001c0001t0005g0029a0001c0001t0005g0031others(3): Show | 6 | HG00621.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+297_4065+312d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(11): Show |
C | 20 | a0001c0001t0002g0128a0001c0005t0001g0125a0001c0005t0005g0108others(17): Show | 20 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.4065+295_4065+312d others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(13): Show |
C | 83 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.4065+293_4065+312d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(15): Show |
C | 2 | a0001c0001t0003g0185a0011c0017t0003g0342 | 2 | HG02523.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4065+291_4065+312d others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(17): Show |
C | 6 | a0001c0001t0003g0176a0001c0005t0001g0247a0002c0031t0009g0045others(3): Show | 6 | HG00140.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4065+289_4065+312d others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(21): Show |
C | 1 | a0001c0001t0001g0166 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4065+285_4065+312d others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017501
|
CTATATAT others(23): Show |
C | 8 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336others(5): Show | 8 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.4065+283_4065+312d others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017501 | |||||
| chr15:40017502
|
TATATATA others(12): Show |
T | 1 | a0004c0007t0001g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4065+261_4065+279d others(21): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017502 | ||||||
| chr15:40017503
|
A | T | 76 | a0001c0001t0002g0129a0001c0001t0002g0138a0001c0001t0002g0148others(73): Show | 78 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.4065+261A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017503 | ||||||
| chr15:40017509
|
A | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0220a0001c0001t0002g0223others(3): Show | 6 | HG00597.hp1 HG03927.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.4065+267A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017509 | ||||||
| chr15:40017511
|
A | T | 4 | a0001c0001t0002g0009a0002c0002t0002g0243a0006c0012t0002g0177others(1): Show | 4 | HG02965.hp1 HG03669.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.4065+269A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017511 | ||||||
| chr15:40017513
|
A | T | 2 | a0001c0001t0001g0244a0003c0003t0002g0072 | 2 | HG02895.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4065+271A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017513 | ||||||
| chr15:40017515
|
A | T | 2 | a0003c0003t0002g0055a0003c0003t0002g0076 | 2 | NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4065+273A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017515 | ||||||
| chr15:40017517
|
A | T | 2 | a0001c0005t0001g0181a0001c0020t0001g0174 | 2 | NA18974.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.4065+275A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017517 | ||||||
| chr15:40017519
|
A | T | 3 | a0002c0002t0010g0046a0003c0010t0001g0079a0004c0007t0001g0216 | 3 | HG00621.hp2 HG02572.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.4065+277A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017519 | ||||||
| chr15:40017521
|
A | T | 18 | a0001c0005t0001g0125a0001c0005t0005g0108a0001c0005t0005g0123others(15): Show | 18 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.4065+279A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017521 | ||||||
| chr15:40017522
|
T | TATATATA others(17): Show |
2 | a0001c0001t0001g0001a0001c0001t0001g0140 | 3 | NA18962.hp1 NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4065+303_4065+304i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017522 | |||||
| chr15:40017523
|
A | T | 69 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0132others(66): Show | 70 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.4065+281A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017523 | ||||||
| chr15:40017527
|
A | T | 3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048 | 3 | HG02258.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4065+285A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017527 | ||||||
| chr15:40017533
|
A | T | 5 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+291A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017533 | ||||||
| chr15:40017543
|
A | G | 16 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(13): Show | 16 | HG00438.hp2 HG00673.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.4065+301A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017543 | ||||||
| chr15:40017545
|
A | G | 14 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0220others(11): Show | 14 | HG00597.hp1 HG01975.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4065+303A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017545 | ||||||
| chr15:40017546
|
T | C | 1 | a0002c0013t0001g0283 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4065+304T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017546 | ||||||
| chr15:40017547
|
A | ATATGTAT others(1): Show |
3 | a0001c0001t0002g0143a0003c0003t0001g0106a0005c0008t0004g0004 | 4 | HG02165.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+308_4065+309i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017547 | |||||
| chr15:40017547
|
A | G | 20 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 21 | HG00438.hp2 HG00673.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.4065+305A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017547 | ||||||
| chr15:40017548
|
T | C | 100 | a0001c0001t0001g0244a0001c0005t0001g0032a0001c0005t0001g0034others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.4065+306T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017548 | ||||||
| chr15:40017551
|
A | ATATATAC others(3): Show |
1 | a0002c0002t0004g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(7): Show |
2 | a0003c0003t0003g0091a0007c0009t0003g0232 | 2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(9): Show |
3 | a0002c0002t0004g0016a0007c0009t0003g0234a0013c0023t0003g0233 | 3 | HG03579.hp2 NA18974.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(15): Show |
1 | a0007c0009t0003g0235 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(17): Show |
1 | a0007c0009t0003g0230 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(23): Show |
1 | a0003c0003t0002g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(32): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(21): Show |
2 | a0003c0003t0002g0082a0011c0017t0002g0240 | 2 | HG02145.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0127a0002c0002t0001g0300 | 2 | HG03654.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(19): Show |
