Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83939 |
| ensemblid | ENSG00000144895.12 |
| hgncid | 3254 |
| symbol | EIF2A |
| name | eukaryotic translation initiation factor 2A |
| refseq_nuc | NM_032025.5 |
| refseq_prot | NP_114414.2 |
| ensembl_nuc | ENST00000460851.6 |
| ensembl_prot | ENSP00000417229.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 150546787 |
| end | 150586016 |
| strand | + |
| ver | v1.2 |
| region | chr3:150546787-150586016 |
| region5000 | chr3:150541787-150591016 |
| regionname0 | EIF2A_chr3_150546787_150586016 |
| regionname5000 | EIF2A_chr3_150541787_150591016 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 585 | 253 | 85 | 51 | 89 | 6 | 21 | 71 | EIF2A_chr3_150541787_150591016 | EIF2A | MAPST others(580): Show |
chr3 | 150541787 | 150591016 |
| a0002 | 0/1 | 585 | 138 | 6 | 25 | 81 | 6 | 19 | 66 | EIF2A_chr3_150541787_150591016 | EIF2A | MAPST others(580): Show |
chr3 | 150541787 | 150591016 |
| a0003 | 0/0 | 585 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | MAPST others(580): Show |
chr3 | 150541787 | 150591016 |
| a0004 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | MAPST others(580): Show |
chr3 | 150541787 | 150591016 |
| a0005 | 0/0 | 585 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | MAPST others(580): Show |
chr3 | 150541787 | 150591016 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1755 | 198 | 54 | 38 | 85 | 5 | 15 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0001c0003 | 0/0 | 1755 | 49 | 25 | 13 | 4 | 1 | 6 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0001c0004 | 0/0 | 1755 | 5 | 5 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0001c0005 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0002c0002 | 0/1 | 1755 | 138 | 6 | 25 | 81 | 6 | 19 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0003c0008 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0004c0006 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 | ||
| a0005c0007 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | ATGGC others(1750): Show |
chr3 | 150541787 | 150591016 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3875 | 106 | 18 | 15 | 61 | 3 | 9 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0003 | 1/0 | 3879 | 61 | 20 | 15 | 21 | 1 | 3 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0005 | 0/0 | 3879 | 12 | 1 | 7 | 0 | 1 | 3 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0006 | 0/0 | 3873 | 10 | 9 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3868): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0009 | 0/0 | 3879 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0012 | 0/0 | 3879 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0013 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0014 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0015 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0001t0020 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0002 | 0/0 | 3875 | 8 | 6 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0004 | 0/0 | 3875 | 28 | 10 | 9 | 2 | 1 | 6 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0007 | 0/0 | 3875 | 8 | 7 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0011 | 0/0 | 3875 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0016 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0017 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0003t0018 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0001c0004t0003 | 0/0 | 3879 | 5 | 5 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0001c0005t0003 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0002c0002t0001 | 0/1 | 3875 | 129 | 6 | 22 | 79 | 5 | 16 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0002c0002t0002 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0002c0002t0008 | 0/0 | 3879 | 4 | 0 | 1 | 0 | 0 | 3 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3874): Show |
chr3 | 150541787 | 150591016 |
| a0002c0002t0010 | 0/0 | 3875 | 3 | 0 | 1 | 1 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0002c0002t0019 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0003c0008t0001 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0004c0006t0002 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| a0005c0007t0001 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | CTCTT others(3870): Show |
chr3 | 150541787 | 150591016 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 24 | 8 | 3 | 10 | 0 | 3 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0003 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0006g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0002g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0008 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0007g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0007g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0011g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0017g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0003t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0004t0003g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0004t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0001c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0002 | 0/0 | 22 | 0 | 7 | 10 | 1 | 4 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0006 | 0/0 | 7 | 3 | 0 | 0 | 0 | 4 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0056 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0008g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0008g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0010g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0010g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0002c0002t0019g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0003c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0004c0006t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| a0005c0007t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | FIN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0013 | EUR | FIN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00323 | hp1 | a0001 | c0003 | t0004 | g0163 | EUR | FIN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00323 | hp2 | a0002 | c0002 | t0010 | g0075 | EUR | FIN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00408 | hp2 | a0003 | c0008 | t0001 | g0102 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00438 | hp2 | a0001 | c0001 | t0014 | g0047 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00735 | hp1 | a0001 | c0003 | t0004 | g0008 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG00741 | hp2 | a0002 | c0002 | t0008 | g0017 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01070 | hp1 | a0001 | c0003 | t0004 | g0176 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01070 | hp2 | a0002 | c0002 | t0010 | g0069 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0177 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0121 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01168 | hp2 | a0001 | c0003 | t0017 | g0180 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01243 | hp2 | a0001 | c0003 | t0007 | g0043 | AMR | PUR | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01361 | hp1 | a0002 | c0002 | t0019 | g0002 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0010 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0010 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01496 | hp2 | a0001 | c0003 | t0004 | g0008 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0035 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0035 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01884 | hp2 | a0001 | c0003 | t0007 | g0011 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01891 | hp1 | a0001 | c0003 | t0007 | g0011 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01952 | hp2 | a0001 | c0003 | t0004 | g0008 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01975 | hp2 | a0001 | c0003 | t0004 | g0159 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0064 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02145 | hp2 | a0004 | c0006 | t0002 | g0068 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0161 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0010 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0184 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02300 | hp1 | a0001 | c0003 | t0004 | g0059 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02451 | hp2 | a0001 | c0004 | t0003 | g0014 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02572 | hp1 | a0001 | c0001 | t0015 | g0066 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02602 | hp2 | a0001 | c0003 | t0004 | g0162 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02622 | hp2 | a0001 | c0003 | t0016 | g0164 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02630 | hp2 | a0001 | c0004 | t0003 | g0186 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02683 | hp1 | a0002 | c0002 | t0008 | g0087 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02698 | hp2 | a0001 | c0003 | t0004 | g0008 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02723 | hp2 | a0001 | c0005 | t0003 | g0015 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02735 | hp2 | a0001 | c0003 | t0004 | g0178 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0014 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02886 | hp2 | a0001 | c0003 | t0007 | g0011 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0014 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0165 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0010 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0026 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0202 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0026 | AFR | GWD | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0169 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03195 | hp1 | a0001 | c0004 | t0003 | g0014 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03195 | hp2 | a0001 | c0003 | t0007 | g0011 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0026 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0181 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03486 | hp2 | a0001 | c0003 | t0018 | g0170 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03490 | hp2 | a0001 | c0003 | t0004 | g0179 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0157 | AFR | ESN | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0156 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03654 | hp2 | a0002 | c0002 | t0008 | g0017 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03688 | hp2 | a0001 | c0003 | t0004 | g0158 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0057 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0116 | SAS | BEB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04204 | hp1 | a0002 | c0002 | t0008 | g0017 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04204 | hp2 | a0001 | c0003 | t0004 | g0008 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | STU | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18747 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | CHB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18906 | hp2 | a0001 | c0003 | t0007 | g0043 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18951 | hp1 | a0001 | c0003 | t0004 | g0175 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18984 | hp2 | a0001 | c0003 | t0011 | g0045 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA18999 | hp2 | a0002 | c0002 | t0010 | g0103 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | LWK | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0010 | AFR | LWK | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19059 | hp1 | a0005 | c0007 | t0001 | g0085 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19078 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19081 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19091 | hp2 | a0001 | c0003 | t0011 | g0045 | EAS | JPT | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19240 | hp1 | a0001 | c0003 | t0007 | g0011 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0065 | AFR | YRI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ASW | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ASW | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | TSI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0027 | EUR | TSI | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | GIH | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG01123 | hp2 | a0001 | c0003 | t0004 | g0160 | AMR | CLM | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0171 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0166 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0168 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | MSL | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG06807 | hp1 | a0001 | c0003 | t0007 | g0172 | AFR | USA | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| HG06807 | hp2 | a0001 | c0003 | t0004 | g0167 | AFR | USA | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | USA | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0089 | REF | REF | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0206 | REF | REF | EIF2A_chr3_150541787_150591016 | EIF2A | chr3 | 150541787 | 150591016 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150562658 | C | G | 3 | a0002 a0003 a0005 |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
