Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1977 |
| ensemblid | ENSG00000151247.13 |
| hgncid | 3287 |
| symbol | EIF4E |
| name | eukaryotic translation initiation factor 4E |
| refseq_nuc | NM_001968.5 |
| refseq_prot | NP_001959.1 |
| ensembl_nuc | ENST00000450253.7 |
| ensembl_prot | ENSP00000389624.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 98879276 |
| end | 98929133 |
| strand | - |
| ver | v1.2 |
| region | chr4:98879276-98929133 |
| region5000 | chr4:98874276-98934133 |
| regionname0 | EIF4E_chr4_98879276_98929133 |
| regionname5000 | EIF4E_chr4_98874276_98934133 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 651 | 283 | 89 | 50 | 116 | 3 | 23 | EIF4E_chr4_98874276_98934133 | EIF4E | ATGGC others(646): Show |
chr4 | 98874276 | 98934133 | ||
| a0001c0002 | 0/0 | 651 | 16 | 3 | 6 | 0 | 1 | 6 | EIF4E_chr4_98874276_98934133 | EIF4E | ATGGC others(646): Show |
chr4 | 98874276 | 98934133 | ||
| a0001c0003 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | ATGGC others(646): Show |
chr4 | 98874276 | 98934133 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2427 | 204 | 78 | 45 | 59 | 3 | 17 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0002 | 0/0 | 2427 | 60 | 1 | 3 | 51 | 0 | 5 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0003 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2423): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0004 | 0/0 | 2427 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | CTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0005 | 0/0 | 2428 | 6 | 1 | 2 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2423): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0006 | 0/0 | 2427 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0001t0008 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0002t0003 | 0/0 | 2428 | 13 | 2 | 6 | 0 | 1 | 4 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2423): Show |
chr4 | 98874276 | 98934133 |
| a0001c0002t0007 | 0/0 | 2427 | 3 | 1 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| a0001c0003t0001 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | GTGCG others(2422): Show |
chr4 | 98874276 | 98934133 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0002t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0080 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0079 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0077 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0084 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0078 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0073 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0074 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0072 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0007 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0007 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03491 | hp2 | a0001 | c0002 | t0007 | g0082 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03492 | hp2 | a0001 | c0002 | t0007 | g0081 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0266 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0083 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0159 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | GIH | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02486 | hp1 | a0001 | c0002 | t0007 | g0076 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0085 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0263 | REF | REF | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0211 | REF | REF | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98887103 | G | A | 1 | a0001c0002 | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
synonymous_variant | LOW | c.375C>T | p.Asp125Asp | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/7 | 396/2427 | 375/654 | 125/217 | chr4 | 98887103 | |||
| chr4:98901953 | A | C | 1 | a0001c0003 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.48T>G | p.Thr16Thr | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/7 | 69/2427 | 48/654 | 16/217 | chr4 | 98901953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98879493 | G | A | 1 | a0001c0001t0006 | 3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 1535 | chr4 | 98879493 | ||||||
| chr4:98879999 | G | C | 1 | a0001c0001t0008 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 1029 | chr4 | 98879999 | ||||||
| chr4:98880282 | A | G | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0007 |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*746T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 746 | chr4 | 98880282 | ||||||
| chr4:98880501 | G | A | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0007 |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*527C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 527 | chr4 | 98880501 | ||||||
| chr4:98880835 | C | CA | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0002t0003 |
20 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*192dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 192 | chr4 | 98880835 | ||||||
| chr4:98880919 | A | C | 1 | a0001c0001t0002 | 60 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*109T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 109 | chr4 | 98880919 | ||||||
| chr4:98929133 | C | G | 1 | a0001c0001t0004 | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/7 | chr4 | 98929133 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98881158 | AAAG | A | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.540-19_540-17delCT others(1): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881158 | |||||||
| chr4:98881160 | A | AG | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0141 others(1): Show |
4 | HG03491.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-19dupC | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881160 | |||||||
| chr4:98881194 | A | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.540-52T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881194 | |||||||
| chr4:98881244 | C | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.540-102G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881244 | |||||||
| chr4:98881281 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.540-139G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881281 | |||||||
| chr4:98881542 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540-400A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881542 | |||||||
| chr4:98881583 | G | GTTTAT | 128 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
133 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(130): Show |
intron_variant | MODIFIER | c.540-442_540-441ins others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881583 | |||||||
| chr4:98881709 | G | A | 1 | a0001c0001t0005g0144 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.540-567C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881709 | |||||||
| chr4:98881725 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.540-583G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881725 | |||||||
| chr4:98881800 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.540-658T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881800 | |||||||
| chr4:98881866 | G | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.540-724C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881866 | |||||||
| chr4:98881949 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0261 |
2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.540-807T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881949 | |||||||
| chr4:98882100 | T | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): Show |
78 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.540-958A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882100 | |||||||
| chr4:98882336 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540-1194C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882336 | |||||||
| chr4:98882396 | CA | C | 185 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
209 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.540-1255delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882396 | |||||||
| chr4:98882532 | GT | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-1391delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882532 | |||||||
| chr4:98882575 | A | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-1433T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882575 | |||||||
| chr4:98882703 | T | C | 1 | a0001c0001t0005g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540-1561A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882703 | |||||||
| chr4:98882862 | T | C | 3 | a0001c0002t0003g0079 a0001c0002t0003g0084 a0001c0002t0003g0085 |
3 | HG01081.hp1 HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.540-1720A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882862 | |||||||
| chr4:98882947 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540-1805C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882947 | |||||||
| chr4:98883129 | T | C | 3 | a0001c0002t0003g0072 a0001c0002t0003g0073 a0001c0002t0003g0080 |
3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.539+1793A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883129 | |||||||
| chr4:98883166 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.539+1756C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883166 | |||||||
| chr4:98883172 | TGA | T | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1748_539+1749d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883172 | |||||||
| chr4:98883228 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.539+1694G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883228 | |||||||
| chr4:98883275 | AAATT | A | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1643_539+1646d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883275 | |||||||
| chr4:98883333 | A | C | 1 | a0001c0001t0002g0021 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.539+1589T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883333 | |||||||
| chr4:98883335 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.539+1587G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883335 | |||||||
| chr4:98883392 | A | AT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0103 |
3 | HG01515.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.539+1529_539+1530i others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883392 | |||||||
| chr4:98883393 | A | AT | 183 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(180): Show |
206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.539+1528dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | |||||||
| chr4:98883393 | A | ATT | 51 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(48): Show |
53 | HG00621.hp1 HG00733.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+1527_539+1528d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | |||||||
| chr4:98883393 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0106 |
4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+1529T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | |||||||
| chr4:98883393 | ATTTTTT | A | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.539+1523_539+1528d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | |||||||
| chr4:98883596 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.539+1326C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883596 | |||||||
| chr4:98883605 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.539+1317C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883605 | |||||||
| chr4:98883703 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.539+1219A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883703 | |||||||
| chr4:98883739 | C | CTTAG | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.539+1179_539+1182d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883739 | |||||||
| chr4:98884038 | C | CA | 92 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