8 | a0002c0002t0002g0309a0003c0003t0002g0083a0003c0003t0002g0084others(5): Show | 8 | HG01346.hp2 HG03139.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(28): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(21): Show |
1 | a0008c0015t0005g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4065+312_4065+313i others(30): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0112a0001c0001t0001g0139a0002c0002t0001g0298others(2): Show | 5 | HG00280.hp2 HG02056.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(17): Show |
2 | a0003c0003t0002g0075a0003c0003t0002g0095 | 2 | NA18949.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(26): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0011g0164a0002c0019t0001g0285a0004c0037t0001g0274 | 3 | HG01106.hp2 HG01175.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(15): Show |
3 | a0003c0003t0002g0059a0003c0003t0002g0070a0003c0003t0002g0081 | 3 | NA18979.hp2 NA19030.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0207a0002c0002t0001g0288a0002c0002t0001g0291 | 3 | HG01361.hp1 HG03927.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(13): Show |
7 | a0002c0002t0002g0242a0002c0002t0002g0310a0003c0003t0002g0054others(4): Show | 7 | HG02273.hp2 HG03704.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(24): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(5): Show |
5 | a0001c0001t0001g0130a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02004.hp1 HG02074.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(11): Show |
10 | a0002c0002t0002g0311a0003c0003t0001g0067a0003c0003t0001g0099others(7): Show | 10 | HG02027.hp2 HG02071.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(13): Show |
3 | a0002c0002t0001g0160a0005c0008t0001g0299a0005c0008t0004g0340 | 3 | HG02074.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(3): Show |
4 | a0002c0002t0001g0003a0002c0002t0001g0289a0002c0002t0001g0361others(1): Show | 5 | HG00639.hp1 HG01069.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(9): Show |
9 | a0001c0001t0002g0129a0001c0001t0002g0148a0002c0002t0001g0035others(6): Show | 9 | HG00408.hp1 HG00408.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0145a0002c0002t0001g0163 | 2 | NA18991.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(1): Show |
3 | a0002c0002t0001g0022a0002c0002t0001g0287a0004c0006t0004g0249 | 3 | HG01074.hp2 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(7): Show |
2 | a0003c0003t0002g0008a0004c0006t0002g0254 | 2 | HG04184.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATAT others(9): Show |
3 | a0002c0002t0001g0161a0003c0003t0006g0105a0004c0006t0006g0252 | 3 | HG00673.hp1 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4065+312_4065+313i others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATG | 4 | a0001c0001t0001g0165a0002c0002t0001g0271a0004c0006t0001g0211others(1): Show | 4 | HG00140.hp2 HG00609.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATGT others(5): Show |
7 | a0001c0001t0002g0138a0002c0002t0002g0337a0002c0002t0002g0338others(4): Show | 7 | HG01123.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0133 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATGT others(7): Show |
5 | a0001c0001t0002g0144a0001c0001t0012g0156a0002c0019t0001g0282others(2): Show | 5 | HG01099.hp1 HG01169.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4065+312_4065+313i others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATATGT others(11): Show |
1 | a0002c0002t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4065+312_4065+313i others(20): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATGTAT others(3): Show |
3 | a0003c0003t0002g0062a0003c0003t0002g0066a0003c0003t0003g0063 | 3 | HG01099.hp2 HG01109.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.4065+316_4065+317i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATATGTAT others(5): Show |
3 | a0001c0001t0002g0142a0004c0006t0006g0253a0005c0008t0001g0297 | 3 | HG01516.hp2 HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.4065+316_4065+317i others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATGTATAT others(1): Show |
10 | a0002c0002t0002g0040a0002c0002t0002g0314a0002c0002t0002g0351others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.4065+310_4065+311i others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | ATGTATGT others(3): Show |
2 | a0001c0001t0002g0157a0008c0015t0006g0027 | 2 | HG02135.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4065+310_4065+311i others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40017551 | |||||
| chr15:40017551
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(162): Show | 169 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.4065+309A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017551 | ||||||
| chr15:40017655
|
C | G | 3 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0004g0237 | 3 | HG01109.hp1 HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4065+413C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017655 | ||||||
| chr15:40017670
|
C | T | 1 | a0002c0004t0001g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4065+428C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017670 | ||||||
| chr15:40017683
|
C | T | 1 | a0004c0006t0001g0256 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4065+441C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017683 | ||||||
| chr15:40017775
|
G | A | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4065+533G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017775 | ||||||
| chr15:40017821
|
A | T | 1 | a0002c0004t0001g0327 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4065+579A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017821 | ||||||
| chr15:40017953
|
A | G | 1 | a0002c0004t0001g0343 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4065+711A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40017953 | ||||||
| chr15:40018030
|
G | T | 8 | a0001c0005t0001g0247a0002c0004t0003g0036a0002c0004t0003g0038others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4065+788G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018030 | ||||||
| chr15:40018334
|
C | T | 15 | a0001c0005t0001g0125a0001c0005t0001g0134a0001c0005t0001g0135others(12): Show | 15 | HG00280.hp1 HG00741.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.4066-759C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018334 | ||||||
| chr15:40018392
|
A | G | 1 | a0002c0002t0010g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4066-701A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018392 | ||||||
| chr15:40018442
|
AT | A | 21 | a0001c0001t0001g0244a0001c0001t0003g0246a0001c0001t0004g0245others(18): Show | 23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4066-641delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | INFO_REALIGN_3_PRIME | chr15 | 40018442 | |||||
| chr15:40018600
|
G | A | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4066-493G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40018600 | ||||||