missense_variant&splice_region_variant | MODERATE | c.290C>G | p.Thr97Ser | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/14 | 306/3879 | 290/1758 | 97/585 | chr3 | 150562658 | |||
| chr3:150572210 | C | T | 1 | a0003 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1064C>T | p.Pro355Leu | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/14 | 1080/3879 | 1064/1758 | 355/585 | chr3 | 150572210 | |||
| chr3:150572522 | C | G | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1376C>G | p.Ser459Cys | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/14 | 1392/3879 | 1376/1758 | 459/585 | chr3 | 150572522 | |||
| chr3:150575656 | A | T | 1 | a0005 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.1391A>T | p.Glu464Val | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/14 | 1407/3879 | 1391/1758 | 464/585 | chr3 | 150575656 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150567733 | T | C | 1 | a0001c0003 | 49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
synonymous_variant | LOW | c.516T>C | p.Asp172Asp | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 7/14 | 532/3879 | 516/1758 | 172/585 | chr3 | 150567733 | |||
| chr3:150572025 | T | C | 1 | a0001c0005 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.879T>C | p.Gly293Gly | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/14 | 895/3879 | 879/1758 | 293/585 | chr3 | 150572025 | |||
| chr3:150572527 | T | C | 1 | a0001c0004 | 5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1381T>C | p.Leu461Leu | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/14 | 1397/3879 | 1381/1758 | 461/585 | chr3 | 150572527 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150584126 | T | C | 1 | a0001c0003t0011 | 2 | NA18984.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*215T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 215 | chr3 | 150584126 | ||||||
| chr3:150584223 | C | T | 20 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(17): Show |
317 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*312C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 312 | chr3 | 150584223 | ||||||
| chr3:150584227 | GAC | G | 1 | a0001c0001t0006 | 10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*318_*319delCA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 318 | INFO_REALIGN_3_PRIME | chr3 | 150584227 | |||||
| chr3:150584373 | A | G | 20 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(17): Show |
309 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*462A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 462 | chr3 | 150584373 | ||||||
| chr3:150584910 | A | G | 1 | a0002c0002t0010 | 3 | HG00323.hp2 HG01070.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 999 | chr3 | 150584910 | ||||||
| chr3:150585035 | A | C | 20 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(17): Show |
309 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1124A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1124 | chr3 | 150585035 | ||||||
| chr3:150585130 | A | C | 1 | a0001c0001t0012 | 2 | HG02145.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1219A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1219 | chr3 | 150585130 | ||||||
| chr3:150585289 | G | A | 1 | a0001c0001t0015 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1378G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1378 | chr3 | 150585289 | ||||||
| chr3:150585306 | G | T | 1 | a0001c0001t0014 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1395G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1395 | chr3 | 150585306 | ||||||
| chr3:150585314 | G | A | 1 | a0001c0001t0009 | 3 | HG02647.hp2 HG03041.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1403G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1403 | chr3 | 150585314 | ||||||
| chr3:150585436 | T | C | 1 | a0001c0003t0016 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1525 | chr3 | 150585436 | ||||||
| chr3:150585517 | TCACA | T | 6 | a0001c0003t0004 a0001c0003t0007 a0001c0003t0011 others(3): Show |
41 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1615_*1618delCACA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1615 | INFO_REALIGN_3_PRIME | chr3 | 150585517 | |||||
| chr3:150585526 | CACAA | C | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0015 others(9): Show |
262 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*1617_*1620delCAAA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1617 | INFO_REALIGN_3_PRIME | chr3 | 150585526 | |||||
| chr3:150585530 | A | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(2): Show |
24 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1619A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1619 | chr3 | 150585530 | ||||||
| chr3:150585571 | T | A | 1 | a0001c0001t0013 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1660T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1660 | chr3 | 150585571 | ||||||
| chr3:150585747 | C | T | 1 | a0001c0003t0018 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1836C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1836 | chr3 | 150585747 | ||||||
| chr3:150585803 | A | C | 1 | a0001c0003t0017 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1892A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1892 | chr3 | 150585803 | ||||||
| chr3:150585808 | T | C | 1 | a0002c0002t0019 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1897T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1897 | chr3 | 150585808 | ||||||
| chr3:150585880 | C | T | 5 | a0002c0002t0001 a0002c0002t0010 a0002c0002t0019 others(2): Show |
134 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1969 | chr3 | 150585880 | ||||||
| chr3:150585899 | A | T | 1 | a0001c0001t0020 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1988A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 1988 | chr3 | 150585899 | ||||||
| chr3:150585918 | C | T | 1 | a0001c0003t0007 | 8 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2007C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 14/14 | 2007 | chr3 | 150585918 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150546920 | A | C | 19 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0056 others(16): Show |
32 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.28+90A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150546920 | |||||||
| chr3:150546924 | T | G | 1 | a0001c0001t0002g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.28+94T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150546924 | |||||||
| chr3:150546992 | G | A | 19 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0056 others(16): Show |
32 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.28+162G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150546992 | |||||||
| chr3:150547596 | T | C | 189 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(186): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.28+766T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547596 | |||||||
| chr3:150547663 | G | C | 1 | a0001c0003t0004g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.28+833G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547663 | |||||||
| chr3:150547690 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.28+860C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547690 | |||||||
| chr3:150547702 | A | G | 1 | a0002c0002t0001g0182 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.28+872A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547702 | |||||||
| chr3:150547722 | T | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0060 a0001c0001t0002g0061 |
5 | HG02055.hp2 HG02257.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+892T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547722 | |||||||
| chr3:150547838 | A | G | 1 | a0002c0002t0001g0046 | 2 | NA18986.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.28+1008A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547838 | |||||||
| chr3:150547871 | G | A | 2 | a0002c0002t0001g0027 a0002c0002t0001g0062 |
3 | HG01069.hp2 HG01074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.28+1041G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150547871 | |||||||
| chr3:150548096 | T | C | 93 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(90): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.28+1266T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150548096 | |||||||
| chr3:150548239 | A | G | 83 | a0001c0001t0003g0104 a0002c0002t0001g0002 a0002c0002t0001g0006 others(80): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.28+1409A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150548239 | |||||||
| chr3:150548773 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28+1943G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150548773 | |||||||
| chr3:150548873 | T | C | 83 | a0001c0001t0003g0104 a0002c0002t0001g0002 a0002c0002t0001g0006 others(80): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.28+2043T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150548873 | |||||||
| chr3:150549006 | T | C | 4 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02300.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+2176T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549006 | |||||||
| chr3:150549123 | A | AT | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.28+2304dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150549123 | ||||||
| chr3:150549143 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.28+2313A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549143 | |||||||
| chr3:150549216 | TTC | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0004c0006t0002g0068 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28+2388_28+2389del others(2): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150549216 | ||||||
| chr3:150549222 | C | CT | 9 | a0001c0001t0003g0055 a0001c0001t0003g0212 a0001c0001t0003g0213 others(6): Show |