97 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.539+883dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884038 | |||||||
| chr4:98884292 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.539+630C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884292 | |||||||
| chr4:98884461 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0125 |
2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.539+461C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884461 | |||||||
| chr4:98884511 | C | G | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.539+411G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884511 | |||||||
| chr4:98884514 | G | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.539+408C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884514 | |||||||
| chr4:98884703 | A | C | 19 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0201 others(16): Show |
19 | HG00673.hp1 HG01243.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.539+219T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884703 | |||||||
| chr4:98884732 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539+190A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884732 | |||||||
| chr4:98884744 | C | CA | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.539+177dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884744 | |||||||
| chr4:98884763 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.539+159C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884763 | |||||||
| chr4:98885095 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.400-34A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885095 | |||||||
| chr4:98885364 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-303A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885364 | |||||||
| chr4:98885390 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.400-329G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885390 | |||||||
| chr4:98885475 | T | C | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-414A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885475 | |||||||
| chr4:98885479 | G | C | 1 | a0001c0001t0001g0008 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.400-418C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885479 | |||||||
| chr4:98886056 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.400-995C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886056 | |||||||
| chr4:98886525 | G | A | 1 | a0001c0001t0005g0156 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.399+554C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886525 | |||||||
| chr4:98886531 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.399+548A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886531 | |||||||
| chr4:98886723 | A | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+356T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886723 | |||||||
| chr4:98886727 | G | A | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.399+352C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886727 | |||||||
| chr4:98886817 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399+262C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886817 | |||||||
| chr4:98886923 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
18 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.399+156C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886923 | |||||||
| chr4:98886931 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399+148A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886931 | |||||||
| chr4:98886985 | CTTAAA | C | 15 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(12): Show |
16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.399+89_399+93delTT others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886985 | |||||||
| chr4:98887380 | C | G | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-188G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887380 | |||||||
| chr4:98887542 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(268): Show |
297 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(294): Show |
intron_variant | MODIFIER | c.285+347A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887542 | |||||||
| chr4:98887619 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.285+270C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887619 | |||||||
| chr4:98887628 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.285+261T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887628 | |||||||
| chr4:98887654 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.285+235T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887654 | |||||||
| chr4:98887721 | T | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.285+168A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887721 | |||||||
| chr4:98887990 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.222-38A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98887990 | |||||||
| chr4:98888025 | A | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-73T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888025 | |||||||
| chr4:98888271 | G | A | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-319C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888271 | |||||||
| chr4:98888321 | AAAAAAC | A | 7 | a0001c0001t0001g0086 a0001c0001t0001g0104 a0001c0001t0001g0106 others(4): Show |
7 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-375_222-370del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888321 | |||||||
| chr4:98888350 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.222-398T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888350 | |||||||
| chr4:98888438 | C | T | 15 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(12): Show |
16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.222-486G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888438 | |||||||
| chr4:98888546 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.222-594C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888546 | |||||||
| chr4:98888677 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-725A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888677 | |||||||
| chr4:98888952 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.222-1000T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888952 | |||||||
| chr4:98888957 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.222-1005C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888957 | |||||||
| chr4:98889157 | C | CA | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-1206dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889157 | |||||||
| chr4:98889157 | CA | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
85 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.222-1206delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889157 | |||||||
| chr4:98889340 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0106 others(1): Show |
5 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-1388C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889340 | |||||||
| chr4:98889359 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222-1407T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889359 | |||||||
| chr4:98889406 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.222-1454G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889406 | |||||||
| chr4:98889654 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.221+1583A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889654 | |||||||
| chr4:98889804 | CCT | C | 7 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0220 others(4): Show |
7 | NA18952.hp2 NA18965.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1431_221+1432d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889804 | |||||||
| chr4:98889839 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0002t0007g0076 |
3 | HG02486.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.221+1398A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889839 | |||||||
| chr4:98889844 | G | A | 3 | a0001c0002t0003g0072 a0001c0002t0003g0073 a0001c0002t0003g0080 |
3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.221+1393C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889844 | |||||||
| chr4:98889889 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1348A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889889 | |||||||
| chr4:98890018 | A | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.221+1219T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890018 | |||||||
| chr4:98890771 | T | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.221+466A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890771 | |||||||
| chr4:98890785 | G | C | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
132 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(129): Show |
intron_variant | MODIFIER | c.221+452C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890785 | |||||||
| chr4:98890832 | A | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0122 |
2 | NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.221+405T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890832 | |||||||
| chr4:98890836 | C | T | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.221+401G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890836 | |||||||
| chr4:98891149 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.221+88G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98891149 | |||||||
| chr4:98891645 | C | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-313G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98891645 | |||||||
| chr4:98892104 | T | C | 1 | a0001c0001t0004g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126-772A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892104 | |||||||
| chr4:98892115 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126-783C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892115 | |||||||
| chr4:98892143 | T | C | 1 | a0001c0002t0003g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-811A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892143 | |||||||
| chr4:98892252 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-920T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892252 | |||||||
| chr4:98892277 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0174 others(3): Show |
6 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-945G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892277 | |||||||
| chr4:98892327 | AC | A | 107 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
112 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(109): Show |
intron_variant | MODIFIER | c.126-996delG | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892327 | |||||||
| chr4:98892328 | C | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0091 others(15): Show |
18 | HG01081.hp1 HG01123.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.126-996G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892328 | |||||||
| chr4:98892335 | A | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0091 others(12): Show |
15 | HG01081.hp1 HG01123.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.126-1003T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892335 | |||||||
| chr4:98892337 | A | C | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
116 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.126-1005T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892337 | |||||||
| chr4:98892340 | C | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
131 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(128): Show |
intron_variant | MODIFIER | c.126-1008G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892340 | |||||||
| chr4:98892344 | A | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.126-1012T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892344 | |||||||
| chr4:98892352 | A | C | 1 | a0001c0001t0005g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.126-1020T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892352 | |||||||