| chr15:40019011
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(82): Show | 87 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.4066-82G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 29/38 | chr15 | 40019011 | ||||||
| chr15:40019232
|
C | T | 1 | a0003c0003t0002g0053 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4173+32C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019232 | ||||||
| chr15:40019367
|
A | G | 1 | a0002c0013t0001g0281 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4173+167A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019367 | ||||||
| chr15:40019434
|
C | T | 1 | a0001c0005t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4173+234C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019434 | ||||||
| chr15:40019435
|
C | T | 1 | a0001c0005t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4173+235C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019435 | ||||||
| chr15:40019442
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4173+242G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019442 | ||||||
| chr15:40019698
|
C | T | 1 | a0001c0005t0005g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4173+498C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019698 | ||||||
| chr15:40019699
|
G | A | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4173+499G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40019699 | ||||||
| chr15:40020082
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4174-817G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020082 | ||||||
| chr15:40020165
|
C | CA | 225 | a0001c0001t0001g0001a0001c0001t0001g0140a0001c0001t0001g0244others(222): Show | 229 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.4174-721dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020165 | |||||
| chr15:40020342
|
A | AT | 8 | a0001c0001t0002g0145a0001c0005t0005g0154a0002c0002t0001g0160others(5): Show | 8 | HG00741.hp1 HG02056.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4174-543dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020342 | |||||
| chr15:40020342
|
AT | A | 6 | a0001c0001t0003g0012a0001c0005t0001g0226a0002c0004t0001g0325others(3): Show | 6 | HG00099.hp2 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.4174-543delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020342 | |||||
| chr15:40020414
|
A | G | 21 | a0001c0001t0001g0244a0001c0001t0003g0246a0001c0001t0004g0245others(18): Show | 23 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4174-485A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020414 | ||||||
| chr15:40020512
|
A | ATATT | 4 | a0001c0001t0002g0111a0001c0001t0002g0206a0001c0021t0003g0224others(1): Show | 4 | HG00621.hp1 HG02040.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.4174-361_4174-358d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | |||||
| chr15:40020512
|
ATATT | A | 33 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.4174-361_4174-358d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | |||||
| chr15:40020512
|
ATATTTAT others(1): Show |
A | 227 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(224): Show | 230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.4174-365_4174-358d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020512 | |||||
| chr15:40020520
|
T | A | 29 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4174-379T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020520 | ||||||
| chr15:40020524
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4174-375T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020524 | ||||||
| chr15:40020528
|
T | C | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0163 | 3 | HG02622.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4174-371T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020528 | ||||||
| chr15:40020637
|
G | A | 33 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.4174-262G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020637 | ||||||
| chr15:40020682
|
C | CT | 3 | a0002c0002t0007g0043a0009c0016t0007g0042a0009c0016t0007g0044 | 3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4174-216dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020682 | |||||
| chr15:40020721
|
CT | C | 130 | a0001c0001t0001g0244a0001c0001t0002g0009a0001c0001t0002g0013others(127): Show | 132 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.4174-162delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr15 | 40020721 | |||||
| chr15:40020811
|
A | G | 2 | a0003c0003t0002g0055a0003c0003t0002g0094 | 2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4174-88A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020811 | ||||||
| chr15:40020882
|
G | T | 275 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(272): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.4174-17G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 30/38 | chr15 | 40020882 | ||||||
| chr15:40021039
|
A | G | 1 | a0001c0001t0004g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4302+12A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021039 | ||||||
| chr15:40021185
|
A | G | 12 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0360others(9): Show | 12 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.4302+158A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021185 | ||||||
| chr15:40021473
|
C | A | 1 | a0003c0003t0002g0008 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4302+446C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021473 | ||||||
| chr15:40021644
|
A | C | 1 | a0002c0004t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4302+617A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021644 | ||||||
| chr15:40021829
|
C | T | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4303-690C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021829 | ||||||
| chr15:40021872
|
G | C | 91 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0125others(88): Show | 92 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.4303-647G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021872 | ||||||
| chr15:40021990
|
A | G | 74 | a0001c0005t0001g0032a0001c0005t0001g0034a0001c0005t0001g0132others(71): Show | 75 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4303-529A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40021990 | ||||||
| chr15:40022181
|
C | CGT | 13 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0207others(10): Show | 14 | HG01168.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.4303-305_4303-304d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGT | 32 | a0001c0001t0001g0205a0001c0001t0002g0149a0001c0001t0003g0201others(29): Show | 32 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.4303-307_4303-304d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGT | 26 | a0001c0001t0002g0129a0001c0005t0001g0032a0001c0005t0001g0034others(23): Show | 26 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4303-309_4303-304d others(8): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGTG others(1): Show |
