Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1975 |
| ensemblid | ENSG00000063046.18 |
| hgncid | 3285 |
| symbol | EIF4B |
| name | eukaryotic translation initiation factor 4B |
| refseq_nuc | NM_001417.7 |
| refseq_prot | NP_001408.2 |
| ensembl_nuc | ENST00000262056.14 |
| ensembl_prot | ENSP00000262056.9 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53006456 |
| end | 53042215 |
| strand | + |
| ver | v1.2 |
| region | chr12:53006456-53042215 |
| region5000 | chr12:53001456-53047215 |
| regionname0 | EIF4B_chr12_53006456_53042215 |
| regionname5000 | EIF4B_chr12_53001456_53047215 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 611 | 365 | 95 | 65 | 153 | 10 | 40 | 119 | EIF4B_chr12_53001456_53047215 | EIF4B | MAASA others(606): Show |
chr12 | 53001456 | 53047215 |
| a0002 | 0/0 | 611 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | MAASA others(606): Show |
chr12 | 53001456 | 53047215 |
| a0003 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | MAASA others(606): Show |
chr12 | 53001456 | 53047215 |
| a0004 | 0/0 | 601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | MAASA others(596): Show |
chr12 | 53001456 | 53047215 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1833 | 258 | 40 | 60 | 110 | 10 | 37 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0001c0002 | 0/0 | 1833 | 91 | 43 | 5 | 41 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0001c0003 | 1/0 | 1833 | 8 | 7 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0001c0005 | 0/0 | 1833 | 5 | 5 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0001c0006 | 0/0 | 1833 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0001c0007 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0002c0004 | 0/0 | 1833 | 5 | 0 | 5 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0003c0009 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1828): Show |
chr12 | 53001456 | 53047215 | ||
| a0004c0008 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | ATGGC others(1798): Show |
chr12 | 53001456 | 53047215 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3859 | 133 | 4 | 41 | 56 | 7 | 24 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0002 | 0/0 | 3860 | 100 | 28 | 16 | 47 | 1 | 8 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0006 | 0/0 | 3862 | 7 | 2 | 1 | 0 | 1 | 3 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3857): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0008 | 0/0 | 3860 | 5 | 0 | 0 | 4 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0010 | 0/0 | 3856 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0014 | 0/0 | 3859 | 2 | 0 | 1 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0016 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0017 | 0/0 | 3859 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0021 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0022 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0023 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0024 | 0/0 | 3860 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0027 | 0/0 | 3860 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0028 | 0/0 | 3860 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0001t0029 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0003 | 0/0 | 3859 | 34 | 1 | 1 | 32 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0004 | 0/0 | 3859 | 27 | 18 | 3 | 4 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0005 | 0/0 | 3856 | 9 | 8 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0007 | 0/0 | 3856 | 6 | 6 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0009 | 0/0 | 3856 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTCT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0011 | 0/0 | 3859 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0012 | 0/0 | 3859 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0015 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0018 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0019 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0020 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0025 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0002t0026 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3855): Show |
chr12 | 53001456 | 53047215 |
| a0001c0003t0005 | 1/0 | 3856 | 8 | 7 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0005t0005 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0005t0013 | 0/0 | 3856 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0001c0006t0001 | 0/0 | 3859 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0001c0007t0001 | 0/0 | 3859 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0002c0004t0001 | 0/0 | 3859 | 4 | 0 | 4 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0002c0004t0010 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3851): Show |
chr12 | 53001456 | 53047215 |
| a0003c0009t0015 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3854): Show |
chr12 | 53001456 | 53047215 |
| a0004c0008t0001 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | CTTTT others(3824): Show |
chr12 | 53001456 | 53047215 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0016g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0017g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0021g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0023g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0027g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0028g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0029g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0015g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0018g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0020g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0025g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0026g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0316 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0010g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0003c0009t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0004c0008t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00423 | hp1 | a0001 | c0002 | t0012 | g0289 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0309 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00438 | hp1 | a0001 | c0006 | t0001 | g0156 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00544 | hp1 | a0001 | c0001 | t0029 | g0214 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01070 | hp1 | a0002 | c0004 | t0010 | g0052 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0314 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0012 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0008 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01169 | hp1 | a0001 | c0002 | t0004 | g0008 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0054 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0273 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0019 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0106 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01258 | hp2 | a0002 | c0004 | t0001 | g0108 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01884 | hp1 | a0001 | c0002 | t0009 | g0318 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01891 | hp1 | a0001 | c0002 | t0011 | g0351 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0331 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0307 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0317 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0329 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02148 | hp1 | a0001 | c0001 | t0017 | g0075 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0283 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0327 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0120 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02451 | hp1 | a0001 | c0002 | t0018 | g0291 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0162 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0312 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02572 | hp1 | a0001 | c0002 | t0011 | g0353 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0274 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0322 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0320 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0204 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0276 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0279 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0203 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0326 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0334 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0285 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0275 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0030 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0336 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0298 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0293 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0296 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0278 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0294 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02970 | hp2 | a0001 | c0005 | t0005 | g0013 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0297 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0270 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0042 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0299 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0184 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03195 | hp1 | a0001 | c0002 | t0019 | g0277 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03209 | hp2 | a0001 | c0002 | t0020 | g0339 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03225 | hp1 | a0001 | c0002 | t0009 | g0338 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0324 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0014 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0328 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03486 | hp2 | a0001 | c0002 | t0011 | g0352 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03516 | hp1 | a0003 | c0009 | t0015 | g0301 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03540 | hp1 | a0001 | c0003 | t0005 | g0325 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0337 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0321 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0246 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03688 | hp2 | a0001 | c0007 | t0001 | g0104 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0245 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0286 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0288 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04204 | hp2 | a0001 | c0001 | t0028 | g0179 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18522 | hp1 | a0001 | c0005 | t0005 | g0013 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0014 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0282 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0342 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18952 | hp1 | a0001 | c0006 | t0001 | g0128 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18954 | hp1 | a0001 | c0002 | t0026 | g0340 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0153 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0349 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18969 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0304 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18990 | hp2 | a0001 | c0002 | t0012 | g0284 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0305 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19000 | hp1 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19000 | hp2 | a0004 | c0008 | t0001 | g0155 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19001 | hp2 | a0001 | c0002 | t0025 | g0347 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0310 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0263 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19030 | hp2 | a0001 | c0005 | t0013 | g0271 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0292 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0332 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0346 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19091 | hp1 | a0001 | c0002 | t0012 | g0272 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19240 | hp2 | a0001 | c0002 | t0015 | g0280 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20129 | hp1 | a0001 | c0005 | t0013 | g0311 | AFR | ASW | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ASW | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0073 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0037 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0185 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0323 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0290 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0295 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0302 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG06807 | hp1 | a0001 | c0005 | t0013 | g0333 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0330 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0095 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA21309 | hp2 | a0001 | c0002 | t0007 | g0335 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0005 | g0316 | REF | REF | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53037514 | T | A | 1 | a0002 | 5 | HG01070.hp1 HG01192.hp2 HG01257.hp1 others(2): Show |
missense_variant | MODERATE | c.1412T>A | p.Leu471Gln | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/15 | 1440/3856 | 1412/1836 | 471/611 | chr12 | 53037514 | |||
| chr12:53039625 | TGCAGGAA others(27): Show |
T | 1 | a0004 | 1 | NA19000.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1683-4_1712delGCAG others(30): Show |
p.Lys562_Arg571del | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/15 | 1683/1836 | 561/611 | chr12 | 53039625 | ||||
| chr12:53040177 | C | T | 1 | a0003 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1790C>T | p.Ser597Phe | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1818/3856 | 1790/1836 | 597/611 | chr12 | 53040177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53028118 | C | T | 1 | a0001c0006 | 2 | HG00438.hp1 NA18952.hp1 |