| chr4:98892353 | C | A | 1 | a0001c0001t0005g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.126-1021G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892353 | |||||||
| chr4:98892357 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-1025T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892357 | |||||||
| chr4:98892453 | C | T | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-1121G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892453 | |||||||
| chr4:98892477 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126-1145C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892477 | |||||||
| chr4:98892498 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.126-1166C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892498 | |||||||
| chr4:98892553 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-1221C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892553 | |||||||
| chr4:98892609 | G | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126-1277C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892609 | |||||||
| chr4:98892610 | T | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-1278A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892610 | |||||||
| chr4:98892681 | C | CA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0238 a0001c0001t0001g0242 others(5): Show |
8 | HG01074.hp2 HG01934.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-1350dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | |||||||
| chr4:98892681 | CA | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0089 others(24): Show |
28 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-1350delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | |||||||
| chr4:98892681 | CAA | C | 159 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
182 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.126-1351_126-1350d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | |||||||
| chr4:98892888 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG00423.hp2 NA18955.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.126-1556T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892888 | |||||||
| chr4:98893032 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.126-1700T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893032 | |||||||
| chr4:98893147 | TA | T | 8 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0073 others(5): Show |
9 | HG01358.hp1 HG01515.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-1816delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893147 | |||||||
| chr4:98893148 | A | AAAAAAAA others(3301): Show |
2 | a0001c0002t0003g0072 a0001c0002t0003g0080 |
2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | |||||||
| chr4:98893148 | A | AAAAAAAA others(3301): Show |
5 | a0001c0002t0003g0077 a0001c0002t0003g0078 a0001c0002t0003g0079 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | |||||||
| chr4:98893148 | A | AAAAAAAA others(3301): Show |
1 | a0001c0002t0003g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | |||||||
| chr4:98893163 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.126-1831A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893163 | |||||||
| chr4:98893165 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-1833G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893165 | |||||||
| chr4:98893258 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126-1926G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893258 | |||||||
| chr4:98893291 | T | C | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-1959A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893291 | |||||||
| chr4:98893366 | T | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2034A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893366 | |||||||
| chr4:98893379 | T | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2047A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893379 | |||||||
| chr4:98893393 | T | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126-2061A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893393 | |||||||
| chr4:98893470 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126-2138C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893470 | |||||||
| chr4:98893728 | C | CGGGTTGG others(3302): Show |
1 | a0001c0002t0003g0073 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.126-2397_126-2396i others(3311): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893728 | |||||||
| chr4:98893763 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.126-2431A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893763 | |||||||
| chr4:98893852 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126-2520A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893852 | |||||||
| chr4:98893907 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-2575A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893907 | |||||||
| chr4:98894035 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126-2703C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894035 | |||||||
| chr4:98894096 | C | T | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2764G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894096 | |||||||
| chr4:98894799 | T | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0129 others(4): Show |
8 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-3467A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894799 | |||||||
| chr4:98895008 | G | A | 1 | a0001c0002t0003g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.126-3676C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895008 | |||||||
| chr4:98895076 | C | G | 192 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.126-3744G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895076 | |||||||
| chr4:98895156 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.126-3824T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895156 | |||||||
| chr4:98895198 | G | A | 34 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(31): Show |
35 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.126-3866C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895198 | |||||||
| chr4:98895319 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-3987G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895319 | |||||||
| chr4:98895370 | A | G | 1 | a0001c0002t0003g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-4038T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895370 | |||||||
| chr4:98895590 | A | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0005g0193 others(1): Show |
4 | HG01943.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-4258T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895590 | |||||||
| chr4:98895674 | G | C | 1 | a0001c0001t0002g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126-4342C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895674 | |||||||
| chr4:98895982 | G | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.126-4650C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895982 | |||||||
| chr4:98895984 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126-4652A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895984 | |||||||
| chr4:98895990 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126-4658C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895990 | |||||||
| chr4:98896020 | ACC | A | 17 | a0001c0001t0001g0068 a0001c0001t0003g0087 a0001c0002t0003g0007 others(14): Show |
18 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.126-4690_126-4689d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896020 | |||||||
| chr4:98896025 | G | A | 3 | a0001c0001t0006g0227 a0001c0001t0006g0228 a0001c0001t0006g0247 |
3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.126-4693C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896025 | |||||||
| chr4:98896068 | C | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.126-4736G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896068 | |||||||
| chr4:98896111 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0129 others(4): Show |
8 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-4779C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896111 | |||||||
| chr4:98896128 | G | A | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4796C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896128 | |||||||
| chr4:98896150 | C | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG01261.hp2 HG01934.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-4818G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896150 | |||||||
| chr4:98896195 | C | CAATAA | 6 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0123 others(3): Show |
6 | HG01109.hp1 HG01109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-4868_126-4864d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896195 | |||||||
| chr4:98896224 | A | AAAATAAA others(98): Show |
1 | a0001c0001t0001g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(107): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(93): Show |
1 | a0001c0001t0001g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(102): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(83): Show |
1 | a0001c0001t0004g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(92): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(53): Show |
1 | a0001c0001t0001g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(62): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(43): Show |
1 | a0001c0001t0001g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(52): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(38): Show |
13 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
13 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-4893_126-4892i others(47): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(33): Show |
4 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0001t0004g0167 others(1): Show |
4 | HG02622.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-4893_126-4892i others(42): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(28): Show |
1 | a0001c0001t0001g0190 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(37): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(23): Show |
1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(32): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896224 | A | AAAATAAA others(13): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0177 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.126-4893_126-4892i others(22): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | |||||||
| chr4:98896363 | C | T | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.126-5031G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896363 | |||||||
| chr4:98896486 | C | CA | 99 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0046 others(96): Show |
117 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.126-5155dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAA | 39 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0070 others(36): Show |
42 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.126-5156_126-5155d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAAA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0135 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-5157_126-5155d others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAAAAA | 9 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0088 others(6): Show |
9 | HG01123.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.126-5159_126-5155d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAAAAAA | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0004g0179 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-5160_126-5155d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAAAAAAA | 10 | a0001c0001t0001g0090 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