48 | a0001c0001t0002g0117a0001c0001t0002g0141a0001c0001t0002g0159others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.4303-311_4303-304d others(10): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGTG others(3): Show |
53 | a0001c0001t0001g0356a0001c0001t0002g0118a0001c0001t0002g0120others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.4303-313_4303-304d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGTG others(5): Show |
70 | a0001c0001t0001g0170a0001c0001t0002g0119a0001c0001t0002g0142others(67): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4303-315_4303-304d others(14): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGTG others(7): Show |
5 | a0001c0001t0012g0156a0002c0004t0001g0258a0002c0004t0001g0329others(2): Show | 5 | HG00544.hp1 HG01168.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303-317_4303-304d others(16): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022181
|
C | CGTGTGTG others(9): Show |
8 | a0001c0005t0001g0181a0001c0020t0001g0174a0002c0004t0001g0210others(5): Show | 8 | HG00621.hp2 HG01257.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.4303-319_4303-304d others(18): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022181 | |||||
| chr15:40022196
|
GTGTGTGT others(13): Show |
G | 1 | a0002c0029t0002g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4303-319_4303-300d others(22): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022196 | |||||
| chr15:40022206
|
GTGTGTGT others(3): Show |
G | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4303-309_4303-300d others(12): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022206 | |||||
| chr15:40022208
|
GTGTGTGT others(4): Show |
G | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4303-305_4303-295d others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022208 | |||||
| chr15:40022214
|
GTA | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0220others(3): Show | 6 | HG00597.hp1 HG03927.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303-303_4303-302d others(4): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 40022214 | |||||
| chr15:40022215
|
TATG | T | 7 | a0001c0005t0001g0247a0002c0004t0003g0036a0002c0004t0003g0038others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-303_4303-301d others(5): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022215 | ||||||
| chr15:40022216
|
A | G | 120 | a0001c0001t0001g0244a0001c0001t0002g0090a0001c0001t0002g0117others(117): Show | 122 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.4303-303A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022216 | ||||||
| chr15:40022219
|
T | G | 7 | a0001c0005t0001g0247a0002c0004t0003g0036a0002c0004t0003g0038others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-300T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022219 | ||||||
| chr15:40022219
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0002g0090 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.4303-300_4303-299i others(13): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022219 | ||||||
| chr15:40022318
|
G | C | 1 | a0004c0007t0002g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4303-201G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022318 | ||||||
| chr15:40022325
|
G | A | 253 | a0001c0001t0001g0170a0001c0001t0001g0244a0001c0001t0001g0356others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.4303-194G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022325 | ||||||
| chr15:40022510
|
T | G | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4303-9T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 31/38 | chr15 | 40022510 | ||||||
| chr15:40022683
|
G | C | 4 | a0002c0004t0001g0272a0002c0004t0003g0257a0002c0004t0003g0264others(1): Show | 4 | HG00544.hp2 HG02135.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.4389+78G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022683 | ||||||
| chr15:40022741
|
CT | C | 9 | a0001c0001t0003g0193a0003c0003t0002g0104a0003c0003t0003g0091others(6): Show | 9 | HG02027.hp2 HG02523.hp2 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.4389+148delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40022741 | |||||
| chr15:40022766
|
C | G | 206 | a0001c0001t0001g0133a0001c0001t0001g0244a0001c0001t0002g0009others(203): Show | 207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.4389+161C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022766 | ||||||
| chr15:40022797
|
A | T | 7 | a0001c0001t0001g0205a0001c0001t0003g0201a0001c0001t0003g0202others(4): Show | 7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.4389+192A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022797 | ||||||
| chr15:40022819
|
C | T | 1 | a0004c0007t0002g0267 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4389+214C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022819 | ||||||
| chr15:40022873
|
G | A | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389+268G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022873 | ||||||
| chr15:40022884
|
C | A | 1 | a0003c0003t0002g0103 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4389+279C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40022884 | ||||||
| chr15:40023016
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | NA19075.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4389+411C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023016 | ||||||
| chr15:40023022
|
C | T | 1 | a0002c0004t0002g0349 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4389+417C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023022 | ||||||
| chr15:40023023
|
G | A | 4 | a0002c0004t0003g0036a0002c0004t0003g0039a0002c0004t0005g0037others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+418G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023023 | ||||||
| chr15:40023076
|
T | G | 3 | a0002c0002t0007g0043a0009c0016t0007g0042a0009c0016t0007g0044 | 3 | HG01255.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4389+471T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023076 | ||||||
| chr15:40023179
|
G | T | 1 | a0016c0034t0001g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4389+574G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023179 | ||||||
| chr15:40023195
|
A | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0176a0001c0001t0003g0227others(1): Show | 5 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.4389+590A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023195 | ||||||
| chr15:40023274
|
T | C | 1 | a0003c0003t0001g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4389+669T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023274 | ||||||
| chr15:40023335
|