synonymous_variant | LOW | c.909C>T | p.Asp303Asp | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/15 | 937/3856 | 909/1836 | 303/611 | chr12 | 53028118 | |||
| chr12:53033813 | C | G | 1 | a0001c0005 | 5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
synonymous_variant | LOW | c.987C>G | p.Pro329Pro | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/15 | 1015/3856 | 987/1836 | 329/611 | chr12 | 53033813 | |||
| chr12:53034032 | G | A | 1 | a0001c0007 | 1 | HG03688.hp2 | splice_region_variant&synonymous_variant | LOW | c.1206G>A | p.Glu402Glu | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/15 | 1234/3856 | 1206/1836 | 402/611 | chr12 | 53034032 | |||
| chr12:53039305 | C | A | 8 | a0001c0001 a0001c0002 a0001c0005 others(5): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
synonymous_variant | LOW | c.1644C>A | p.Gly548Gly | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/15 | 1672/3856 | 1644/1836 | 548/611 | chr12 | 53039305 | |||
| chr12:53039702 | C | T | 5 | a0001c0001 a0001c0006 a0001c0007 others(2): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
splice_region_variant&synonymous_variant | LOW | c.1755C>T | p.Ser585Ser | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/15 | 1783/3856 | 1755/1836 | 585/611 | chr12 | 53039702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53006459 | T | C | 1 | a0001c0002t0009 | 3 | HG01884.hp1 HG02145.hp1 HG03225.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/15 | chr12 | 53006459 | |||||||
| chr12:53040260 | C | T | 2 | a0001c0002t0015 a0003c0009t0015 |
2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*37C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 37 | chr12 | 53040260 | ||||||
| chr12:53040321 | C | A | 11 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(8): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*98C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 98 | chr12 | 53040321 | ||||||
| chr12:53040477 | G | A | 1 | a0001c0002t0011 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*254G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 254 | chr12 | 53040477 | ||||||
| chr12:53040543 | T | C | 1 | a0001c0002t0012 | 3 | HG00423.hp1 NA18990.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 320 | chr12 | 53040543 | ||||||
| chr12:53040788 | C | CT | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0024 others(5): Show |
111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*577dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 578 | INFO_REALIGN_3_PRIME | chr12 | 53040788 | |||||
| chr12:53040788 | C | CTTT | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(6): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*575_*577dupTTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 578 | INFO_REALIGN_3_PRIME | chr12 | 53040788 | |||||
| chr12:53040990 | G | A | 1 | a0001c0001t0008 | 5 | HG02683.hp1 NA18944.hp1 NA18978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*767G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 767 | chr12 | 53040990 | ||||||
| chr12:53041006 | C | T | 2 | a0001c0001t0017 a0001c0001t0029 |
2 | HG00544.hp1 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 783 | chr12 | 53041006 | ||||||
| chr12:53041127 | T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 904 | chr12 | 53041127 | ||||||
| chr12:53041128 | C | T | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 905 | chr12 | 53041128 | ||||||
| chr12:53041129 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(22): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 906 | chr12 | 53041129 | ||||||
| chr12:53041211 | C | G | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(17): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*988C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 988 | chr12 | 53041211 | ||||||
| chr12:53041240 | C | T | 1 | a0001c0005t0013 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1017 | chr12 | 53041240 | ||||||
| chr12:53041398 | T | G | 1 | a0001c0001t0027 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1175 | chr12 | 53041398 | ||||||
| chr12:53041458 | A | G | 1 | a0001c0001t0014 | 2 | HG01256.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1235A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1235 | chr12 | 53041458 | ||||||
| chr12:53041500 | T | TTTG | 6 | a0001c0002t0004 a0001c0002t0012 a0001c0002t0015 others(3): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1286_*1288dupGTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1289 | INFO_REALIGN_3_PRIME | chr12 | 53041500 | |||||
| chr12:53041509 | G | GTTT | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(21): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1291_*1293dupTTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1294 | INFO_REALIGN_3_PRIME | chr12 | 53041509 | |||||
| chr12:53041509 | G | T | 1 | a0001c0002t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1286 | chr12 | 53041509 | ||||||
| chr12:53041575 | T | C | 1 | a0001c0002t0011 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1352 | chr12 | 53041575 | ||||||
| chr12:53041838 | TAAG | T | 10 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(7): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1619_*1621delAAG | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1619 | INFO_REALIGN_3_PRIME | chr12 | 53041838 | |||||
| chr12:53041915 | G | A | 1 | a0001c0001t0021 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1692 | chr12 | 53041915 | ||||||
| chr12:53041952 | A | G | 1 | a0001c0002t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1729 | chr12 | 53041952 | ||||||
| chr12:53041967 | C | G | 1 | a0001c0001t0028 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1744 | chr12 | 53041967 | ||||||
| chr12:53041978 | T | C | 2 | a0001c0002t0003 a0001c0002t0025 |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1755T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1755 | chr12 | 53041978 | ||||||
| chr12:53041997 | C | G | 2 | a0001c0001t0021 a0001c0001t0023 |
2 | HG02451.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1774C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1774 | chr12 | 53041997 | ||||||
| chr12:53042017 | C | G | 1 | a0001c0002t0018 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1794 | chr12 | 53042017 | ||||||
| chr12:53042112 | T | C | 2 | a0001c0002t0007 a0001c0002t0009 |
9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1889T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1889 | chr12 | 53042112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53006656 | T | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+160T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006656 | |||||||
| chr12:53006712 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.13+216C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006712 | |||||||
| chr12:53006785 | G | A | 1 | a0001c0002t0007g0270 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13+289G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006785 | |||||||
| chr12:53006913 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.13+417T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006913 | |||||||
| chr12:53006929 | G | C | 1 | a0001c0002t0003g0303 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.13+433G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006929 | |||||||
| chr12:53006929 | G | T | 1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.13+433G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006929 | |||||||
| chr12:53006944 | A | T | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.13+448A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006944 | |||||||
| chr12:53007062 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.13+566A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007062 | |||||||
| chr12:53007070 | G | C | 1 | a0001c0005t0013g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13+574G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007070 | |||||||
| chr12:53007122 | C | T | 13 | a0001c0002t0003g0001 a0001c0002t0003g0015 a0001c0002t0003g0341 others(10): Show |
18 | HG00544.hp2 NA18939.hp1 NA18950.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+626C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007122 | |||||||
| chr12:53007224 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.13+728T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007224 | |||||||
| chr12:53007233 | G | A | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.13+737G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007233 | |||||||
| chr12:53007278 | C | T | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.13+782C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007278 | |||||||
| chr12:53007310 | A | G | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.13+814A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007310 | |||||||
| chr12:53007364 | G | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+868G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007364 | |||||||
| chr12:53007420 | C | CT | 38 | a0001c0002t0003g0319 a0001c0002t0003g0348 a0001c0002t0003g0349 others(35): Show |
40 | HG00423.hp1 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.13+952dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | ||||||
| chr12:53007420 | C | CTT | 16 | a0001c0002t0004g0009 a0001c0002t0004g0297 a0001c0002t0004g0298 others(13): Show |
19 | HG02818.hp1 HG02895.hp1 HG02896.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+951_13+952dupTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | ||||||
| chr12:53007420 | CT | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.13+952delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | ||||||
| chr12:53007420 | CTT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG01070.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+951_13+952delTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | ||||||
| chr12:53007444 | T | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0014g0019 |
4 | HG01256.hp1 HG01258.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+948T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007444 | |||||||
| chr12:53007445 | T | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.13+949T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007445 | |||||||
| chr12:53007445 | T | TA | 5 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0266 others(2): Show |
5 | HG00558.hp1 HG02559.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+949_13+950insA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007445 | |||||||
| chr12:53007697 | G | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.13+1201G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007697 | |||||||
| chr12:53007896 | T | C | 11 | a0001c0002t0004g0273 a0001c0002t0004g0281 a0001c0002t0004g0282 others(8): Show |
11 | HG00423.hp1 HG01255.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+1400T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007896 | |||||||
| chr12:53007934 | G | C | 2 | a0001c0005t0013g0271 a0001c0005t0013g0333 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.13+1438G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007934 | |||||||
| chr12:53007995 | A | G | 1 | a0001c0002t0012g0289 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.13+1499A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007995 | |||||||
| chr12:53008083 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.13+1587A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008083 | |||||||
| chr12:53008310 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.13+1814A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008310 | |||||||
| chr12:53008379 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.13+1883C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008379 | |||||||
| chr12:53008711 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.13+2215G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008711 | |||||||
| chr12:53008986 | G | A | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.13+2490G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008986 | |||||||
| chr12:53009083 | A | G | 2 | a0001c0002t0015g0280 a0003c0009t0015g0301 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.13+2587A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009083 | |||||||
| chr12:53009149 | C | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.13+2653C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009149 | |||||||
| chr12:53009162 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+2666A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009162 | |||||||
| chr12:53009164 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+2668T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009164 | |||||||
| chr12:53009204 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.13+2708G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009204 | |||||||
| chr12:53009243 | G | A | 1 | a0001c0002t0004g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13+2747G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009243 | |||||||
| chr12:53009329 | G | T | 1 | a0001c0001t0002g0251 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.13+2833G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009329 | |||||||
| chr12:53009399 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.13+2903G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009399 | |||||||
| chr12:53009474 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.13+2978G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009474 | |||||||
| chr12:53009489 | C | T | 8 | a0001c0002t0007g0014 a0001c0002t0007g0270 a0001c0002t0007g0335 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+2993C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009489 | |||||||
| chr12:53009494 | C | CA | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.13+3010dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53009494 | ||||||
| chr12:53009494 | CAAAAAA | C | 30 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(27): Show |
32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.13+3005_13+3010del others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53009494 | ||||||