10 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.126-5161_126-5155d others(9): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896486 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0001t0001g0172 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-5162_126-5155d others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | |||||||
| chr4:98896502 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126-5170T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896502 | |||||||
| chr4:98896667 | C | CA | 33 | a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0201 others(30): Show |
33 | HG00423.hp2 HG00621.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+5208dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAA | C | 28 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(25): Show |
31 | HG00673.hp2 HG01884.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.125+5207_125+5208d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAAA | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
104 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.125+5206_125+5208d others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAAAA | C | 9 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0123 others(6): Show |
9 | HG01109.hp2 HG01934.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+5205_125+5208d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAAAAA | C | 28 | a0001c0001t0001g0068 a0001c0001t0001g0088 a0001c0001t0001g0089 others(25): Show |
29 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.125+5204_125+5208d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAAAAAA | C | 22 | a0001c0001t0001g0091 a0001c0001t0001g0168 a0001c0001t0001g0169 others(19): Show |
22 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.125+5203_125+5208d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896667 | CAAAAAAA others(6): Show |
C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0115 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.125+5196_125+5208d others(15): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | |||||||
| chr4:98896738 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+5138C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896738 | |||||||
| chr4:98896801 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+5075G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896801 | |||||||
| chr4:98896918 | C | T | 1 | a0001c0002t0007g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125+4958G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896918 | |||||||
| chr4:98896946 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+4930G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896946 | |||||||
| chr4:98896972 | C | T | 6 | a0001c0002t0003g0072 a0001c0002t0003g0073 a0001c0002t0003g0079 others(3): Show |
6 | HG00733.hp2 HG01081.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+4904G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896972 | |||||||
| chr4:98897108 | G | T | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+4768C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897108 | |||||||
| chr4:98897275 | T | TAAGAATG others(311): Show |
22 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.125+4600_125+4601i others(320): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897275 | |||||||
| chr4:98897275 | T | TAAGAATG others(312): Show |
4 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0191 others(1): Show |
4 | HG00735.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+4600_125+4601i others(321): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897275 | |||||||
| chr4:98897318 | T | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
133 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(130): Show |
intron_variant | MODIFIER | c.125+4558A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897318 | |||||||
| chr4:98897482 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+4394T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897482 | |||||||
| chr4:98897497 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.125+4379G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897497 | |||||||
| chr4:98897670 | T | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+4206A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897670 | |||||||
| chr4:98897682 | A | C | 192 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.125+4194T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897682 | |||||||
| chr4:98897807 | A | G | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+4069T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897807 | |||||||
| chr4:98898123 | GA | G | 6 | a0001c0001t0001g0086 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG01070.hp2 HG01243.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+3752delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898123 | |||||||
| chr4:98898124 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.125+3752T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898124 | |||||||
| chr4:98898238 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.125+3638A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898238 | |||||||
| chr4:98898429 | A | G | 5 | a0001c0001t0001g0238 a0001c0001t0001g0242 a0001c0001t0001g0258 others(2): Show |
5 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+3447T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898429 | |||||||
| chr4:98898448 | A | C | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+3428T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898448 | |||||||
| chr4:98898465 | G | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.125+3411C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898465 | |||||||
| chr4:98898492 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.125+3384G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898492 | |||||||
| chr4:98898533 | G | A | 1 | a0001c0002t0003g0007 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.125+3343C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898533 | |||||||
| chr4:98898782 | A | C | 6 | a0001c0001t0001g0201 a0001c0001t0001g0210 a0001c0001t0001g0243 others(3): Show |
6 | HG02027.hp2 HG02083.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+3094T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898782 | |||||||
| chr4:98898897 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+2979A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898897 | |||||||
| chr4:98898916 | G | A | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+2960C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898916 | |||||||
| chr4:98899054 | T | TA | 7 | a0001c0001t0001g0114 a0001c0001t0001g0121 a0001c0001t0001g0154 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+2821dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899054 | |||||||
| chr4:98899054 | TA | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0004g0167 others(8): Show |
11 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+2821delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899054 | |||||||
| chr4:98899105 | T | A | 13 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(10): Show |
14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.125+2771A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899105 | |||||||
| chr4:98899209 | T | C | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+2667A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899209 | |||||||
| chr4:98899318 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+2558A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899318 | |||||||
| chr4:98899389 | G | A | 17 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.125+2487C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899389 | |||||||
| chr4:98899396 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.125+2480T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899396 | |||||||
| chr4:98899427 | A | C | 2 | a0001c0001t0006g0227 a0001c0001t0006g0247 |
2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.125+2449T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899427 | |||||||
| chr4:98899456 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.125+2420C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899456 | |||||||
| chr4:98899819 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.125+2057A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899819 | |||||||
| chr4:98899883 | T | C | 1 | a0001c0002t0003g0077 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125+1993A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899883 | |||||||
| chr4:98899945 | T | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+1931A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899945 | |||||||
| chr4:98900048 | T | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+1828A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900048 | |||||||
| chr4:98900313 | C | T | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.125+1563G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900313 | |||||||
| chr4:98900462 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+1414T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900462 | |||||||
| chr4:98900471 | G | A | 193 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
217 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.125+1405C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900471 | |||||||
| chr4:98900478 | TA | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.125+1397delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900478 | |||||||
| chr4:98900518 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125+1358C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900518 | |||||||
| chr4:98900525 | CTT | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+1349_125+1350d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900525 | |||||||
| chr4:98900634 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+1242G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900634 | |||||||
| chr4:98900825 | A | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): Show |
78 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.125+1051T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900825 | |||||||
| chr4:98900902 | C | T | 1 | a0001c0002t0003g0077 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125+974G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900902 | |||||||
| chr4:98901030 | T | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+846A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901030 | |||||||
| chr4:98901120 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+756A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901120 | |||||||
| chr4:98901123 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+753G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901123 | |||||||
| chr4:98901200 | C | CT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.125+675dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901200 | |||||||
| chr4:98901259 | G | A | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+617C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901259 | |||||||
| chr4:98901323 | G | A | 1 | a0001c0002t0007g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125+553C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901323 | |||||||
| chr4:98901436 | T | G | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+440A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901436 | |||||||
| chr4:98901443 | CCCGCCT | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0098 others(7): Show |
10 | HG00735.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+427_125+432del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901443 | |||||||
| chr4:98901491 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.125+385C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901491 | |||||||
| chr4:98901754 | T | C | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+122A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901754 | |||||||
| chr4:98902030 | T | C | 7 | a0001c0001t0001g0235 a0001c0001t0001g0238 a0001c0001t0001g0242 others(4): Show |