T | G | 6 | a0002c0002t0001g0360a0002c0002t0001g0362a0002c0002t0003g0162others(3): Show | 6 | HG01109.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4389+730T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023335 | ||||||
| chr15:40023416
|
C | T | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4389+811C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023416 | ||||||
| chr15:40023435
|
A | G | 7 | a0001c0005t0001g0125a0001c0005t0005g0123a0001c0005t0005g0124others(4): Show | 7 | HG00741.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4389+830A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023435 | ||||||
| chr15:40023534
|
A | G | 1 | a0003c0003t0002g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4389+929A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023534 | ||||||
| chr15:40023675
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4389+1070C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023675 | ||||||
| chr15:40023837
|
C | CT | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389+1239dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40023837 | |||||
| chr15:40023967
|
A | G | 3 | a0008c0015t0005g0026a0008c0015t0006g0025a0008c0015t0006g0027 | 3 | HG02976.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4389+1362A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023967 | ||||||
| chr15:40023970
|
A | C | 95 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4389+1365A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40023970 | ||||||
| chr15:40024161
|
A | C | 1 | a0003c0003t0002g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4389+1556A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024161 | ||||||
| chr15:40024218
|
C | CT | 12 | a0002c0002t0002g0040a0002c0002t0002g0309a0002c0002t0002g0310others(9): Show | 12 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4389+1623dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024218 | |||||
| chr15:40024228
|
T | TAAGAGAT others(313): Show |
3 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0026t0001g0011 | 3 | HG02258.hp1 HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4389+1639_4389+164 others(324): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024228 | |||||
| chr15:40024228
|
T | TAAGAGAT others(314): Show |
1 | a0003c0010t0001g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4389+1639_4389+164 others(325): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024228 | |||||
| chr15:40024403
|
C | CT | 13 | a0001c0001t0001g0205a0001c0001t0003g0187a0001c0001t0003g0197others(10): Show | 13 | HG01516.hp1 HG01884.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.4390-1551dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | |||||
| chr15:40024403
|
CT | C | 90 | a0001c0001t0002g0013a0001c0001t0002g0129a0001c0001t0002g0138others(87): Show | 92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.4390-1551delT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | |||||
| chr15:40024403
|
CTT | C | 10 | a0001c0001t0002g0009a0001c0001t0002g0128a0001c0001t0004g0195others(7): Show | 10 | HG00597.hp2 HG01255.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.4390-1552_4390-155 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | |||||
| chr15:40024403
|
CTTTTTTT | C | 24 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0035others(21): Show | 24 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.4390-1557_4390-155 others(11): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024403 | |||||
| chr15:40024479
|
A | T | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4390-1498A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024479 | ||||||
| chr15:40024649
|
C | T | 102 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-1328C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024649 | ||||||
| chr15:40024677
|
C | T | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1300C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024677 | ||||||
| chr15:40024700
|
C | CT | 147 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(144): Show | 151 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.4390-1264dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024700 | |||||
| chr15:40024737
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4390-1240T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024737 | ||||||
| chr15:40024739
|
G | GTT | 7 | a0002c0002t0001g0160a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02809.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4390-1228_4390-122 others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40024739 | |||||
| chr15:40024764
|
A | T | 5 | a0002c0002t0001g0360a0002c0002t0003g0162a0002c0002t0003g0335others(2): Show | 5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4390-1213A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024764 | ||||||
| chr15:40024782
|
G | A | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1195G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024782 | ||||||
| chr15:40024809
|
A | G | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1168A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024809 | ||||||
| chr15:40024874
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(119): Show | 126 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.4390-1103G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024874 | ||||||
| chr15:40024916
|
G | A | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4390-1061G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40024916 | ||||||
| chr15:40025314
|
C | T | 102 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-663C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025314 | ||||||
| chr15:40025407
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(104): Show | 109 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.4390-570G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025407 | ||||||
| chr15:40025500
|
A | G | 1 | a0002c0004t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4390-477A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025500 | ||||||
| chr15:40025591
|
T | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(128): Show | 135 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.4390-386T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025591 | ||||||
| chr15:40025608
|
A | G | 102 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.4390-369A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025608 | ||||||
| chr15:40025647
|
TA | T | 22 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(19): Show | 22 | HG00438.hp2 HG02056.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.4390-318delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr15 | 40025647 | |||||
| chr15:40025782
|
G | A | 1 | a0004c0006t0001g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4390-195G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 32/38 | chr15 | 40025782 | ||||||