10 | HG01169.hp1 HG02300.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.28+2407dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150549222 | ||||||
| chr3:150549222 | CT | C | 174 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(171): Show |
304 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.28+2407delT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150549222 | ||||||
| chr3:150549222 | CTT | C | 5 | a0001c0001t0002g0119 a0001c0001t0005g0013 a0001c0001t0005g0120 others(2): Show |
8 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.28+2406_28+2407del others(2): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150549222 | ||||||
| chr3:150549293 | G | A | 2 | a0002c0002t0001g0070 a0002c0002t0001g0071 |
2 | HG02074.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.28+2463G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549293 | |||||||
| chr3:150549316 | G | T | 189 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(186): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.28+2486G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549316 | |||||||
| chr3:150549363 | C | T | 2 | a0001c0003t0004g0175 a0001c0003t0011g0045 |
3 | NA18951.hp1 NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+2533C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549363 | |||||||
| chr3:150549479 | A | C | 1 | a0001c0001t0005g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.28+2649A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549479 | |||||||
| chr3:150549502 | G | A | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.28+2672G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549502 | |||||||
| chr3:150549546 | T | A | 1 | a0001c0004t0003g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.28+2716T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549546 | |||||||
| chr3:150549559 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.28+2729C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549559 | |||||||
| chr3:150549798 | A | T | 10 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(7): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-2558A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549798 | |||||||
| chr3:150549838 | C | T | 1 | a0001c0001t0015g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.29-2518C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549838 | |||||||
| chr3:150549939 | G | C | 1 | a0002c0002t0001g0074 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.29-2417G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150549939 | |||||||
| chr3:150550031 | A | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0120 a0001c0001t0005g0121 others(1): Show |
7 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2325A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550031 | |||||||
| chr3:150550079 | T | C | 1 | a0001c0001t0006g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.29-2277T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550079 | |||||||
| chr3:150550098 | T | C | 1 | a0002c0002t0010g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.29-2258T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550098 | |||||||
| chr3:150550137 | G | T | 1 | a0001c0001t0003g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.29-2219G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550137 | |||||||
| chr3:150550141 | T | TAATG | 189 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(186): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.29-2213_29-2212ins others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150550141 | ||||||
| chr3:150550605 | G | A | 2 | a0002c0002t0001g0070 a0002c0002t0001g0071 |
2 | HG02074.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.29-1751G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550605 | |||||||
| chr3:150550680 | C | T | 1 | a0001c0003t0004g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-1676C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550680 | |||||||
| chr3:150550791 | C | T | 1 | a0002c0002t0010g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.29-1565C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550791 | |||||||
| chr3:150550977 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0211 |
3 | HG02615.hp2 HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.29-1379C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150550977 | |||||||
| chr3:150551018 | C | G | 1 | a0001c0001t0003g0210 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.29-1338C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551018 | |||||||
| chr3:150551046 | A | G | 1 | a0001c0001t0002g0044 | 2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.29-1310A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551046 | |||||||
| chr3:150551316 | G | T | 83 | a0001c0001t0003g0104 a0002c0002t0001g0002 a0002c0002t0001g0006 others(80): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.29-1040G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551316 | |||||||
| chr3:150551405 | C | G | 10 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(7): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-951C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551405 | |||||||
| chr3:150551461 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.29-895G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551461 | |||||||
| chr3:150551492 | T | A | 191 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(188): Show |
327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.29-864T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551492 | |||||||
| chr3:150551567 | C | CA | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(89): Show |
154 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.29-777dupA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 150551567 | ||||||
| chr3:150551638 | G | C | 1 | a0001c0001t0003g0187 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-718G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551638 | |||||||
| chr3:150551639 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-717C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551639 | |||||||
| chr3:150551682 | C | T | 6 | a0002c0002t0001g0009 a0002c0002t0001g0110 a0002c0002t0001g0111 others(3): Show |
10 | HG01433.hp1 HG01981.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-674C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150551682 | |||||||
| chr3:150552135 | C | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-221C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150552135 | |||||||
| chr3:150552290 | C | G | 125 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(122): Show |
205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.29-66C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 1/13 | chr3 | 150552290 | |||||||
| chr3:150552642 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.98+217G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150552642 | |||||||
| chr3:150552852 | T | C | 2 | a0002c0002t0001g0028 a0002c0002t0001g0076 |
3 | HG01952.hp1 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.98+427T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150552852 | |||||||
| chr3:150553035 | A | G | 191 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(188): Show |
327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.98+610A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553035 | |||||||
| chr3:150553228 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98+803C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553228 | |||||||
| chr3:150553287 | C | T | 18 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0005g0013 others(15): Show |
27 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.98+862C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553287 | |||||||
| chr3:150553288 | A | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+863A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553288 | |||||||
| chr3:150553322 | C | CA | 20 | a0001c0001t0003g0055 a0001c0001t0003g0188 a0001c0001t0003g0189 others(17): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.98+917dupA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150553322 | ||||||
| chr3:150553322 | C | CAA | 9 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0012g0064 others(6): Show |
13 | HG01433.hp2 HG01496.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.98+916_98+917dupAA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150553322 | ||||||
| chr3:150553322 | CA | C | 59 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(56): Show |
109 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.98+917delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150553322 | ||||||
| chr3:150553378 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+953C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553378 | |||||||
| chr3:150553380 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+955G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553380 | |||||||
| chr3:150553381 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+956G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553381 | |||||||
| chr3:150553384 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+959G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553384 | |||||||
| chr3:150553387 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+962G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553387 | |||||||
| chr3:150553388 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+963G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553388 | |||||||
| chr3:150553390 | A | C | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+965A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553390 | |||||||
| chr3:150553391 | T | C | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+966T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553391 | |||||||
| chr3:150553394 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+969C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553394 | |||||||
| chr3:150553396 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+971A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553396 | |||||||
| chr3:150553398 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+973G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553398 | |||||||
| chr3:150553405 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+980C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553405 | |||||||
| chr3:150553408 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+983G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553408 | |||||||
| chr3:150553412 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+987A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553412 | |||||||
| chr3:150553431 | T | G | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1006T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553431 | |||||||
| chr3:150553439 | G | C | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1014G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553439 | |||||||
| chr3:150553441 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1016C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553441 | |||||||
| chr3:150553445 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1020G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553445 | |||||||
| chr3:150553465 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1040G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553465 | |||||||
| chr3:150553468 | G | C | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1043G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553468 | |||||||
| chr3:150553473 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1048A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553473 | |||||||