7 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-48A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902030 | |||||||
| chr4:98902159 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19-177G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902159 | |||||||
| chr4:98902376 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-394C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902376 | |||||||
| chr4:98902391 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-409T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902391 | |||||||
| chr4:98902554 | T | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.19-572A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902554 | |||||||
| chr4:98902620 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19-638A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902620 | |||||||
| chr4:98902640 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-658C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902640 | |||||||
| chr4:98902864 | CA | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-883delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902864 | |||||||
| chr4:98903049 | A | G | 1 | a0001c0002t0003g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-1067T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903049 | |||||||
| chr4:98903210 | A | G | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-1228T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903210 | |||||||
| chr4:98903275 | C | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-1293G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903275 | |||||||
| chr4:98903360 | G | GT | 16 | a0001c0001t0001g0168 a0001c0001t0001g0268 a0001c0001t0002g0029 others(13): Show |
17 | HG00735.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-1379dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903360 | |||||||
| chr4:98903435 | T | C | 31 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0002g0001 others(28): Show |
48 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-1453A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903435 | |||||||
| chr4:98903452 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.19-1470A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903452 | |||||||
| chr4:98903486 | T | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-1504A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903486 | |||||||
| chr4:98903514 | T | C | 13 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(10): Show |
14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-1532A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903514 | |||||||
| chr4:98903677 | G | A | 3 | a0001c0002t0003g0007 a0001c0002t0007g0081 a0001c0002t0007g0082 |
4 | HG03017.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1695C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903677 | |||||||
| chr4:98904122 | GAGA | G | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-2143_19-2141del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904122 | |||||||
| chr4:98904455 | AT | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-2474delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904455 | |||||||
| chr4:98904488 | C | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-2506G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904488 | |||||||
| chr4:98904502 | G | A | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-2520C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904502 | |||||||
| chr4:98904552 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-2570G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904552 | |||||||
| chr4:98904640 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
132 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(129): Show |
intron_variant | MODIFIER | c.19-2658T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904640 | |||||||
| chr4:98904643 | C | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-2661G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904643 | |||||||
| chr4:98904831 | T | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-2849A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904831 | |||||||
| chr4:98905096 | G | T | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-3114C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905096 | |||||||
| chr4:98905206 | C | T | 17 | a0001c0001t0001g0068 a0001c0001t0003g0087 a0001c0002t0003g0007 others(14): Show |
18 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-3224G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905206 | |||||||
| chr4:98905231 | T | TAA | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
74 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.19-3251_19-3250dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905231 | |||||||
| chr4:98905231 | TA | T | 28 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(25): Show |
28 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.19-3250delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905231 | |||||||
| chr4:98905233 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-3251T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905233 | |||||||
| chr4:98905416 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-3434C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905416 | |||||||
| chr4:98905432 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-3450G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905432 | |||||||
| chr4:98905727 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.19-3745G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905727 | |||||||
| chr4:98906163 | T | A | 1 | a0001c0001t0006g0247 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-4181A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906163 | |||||||
| chr4:98906264 | G | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-4282C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906264 | |||||||
| chr4:98906509 | A | G | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-4527T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906509 | |||||||
| chr4:98906642 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19-4660G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906642 | |||||||
| chr4:98906651 | C | T | 15 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(12): Show |
16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.19-4669G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906651 | |||||||
| chr4:98906796 | C | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-4814G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906796 | |||||||
| chr4:98906888 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-4906A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906888 | |||||||
| chr4:98906956 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.19-4974A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906956 | |||||||
| chr4:98907176 | A | G | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-5194T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907176 | |||||||
| chr4:98907217 | A | G | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-5235T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907217 | |||||||
| chr4:98907396 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-5414G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907396 | |||||||
| chr4:98907431 | T | TCAAAAAA others(4): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-5460_19-5450dup others(11): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907431 | |||||||
| chr4:98907523 | T | C | 1 | a0001c0002t0003g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-5541A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907523 | |||||||
| chr4:98907605 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19-5623C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907605 | |||||||
| chr4:98907755 | T | A | 1 | a0001c0001t0006g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-5773A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907755 | |||||||
| chr4:98907855 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-5873T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907855 | |||||||
| chr4:98908103 | A | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-6121T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908103 | |||||||
| chr4:98908154 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.19-6172G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908154 | |||||||
| chr4:98908224 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-6242T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908224 | |||||||
| chr4:98908525 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-6543A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908525 | |||||||
| chr4:98908711 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-6729G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908711 | |||||||
| chr4:98908815 | C | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-6833G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908815 | |||||||
| chr4:98909114 | G | A | 17 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-7132C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909114 | |||||||
| chr4:98909203 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-7221C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909203 | |||||||
| chr4:98909528 | A | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-7546T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909528 | |||||||
| chr4:98909689 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-7707C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909689 | |||||||
| chr4:98909855 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.19-7873G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909855 | |||||||
| chr4:98909943 | C | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-7961G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909943 | |||||||
| chr4:98910153 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-8171A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910153 | |||||||
| chr4:98910311 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02809.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-8329C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910311 | |||||||
| chr4:98910349 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19-8367T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910349 | |||||||
| chr4:98910383 | A | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-8401T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910383 | |||||||
| chr4:98910458 | T | A | 1 | a0001c0001t0002g0033 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19-8476A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910458 | |||||||
| chr4:98910508 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-8526T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910508 | |||||||
| chr4:98910704 | A | C | 3 | a0001c0001t0006g0227 a0001c0001t0006g0228 a0001c0001t0006g0247 |
3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.19-8722T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910704 | |||||||
| chr4:98910734 | C | CT | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.19-8753dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910734 | |||||||
| chr4:98910799 | G | A | 17 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-8817C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910799 | |||||||
| chr4:98910832 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-8850G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910832 | |||||||
| chr4:98910854 | C | G | 1 | a0001c0001t0002g0013 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.19-8872G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910854 | |||||||
| chr4:98910919 | C | T | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8937G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910919 | |||||||