| chr15:40026111
|
G | A | 8 | a0002c0002t0001g0160a0003c0003t0003g0091a0003c0025t0004g0010others(5): Show | 8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4502+22G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026111 | ||||||
| chr15:40026146
|
C | G | 1 | a0003c0025t0004g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4502+57C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026146 | ||||||
| chr15:40026187
|
G | C | 9 | a0001c0001t0003g0246a0002c0002t0001g0360a0002c0002t0003g0162others(6): Show | 9 | HG01081.hp1 HG02055.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.4502+98G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026187 | ||||||
| chr15:40026264
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4502+175G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026264 | ||||||
| chr15:40026289
|
TA | T | 8 | a0002c0002t0001g0160a0003c0003t0003g0091a0003c0025t0004g0010others(5): Show | 8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4502+210delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40026289 | |||||
| chr15:40026290
|
A | G | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4502+201A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026290 | ||||||
| chr15:40026300
|
T | A | 5 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336others(2): Show | 5 | HG02630.hp2 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4502+211T>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026300 | ||||||
| chr15:40026335
|
A | G | 4 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+246A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026335 | ||||||
| chr15:40026480
|
A | G | 1 | a0003c0003t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4502+391A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026480 | ||||||
| chr15:40026518
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4502+429C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026518 | ||||||
| chr15:40026731
|
T | C | 2 | a0002c0002t0001g0161a0002c0002t0001g0163 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4502+642T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026731 | ||||||
| chr15:40026887
|
T | C | 5 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(2): Show | 5 | NA18984.hp1 NA19074.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.4502+798T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40026887 | ||||||
| chr15:40027102
|
C | T | 1 | a0002c0002t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4502+1013C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027102 | ||||||
| chr15:40027150
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4502+1061C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027150 | ||||||
| chr15:40027306
|
T | C | 5 | a0002c0002t0001g0360a0002c0002t0003g0162a0002c0002t0003g0335others(2): Show | 5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4502+1217T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027306 | ||||||
| chr15:40027316
|
G | A | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+1227G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027316 | ||||||
| chr15:40027432
|
C | T | 1 | a0004c0007t0002g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4502+1343C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027432 | ||||||
| chr15:40027571
|
TG | T | 14 | a0001c0001t0001g0244a0001c0001t0003g0246a0002c0002t0001g0035others(11): Show | 14 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.4502+1483delG | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027571 | ||||||
| chr15:40027613
|
G | A | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4502+1524G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027613 | ||||||
| chr15:40027617
|
G | A | 6 | a0003c0003t0002g0072a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | NA18964.hp1 NA18974.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.4502+1528G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027617 | ||||||
| chr15:40027699
|
G | A | 6 | a0003c0003t0003g0091a0007c0009t0003g0230a0007c0009t0003g0232others(3): Show | 6 | HG02523.hp2 NA18964.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.4502+1610G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027699 | ||||||
| chr15:40027704
|
C | T | 1 | a0002c0002t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4502+1615C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027704 | ||||||
| chr15:40027760
|
G | A | 4 | a0001c0005t0001g0247a0003c0010t0001g0047a0003c0010t0001g0048others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4503-1646G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027760 | ||||||
| chr15:40027845
|
C | A | 95 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4503-1561C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027845 | ||||||
| chr15:40027889
|
C | CA | 39 | a0001c0001t0001g0170a0001c0001t0001g0356a0001c0001t0002g0129others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.4503-1506dupA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40027889 | |||||
| chr15:40027900
|
A | C | 8 | a0002c0002t0001g0160a0003c0003t0003g0091a0003c0025t0004g0010others(5): Show | 8 | HG02523.hp2 HG02809.hp2 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.4503-1506A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40027900 | ||||||
| chr15:40028031
|
A | G | 29 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4503-1375A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028031 | ||||||
| chr15:40028066
|
A | G | 29 | a0001c0001t0001g0170a0001c0001t0001g0356a0002c0002t0001g0003others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.4503-1340A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028066 | ||||||
| chr15:40028079
|
C | CT | 118 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.4503-1314dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 40028079 | |||||
| chr15:40028081
|
T | C | 1 | a0002c0002t0001g0300 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4503-1325T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028081 | ||||||
| chr15:40028114
|
C | G | 1 | a0002c0002t0005g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4503-1292C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028114 | ||||||
| chr15:40028114
|
C | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4503-1292C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028114 | ||||||
| chr15:40028163
|
C | T | 7 | a0001c0001t0001g0205a0001c0001t0003g0201a0001c0001t0003g0202others(4): Show | 7 | NA18949.hp1 NA18970.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.4503-1243C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028163 | ||||||
| chr15:40028540
|
T | C | 9 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0003g0179others(6): Show | 9 | HG02155.hp2 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.4503-866T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028540 | ||||||