| chr3:150553495 | G | C | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1070G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553495 | |||||||
| chr3:150553499 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98+1074C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553499 | |||||||
| chr3:150553500 | C | A | 15 | a0001c0003t0004g0008 a0001c0003t0004g0059 a0001c0003t0004g0158 others(12): Show |
21 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.98+1075C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553500 | |||||||
| chr3:150553511 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98+1086C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553511 | |||||||
| chr3:150553555 | C | G | 1 | a0001c0001t0005g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.98+1130C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553555 | |||||||
| chr3:150553565 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.98+1140T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553565 | |||||||
| chr3:150553839 | C | T | 93 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(90): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.98+1414C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150553839 | |||||||
| chr3:150554040 | TGTACAAG others(5): Show |
T | 1 | a0002c0002t0001g0113 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.98+1619_98+1630del others(12): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150554040 | ||||||
| chr3:150554043 | A | G | 4 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
8 | HG01433.hp2 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+1618A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554043 | |||||||
| chr3:150554091 | CTAA | C | 3 | a0001c0003t0007g0011 a0001c0003t0007g0043 a0001c0003t0007g0172 |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+1668_98+1670del others(3): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150554091 | ||||||
| chr3:150554162 | T | A | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.98+1737T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554162 | |||||||
| chr3:150554230 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.98+1805G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554230 | |||||||
| chr3:150554284 | T | G | 15 | a0001c0003t0004g0008 a0001c0003t0004g0059 a0001c0003t0004g0158 others(12): Show |
21 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.98+1859T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554284 | |||||||
| chr3:150554439 | C | A | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+2014C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554439 | |||||||
| chr3:150554448 | A | T | 1 | a0001c0003t0004g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.98+2023A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554448 | |||||||
| chr3:150554518 | G | A | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+2093G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554518 | |||||||
| chr3:150554559 | T | TCATTAGA others(14): Show |
1 | a0001c0001t0002g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98+2137_98+2157dup others(21): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150554559 | ||||||
| chr3:150554716 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.98+2291G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554716 | |||||||
| chr3:150554778 | G | T | 89 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0003g0104 others(86): Show |
146 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.98+2353G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554778 | |||||||
| chr3:150554802 | C | T | 10 | a0002c0002t0001g0007 a0002c0002t0001g0217 a0002c0002t0001g0218 others(7): Show |
15 | HG00597.hp2 HG00673.hp2 NA18942.hp1 others(12): Show |
intron_variant | MODIFIER | c.98+2377C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150554802 | |||||||
| chr3:150554938 | CT | C | 83 | a0001c0001t0003g0104 a0002c0002t0001g0002 a0002c0002t0001g0006 others(80): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.98+2523delT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150554938 | ||||||
| chr3:150555477 | C | T | 1 | a0001c0001t0003g0054 | 2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.99-2911C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150555477 | |||||||
| chr3:150555613 | G | T | 1 | a0001c0001t0002g0152 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.99-2775G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150555613 | |||||||
| chr3:150555616 | C | T | 29 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(26): Show |
41 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.99-2772C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150555616 | |||||||
| chr3:150555851 | A | C | 7 | a0001c0001t0005g0013 a0001c0001t0005g0120 a0001c0001t0005g0121 others(4): Show |
15 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2537A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150555851 | |||||||
| chr3:150556621 | T | TAAAC | 191 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(188): Show |
327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.99-1764_99-1763ins others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150556621 | ||||||
| chr3:150556702 | G | A | 25 | a0001c0003t0004g0008 a0001c0003t0004g0026 a0001c0003t0004g0059 others(22): Show |
33 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-1686G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150556702 | |||||||
| chr3:150556762 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.99-1626C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150556762 | |||||||
| chr3:150556816 | T | G | 11 | a0002c0002t0001g0029 a0002c0002t0001g0070 a0002c0002t0001g0071 others(8): Show |
12 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.99-1572T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150556816 | |||||||
| chr3:150556828 | C | T | 1 | a0002c0002t0001g0084 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.99-1560C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150556828 | |||||||
| chr3:150556993 | A | G | 1 | a0001c0001t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.99-1395A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150556993 | |||||||
| chr3:150557010 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.99-1378A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557010 | |||||||
| chr3:150557035 | A | G | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.99-1353A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557035 | |||||||
| chr3:150557437 | C | T | 16 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0025 others(13): Show |
26 | HG00423.hp2 HG00673.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.99-951C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557437 | |||||||
| chr3:150557498 | T | TGAAGCAA others(12): Show |
1 | a0001c0001t0003g0192 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.99-889_99-871dupGA others(17): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150557498 | ||||||
| chr3:150557552 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99-836A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557552 | |||||||
| chr3:150557607 | C | G | 2 | a0001c0003t0004g0162 a0001c0003t0004g0163 |
2 | HG00323.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.99-781C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557607 | |||||||
| chr3:150557685 | C | T | 1 | a0002c0002t0010g0069 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.99-703C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557685 | |||||||
| chr3:150557709 | TA | T | 3 | a0002c0002t0010g0069 a0002c0002t0010g0075 a0002c0002t0010g0103 |
3 | HG00323.hp2 HG01070.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.99-674delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150557709 | ||||||
| chr3:150557732 | A | G | 2 | a0001c0001t0012g0064 a0001c0001t0012g0065 |
2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.99-656A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557732 | |||||||
| chr3:150557959 | T | G | 1 | a0001c0001t0005g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-429T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150557959 | |||||||
| chr3:150558008 | A | G | 83 | a0001c0001t0003g0104 a0002c0002t0001g0002 a0002c0002t0001g0006 others(80): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.99-380A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150558008 | |||||||
| chr3:150558345 | T | TTAA | 3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0004c0006t0002g0068 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99-41_99-39dupAAT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150558345 | ||||||
| chr3:150558364 | A | AT | 25 | a0001c0003t0004g0008 a0001c0003t0004g0059 a0001c0003t0004g0158 others(22): Show |
36 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.99-24_99-23insT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150558364 | |||||||
| chr3:150558365 | C | T | 3 | a0001c0003t0004g0026 a0001c0003t0004g0165 a0001c0003t0016g0164 |
5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-23C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150558365 | |||||||
| chr3:150558366 | C | CT | 22 | a0001c0001t0002g0041 a0001c0001t0002g0063 a0001c0001t0002g0067 others(19): Show |
35 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.99-12dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 150558366 | ||||||
| chr3:150558366 | C | T | 25 | a0001c0003t0004g0008 a0001c0003t0004g0059 a0001c0003t0004g0158 others(22): Show |
36 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.99-22C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 2/13 | chr3 | 150558366 | |||||||
| chr3:150558487 | T | C | 4 | a0001c0001t0003g0047 a0001c0001t0003g0188 a0001c0001t0003g0193 others(1): Show |
4 | HG00438.hp2 HG02027.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+25T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558487 | |||||||
| chr3:150558604 | A | G | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.173+142A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558604 | |||||||
| chr3:150558679 | T | A | 1 | a0001c0001t0015g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.173+217T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558679 | |||||||
| chr3:150558767 | C | T | 4 | a0001c0001t0002g0025 a0001c0001t0002g0148 a0001c0001t0002g0149 others(1): Show |
6 | HG02523.hp2 NA18953.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.173+305C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558767 | |||||||
| chr3:150558905 | A | G | 8 | a0001c0003t0004g0026 a0001c0003t0004g0165 a0001c0003t0004g0167 others(5): Show |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+443A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558905 | |||||||
| chr3:150558911 | C | T | 1 | a0003c0008t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.173+449C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150558911 | |||||||
| chr3:150559380 | TA | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+919delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559380 | |||||||
| chr3:150559479 | T | G | 1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.173+1017T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559479 | |||||||
| chr3:150559492 | C | G | 1 | a0001c0001t0002g0040 | 2 | NA18980.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.173+1030C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559492 | |||||||
| chr3:150559498 | C | CT | 103 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(100): Show |