| chr12:53009507 | C | A | 1 | a0001c0001t0002g0164 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.13+3011C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009507 | |||||||
| chr12:53009586 | A | C | 2 | a0001c0002t0004g0296 a0001c0002t0004g0300 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.13+3090A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009586 | |||||||
| chr12:53009639 | G | A | 1 | a0001c0002t0004g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+3143G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009639 | |||||||
| chr12:53009740 | T | C | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.13+3244T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009740 | |||||||
| chr12:53009796 | T | C | 3 | a0001c0001t0021g0030 a0001c0001t0023g0162 a0001c0002t0004g0297 |
3 | HG02451.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.13+3300T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009796 | |||||||
| chr12:53009837 | A | T | 2 | a0001c0002t0004g0008 a0001c0002t0004g0295 |
3 | HG01167.hp1 HG01169.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.13+3341A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009837 | |||||||
| chr12:53009864 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+3368T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009864 | |||||||
| chr12:53009934 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+3438T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009934 | |||||||
| chr12:53010037 | T | C | 336 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(333): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.13+3541T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010037 | |||||||
| chr12:53010137 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.13+3641A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010137 | |||||||
| chr12:53010151 | T | C | 1 | a0001c0002t0018g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.13+3655T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010151 | |||||||
| chr12:53010392 | G | A | 2 | a0001c0002t0004g0281 a0001c0002t0004g0282 |
2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.13+3896G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010392 | |||||||
| chr12:53010399 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.13+3903C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010399 | |||||||
| chr12:53010454 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.13+3958A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010454 | |||||||
| chr12:53010564 | C | CTGTT | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+4070_13+4071ins others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53010564 | ||||||
| chr12:53010727 | A | G | 1 | a0001c0002t0004g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+4231A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010727 | |||||||
| chr12:53010754 | C | T | 1 | a0001c0002t0005g0012 | 2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.13+4258C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010754 | |||||||
| chr12:53010872 | C | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
79 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.13+4376C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010872 | |||||||
| chr12:53010916 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.13+4420T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010916 | |||||||
| chr12:53011289 | C | T | 1 | a0001c0002t0025g0347 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.13+4793C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011289 | |||||||
| chr12:53011467 | C | A | 4 | a0001c0002t0004g0283 a0001c0002t0012g0272 a0001c0002t0012g0284 others(1): Show |
4 | HG00423.hp1 HG02165.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+4971C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011467 | |||||||
| chr12:53011502 | T | C | 2 | a0001c0001t0002g0165 a0001c0001t0002g0268 |
2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.14-4971T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011502 | |||||||
| chr12:53011537 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-4936A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011537 | |||||||
| chr12:53011598 | C | T | 2 | a0001c0002t0004g0274 a0001c0002t0004g0279 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.14-4875C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011598 | |||||||
| chr12:53011613 | C | G | 1 | a0001c0002t0003g0315 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.14-4860C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011613 | |||||||
| chr12:53012101 | G | A | 1 | a0001c0002t0003g0310 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.14-4372G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012101 | |||||||
| chr12:53012319 | CAG | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.14-4151_14-4150del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53012319 | ||||||
| chr12:53012321 | G | C | 1 | a0001c0001t0002g0166 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.14-4152G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012321 | |||||||
| chr12:53012370 | C | G | 3 | a0001c0002t0009g0317 a0001c0002t0009g0318 a0001c0002t0009g0338 |
3 | HG01884.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14-4103C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012370 | |||||||
| chr12:53012429 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.14-4044C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012429 | |||||||
| chr12:53012469 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14-4004G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012469 | |||||||
| chr12:53012478 | C | T | 2 | a0001c0002t0015g0280 a0003c0009t0015g0301 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.14-3995C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012478 | |||||||
| chr12:53012503 | G | A | 1 | a0001c0005t0005g0013 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.14-3970G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012503 | |||||||
| chr12:53012567 | C | T | 1 | a0001c0002t0004g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.14-3906C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012567 | |||||||
| chr12:53012569 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-3904T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012569 | |||||||
| chr12:53012597 | C | CT | 6 | a0001c0002t0003g0350 a0001c0002t0004g0288 a0001c0002t0005g0331 others(3): Show |
6 | HG02055.hp2 HG03516.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-3863dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53012597 | ||||||
| chr12:53012614 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-3859T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012614 | |||||||
| chr12:53012629 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.14-3844G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012629 | |||||||
| chr12:53012669 | G | A | 30 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(27): Show |
32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.14-3804G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012669 | |||||||
| chr12:53012796 | C | T | 23 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(20): Show |
30 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.14-3677C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012796 | |||||||
| chr12:53012827 | C | T | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-3646C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012827 | |||||||
| chr12:53012874 | G | T | 1 | a0001c0001t0002g0039 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.14-3599G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012874 | |||||||
| chr12:53012881 | C | T | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-3592C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012881 | |||||||
| chr12:53013054 | A | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.14-3419A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013054 | |||||||
| chr12:53013228 | A | G | 3 | a0001c0001t0001g0107 a0002c0004t0001g0106 a0002c0004t0001g0108 |
3 | HG01257.hp1 HG01258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.14-3245A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013228 | |||||||
| chr12:53013256 | G | A | 1 | a0001c0001t0022g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.14-3217G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013256 | |||||||
| chr12:53013263 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01081.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.14-3210C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013263 | |||||||
| chr12:53013783 | T | TA | 51 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0047 others(48): Show |
58 | HG00423.hp2 HG00544.hp2 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.14-2675dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53013783 | ||||||
| chr12:53013885 | A | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-2588A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013885 | |||||||
| chr12:53013904 | T | C | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-2569T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013904 | |||||||
| chr12:53013920 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.14-2553G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013920 | |||||||
| chr12:53014065 | A | G | 106 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(103): Show |
110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.14-2408A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014065 | |||||||
| chr12:53014157 | C | T | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.14-2316C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014157 | |||||||
| chr12:53014160 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-2313G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014160 | |||||||
| chr12:53014246 | TA | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0158 a0001c0001t0002g0243 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-2211delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53014246 | ||||||
| chr12:53014285 | G | A | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14-2188G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014285 | |||||||
| chr12:53014381 | C | G | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.14-2092C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014381 | |||||||
| chr12:53014412 | C | CA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0113 others(12): Show |
16 | HG01358.hp1 HG01358.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-2045dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53014412 | ||||||
| chr12:53014603 | T | G | 6 | a0001c0002t0003g0010 a0001c0002t0003g0011 a0001c0002t0003g0308 others(3): Show |
8 | HG02071.hp1 HG02083.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-1870T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014603 | |||||||
| chr12:53014739 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-1734T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014739 | |||||||
| chr12:53014796 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.14-1677A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014796 | |||||||
| chr12:53014869 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.14-1604G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014869 | |||||||
| chr12:53014900 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.14-1573C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014900 | |||||||
| chr12:53015116 | A | G | 1 | a0001c0002t0007g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-1357A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015116 | |||||||
| chr12:53015141 | T | C | 1 | a0001c0001t0006g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.14-1332T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015141 | |||||||
| chr12:53015273 | G | A | 6 | a0001c0002t0004g0274 a0001c0002t0004g0276 a0001c0002t0004g0279 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-1200G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015273 | |||||||
| chr12:53015309 | C | T | 1 | a0001c0007t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.14-1164C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015309 | |||||||
| chr12:53015470 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-1003G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015470 | |||||||
| chr12:53015526 | T | C | 4 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-947T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015526 | |||||||
| chr12:53015630 | G | A | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.14-843G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015630 | |||||||
| chr12:53015680 | C | CA | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.14-781dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015680 | ||||||
| chr12:53015680 | C | CAA | 10 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(7): Show |
10 | HG00735.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-782_14-781dupAA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015680 | ||||||
| chr12:53015709 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG02698.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.14-764G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015709 | |||||||
| chr12:53015718 | C | T | 2 | a0001c0002t0004g0290 a0001c0002t0018g0291 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.14-755C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015718 | |||||||
| chr12:53015806 | G | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.14-667G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015806 | |||||||
| chr12:53015978 | C | CAA | 23 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(20): Show |
29 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.14-479_14-478dupAA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015978 | ||||||
| chr12:53015978 | CA | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.14-478delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015978 | ||||||
| chr12:53016266 | CAT | C | 106 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(103): Show |
110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.14-206_14-205delAT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53016266 | |||||||