| chr15:40028565
|
C | G | 2 | a0002c0004t0001g0304a0002c0004t0001g0313 | 2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4503-841C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028565 | ||||||
| chr15:40028632
|
TC | T | 5 | a0001c0005t0001g0247a0002c0002t0001g0160a0003c0010t0001g0047others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-773delC | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028632 | ||||||
| chr15:40028635
|
C | T | 13 | a0001c0001t0002g0159a0002c0002t0001g0161a0002c0002t0001g0163others(10): Show | 13 | HG00673.hp1 HG01099.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.4503-771C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028635 | ||||||
| chr15:40028825
|
G | T | 1 | a0002c0031t0009g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4503-581G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028825 | ||||||
| chr15:40028871
|
C | T | 5 | a0001c0005t0001g0247a0002c0002t0001g0160a0003c0010t0001g0047others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-535C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028871 | ||||||
| chr15:40028882
|
G | C | 1 | a0003c0003t0003g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4503-524G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028882 | ||||||
| chr15:40028973
|
G | A | 12 | a0001c0001t0002g0148a0002c0004t0002g0312a0003c0003t0002g0056others(9): Show | 12 | HG00408.hp2 HG00544.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.4503-433G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40028973 | ||||||
| chr15:40029150
|
C | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(151): Show | 158 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.4503-256C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029150 | ||||||
| chr15:40029235
|
C | G | 5 | a0002c0002t0001g0360a0002c0002t0003g0162a0002c0002t0003g0335others(2): Show | 5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4503-171C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029235 | ||||||
| chr15:40029240
|
C | T | 2 | a0003c0003t0002g0055a0003c0003t0002g0094 | 2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4503-166C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029240 | ||||||
| chr15:40029331
|
G | A | 7 | a0003c0003t0003g0091a0003c0025t0004g0010a0007c0009t0003g0230others(4): Show | 7 | HG02523.hp2 NA18522.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.4503-75G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 33/38 | chr15 | 40029331 | ||||||
| chr15:40029579
|
C | T | 3 | a0004c0007t0002g0267a0004c0007t0003g0259a0011c0017t0003g0342 | 3 | HG03098.hp1 NA18972.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4561+115C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029579 | ||||||
| chr15:40029731
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4561+267G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029731 | ||||||
| chr15:40029923
|
T | C | 36 | a0001c0001t0001g0170a0001c0001t0001g0356a0001c0001t0003g0002others(33): Show | 38 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.4562-436T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029923 | ||||||
| chr15:40029966
|
C | T | 109 | a0001c0001t0001g0133a0001c0001t0002g0009a0001c0001t0002g0013others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.4562-393C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40029966 | ||||||
| chr15:40030095
|
G | A | 4 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336others(1): Show | 4 | HG02965.hp2 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4562-264G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030095 | ||||||
| chr15:40030198
|
C | T | 1 | a0003c0003t0006g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4562-161C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030198 | ||||||
| chr15:40030259
|
C | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0012a0001c0001t0003g0109others(41): Show | 45 | HG00438.hp1 HG01256.hp1 HG01258.hp2 others(42): Show |
intron_variant | MODIFIER | c.4562-100C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030259 | ||||||
| chr15:40030347
|
T | G | 5 | a0001c0005t0001g0247a0002c0002t0001g0160a0003c0010t0001g0047others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4562-12T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030347 | ||||||
| chr15:40030351
|
G | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(308): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
splice_region_variant&intron_variant | LOW | c.4562-8G>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 34/38 | chr15 | 40030351 | ||||||
| chr15:40030584
|
T | C | 2 | a0002c0002t0002g0337a0002c0002t0002g0338 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4659+128T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40030584 | ||||||
| chr15:40031009
|
G | A | 5 | a0001c0005t0001g0247a0002c0002t0001g0160a0003c0010t0001g0047others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4659+553G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031009 | ||||||
| chr15:40031015
|
G | A | 3 | a0004c0006t0006g0252a0004c0006t0006g0253a0004c0006t0006g0261 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4659+559G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031015 | ||||||
| chr15:40031037
|
C | T | 10 | a0001c0001t0003g0209a0001c0021t0003g0224a0002c0002t0001g0360others(7): Show | 10 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.4659+581C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031037 | ||||||
| chr15:40031121
|
T | C | 2 | a0002c0002t0004g0018a0002c0002t0004g0019 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4659+665T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031121 | ||||||
| chr15:40031197
|
G | C | 120 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(117): Show | 120 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.4659+741G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031197 | ||||||
| chr15:40031339
|
G | A | 1 | a0017c0035t0003g0236 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4660-830G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031339 | ||||||
| chr15:40031392
|
T | C | 1 | a0002c0004t0002g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4660-777T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031392 | ||||||
| chr15:40031491
|
A | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.4660-678A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031491 | ||||||
| chr15:40031508
|
GCCAC | G | 3 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039 | 3 | HG01891.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4660-659_4660-656d others(6): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 40031508 | |||||
| chr15:40031686
|
C | T | 1 | a0002c0002t0001g0361 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4660-483C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031686 | ||||||
| chr15:40031731