178 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.173+1056dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150559498 | ||||||
| chr3:150559498 | C | CTT | 82 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0061 others(79): Show |
136 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.173+1055_173+1056d others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150559498 | ||||||
| chr3:150559525 | G | A | 3 | a0001c0003t0004g0026 a0001c0003t0004g0165 a0001c0003t0016g0164 |
5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.173+1063G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559525 | |||||||
| chr3:150559552 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.173+1090G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559552 | |||||||
| chr3:150559731 | T | C | 2 | a0001c0001t0002g0148 a0001c0001t0002g0149 |
2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.173+1269T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559731 | |||||||
| chr3:150559757 | A | C | 1 | a0001c0003t0004g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.173+1295A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150559757 | |||||||
| chr3:150560014 | G | C | 1 | a0002c0002t0010g0103 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.173+1552G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560014 | |||||||
| chr3:150560027 | TC | T | 1 | a0002c0002t0001g0012 | 4 | NA18946.hp2 NA18975.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+1566delC | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560027 | |||||||
| chr3:150560160 | C | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0046 |
4 | NA18986.hp1 NA18997.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+1698C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560160 | |||||||
| chr3:150560240 | GT | G | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+1780delT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150560240 | ||||||
| chr3:150560316 | T | G | 55 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(52): Show |
105 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.173+1854T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560316 | |||||||
| chr3:150560439 | T | C | 1 | a0002c0002t0001g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.173+1977T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560439 | |||||||
| chr3:150560716 | C | CT | 15 | a0001c0001t0002g0023 a0001c0001t0002g0140 a0001c0001t0002g0142 others(12): Show |
23 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.174-1806dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150560716 | ||||||
| chr3:150560716 | CT | C | 118 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(115): Show |
198 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.174-1806delT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150560716 | ||||||
| chr3:150560837 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.174-1705C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560837 | |||||||
| chr3:150560891 | T | G | 2 | a0001c0001t0003g0054 a0001c0001t0003g0211 |
3 | HG02615.hp2 HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.174-1651T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150560891 | |||||||
| chr3:150561000 | G | T | 3 | a0001c0003t0007g0011 a0001c0003t0007g0043 a0001c0003t0007g0172 |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.174-1542G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561000 | |||||||
| chr3:150561026 | A | G | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0173 |
3 | HG01099.hp1 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.174-1516A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561026 | |||||||
| chr3:150561104 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.174-1438C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561104 | |||||||
| chr3:150561109 | A | G | 1 | a0004c0006t0002g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.174-1433A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561109 | |||||||
| chr3:150561134 | T | A | 187 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(184): Show |
320 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.174-1408T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561134 | |||||||
| chr3:150561135 | T | A | 3 | a0001c0001t0002g0142 a0001c0001t0012g0064 a0001c0003t0004g0176 |
3 | HG01070.hp1 HG02145.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.174-1407T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561135 | |||||||
| chr3:150561172 | C | T | 2 | a0002c0002t0008g0017 a0002c0002t0008g0087 |
4 | HG00741.hp2 HG02683.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-1370C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561172 | |||||||
| chr3:150561173 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.174-1369G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561173 | |||||||
| chr3:150561191 | TG | T | 2 | a0001c0003t0004g0175 a0001c0003t0011g0045 |
3 | NA18951.hp1 NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.174-1348delG | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150561191 | ||||||
| chr3:150561438 | C | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0004c0006t0002g0068 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.174-1104C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561438 | |||||||
| chr3:150561501 | C | T | 5 | a0001c0001t0002g0022 a0001c0001t0002g0039 a0001c0001t0002g0044 others(2): Show |
9 | HG01106.hp2 HG01361.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.174-1041C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561501 | |||||||
| chr3:150561592 | A | G | 1 | a0002c0002t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.174-950A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561592 | |||||||
| chr3:150561795 | A | AT | 80 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(77): Show |
137 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.174-734dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150561795 | ||||||
| chr3:150561919 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0061 |
4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-623C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561919 | |||||||
| chr3:150561920 | G | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(79): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.174-622G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150561920 | |||||||
| chr3:150562219 | A | G | 5 | a0001c0001t0002g0137 a0001c0003t0002g0010 a0001c0003t0002g0155 others(2): Show |
9 | HG01433.hp2 HG01496.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.174-323A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562219 | |||||||
| chr3:150562230 | G | C | 229 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(226): Show |
380 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(377): Show |
intron_variant | MODIFIER | c.174-312G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562230 | |||||||
| chr3:150562257 | C | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.174-285C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562257 | |||||||
| chr3:150562278 | C | T | 20 | a0001c0003t0004g0008 a0001c0003t0004g0059 a0001c0003t0004g0158 others(17): Show |
31 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.174-264C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562278 | |||||||
| chr3:150562281 | G | C | 1 | a0001c0001t0005g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.174-261G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562281 | |||||||
| chr3:150562295 | A | G | 58 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(55): Show |
100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.174-247A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562295 | |||||||
| chr3:150562296 | C | G | 2 | a0001c0001t0003g0052 a0001c0001t0003g0205 |
3 | HG01255.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174-246C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562296 | |||||||
| chr3:150562296 | C | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.174-246C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562296 | |||||||
| chr3:150562345 | C | T | 5 | a0002c0002t0001g0217 a0002c0002t0001g0225 a0002c0002t0001g0228 others(2): Show |
5 | NA18969.hp2 NA18993.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-197C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562345 | |||||||
| chr3:150562419 | CA | C | 81 | a0001c0001t0002g0147 a0002c0002t0001g0002 a0002c0002t0001g0006 others(78): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.174-110delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 150562419 | ||||||
| chr3:150562466 | A | T | 82 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(79): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.174-76A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562466 | |||||||
| chr3:150562516 | G | A | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-26G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 3/13 | chr3 | 150562516 | |||||||
| chr3:150562719 | GA | G | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.292+64delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 150562719 | ||||||
| chr3:150562845 | A | C | 2 | a0001c0003t0004g0176 a0001c0003t0004g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.292+185A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/13 | chr3 | 150562845 | |||||||
| chr3:150562968 | A | C | 1 | a0001c0001t0005g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.292+308A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/13 | chr3 | 150562968 | |||||||
| chr3:150563135 | C | T | 2 | a0002c0002t0001g0082 a0002c0002t0001g0083 |
2 | HG00621.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.293-380C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/13 | chr3 | 150563135 | |||||||
| chr3:150563419 | T | A | 1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.293-96T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 4/13 | chr3 | 150563419 | |||||||
| chr3:150564050 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393-249C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 5/13 | chr3 | 150564050 | |||||||
| chr3:150564120 | T | C | 17 | a0001c0001t0003g0003 a0001c0001t0003g0047 a0001c0001t0003g0048 others(14): Show |
31 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.393-179T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 5/13 | chr3 | 150564120 | |||||||
| chr3:150564209 | A | G | 1 | a0002c0002t0001g0019 | 3 | HG00280.hp1 HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.393-90A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 5/13 | chr3 | 150564209 | |||||||
| chr3:150564424 | C | G | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.475+43C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564424 | |||||||
| chr3:150564551 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.475+170G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564551 | |||||||
| chr3:150564575 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.475+194A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564575 | |||||||
| chr3:150564669 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0127 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.475+288G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564669 | |||||||
| chr3:150564855 | T | C | 1 | a0002c0002t0001g0079 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.475+474T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564855 | |||||||
| chr3:150564860 | G | A | 2 | a0001c0003t0004g0176 a0001c0003t0004g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.475+479G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564860 | |||||||