| chr12:53017252 | CA | C | 30 | a0001c0001t0021g0030 a0001c0001t0023g0162 a0001c0002t0003g0001 others(27): Show |
37 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.151+657delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017252 | ||||||
| chr12:53017252 | CAA | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.151+656_151+657del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017252 | ||||||
| chr12:53017295 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0006g0021 a0001c0002t0004g0283 others(5): Show |
8 | HG00423.hp1 HG01070.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+685A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017295 | |||||||
| chr12:53017348 | CAG | C | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0251 |
3 | HG02015.hp1 HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.151+741_151+742del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017348 | ||||||
| chr12:53017518 | C | T | 6 | a0001c0002t0004g0283 a0001c0002t0004g0286 a0001c0002t0004g0287 others(3): Show |
6 | HG00423.hp1 HG02040.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+908C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017518 | |||||||
| chr12:53017697 | G | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.151+1087G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017697 | |||||||
| chr12:53017748 | C | T | 2 | a0001c0002t0004g0290 a0001c0002t0018g0291 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.152-1050C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017748 | |||||||
| chr12:53017938 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152-860C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017938 | |||||||
| chr12:53018174 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.152-624A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018174 | |||||||
| chr12:53018194 | A | G | 1 | a0001c0002t0004g0285 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.152-604A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018194 | |||||||
| chr12:53018238 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-560T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018238 | |||||||
| chr12:53018383 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.152-415T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018383 | |||||||
| chr12:53018526 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.152-272A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018526 | |||||||
| chr12:53018538 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.152-260G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018538 | |||||||
| chr12:53018543 | T | C | 21 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(18): Show |
28 | HG00544.hp2 HG02071.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-255T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018543 | |||||||
| chr12:53018678 | T | C | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-120T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018678 | |||||||
| chr12:53018702 | A | G | 21 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0045 others(18): Show |
21 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-96A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018702 | |||||||
| chr12:53018753 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.152-45G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018753 | |||||||
| chr12:53019134 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.360+128C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019134 | |||||||
| chr12:53019147 | C | G | 1 | a0001c0002t0003g0306 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.360+141C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019147 | |||||||
| chr12:53019423 | TTA | T | 6 | a0001c0001t0002g0174 a0001c0001t0002g0196 a0001c0001t0002g0197 others(3): Show |
6 | HG00609.hp1 HG02717.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+431_360+432del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019423 | ||||||
| chr12:53019423 | TTATA | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0138 others(5): Show |
8 | HG01074.hp2 HG01123.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+429_360+432del others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019423 | ||||||
| chr12:53019432 | TATA | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(37): Show |
41 | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.360+427_360+429del others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019432 | |||||||
| chr12:53019433 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0082 |
2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.360+428_360+429ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019433 | ||||||
| chr12:53019433 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0081 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+428_360+429ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019433 | ||||||
| chr12:53019433 | A | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0057 |
3 | HG01167.hp2 HG01169.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.360+427A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019433 | |||||||
| chr12:53019434 | TATA | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0109 others(40): Show |
44 | HG00140.hp2 HG01081.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.360+429_360+431del others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019434 | |||||||
| chr12:53019435 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+429A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019435 | |||||||
| chr12:53019435 | A | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
76 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.360+429A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019435 | |||||||
| chr12:53019436 | T | TTTTTTTT others(4): Show |
5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG02040.hp1 NA18948.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+430_360+431ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019436 | |||||||
| chr12:53019436 | TA | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0018 others(68): Show |
75 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.360+431delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019436 | |||||||
| chr12:53019437 | A | ATATATTT others(9): Show |
6 | a0001c0002t0003g0001 a0001c0002t0003g0308 a0001c0002t0003g0312 others(3): Show |
6 | HG02071.hp1 HG02523.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATATTT others(10): Show |
9 | a0001c0002t0003g0001 a0001c0002t0003g0310 a0001c0002t0003g0319 others(6): Show |
9 | HG00544.hp2 NA18950.hp2 NA18992.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATATTT others(11): Show |
4 | a0001c0002t0003g0001 a0001c0002t0003g0015 a0001c0002t0003g0315 others(1): Show |
5 | HG02083.hp2 NA18939.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(8): Show |
1 | a0001c0002t0003g0305 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(9): Show |
3 | a0001c0002t0003g0001 a0001c0002t0003g0304 a0001c0002t0003g0306 |
3 | NA18975.hp1 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.360+432_360+433ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(10): Show |
2 | a0001c0002t0003g0011 a0001c0002t0003g0349 |
3 | NA18944.hp2 NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.360+432_360+433ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(11): Show |
4 | a0001c0002t0003g0010 a0001c0002t0003g0303 a0001c0002t0003g0309 others(1): Show |
5 | HG00423.hp2 HG01099.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(12): Show |
1 | a0001c0002t0003g0001 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | ATATTTTT others(13): Show |
1 | a0001c0002t0003g0343 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | ||||||
| chr12:53019437 | A | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0082 |
2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.360+431A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019437 | |||||||
| chr12:53019437 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(136): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.360+431A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019437 | |||||||
| chr12:53019438 | T | TA | 5 | a0001c0002t0005g0012 a0001c0002t0005g0323 a0001c0002t0005g0330 others(2): Show |
6 | HG01109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(1): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019438 | |||||||
| chr12:53019439 | T | A | 16 | a0001c0002t0004g0009 a0001c0002t0004g0275 a0001c0002t0004g0278 others(13): Show |
17 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.360+433T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019439 | |||||||
| chr12:53019440 | T | TTTTTTTC | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG01952.hp2 HG01975.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(7): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019440 | ||||||
| chr12:53019441 | T | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.360+435T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019441 | |||||||
| chr12:53019441 | T | TTTTTTC | 11 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01070.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019441 | ||||||
| chr12:53019442 | T | TTTTTC | 7 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
7 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019442 | ||||||
| chr12:53019443 | T | A | 1 | a0001c0002t0011g0351 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.360+437T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019443 | |||||||
| chr12:53019443 | T | TTTTC | 23 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0045 others(20): Show |
23 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019443 | ||||||
| chr12:53019446 | T | C | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.360+440T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019446 | |||||||
| chr12:53019447 | T | C | 7 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0002g0178 others(4): Show |
7 | HG00438.hp2 HG02723.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+441T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019447 | |||||||
| chr12:53019448 | T | C | 81 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0018 others(78): Show |
84 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.360+442T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019448 | |||||||
| chr12:53019449 | T | C | 12 | a0001c0001t0001g0029 a0001c0001t0006g0037 a0001c0001t0006g0042 others(9): Show |
13 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+443T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019449 | |||||||
| chr12:53019449 | TC | T | 8 | a0001c0001t0002g0173 a0001c0001t0002g0178 a0001c0002t0007g0335 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+444delC | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019449 | |||||||
| chr12:53019450 | C | CT | 22 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0127 others(19): Show |
22 | HG00423.hp1 HG00438.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-436dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | ||||||
| chr12:53019450 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0003g0307 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.361-450_361-436dup others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | ||||||
| chr12:53019450 | C | T | 203 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(200): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.360+444C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019450 | |||||||
| chr12:53019450 | CT | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00140.hp2 HG02258.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-436delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | ||||||
| chr12:53019453 | T | C | 1 | a0001c0007t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.360+447T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019453 | |||||||
| chr12:53019454 | T | C | 1 | a0001c0002t0003g0341 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.360+448T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019454 | |||||||
| chr12:53019456 | T | C | 5 | a0001c0001t0002g0170 a0001c0001t0002g0180 a0001c0001t0002g0181 others(2): Show |
5 | HG00438.hp2 HG03831.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+450T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019456 | |||||||
| chr12:53019457 | T | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0018 others(77): Show |
83 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.360+451T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019457 | |||||||
| chr12:53019457 | T | TTC | 23 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0175 others(20): Show |
23 | HG02015.hp1 HG02074.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.360+452_361-451ins others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019457 | ||||||
| chr12:53019458 | T | TC | 3 | a0001c0001t0002g0006 a0001c0001t0002g0165 a0001c0001t0002g0268 |
4 | HG01934.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+452_361-451ins others(1): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019458 | |||||||
| chr12:53019641 | C | T | 108 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(105): Show |
112 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.361-269C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019641 | |||||||
| chr12:53019653 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.361-257A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019653 | |||||||
| chr12:53019675 | C | CT | 111 | a0001c0001t0001g0022 a0001c0001t0001g0085 a0001c0001t0001g0142 others(108): Show |
115 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.361-218dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | ||||||
| chr12:53019675 | C | CTT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.361-219_361-218dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | ||||||
| chr12:53019675 | C | CTTT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01074.hp2 HG01978.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-220_361-218dup others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | ||||||