|
C | CT | 22 | a0001c0001t0004g0195a0001c0001t0004g0245a0001c0005t0004g0121others(19): Show | 24 | HG00408.hp1 HG01074.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.4660-426dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 40031731 | |||||
| chr15:40031731
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(81): Show | 86 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.4660-438C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031731 | ||||||
| chr15:40031874
|
G | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.4660-295G>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40031874 | ||||||
| chr15:40032079
|
C | T | 1 | a0003c0003t0002g0100 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4660-90C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40032079 | ||||||
| chr15:40032121
|
A | G | 3 | a0002c0004t0003g0036a0002c0004t0003g0038a0002c0004t0003g0039 | 3 | HG01891.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4660-48A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 35/38 | chr15 | 40032121 | ||||||
| chr15:40032280
|
T | C | 116 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(113): Show | 116 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.4728+43T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032280 | ||||||
| chr15:40032528
|
G | A | 119 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(116): Show | 119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.4729-229G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032528 | ||||||
| chr15:40032592
|
C | T | 1 | a0002c0002t0001g0362 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4729-165C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032592 | ||||||
| chr15:40032604
|
C | G | 1 | a0004c0006t0001g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4729-153C>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032604 | ||||||
| chr15:40032626
|
A | C | 9 | a0001c0001t0003g0209a0001c0021t0003g0224a0003c0003t0003g0063others(6): Show | 9 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.4729-131A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032626 | ||||||
| chr15:40032636
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(305): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.4729-121C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 36/38 | chr15 | 40032636 | ||||||
| chr15:40033147
|
T | C | 1 | a0003c0026t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4773+346T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033147 | ||||||
| chr15:40033267
|
G | A | 21 | a0001c0001t0005g0014a0001c0001t0005g0023a0001c0001t0005g0028others(18): Show | 21 | HG00741.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.4773+466G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033267 | ||||||
| chr15:40033293
|
A | C | 2 | a0008c0015t0006g0025a0008c0015t0006g0027 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4773+492A>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033293 | ||||||
| chr15:40033490
|
C | T | 119 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(116): Show | 119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.4773+689C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033490 | ||||||
| chr15:40033628
|
T | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0115others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.4774-698T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033628 | ||||||
| chr15:40033629
|
T | C | 1 | a0002c0004t0001g0320 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4774-697T>C | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033629 | ||||||
| chr15:40033659
|
A | G | 165 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0090others(162): Show | 167 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.4774-667A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033659 | ||||||
| chr15:40033706
|
T | G | 1 | a0016c0034t0001g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4774-620T>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033706 | ||||||
| chr15:40033721
|
A | G | 3 | a0002c0002t0003g0162a0002c0002t0003g0335a0002c0002t0003g0336 | 3 | HG02965.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-605A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033721 | ||||||
| chr15:40033821
|
G | A | 9 | a0001c0001t0003g0209a0001c0021t0003g0224a0003c0003t0003g0063others(6): Show | 9 | HG01109.hp2 HG02040.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-505G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033821 | ||||||
| chr15:40033848
|
G | A | 1 | a0009c0016t0007g0042 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4774-478G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033848 | ||||||
| chr15:40033849
|
A | G | 5 | a0001c0005t0001g0247a0002c0002t0001g0160a0003c0010t0001g0047others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-477A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033849 | ||||||
| chr15:40033977
|
G | A | 2 | a0002c0004t0001g0320a0004c0006t0001g0262 | 2 | HG01981.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.4774-349G>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40033977 | ||||||
| chr15:40034015
|
C | T | 3 | a0004c0006t0006g0252a0004c0006t0006g0253a0004c0006t0006g0261 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4774-311C>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40034015 | ||||||
| chr15:40034028
|
CA | C | 14 | a0001c0001t0003g0209a0001c0001t0012g0156a0001c0005t0005g0124others(11): Show | 14 | HG01109.hp2 HG01975.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-279delA | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 40034028 | |||||
| chr15:40034166
|
A | G | 1 | a0003c0010t0001g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4774-160A>G | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 37/38 | chr15 | 40034166 | ||||||
| chr15:40034552
|
C | A | 1 | a0001c0005t0004g0121 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4892+108C>A | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | chr15 | 40034552 | ||||||
| chr15:40034943
|
C | CT | 5 | a0001c0001t0002g0128a0003c0003t0002g0054a0003c0003t0002g0070others(2): Show | 5 | HG00597.hp2 HG02015.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.4893-83dupT | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 40034943 | |||||
| chr15:40035004
|
A | T | 1 | a0001c0001t0003g0199 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4893-23A>T | EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | chr15 | 40035004 | ||||||
| chr15:40035006
|
ATCTTT | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0116others(17): Show | 21 | HG00609.hp1 HG00609.hp2 HG01168.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.4893-9_4893-5delCT others(3): Show |
EIF2AK4 | ENSG00000128829.12 | transcript | ENST00000263791.10 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 40035006 |