| chr3:150564955 | C | T | 1 | a0001c0001t0003g0051 | 2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.475+574C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150564955 | |||||||
| chr3:150565163 | T | A | 1 | a0001c0001t0006g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.475+782T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565163 | |||||||
| chr3:150565167 | C | T | 3 | a0001c0003t0007g0011 a0001c0003t0007g0043 a0001c0003t0007g0172 |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.475+786C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565167 | |||||||
| chr3:150565186 | G | T | 1 | a0001c0001t0002g0152 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.475+805G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565186 | |||||||
| chr3:150565245 | A | G | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+864A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565245 | |||||||
| chr3:150565263 | C | A | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.475+882C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565263 | |||||||
| chr3:150565288 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.475+907A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565288 | |||||||
| chr3:150565396 | C | G | 1 | a0001c0003t0018g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.475+1015C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565396 | |||||||
| chr3:150565775 | T | C | 60 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(57): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.475+1394T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565775 | |||||||
| chr3:150565788 | C | CT | 86 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0142 others(83): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.475+1431dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 150565788 | ||||||
| chr3:150565788 | C | CTT | 19 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0005g0116 others(16): Show |
26 | HG00408.hp2 HG00735.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.475+1430_475+1431d others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 150565788 | ||||||
| chr3:150565818 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.475+1437G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565818 | |||||||
| chr3:150565846 | A | G | 3 | a0001c0001t0009g0201 a0001c0001t0009g0202 a0001c0001t0009g0203 |
3 | HG02647.hp2 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475+1465A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565846 | |||||||
| chr3:150565864 | C | T | 1 | a0001c0001t0015g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.475+1483C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565864 | |||||||
| chr3:150565872 | C | G | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.475+1491C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565872 | |||||||
| chr3:150565902 | TCTCCTGC others(20): Show |
T | 1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.475+1522_475+1548d others(29): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565902 | |||||||
| chr3:150565976 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.475+1595G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150565976 | |||||||
| chr3:150566022 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.475+1641C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566022 | |||||||
| chr3:150566025 | C | A | 90 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(87): Show |
151 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.475+1644C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566025 | |||||||
| chr3:150566052 | C | G | 1 | a0001c0001t0003g0192 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.476-1641C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566052 | |||||||
| chr3:150566309 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.476-1384C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566309 | |||||||
| chr3:150566540 | T | G | 2 | a0001c0001t0003g0197 a0001c0001t0003g0204 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.476-1153T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566540 | |||||||
| chr3:150566642 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.476-1051C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566642 | |||||||
| chr3:150566771 | CACTGTT | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(52): Show |
105 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.476-917_476-912del others(6): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr3 | 150566771 | ||||||
| chr3:150566893 | A | C | 1 | a0002c0002t0001g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.476-800A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566893 | |||||||
| chr3:150566979 | C | T | 1 | a0001c0001t0002g0038 | 2 | NA18944.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.476-714C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150566979 | |||||||
| chr3:150567135 | C | T | 4 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02300.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-558C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150567135 | |||||||
| chr3:150567137 | CTT | C | 1 | a0001c0003t0007g0011 | 5 | HG01884.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-555_476-554del others(2): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 6/13 | chr3 | 150567137 | |||||||
| chr3:150567774 | C | G | 2 | a0002c0002t0001g0032 a0002c0002t0001g0093 |
3 | NA18972.hp2 NA18979.hp2 NA18994.hp2 |
splice_region_variant&intron_variant | LOW | c.549+8C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 7/13 | chr3 | 150567774 | |||||||
| chr3:150567877 | A | G | 28 | a0001c0003t0004g0008 a0001c0003t0004g0026 a0001c0003t0004g0059 others(25): Show |
41 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.550-25A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 7/13 | chr3 | 150567877 | |||||||
| chr3:150568085 | G | T | 4 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(1): Show |
4 | NA18951.hp2 NA18952.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+39G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 8/13 | chr3 | 150568085 | |||||||
| chr3:150568301 | T | A | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.811+9T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150568301 | |||||||
| chr3:150568423 | A | T | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.811+131A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150568423 | |||||||
| chr3:150568751 | A | G | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.811+459A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150568751 | |||||||
| chr3:150568883 | C | T | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.811+591C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150568883 | |||||||
| chr3:150569072 | T | A | 1 | a0001c0001t0003g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.811+780T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569072 | |||||||
| chr3:150569098 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.811+806G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569098 | |||||||
| chr3:150569113 | C | G | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.811+821C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569113 | |||||||
| chr3:150569275 | A | G | 2 | a0001c0003t0004g0026 a0001c0003t0004g0165 |
4 | HG02896.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+983A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569275 | |||||||
| chr3:150569279 | A | G | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.811+987A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569279 | |||||||
| chr3:150569299 | A | G | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.811+1007A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569299 | |||||||
| chr3:150569333 | A | G | 1 | a0001c0003t0007g0043 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.811+1041A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569333 | |||||||
| chr3:150569394 | C | G | 1 | a0001c0003t0004g0161 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.811+1102C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569394 | |||||||
| chr3:150569420 | A | AT | 74 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(71): Show |
124 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.811+1140dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 150569420 | ||||||
| chr3:150569420 | A | ATT | 16 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0056 others(13): Show |
29 | HG00597.hp2 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.811+1139_811+1140d others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 150569420 | ||||||
| chr3:150569420 | AT | A | 58 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(55): Show |
112 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.811+1140delT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 150569420 | ||||||
| chr3:150569653 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.811+1361A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569653 | |||||||
| chr3:150569669 | G | T | 28 | a0001c0003t0004g0008 a0001c0003t0004g0026 a0001c0003t0004g0059 others(25): Show |
41 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.811+1377G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569669 | |||||||
| chr3:150569708 | G | A | 2 | a0001c0003t0004g0176 a0001c0003t0004g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.811+1416G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569708 | |||||||
| chr3:150569720 | C | T | 3 | a0002c0002t0001g0031 a0002c0002t0001g0097 a0002c0002t0001g0101 |
4 | NA18953.hp1 NA18974.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+1428C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569720 | |||||||
| chr3:150569759 | G | A | 2 | a0002c0002t0001g0218 a0002c0002t0001g0227 |
2 | HG00597.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.811+1467G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569759 | |||||||
| chr3:150569778 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.811+1486G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569778 | |||||||
| chr3:150569797 | G | A | 2 | a0002c0002t0008g0017 a0002c0002t0008g0087 |
4 | HG00741.hp2 HG02683.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+1505G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150569797 | |||||||
| chr3:150570216 | A | G | 1 | a0001c0001t0009g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.812-1742A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570216 | |||||||
| chr3:150570232 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0136 |
4 | NA18948.hp2 NA18969.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.812-1726A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570232 | |||||||
| chr3:150570314 | A | T | 1 | a0001c0001t0002g0136 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.812-1644A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570314 | |||||||
| chr3:150570522 | T | C | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.812-1436T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570522 | |||||||
| chr3:150570584 | G | A | 54 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(51): Show |
104 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.812-1374G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570584 | |||||||
| chr3:150570672 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.812-1286A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570672 | |||||||