| chr12:53019754 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-156A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019754 | |||||||
| chr12:53020223 | C | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02027.hp2 HG02155.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+197C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020223 | |||||||
| chr12:53020226 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.477+200A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020226 | |||||||
| chr12:53020266 | A | T | 1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.477+240A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020266 | |||||||
| chr12:53020542 | A | G | 2 | a0001c0002t0015g0280 a0003c0009t0015g0301 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.477+516A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020542 | |||||||
| chr12:53020654 | A | G | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.477+628A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020654 | |||||||
| chr12:53020907 | G | A | 3 | a0001c0002t0004g0274 a0001c0002t0004g0276 a0001c0002t0004g0279 |
3 | HG02572.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.477+881G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020907 | |||||||
| chr12:53020985 | A | C | 2 | a0001c0001t0002g0238 a0001c0001t0002g0239 |
2 | NA19002.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.478-821A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020985 | |||||||
| chr12:53020988 | G | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.478-818G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020988 | |||||||
| chr12:53021255 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.478-551A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021255 | |||||||
| chr12:53021350 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.478-456T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021350 | |||||||
| chr12:53021565 | G | T | 1 | a0001c0007t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.478-241G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021565 | |||||||
| chr12:53021622 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.478-184T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021622 | |||||||
| chr12:53021664 | A | G | 2 | a0001c0002t0004g0290 a0001c0002t0018g0291 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.478-142A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021664 | |||||||
| chr12:53021732 | A | C | 2 | a0001c0001t0002g0235 a0001c0001t0002g0236 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.478-74A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021732 | |||||||
| chr12:53022216 | G | A | 1 | a0001c0001t0008g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.533-277G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022216 | |||||||
| chr12:53022291 | A | T | 1 | a0001c0001t0014g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.533-202A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022291 | |||||||
| chr12:53022335 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.533-158T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022335 | |||||||
| chr12:53022338 | A | C | 24 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(21): Show |
26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.533-155A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022338 | |||||||
| chr12:53022467 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.533-26C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022467 | |||||||
| chr12:53022479 | T | C | 1 | a0001c0002t0003g0306 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.533-14T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022479 | |||||||
| chr12:53022841 | G | A | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.667+214G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022841 | |||||||
| chr12:53022915 | A | G | 107 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(104): Show |
111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.667+288A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022915 | |||||||
| chr12:53022989 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0067 |
2 | NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.667+362C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022989 | |||||||
| chr12:53023023 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.667+396G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023023 | |||||||
| chr12:53023271 | C | T | 1 | a0001c0002t0004g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.667+644C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023271 | |||||||
| chr12:53023313 | A | G | 3 | a0001c0001t0002g0182 a0001c0001t0002g0195 a0001c0001t0002g0234 |
3 | HG01106.hp2 HG03490.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.667+686A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023313 | |||||||
| chr12:53023378 | G | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.667+751G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023378 | |||||||
| chr12:53023381 | C | T | 4 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+754C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023381 | |||||||
| chr12:53023420 | A | C | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.667+793A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023420 | |||||||
| chr12:53023420 | A | G | 1 | a0001c0002t0004g0288 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.667+793A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023420 | |||||||
| chr12:53023437 | T | TGGCCAGG others(20): Show |
1 | a0001c0002t0004g0283 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667+811_667+837dup others(27): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023437 | ||||||
| chr12:53023463 | C | G | 1 | a0001c0002t0003g0309 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.667+836C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023463 | |||||||
| chr12:53023578 | A | AT | 21 | a0001c0001t0001g0024 a0001c0001t0001g0066 a0001c0001t0001g0083 others(18): Show |
22 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.667+973dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | ||||||
| chr12:53023578 | A | ATT | 99 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(96): Show |
104 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.667+972_667+973dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | ||||||
| chr12:53023578 | A | ATTT | 37 | a0001c0001t0002g0173 a0001c0001t0002g0175 a0001c0001t0002g0181 others(34): Show |
44 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.667+971_667+973dup others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | ||||||
| chr12:53023578 | A | ATTTT | 7 | a0001c0001t0002g0244 a0001c0002t0003g0304 a0001c0002t0003g0307 others(4): Show |
7 | HG02056.hp1 HG02083.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+970_667+973dup others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | ||||||
| chr12:53023578 | AT | A | 13 | a0001c0001t0001g0029 a0001c0001t0001g0090 a0001c0001t0001g0130 others(10): Show |
13 | HG01070.hp1 HG01515.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.667+973delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | ||||||
| chr12:53023617 | C | G | 2 | a0001c0002t0004g0296 a0001c0002t0004g0300 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.667+990C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023617 | |||||||
| chr12:53023686 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.667+1059C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023686 | |||||||
| chr12:53023763 | A | T | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.667+1136A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023763 | |||||||
| chr12:53023802 | C | T | 1 | a0001c0002t0004g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.667+1175C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023802 | |||||||
| chr12:53023919 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.667+1292C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023919 | |||||||
| chr12:53023964 | G | C | 2 | a0001c0001t0006g0038 a0001c0001t0006g0041 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.667+1337G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023964 | |||||||
| chr12:53024047 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0074 others(2): Show |
5 | HG01952.hp2 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+1420G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024047 | |||||||
| chr12:53024097 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.667+1470C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024097 | |||||||
| chr12:53024199 | T | C | 1 | a0001c0001t0006g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.667+1572T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024199 | |||||||
| chr12:53024314 | A | T | 1 | a0001c0002t0004g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.667+1687A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024314 | |||||||
| chr12:53024315 | TAAC | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0130 others(2): Show |
5 | HG00140.hp2 HG01081.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.667+1693_667+1695d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53024315 | ||||||
| chr12:53024408 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00140.hp2 HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.667+1781G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024408 | |||||||
| chr12:53024429 | G | A | 105 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(102): Show |
109 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.667+1802G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024429 | |||||||
| chr12:53024448 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.667+1821C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024448 | |||||||
| chr12:53024467 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.667+1840A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024467 | |||||||
| chr12:53024490 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.667+1863C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024490 | |||||||
| chr12:53024510 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.667+1883A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024510 | |||||||
| chr12:53024648 | CTTTGTTT others(3): Show |
C | 6 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 others(3): Show |
6 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+2041_667+2050d others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53024648 | ||||||
| chr12:53024791 | G | T | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.667+2164G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024791 | |||||||
| chr12:53024800 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.667+2173T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024800 | |||||||
| chr12:53024946 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.667+2319G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024946 | |||||||
| chr12:53025453 | A | C | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.668-2329A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025453 | |||||||
| chr12:53025654 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.668-2128T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025654 | |||||||
| chr12:53025827 | G | T | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1955G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025827 | |||||||
| chr12:53025831 | G | T | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1951G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025831 | |||||||
| chr12:53025974 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0136 a0001c0001t0001g0262 |
3 | HG03831.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.668-1808G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025974 | |||||||
| chr12:53026066 | C | G | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.668-1716C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026066 | |||||||
| chr12:53026144 | A | G | 1 | a0001c0002t0004g0273 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.668-1638A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026144 | |||||||
| chr12:53026267 | C | G | 1 | a0001c0003t0005g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.668-1515C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026267 | |||||||
| chr12:53026435 | AAAC | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1342_668-1340d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53026435 | ||||||
| chr12:53026496 | C | T | 1 | a0001c0002t0003g0341 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.668-1286C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026496 | |||||||
| chr12:53026497 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.668-1285A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026497 | |||||||
| chr12:53026602 | GATTT | G | 3 | a0001c0002t0004g0274 a0001c0002t0004g0276 a0001c0002t0004g0279 |
3 | HG02572.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.668-1167_668-1164d others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53026602 | ||||||
| chr12:53026606 | T | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.668-1176T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026606 | |||||||
| chr12:53026726 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.668-1056C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026726 | |||||||
| chr12:53026840 | C | G | 3 | a0001c0001t0002g0035 a0001c0001t0002g0229 a0001c0001t0002g0237 |
3 | HG00735.hp2 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.668-942C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026840 | |||||||
| chr12:53026841 | A | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.668-941A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026841 | |||||||
| chr12:53026879 | A | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0027g0204 |
3 | HG01891.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.668-903A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026879 | |||||||
| chr12:53026879 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.668-903A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026879 | |||||||
| chr12:53027124 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.668-658A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027124 | |||||||