| chr4:98910943 | C | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-8961G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910943 | |||||||
| chr4:98911016 | G | A | 17 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-9034C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911016 | |||||||
| chr4:98911022 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-9040G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911022 | |||||||
| chr4:98911193 | C | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG01070.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9211G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911193 | |||||||
| chr4:98911195 | C | T | 13 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(10): Show |
14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-9213G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911195 | |||||||
| chr4:98911206 | G | A | 1 | a0001c0002t0007g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-9224C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911206 | |||||||
| chr4:98911210 | G | A | 17 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-9228C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911210 | |||||||
| chr4:98911221 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-9239C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911221 | |||||||
| chr4:98911294 | C | T | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-9312G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911294 | |||||||
| chr4:98911426 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-9444C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911426 | |||||||
| chr4:98911489 | A | G | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-9507T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911489 | |||||||
| chr4:98911583 | C | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-9601G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911583 | |||||||
| chr4:98911661 | C | CA | 18 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0114 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-9680dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | C | CAA | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0104 others(44): Show |
49 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.19-9681_19-9680dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | C | CAAA | 8 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0109 others(5): Show |
8 | HG00733.hp1 HG02074.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-9682_19-9680dup others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | C | CAAAA | 4 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0162 others(1): Show |
6 | HG01515.hp1 HG01517.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-9683_19-9680dup others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | CA | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(68): Show |
90 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.19-9680delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | CAA | C | 27 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0071 others(24): Show |
28 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.19-9681_19-9680del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | CAAA | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-9682_19-9680del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-9692_19-9680del others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911661 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19-9693_19-9680del others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | |||||||
| chr4:98911979 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-9997C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911979 | |||||||
| chr4:98911992 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-10010G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911992 | |||||||
| chr4:98912177 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-10195C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912177 | |||||||
| chr4:98912228 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-10246C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912228 | |||||||
| chr4:98912269 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-10287T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912269 | |||||||
| chr4:98912470 | G | A | 1 | a0001c0001t0004g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19-10488C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912470 | |||||||
| chr4:98912524 | T | C | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-10542A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912524 | |||||||
| chr4:98912525 | G | A | 13 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(10): Show |
14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-10543C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912525 | |||||||
| chr4:98912586 | CAAAGA | C | 45 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(42): Show |
48 | HG00558.hp2 HG00733.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-10609_19-10605d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912586 | |||||||
| chr4:98912636 | A | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-10654T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912636 | |||||||
| chr4:98912636 | AT | A | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-10655delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912636 | |||||||
| chr4:98912763 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-10781A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912763 | |||||||
| chr4:98912929 | G | A | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-10947C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912929 | |||||||
| chr4:98913081 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.19-11099C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913081 | |||||||
| chr4:98913098 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19-11116G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913098 | |||||||
| chr4:98913099 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-11117C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913099 | |||||||
| chr4:98913130 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-11148G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913130 | |||||||
| chr4:98913207 | C | CA | 9 | a0001c0001t0001g0071 a0001c0001t0004g0167 a0001c0001t0004g0179 others(6): Show |
9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-11226dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913207 | |||||||
| chr4:98913207 | CA | C | 17 | a0001c0001t0001g0249 a0001c0001t0001g0261 a0001c0002t0003g0007 others(14): Show |
18 | HG00733.hp2 HG01081.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-11226delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913207 | |||||||
| chr4:98913226 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.19-11244T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913226 | |||||||
| chr4:98913324 | T | G | 1 | a0001c0002t0007g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-11342A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913324 | |||||||
| chr4:98913436 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0255 |
2 | HG00673.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.19-11454G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913436 | |||||||
| chr4:98913802 | A | C | 1 | a0001c0001t0006g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-11820T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913802 | |||||||
| chr4:98913859 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19-11877A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913859 | |||||||
| chr4:98913964 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19-11982G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913964 | |||||||
| chr4:98914033 | C | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-12051G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914033 | |||||||
| chr4:98914064 | TA | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-12083delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914064 | |||||||
| chr4:98914228 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-12246A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914228 | |||||||
| chr4:98914274 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-12292A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914274 | |||||||
| chr4:98914337 | T | TG | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-12356dupC | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914337 | |||||||
| chr4:98914361 | C | CA | 21 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG01192.hp1 HG01243.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-12380dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | C | CAA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0091 others(3): Show |
6 | HG01123.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-12381_19-12380d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-12391_19-12380d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0003g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-12393_19-12380d others(16): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0003g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-12398_19-12380d others(21): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | C | CAAAAAAA others(34): Show |
1 | a0001c0002t0007g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-12380_19-12379i others(43): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | CA | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0042 others(104): Show |
125 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.19-12380delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | CAA | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(58): Show |
64 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.19-12381_19-12380d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914361 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-12389_19-12380d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | |||||||
| chr4:98914392 | CT | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
71 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.19-12411delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914392 | |||||||
| chr4:98914508 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19-12526C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914508 | |||||||
| chr4:98914655 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02809.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-12673A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914655 | |||||||
| chr4:98914810 | A | G | 1 | a0001c0002t0003g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-12828T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914810 | |||||||
| chr4:98914860 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-12878C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914860 | |||||||
| chr4:98915002 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-13020C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915002 | |||||||
| chr4:98915017 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-13035G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915017 | |||||||
| chr4:98915099 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19-13117T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915099 | |||||||
| chr4:98915253 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-13271C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915253 | |||||||
| chr4:98915256 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-13274G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915256 | |||||||
| chr4:98915387 | A | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.19-13405T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915387 | |||||||
| chr4:98915545 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+13539_18+13549d others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915545 | |||||||