| chr3:150570702 | A | G | 60 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0012 others(57): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.812-1256A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570702 | |||||||
| chr3:150570754 | C | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(53): Show |
106 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.812-1204C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570754 | |||||||
| chr3:150570864 | C | CA | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.812-1090dupA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 150570864 | ||||||
| chr3:150570893 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.812-1065C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150570893 | |||||||
| chr3:150571015 | G | A | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.812-943G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571015 | |||||||
| chr3:150571181 | C | T | 91 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0005g0124 others(88): Show |
152 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.812-777C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571181 | |||||||
| chr3:150571213 | C | T | 1 | a0001c0001t0015g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.812-745C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571213 | |||||||
| chr3:150571402 | A | T | 1 | a0001c0001t0002g0024 | 3 | HG02015.hp1 HG02027.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.812-556A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571402 | |||||||
| chr3:150571430 | G | A | 2 | a0001c0001t0012g0064 a0001c0001t0012g0065 |
2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.812-528G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571430 | |||||||
| chr3:150571489 | C | G | 1 | a0002c0002t0001g0095 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.812-469C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571489 | |||||||
| chr3:150571586 | C | CACAAAGT others(70): Show |
1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.812-371_812-295dup others(77): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 150571586 | ||||||
| chr3:150571701 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.812-257T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571701 | |||||||
| chr3:150571762 | A | G | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.812-196A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571762 | |||||||
| chr3:150571822 | G | T | 1 | a0001c0001t0003g0213 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.812-136G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571822 | |||||||
| chr3:150571944 | T | C | 1 | a0002c0002t0001g0094 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.812-14T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 9/13 | chr3 | 150571944 | |||||||
| chr3:150572588 | TTCACATC others(4): Show |
T | 1 | a0001c0003t0004g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1383+60_1383+70del others(11): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572588 | |||||||
| chr3:150572601 | T | A | 1 | a0001c0003t0004g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1383+72T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572601 | |||||||
| chr3:150572626 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0136 a0001c0001t0003g0196 |
5 | HG01978.hp1 NA18948.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+97G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572626 | |||||||
| chr3:150572725 | G | A | 2 | a0001c0003t0004g0176 a0001c0003t0004g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1383+196G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572725 | |||||||
| chr3:150572781 | G | A | 2 | a0001c0001t0003g0054 a0001c0001t0003g0211 |
3 | HG02615.hp2 HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1383+252G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572781 | |||||||
| chr3:150572800 | G | A | 1 | a0001c0003t0004g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1383+271G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572800 | |||||||
| chr3:150572855 | C | CA | 84 | a0001c0001t0002g0020 a0001c0001t0002g0063 a0001c0001t0002g0119 others(81): Show |
145 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1383+343dupA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 150572855 | ||||||
| chr3:150572855 | C | CAA | 20 | a0001c0001t0002g0067 a0001c0001t0006g0185 a0001c0001t0015g0066 others(17): Show |
25 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1383+342_1383+343d others(4): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 150572855 | ||||||
| chr3:150572855 | CA | C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0120 a0001c0001t0005g0121 others(2): Show |
8 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1383+343delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 150572855 | ||||||
| chr3:150572932 | C | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(52): Show |
105 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.1383+403C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150572932 | |||||||
| chr3:150573013 | A | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0133 |
4 | NA18939.hp1 NA18975.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+484A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573013 | |||||||
| chr3:150573088 | A | C | 2 | a0001c0001t0003g0052 a0001c0001t0003g0205 |
3 | HG01255.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1383+559A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573088 | |||||||
| chr3:150573290 | T | A | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1383+761T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573290 | |||||||
| chr3:150573313 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+784C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573313 | |||||||
| chr3:150573788 | A | G | 1 | a0002c0002t0001g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1383+1259A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573788 | |||||||
| chr3:150573818 | G | A | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1383+1289G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573818 | |||||||
| chr3:150573836 | T | C | 2 | a0002c0002t0001g0028 a0002c0002t0001g0076 |
3 | HG01952.hp1 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1383+1307T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573836 | |||||||
| chr3:150573946 | C | T | 2 | a0002c0002t0001g0097 a0002c0002t0001g0101 |
2 | NA18953.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1383+1417C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150573946 | |||||||
| chr3:150574230 | T | C | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1384-1419T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574230 | |||||||
| chr3:150574410 | A | G | 1 | a0002c0002t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1384-1239A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574410 | |||||||
| chr3:150574432 | C | T | 4 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02300.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-1217C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574432 | |||||||
| chr3:150574562 | A | G | 1 | a0002c0002t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1384-1087A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574562 | |||||||
| chr3:150574706 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1384-943G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574706 | |||||||
| chr3:150574862 | C | T | 1 | a0001c0001t0015g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1384-787C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574862 | |||||||
| chr3:150574979 | T | C | 81 | a0001c0001t0002g0144 a0002c0002t0001g0002 a0002c0002t0001g0006 others(78): Show |
136 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1384-670T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574979 | |||||||
| chr3:150574984 | T | C | 188 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(185): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.1384-665T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574984 | |||||||
| chr3:150574985 | C | G | 2 | a0001c0003t0004g0167 a0001c0003t0004g0169 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1384-664C>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150574985 | |||||||
| chr3:150575248 | G | C | 1 | a0001c0001t0005g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1384-401G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150575248 | |||||||
| chr3:150575255 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1384-394A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150575255 | |||||||
| chr3:150575567 | A | G | 1 | a0002c0002t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1384-82A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150575567 | |||||||
| chr3:150575617 | T | C | 3 | a0001c0003t0004g0026 a0001c0003t0004g0165 a0001c0003t0016g0164 |
5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384-32T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 10/13 | chr3 | 150575617 | |||||||
| chr3:150575800 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1497+38C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150575800 | |||||||
| chr3:150576200 | G | A | 3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0004c0006t0002g0068 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1497+438G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576200 | |||||||
| chr3:150576267 | C | A | 3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0004c0006t0002g0068 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1497+505C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576267 | |||||||
| chr3:150576296 | C | T | 3 | a0002c0002t0001g0034 a0002c0002t0001g0074 a0002c0002t0001g0106 |
4 | HG02523.hp1 NA18967.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+534C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576296 | |||||||
| chr3:150576303 | G | A | 1 | a0001c0003t0004g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1497+541G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576303 | |||||||
| chr3:150576439 | A | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+677A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576439 | |||||||
| chr3:150576444 | A | G | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+682A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576444 | |||||||
| chr3:150576608 | A | G | 1 | a0001c0003t0004g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1497+846A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576608 | |||||||
| chr3:150576649 | G | C | 1 | a0002c0002t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1497+887G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576649 | |||||||
| chr3:150576684 | C | T | 4 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02300.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+922C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576684 | |||||||
| chr3:150576742 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1497+980G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576742 | |||||||
| chr3:150576778 | C | T | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+1016C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576778 | |||||||
| chr3:150576837 | C | T | 56 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(53): Show |
106 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1497+1075C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576837 | |||||||
| chr3:150576839 | T | G | 10 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(7): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1497+1077T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576839 | |||||||