| chr12:53027136 | A | ATTT | 3 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0251 |
3 | HG02015.hp1 HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.668-646_668-645ins others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.668-646_668-645ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0002g0173 a0001c0001t0002g0205 |
2 | NA18965.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.668-646_668-645ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(5): Show |
22 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0167 others(19): Show |
23 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(6): Show |
33 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0033 others(30): Show |
36 | HG00438.hp2 HG00544.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(7): Show |
19 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0166 others(16): Show |
19 | HG00558.hp1 HG00558.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(8): Show |
17 | a0001c0001t0001g0255 a0001c0001t0002g0032 a0001c0001t0002g0181 others(14): Show |
17 | HG01106.hp2 HG01952.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(9): Show |
6 | a0001c0001t0001g0254 a0001c0001t0002g0035 a0001c0001t0002g0176 others(3): Show |
6 | HG02300.hp1 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(10): Show |
10 | a0001c0001t0001g0076 a0001c0001t0001g0145 a0001c0001t0001g0261 others(7): Show |
10 | HG02129.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(11): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0053 others(19): Show |
23 | HG01070.hp1 HG01070.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(12): Show |
55 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(52): Show |
56 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(13): Show |
41 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
42 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(14): Show |
14 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0097 others(11): Show |
14 | HG00140.hp2 HG00438.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(21): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(15): Show |
6 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0116 others(3): Show |
6 | HG02056.hp2 HG03239.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0140 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(23): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.668-646_668-645ins others(24): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(25): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(19): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0058 |
2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.668-646_668-645ins others(26): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027136 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0117 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(28): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | |||||||
| chr12:53027137 | A | AAATTTTT others(6): Show |
1 | a0001c0002t0003g0304 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.668-645_668-644ins others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027137 | A | AAATTTTT others(9): Show |
1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.668-645_668-644ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027137 | A | AATTTTTT others(3): Show |
2 | a0001c0002t0003g0305 a0001c0002t0003g0314 |
2 | HG01099.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.668-645_668-644ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027137 | A | AATTTTTT others(4): Show |
14 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0015 others(11): Show |
20 | HG00423.hp2 HG00544.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.668-645_668-644ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027137 | A | AATTTTTT others(5): Show |
11 | a0001c0002t0003g0011 a0001c0002t0003g0310 a0001c0002t0003g0313 others(8): Show |
12 | HG02071.hp1 HG02083.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.668-645_668-644ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027137 | A | AT | 13 | a0001c0002t0004g0281 a0001c0002t0004g0287 a0001c0002t0004g0288 others(10): Show |
14 | HG02040.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.668-625dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | ||||||
| chr12:53027137 | A | ATTTTTTT others(7): Show |
2 | a0001c0002t0011g0352 a0001c0002t0011g0353 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-638_668-625dup others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | ||||||
| chr12:53027137 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.668-644_668-625dup others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | ||||||
| chr12:53027137 | A | ATTTTTTT others(15): Show |
1 | a0001c0002t0011g0351 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.668-625_668-624ins others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | ||||||
| chr12:53027137 | A | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.668-645A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | |||||||
| chr12:53027193 | C | T | 4 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-589C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027193 | |||||||
| chr12:53027279 | G | A | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-503G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027279 | |||||||
| chr12:53027322 | C | G | 4 | a0001c0002t0004g0283 a0001c0002t0012g0272 a0001c0002t0012g0284 others(1): Show |
4 | HG00423.hp1 HG02165.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-460C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027322 | |||||||
| chr12:53027323 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.668-459G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027323 | |||||||
| chr12:53027343 | A | T | 30 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(27): Show |
32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.668-439A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027343 | |||||||
| chr12:53027345 | G | A | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-437G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027345 | |||||||
| chr12:53027354 | G | A | 8 | a0001c0002t0007g0014 a0001c0002t0007g0270 a0001c0002t0007g0335 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.668-428G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027354 | |||||||
| chr12:53027624 | T | G | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-158T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027624 | |||||||
| chr12:53027723 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.668-59G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027723 | |||||||
| chr12:53027962 | CT | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.806-43delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 53027962 | ||||||
| chr12:53028261 | C | T | 2 | a0001c0002t0004g0275 a0001c0002t0005g0334 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.979+73C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028261 | |||||||
| chr12:53028346 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.979+158T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028346 | |||||||
| chr12:53028447 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.979+259A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028447 | |||||||
| chr12:53028556 | C | CA | 6 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0063 others(3): Show |
6 | HG02027.hp2 NA18939.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+383dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53028556 | ||||||
| chr12:53028742 | G | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.979+554G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028742 | |||||||
| chr12:53028820 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.979+632A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028820 | |||||||
| chr12:53028834 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.979+646G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028834 | |||||||
| chr12:53029083 | C | G | 1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979+895C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029083 | |||||||
| chr12:53029094 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.979+906C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029094 | |||||||
| chr12:53029120 | C | CA | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.979+944dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029120 | ||||||
| chr12:53029137 | T | C | 1 | a0001c0002t0004g0008 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979+949T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029137 | |||||||
| chr12:53029177 | A | G | 1 | a0001c0002t0019g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+989A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029177 | |||||||
| chr12:53029204 | C | T | 1 | a0001c0002t0018g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.979+1016C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029204 | |||||||
| chr12:53029220 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.979+1032C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029220 | |||||||
| chr12:53029239 | T | C | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.979+1051T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029239 | |||||||
| chr12:53029274 | T | C | 107 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(104): Show |
111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.979+1086T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029274 | |||||||
| chr12:53029375 | TTA | T | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.979+1189_979+1190d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029375 | ||||||
| chr12:53029376 | TA | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0111 a0001c0001t0001g0158 others(7): Show |
10 | HG01070.hp2 HG01981.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+1189delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029376 | |||||||
| chr12:53029377 | A | T | 2 | a0001c0002t0003g0302 a0001c0002t0020g0339 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.979+1189A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029377 | |||||||
| chr12:53029380 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.979+1192T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029380 | |||||||
| chr12:53029395 | C | T | 1 | a0001c0002t0004g0275 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.979+1207C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029395 | |||||||
| chr12:53029532 | T | C | 1 | a0001c0001t0029g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.979+1344T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029532 | |||||||
| chr12:53029609 | C | T | 4 | a0001c0005t0005g0013 a0001c0005t0013g0271 a0001c0005t0013g0311 others(1): Show |
5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+1421C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029609 | |||||||
| chr12:53029654 | A | G | 324 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(321): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.979+1466A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029654 | |||||||
| chr12:53029695 | T | A | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.979+1507T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029695 | |||||||
| chr12:53029709 | C | T | 29 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(26): Show |
36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.979+1521C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029709 | |||||||
| chr12:53029721 | G | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.979+1533G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029721 | |||||||
| chr12:53029856 | C | T | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.979+1668C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029856 | |||||||
| chr12:53029927 | T | TA | 267 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.979+1747dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029927 | ||||||
| chr12:53030009 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.979+1821T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030009 | |||||||
| chr12:53030021 | A | G | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.979+1833A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030021 | |||||||
| chr12:53030031 | TGGCAACA others(151): Show |
T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0098 others(8): Show |
11 | HG01123.hp1 HG03710.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+1879_979+2036d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030031 | ||||||
| chr12:53030043 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02027.hp2 HG02155.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+1855G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030043 | |||||||
| chr12:53030063 | AATACAAA others(153): Show |
A | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.979+1879_979+2038d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030063 | ||||||
| chr12:53030067 | C | CAAAAGTT others(151): Show |
1 | a0001c0002t0004g0008 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979+2025_979+2182d others(160): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030067 | ||||||
| chr12:53030067 | CAAAAGTT others(151): Show |
C | 4 | a0001c0005t0005g0013 a0001c0005t0013g0271 a0001c0005t0013g0311 others(1): Show |
5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2025_979+2182d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030067 | ||||||
| chr12:53030069 | A | T | 1 | a0001c0001t0002g0242 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.979+1881A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030069 | |||||||
| chr12:53030108 | G | A | 2 | a0001c0002t0007g0014 a0001c0002t0007g0336 |
2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.979+1920G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030108 | |||||||
| chr12:53030162 | CAGTTAGC others(149): Show |
C | 1 | a0001c0001t0002g0242 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.979+1975_979+2130d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030162 | |||||||
| chr12:53030225 | TAA | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0082 a0001c0001t0001g0098 others(8): Show |