| chr4:98915601 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.18+13494G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915601 | |||||||
| chr4:98915645 | A | G | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+13450T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915645 | |||||||
| chr4:98915659 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+13436T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915659 | |||||||
| chr4:98915690 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+13405C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915690 | |||||||
| chr4:98915732 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.18+13363C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915732 | |||||||
| chr4:98916020 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+13075C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916020 | |||||||
| chr4:98916083 | C | T | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+13012G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916083 | |||||||
| chr4:98916206 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+12889C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916206 | |||||||
| chr4:98916254 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18+12841T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916254 | |||||||
| chr4:98916286 | C | CA | 104 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
108 | HG00558.hp2 HG00733.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.18+12808dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | |||||||
| chr4:98916286 | C | CAA | 78 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(75): Show |
98 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+12807_18+12808d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | |||||||
| chr4:98916286 | CA | C | 9 | a0001c0001t0001g0273 a0001c0001t0004g0167 a0001c0001t0004g0179 others(6): Show |
9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12808delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | |||||||
| chr4:98916310 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+12785T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916310 | |||||||
| chr4:98916348 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+12747G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916348 | |||||||
| chr4:98916410 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | HG02055.hp1 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12685G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916410 | |||||||
| chr4:98916493 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+12602C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916493 | |||||||
| chr4:98916534 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12561A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916534 | |||||||
| chr4:98916578 | G | A | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12517C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916578 | |||||||
| chr4:98916661 | G | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12434C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916661 | |||||||
| chr4:98916751 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.18+12344T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916751 | |||||||
| chr4:98916768 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12327A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916768 | |||||||
| chr4:98917005 | A | G | 1 | a0001c0001t0003g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18+12090T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917005 | |||||||
| chr4:98917083 | A | AAC | 8 | a0001c0001t0001g0155 a0001c0001t0001g0230 a0001c0001t0001g0232 others(5): Show |
8 | HG00735.hp2 HG01891.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12010_18+12011d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | |||||||
| chr4:98917083 | A | AACAC | 4 | a0001c0001t0001g0043 a0001c0001t0001g0226 a0001c0001t0001g0254 others(1): Show |
4 | HG00673.hp1 HG02040.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12008_18+12011d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | |||||||
| chr4:98917083 | AAC | A | 6 | a0001c0001t0001g0198 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG01167.hp1 HG01346.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+12010_18+12011d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | |||||||
| chr4:98917083 | AACAC | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0243 a0001c0001t0001g0244 others(5): Show |
8 | HG00423.hp2 HG01123.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12008_18+12011d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | |||||||
| chr4:98917083 | AACACAC | A | 4 | a0001c0001t0001g0202 a0001c0001t0001g0246 a0001c0001t0001g0249 others(1): Show |
4 | HG01168.hp2 HG03834.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+12006_18+12011d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | |||||||
| chr4:98917109 | CACACACA others(21): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11958_18+11985d others(30): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917109 | |||||||
| chr4:98917113 | CACACACA others(17): Show |
C | 2 | a0001c0001t0001g0012 a0001c0001t0002g0004 |
2 | HG01123.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18+11958_18+11981d others(26): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917113 | |||||||
| chr4:98917115 | CACACACA others(15): Show |
C | 16 | a0001c0001t0001g0192 a0001c0001t0003g0087 a0001c0002t0003g0007 others(13): Show |
17 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+11958_18+11979d others(24): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917115 | |||||||
| chr4:98917117 | CACACACA others(13): Show |
C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0146 others(4): Show |
8 | HG00733.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+11958_18+11977d others(22): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917117 | |||||||
| chr4:98917119 | CACACACA others(11): Show |
C | 8 | a0001c0001t0001g0071 a0001c0001t0004g0167 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+11958_18+11975d others(20): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917119 | |||||||
| chr4:98917121 | CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+11958_18+11973d others(18): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917121 | |||||||
| chr4:98917123 | CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0207 a0001c0001t0001g0212 |
3 | HG01261.hp1 HG01517.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+11960_18+11971d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917123 | |||||||
| chr4:98917123 | CACACACA others(7): Show |
C | 6 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0059 others(3): Show |
6 | HG02602.hp1 HG02738.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+11958_18+11971d others(16): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917123 | |||||||
| chr4:98917125 | CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18+11960_18+11969d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917125 | |||||||
| chr4:98917125 | CACACACA others(5): Show |
C | 12 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0132 others(9): Show |
12 | HG01070.hp2 HG03041.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+11958_18+11969d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917125 | |||||||
| chr4:98917127 | CACACACA others(3): Show |
C | 23 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0069 others(20): Show |
23 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.18+11958_18+11967d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917127 | |||||||
| chr4:98917129 | CACACAAA others(1): Show |
C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0042 others(22): Show |
26 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+11958_18+11965d others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917129 | |||||||
| chr4:98917131 | CACAA | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0001t0001g0205 others(16): Show |
20 | HG00438.hp2 HG01934.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+11960_18+11963d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917131 | |||||||
| chr4:98917131 | CACAAAA | C | 36 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0001g0100 others(33): Show |
50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.18+11958_18+11963d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917131 | |||||||
| chr4:98917133 | C | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0221 a0001c0001t0001g0244 |
3 | HG02258.hp2 NA18953.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.18+11962G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | |||||||
| chr4:98917133 | CAA | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(31): Show |
35 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.18+11960_18+11961d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | |||||||
| chr4:98917133 | CAAAA | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0089 others(17): Show |
22 | HG01346.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.18+11958_18+11961d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | |||||||
| chr4:98917135 | A | C | 26 | a0001c0001t0001g0043 a0001c0001t0001g0092 a0001c0001t0001g0093 others(23): Show |
26 | HG00673.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+11960T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917135 | |||||||
| chr4:98917136 | A | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0248 |
2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.18+11959T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917136 | |||||||
| chr4:98917137 | A | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0053 others(36): Show |
40 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.18+11958T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917137 | |||||||
| chr4:98917138 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+11957T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917138 | |||||||
| chr4:98917139 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.18+11956T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917139 | |||||||
| chr4:98917279 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11816T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917279 | |||||||
| chr4:98917363 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.18+11732T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917363 | |||||||
| chr4:98917680 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+11415C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917680 | |||||||
| chr4:98917729 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.18+11366G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917729 | |||||||
| chr4:98918007 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11088G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918007 | |||||||
| chr4:98918071 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+11024T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918071 | |||||||
| chr4:98918360 | G | GA | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.18+10734dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918360 | |||||||
| chr4:98918409 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0225 |
2 | NA18953.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.18+10686A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918409 | |||||||
| chr4:98918502 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+10593A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918502 | |||||||
| chr4:98918536 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+10559C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918536 | |||||||
| chr4:98918639 | A | C | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.18+10456T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918639 | |||||||