| chr3:150576845 | C | T | 2 | a0001c0004t0003g0014 a0001c0004t0003g0186 |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+1083C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576845 | |||||||
| chr3:150576855 | A | C | 1 | a0001c0001t0003g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1497+1093A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150576855 | |||||||
| chr3:150577054 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1497+1292T>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577054 | |||||||
| chr3:150577068 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+1306C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577068 | |||||||
| chr3:150577069 | G | A | 1 | a0001c0001t0003g0050 | 2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1497+1307G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577069 | |||||||
| chr3:150577099 | G | A | 1 | a0001c0003t0016g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1497+1337G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577099 | |||||||
| chr3:150577135 | C | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1497+1373C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577135 | |||||||
| chr3:150577222 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1497+1460A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577222 | |||||||
| chr3:150577477 | A | G | 1 | a0001c0003t0004g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1497+1715A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577477 | |||||||
| chr3:150577589 | C | T | 187 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(184): Show |
321 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.1497+1827C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577589 | |||||||
| chr3:150577592 | G | T | 1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1497+1830G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577592 | |||||||
| chr3:150577980 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(61): Show |
117 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1497+2218A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150577980 | |||||||
| chr3:150578286 | AATT | A | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+2529_1497+253 others(7): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150578286 | ||||||
| chr3:150578317 | T | C | 2 | a0002c0002t0001g0027 a0002c0002t0001g0062 |
3 | HG01069.hp2 HG01074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1497+2555T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150578317 | |||||||
| chr3:150578503 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1497+2741T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150578503 | |||||||
| chr3:150578833 | T | A | 1 | a0002c0002t0001g0226 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1498-2785T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150578833 | |||||||
| chr3:150578916 | T | C | 1 | a0001c0003t0004g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1498-2702T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150578916 | |||||||
| chr3:150579020 | G | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(79): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1498-2598G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579020 | |||||||
| chr3:150579030 | C | T | 55 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(52): Show |
105 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.1498-2588C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579030 | |||||||
| chr3:150579069 | A | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0200 |
2 | HG01978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1498-2549A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579069 | |||||||
| chr3:150579108 | A | G | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1498-2510A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579108 | |||||||
| chr3:150579221 | T | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(79): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1498-2397T>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579221 | |||||||
| chr3:150579356 | T | C | 4 | a0001c0001t0003g0055 a0001c0001t0003g0191 a0001c0001t0003g0213 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-2262T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579356 | |||||||
| chr3:150579476 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1498-2142G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579476 | |||||||
| chr3:150579702 | C | CA | 7 | a0001c0001t0002g0129 a0001c0001t0002g0150 a0001c0001t0003g0052 others(4): Show |
8 | HG00323.hp1 HG01255.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-1901dupA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150579702 | ||||||
| chr3:150579702 | C | CAA | 28 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(25): Show |
45 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1498-1902_1498-190 others(6): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150579702 | ||||||
| chr3:150579702 | CA | C | 83 | a0001c0001t0002g0037 a0001c0001t0003g0195 a0001c0001t0009g0202 others(80): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1498-1901delA | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150579702 | ||||||
| chr3:150579739 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0060 a0001c0001t0002g0061 |
5 | HG02055.hp2 HG02257.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-1879T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579739 | |||||||
| chr3:150579833 | A | C | 3 | a0002c0002t0001g0018 a0002c0002t0001g0100 a0005c0007t0001g0085 |
5 | NA18950.hp2 NA18971.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-1785A>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579833 | |||||||
| chr3:150579890 | T | TTA | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-1718_1498-171 others(6): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150579890 | ||||||
| chr3:150579936 | C | T | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1498-1682C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579936 | |||||||
| chr3:150579972 | C | T | 1 | a0001c0003t0004g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1498-1646C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150579972 | |||||||
| chr3:150579982 | AAT | A | 92 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(89): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1498-1629_1498-162 others(6): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150579982 | ||||||
| chr3:150580010 | A | G | 1 | a0001c0003t0007g0011 | 5 | HG01884.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-1608A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580010 | |||||||
| chr3:150580104 | G | A | 4 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
8 | HG01433.hp2 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-1514G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580104 | |||||||
| chr3:150580112 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1498-1506G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580112 | |||||||
| chr3:150580155 | G | A | 1 | a0001c0003t0004g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1498-1463G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580155 | |||||||
| chr3:150580479 | G | A | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1498-1139G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580479 | |||||||
| chr3:150580487 | C | T | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1498-1131C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580487 | |||||||
| chr3:150580497 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1498-1121A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580497 | |||||||
| chr3:150580530 | A | G | 124 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(121): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1498-1088A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580530 | |||||||
| chr3:150580746 | A | G | 55 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0016 others(52): Show |
105 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.1498-872A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150580746 | |||||||
| chr3:150581012 | CTGCTGTA others(21): Show |
C | 1 | a0005c0007t0001g0085 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1498-604_1498-577d others(30): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 150581012 | ||||||
| chr3:150581092 | C | A | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-526C>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150581092 | |||||||
| chr3:150581118 | A | T | 4 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02300.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498-500A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150581118 | |||||||
| chr3:150581162 | G | A | 28 | a0001c0003t0004g0008 a0001c0003t0004g0026 a0001c0003t0004g0059 others(25): Show |
41 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1498-456G>A | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 11/13 | chr3 | 150581162 | |||||||
| chr3:150581936 | G | C | 1 | a0001c0001t0005g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1626+190G>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150581936 | |||||||
| chr3:150582149 | C | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+403C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582149 | |||||||
| chr3:150582264 | A | G | 124 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0006g0005 others(121): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1626+518A>G | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582264 | |||||||
| chr3:150582306 | TTTTAA | T | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+574_1626+578d others(7): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 150582306 | ||||||
| chr3:150582321 | A | AT | 81 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(78): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1626+586dupT | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 150582321 | ||||||
| chr3:150582377 | C | T | 1 | a0002c0002t0001g0094 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1626+631C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582377 | |||||||
| chr3:150582378 | G | T | 32 | a0001c0003t0002g0010 a0001c0003t0002g0155 a0001c0003t0002g0156 others(29): Show |
49 | HG00323.hp1 HG00735.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1626+632G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582378 | |||||||
| chr3:150582398 | T | C | 1 | a0002c0002t0001g0082 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1626+652T>C | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582398 | |||||||
| chr3:150582403 | C | T | 1 | a0002c0002t0001g0057 | 2 | HG00642.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1626+657C>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582403 | |||||||
| chr3:150582807 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1627-393G>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582807 | |||||||
| chr3:150582971 | A | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0115 a0001c0001t0005g0116 others(5): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1627-229A>T | EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 12/13 | chr3 | 150582971 | |||||||
| chr3:150583685 | ATACCAGA others(14): Show |
A | 4 | a0001c0001t0006g0005 a0001c0001t0006g0183 a0001c0001t0006g0184 others(1): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693-159_1693-139d others(23): Show |
EIF2A | ENSG00000144895.12 | transcript | ENST00000460851.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 150583685 |