11 | HG01123.hp1 HG03710.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+2040_979+2041d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030225 | ||||||
| chr12:53030227 | A | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.979+2039A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030227 | |||||||
| chr12:53030330 | A | G | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.979+2142A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030330 | |||||||
| chr12:53030370 | T | TA | 8 | a0001c0002t0007g0014 a0001c0002t0007g0270 a0001c0002t0007g0335 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+2188dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030370 | ||||||
| chr12:53030413 | C | CT | 10 | a0001c0001t0001g0051 a0001c0001t0001g0093 a0001c0001t0002g0033 others(7): Show |
10 | HG01074.hp1 HG01081.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.979+2250dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0139 a0001c0001t0002g0176 a0001c0001t0002g0188 others(1): Show |
4 | HG01123.hp1 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+2241_979+2250d others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0122 a0001c0001t0002g0189 a0001c0001t0002g0215 |
3 | HG02129.hp2 HG02132.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.979+2240_979+2250d others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0002g0031 a0001c0001t0002g0190 a0001c0001t0002g0194 |
3 | HG02922.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.979+2239_979+2250d others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0154 a0001c0001t0002g0163 |
2 | HG00738.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.979+2237_979+2250d others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0034 a0001c0001t0002g0264 |
2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.979+2236_979+2250d others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(9): Show |
8 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0166 others(5): Show |
8 | HG02273.hp1 HG02280.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+2235_979+2250d others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(10): Show |
9 | a0001c0001t0002g0177 a0001c0001t0002g0192 a0001c0001t0002g0207 others(6): Show |
9 | HG02486.hp2 HG03098.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.979+2234_979+2250d others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(11): Show |
20 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0002 others(17): Show |
22 | HG00544.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.979+2233_979+2250d others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(12): Show |
28 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0090 others(25): Show |
30 | HG00140.hp1 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.979+2232_979+2250d others(21): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(13): Show |
19 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0069 others(16): Show |
19 | HG00438.hp2 HG01169.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.979+2231_979+2250d others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(14): Show |
20 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0057 others(17): Show |
20 | HG01123.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.979+2230_979+2250d others(23): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(15): Show |
22 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0045 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.979+2229_979+2250d others(24): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(16): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(15): Show |
20 | HG00140.hp2 HG00735.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.979+2228_979+2250d others(25): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(17): Show |
11 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0070 others(8): Show |
11 | HG00642.hp2 HG01952.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+2227_979+2250d others(26): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0058 a0001c0001t0001g0088 a0001c0001t0001g0132 others(2): Show |
5 | HG01433.hp2 HG02027.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2226_979+2250d others(27): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0080 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.979+2250_979+2251i others(28): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(20): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG01978.hp1 NA18991.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.979+2250_979+2251i others(29): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(21): Show |
4 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0085 others(1): Show |
4 | HG02165.hp2 NA18978.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2250_979+2251i others(30): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(22): Show |
4 | a0001c0001t0001g0065 a0001c0001t0001g0138 a0001c0001t0001g0140 others(1): Show |
4 | HG01496.hp1 HG01934.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2250_979+2251i others(31): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0099 |
2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.979+2250_979+2251i others(32): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0111 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(33): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(34): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0141 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(35): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | C | CTTTTTTT others(27): Show |
2 | a0001c0001t0001g0148 a0001c0006t0001g0156 |
2 | HG00438.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.979+2250_979+2251i others(36): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | CT | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0109 others(13): Show |
17 | HG00609.hp1 HG02027.hp2 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+2250delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | CTT | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0151 a0001c0001t0001g0256 others(4): Show |
7 | HG00423.hp2 HG03486.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+2249_979+2250d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | CTTT | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0043 others(34): Show |
44 | HG00544.hp2 HG00609.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+2248_979+2250d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030413 | CTTTTTTT others(6): Show |
C | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.979+2238_979+2250d others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | ||||||
| chr12:53030482 | C | T | 5 | a0001c0001t0002g0178 a0001c0001t0002g0200 a0001c0001t0002g0222 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2294C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030482 | |||||||
| chr12:53030490 | C | T | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.979+2302C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030490 | |||||||
| chr12:53030683 | T | A | 2 | a0001c0001t0021g0030 a0001c0001t0023g0162 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.979+2495T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030683 | |||||||
| chr12:53030708 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.979+2520T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030708 | |||||||
| chr12:53030859 | A | C | 1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979+2671A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030859 | |||||||
| chr12:53030906 | C | T | 1 | a0001c0002t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.979+2718C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030906 | |||||||
| chr12:53031019 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-2787T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031019 | |||||||
| chr12:53031182 | TCTC | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(54): Show |
61 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.980-2621_980-2619d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53031182 | ||||||
| chr12:53031460 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.980-2346A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031460 | |||||||
| chr12:53031644 | C | T | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0143 others(3): Show |
6 | HG02056.hp2 NA18956.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2162C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031644 | |||||||
| chr12:53031645 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.980-2161G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031645 | |||||||
| chr12:53031695 | G | A | 3 | a0001c0005t0013g0271 a0001c0005t0013g0311 a0001c0005t0013g0333 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.980-2111G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031695 | |||||||
| chr12:53031709 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0206 a0001c0001t0002g0265 |
3 | NA18945.hp2 NA18947.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.980-2097G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031709 | |||||||
| chr12:53031763 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.980-2043A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031763 | |||||||
| chr12:53031770 | G | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-2036G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031770 | |||||||
| chr12:53031833 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980-1973G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031833 | |||||||
| chr12:53032026 | A | T | 29 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(26): Show |
36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.980-1780A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032026 | |||||||
| chr12:53032052 | ACTGC | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-1747_980-1744d others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032052 | ||||||
| chr12:53032319 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-1487A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032319 | |||||||
| chr12:53032386 | T | G | 1 | a0001c0001t0002g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.980-1420T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032386 | |||||||
| chr12:53032401 | C | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-1405C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032401 | |||||||
| chr12:53032493 | C | T | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-1313C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032493 | |||||||
| chr12:53032669 | G | GT | 124 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0063 others(121): Show |
128 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.980-1122dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032669 | ||||||
| chr12:53032669 | G | GTT | 8 | a0001c0001t0002g0033 a0001c0001t0002g0163 a0001c0001t0002g0199 others(5): Show |
8 | HG00544.hp1 HG01891.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.980-1123_980-1122d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032669 | ||||||
| chr12:53032669 | G | T | 3 | a0001c0001t0002g0166 a0001c0001t0002g0177 a0001c0001t0002g0219 |
3 | NA18998.hp1 NA19004.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.980-1137G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032669 | |||||||
| chr12:53032670 | T | G | 1 | a0001c0002t0003g0314 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.980-1136T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032670 | |||||||
| chr12:53032724 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-1082G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032724 | |||||||
| chr12:53032782 | C | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.980-1024C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032782 | |||||||
| chr12:53032901 | T | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.980-905T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032901 | |||||||
| chr12:53032963 | G | A | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-843G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032963 | |||||||
| chr12:53033007 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.980-799A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033007 | |||||||
| chr12:53033011 | A | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-795A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033011 | |||||||
| chr12:53033164 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-642C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033164 | |||||||
| chr12:53033334 | C | CT | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.980-460dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53033334 | ||||||
| chr12:53033334 | C | CTT | 8 | a0001c0001t0001g0081 a0001c0001t0001g0113 a0001c0001t0001g0129 others(5): Show |
8 | HG01496.hp1 NA18945.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.980-461_980-460dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53033334 | ||||||
| chr12:53033366 | C | T | 1 | a0001c0002t0004g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980-440C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033366 | |||||||
| chr12:53033398 | AG | A | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.980-407delG | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033398 | |||||||
| chr12:53033447 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.980-359A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033447 | |||||||
| chr12:53033543 | A | G | 1 | a0001c0002t0005g0332 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.980-263A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033543 | |||||||
| chr12:53033650 | T | C | 2 | a0001c0002t0003g0304 a0001c0002t0003g0307 |
2 | HG02056.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.980-156T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033650 | |||||||
| chr12:53034042 | G | T | 5 | a0001c0002t0003g0303 a0001c0002t0003g0304 a0001c0002t0003g0305 others(2): Show |
5 | HG02056.hp1 NA18940.hp1 NA18975.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1208+8G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/14 | chr12 | 53034042 | |||||||
| chr12:53034870 | G | A | 1 | a0001c0001t0006g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1306+161G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53034870 | |||||||
| chr12:53034886 | A | C | 1 | a0001c0002t0004g0008 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1306+177A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53034886 | |||||||
| chr12:53034956 | C | CT | 11 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0089 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306+269dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | ||||||
| chr12:53034956 | C | CTT | 29 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(26): Show |
36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1306+268_1306+269d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | ||||||
| chr12:53034956 | CT | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(113): Show |
119 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1306+269delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | ||||||
| chr12:53034956 | CTT | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1306+268_1306+269d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | ||||||
| chr12:53035017 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1306+308T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035017 | |||||||
| chr12:53035287 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1306+578C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035287 | |||||||
| chr12:53035347 | C | G | 1 | a0001c0002t0007g0336 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1306+638C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035347 | |||||||
| chr12:53035371 | A | AT | 4 | a0001c0001t0002g0173 a0001c0001t0002g0175 a0001c0001t0002g0231 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+666dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53035371 | ||||||
| chr12:53035371 | A | T | 8 | a0001c0001t0002g0163 a0001c0001t0002g0167 a0001c0001t0008g0040 others(5): Show |
8 | HG01891.hp2 HG02630.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306+662A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035371 | |||||||
| chr12:53035375 | T | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
131 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1306+666T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035375 | |||||||
| chr12:53035376 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1306+667C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035376 | |||||||
| chr12:53035379 | T | A | 3 | a0001c0001t0006g0021 a0001c0001t0006g0037 a0001c0001t0006g0042 |
3 | HG01070.hp2 HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1306+670T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035379 | |||||||
| chr12:53035432 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1306+723G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035432 | |||||||
| chr12:53035495 | A | C | 5 | a0001c0002t0003g0303 a0001c0002t0003g0304 a0001c0002t0003g0305 others(2): Show |
5 | HG02056.hp1 NA18940.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+786A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035495 | |||||||
| chr12:53035526 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1306+817A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035526 | |||||||
| chr12:53035663 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1306+954C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035663 | |||||||
| chr12:53035812 | C | G | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1306+1103C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035812 | |||||||
| chr12:53035987 | T | TTTTGTAT others(18): Show |
92 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(89): Show |
104 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1306+1282_1306+128 others(29): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53035987 | ||||||
| chr12:53036068 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1307-1341G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036068 | |||||||
| chr12:53036082 | CCTT | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1307-1324_1307-132 others(7): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53036082 | ||||||
| chr12:53036135 | G | A | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307-1274G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036135 | |||||||
| chr12:53036221 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1307-1188T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036221 | |||||||
| chr12:53036230 | A | G | 2 | a0001c0002t0015g0280 a0003c0009t0015g0301 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1307-1179A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036230 | |||||||
| chr12:53036319 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1307-1090G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036319 | |||||||
| chr12:53036408 | G | A | 1 | a0001c0002t0009g0317 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1307-1001G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036408 | |||||||
| chr12:53036469 | C | T | 1 | a0001c0002t0003g0310 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1307-940C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036469 | |||||||
| chr12:53036561 | A | G | 1 | a0001c0002t0003g0309 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1307-848A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036561 | |||||||
| chr12:53036649 | A | T | 108 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(105): Show |
112 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1307-760A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036649 | |||||||
| chr12:53036653 | A | G | 1 | a0001c0001t0006g0041 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1307-756A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036653 | |||||||
| chr12:53036725 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(63): Show |
68 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1307-684C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036725 | |||||||
| chr12:53036840 | C | T | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307-569C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036840 | |||||||
| chr12:53036993 | G | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1307-416G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036993 | |||||||
| chr12:53037025 | A | G | 1 | a0001c0001t0002g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1307-384A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037025 | |||||||
| chr12:53037083 | T | C | 324 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(321): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1307-326T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037083 | |||||||
| chr12:53037226 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1307-183T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037226 | |||||||
| chr12:53037749 | C | T | 8 | a0001c0001t0001g0047 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
8 | HG02040.hp1 NA18948.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+127C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037749 | |||||||
| chr12:53037924 | C | G | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1520+302C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037924 | |||||||
| chr12:53037960 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0209 a0001c0001t0002g0211 others(4): Show |
9 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+338A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037960 | |||||||
| chr12:53037975 | T | C | 1 | a0002c0004t0010g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1520+353T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037975 | |||||||
| chr12:53037984 | G | A | 2 | a0001c0002t0003g0010 a0001c0002t0003g0011 |
4 | NA18944.hp2 NA18956.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+362G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037984 | |||||||
| chr12:53038053 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1521-303C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038053 | |||||||
| chr12:53038100 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1521-256G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038100 | |||||||
| chr12:53038150 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0256 |
3 | NA18990.hp1 NA19009.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1521-206T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038150 | |||||||
| chr12:53038292 | T | G | 29 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(26): Show |
36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1521-64T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038292 | |||||||
| chr12:53038304 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1521-52T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038304 | |||||||
| chr12:53038323 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0027 others(51): Show |
55 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1521-33A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038323 | |||||||
| chr12:53038491 | A | G | 1 | a0001c0001t0002g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1576+80A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038491 | |||||||
| chr12:53038513 | G | A | 28 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(25): Show |
35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1576+102G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038513 | |||||||
| chr12:53038707 | C | T | 32 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(29): Show |
34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1576+296C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038707 | |||||||
| chr12:53038749 | G | A | 13 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0002g0168 others(10): Show |
15 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1576+338G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038749 | |||||||
| chr12:53038816 | C | CA | 24 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(21): Show |
26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1577-412dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 53038816 | ||||||
| chr12:53038816 | CA | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1577-412delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 53038816 | ||||||
| chr12:53039152 | A | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1577-86A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039152 | |||||||
| chr12:53039169 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1577-69G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039169 | |||||||
| chr12:53039176 | T | G | 1 | a0001c0001t0002g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1577-62T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039176 | |||||||
| chr12:53039194 | T | C | 21 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0175 others(18): Show |
21 | HG01106.hp2 HG02015.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1577-44T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039194 | |||||||
| chr12:53039381 | CAT | C | 7 | a0001c0002t0003g0303 a0001c0002t0003g0304 a0001c0002t0003g0305 others(4): Show |
7 | HG02055.hp2 HG02056.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1682+39_1682+40del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039381 | |||||||
| chr12:53039515 | A | C | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1683-115A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039515 | |||||||
| chr12:53039553 | G | T | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1683-77G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039553 | |||||||
| chr12:53039557 | C | T | 1 | a0001c0002t0015g0280 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1683-73C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039557 | |||||||
| chr12:53039570 | CAT | C | 3 | a0001c0005t0013g0271 a0001c0005t0013g0311 a0001c0005t0013g0333 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1683-59_1683-58del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039570 | |||||||
| chr12:53039619 | C | T | 3 | a0001c0001t0008g0036 a0001c0001t0008g0040 a0001c0001t0008g0217 |
3 | NA18944.hp1 NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1683-11C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039619 | |||||||
| chr12:53039746 | T | C | 1 | a0001c0002t0003g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1755+44T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039746 | |||||||
| chr12:53039804 | T | C | 1 | a0001c0005t0005g0013 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1755+102T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039804 | |||||||
| chr12:53039809 | G | A | 1 | a0001c0002t0020g0339 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1755+107G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039809 | |||||||
| chr12:53039861 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1755+159C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039861 | |||||||
| chr12:53039865 | A | AT | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1755+163_1755+164i others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039865 | |||||||
| chr12:53039893 | T | C | 3 | a0001c0002t0011g0351 a0001c0002t0011g0352 a0001c0002t0011g0353 |
3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1755+191T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039893 | |||||||
| chr12:53039925 | C | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1756-218C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039925 | |||||||
| chr12:53039969 | A | G | 24 | a0001c0002t0004g0008 a0001c0002t0004g0009 a0001c0002t0004g0273 others(21): Show |
26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1756-174A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039969 | |||||||
| chr12:53040004 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1756-139A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040004 | |||||||
| chr12:53040011 | A | G | 1 | a0001c0001t0006g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1756-132A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040011 | |||||||
| chr12:53040070 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1756-73A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040070 |