| chr4:98918648 | A | T | 1 | a0001c0002t0003g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+10447T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918648 | |||||||
| chr4:98918652 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+10443A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918652 | |||||||
| chr4:98918918 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.18+10177G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918918 | |||||||
| chr4:98918938 | A | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+10157T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918938 | |||||||
| chr4:98918954 | T | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+10141A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918954 | |||||||
| chr4:98919069 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.18+10026C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919069 | |||||||
| chr4:98919071 | G | T | 1 | a0001c0002t0003g0077 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.18+10024C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919071 | |||||||
| chr4:98919122 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0113 a0001c0001t0001g0114 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+9973G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919122 | |||||||
| chr4:98919162 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+9933A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919162 | |||||||
| chr4:98919175 | C | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.18+9920G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919175 | |||||||
| chr4:98919332 | C | CA | 25 | a0001c0001t0001g0051 a0001c0001t0001g0200 a0001c0001t0001g0226 others(22): Show |
26 | HG00621.hp1 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+9762dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919332 | |||||||
| chr4:98919332 | CAA | C | 25 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(22): Show |
25 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+9761_18+9762del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919332 | |||||||
| chr4:98919337 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0071 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.18+9748_18+9757del others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919337 | |||||||
| chr4:98919342 | A | C | 72 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
76 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+9753T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919342 | |||||||
| chr4:98919345 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+9750T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919345 | |||||||
| chr4:98919429 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+9666C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919429 | |||||||
| chr4:98919452 | C | T | 1 | a0001c0002t0003g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+9643G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919452 | |||||||
| chr4:98919485 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+9610A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919485 | |||||||
| chr4:98919501 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0070 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.18+9594T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919501 | |||||||
| chr4:98919558 | C | CT | 14 | a0001c0001t0001g0086 a0001c0001t0001g0164 a0001c0001t0001g0201 others(11): Show |
14 | HG01243.hp1 HG02027.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.18+9536dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919558 | |||||||
| chr4:98919558 | CT | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0101 a0001c0001t0001g0109 others(4): Show |
7 | HG01123.hp2 HG01168.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+9536delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919558 | |||||||
| chr4:98919850 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+9245A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919850 | |||||||
| chr4:98920231 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.18+8864A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920231 | |||||||
| chr4:98920403 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18+8692G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920403 | |||||||
| chr4:98920452 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+8643C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920452 | |||||||
| chr4:98920460 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.18+8635T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920460 | |||||||
| chr4:98920512 | C | G | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.18+8583G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920512 | |||||||
| chr4:98920608 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18+8487T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920608 | |||||||
| chr4:98920808 | C | A | 1 | a0001c0002t0003g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.18+8287G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920808 | |||||||
| chr4:98920840 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(58): Show |
80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.18+8255G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920840 | |||||||
| chr4:98921028 | C | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+8067G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921028 | |||||||
| chr4:98921051 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+8044T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921051 | |||||||
| chr4:98921055 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+8040A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921055 | |||||||
| chr4:98921100 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+7995A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921100 | |||||||
| chr4:98921185 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+7910T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921185 | |||||||
| chr4:98921205 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+7890A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921205 | |||||||
| chr4:98921378 | TA | T | 18 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.18+7716delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921378 | |||||||
| chr4:98921416 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+7679A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921416 | |||||||
| chr4:98921962 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+7133T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921962 | |||||||
| chr4:98922142 | C | T | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+6953G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922142 | |||||||
| chr4:98922310 | C | A | 1 | a0001c0002t0003g0007 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.18+6785G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922310 | |||||||
| chr4:98922312 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0106 |
4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+6783G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922312 | |||||||
| chr4:98922326 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+6769C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922326 | |||||||
| chr4:98922332 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.18+6763G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922332 | |||||||
| chr4:98922333 | G | A | 1 | a0001c0001t0005g0144 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.18+6762C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922333 | |||||||
| chr4:98922353 | C | T | 8 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+6742G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922353 | |||||||
| chr4:98922413 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+6682C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922413 | |||||||
| chr4:98922463 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.18+6632C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922463 | |||||||
| chr4:98922553 | C | CA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0102 others(16): Show |
19 | HG01123.hp2 HG01192.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.18+6541dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922553 | |||||||
| chr4:98922568 | A | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0146 a0001c0001t0001g0161 others(2): Show |
6 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+6527T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922568 | |||||||
| chr4:98922713 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+6382A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922713 | |||||||
| chr4:98922753 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+6342A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922753 | |||||||
| chr4:98922830 | T | G | 15 | a0001c0002t0003g0007 a0001c0002t0003g0072 a0001c0002t0003g0073 others(12): Show |
16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+6265A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922830 | |||||||
| chr4:98922850 | C | CT | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
66 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+6244dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | |||||||
| chr4:98922850 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.18+6245G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | |||||||
| chr4:98922850 | CT | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0044 others(58): Show |
80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.18+6244delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | |||||||
| chr4:98922865 | TGA | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0164 others(1): Show |
5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6228_18+6229del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922865 | |||||||
| chr4:98922868 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0164 others(1): Show |
5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6227C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922868 | |||||||
| chr4:98922869 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0164 others(1): Show |
5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6226T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922869 | |||||||
| chr4:98922931 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0146 a0001c0001t0001g0161 others(2): Show |
6 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+6164A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922931 | |||||||
| chr4:98922997 | G | A | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+6098C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922997 | |||||||
| chr4:98923094 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+6001C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923094 | |||||||
| chr4:98923157 | C | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+5938G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923157 | |||||||
| chr4:98923204 | C | CA | 39 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0054 others(36): Show |
39 | HG01109.hp1 HG01123.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+5890dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923204 | |||||||
| chr4:98923208 | A | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0155 |
2 | NA18956.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.18+5887T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923208 | |||||||
| chr4:98923283 | G | GAC | 60 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(57): Show |
79 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+5810_18+5811dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923283 | |||||||
| chr4:98923319 | CT | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.18+5775delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923319 | |||||||
| chr4:98923596 | C | T | 3 | a0001c0002t0003g0072 a0001c0002t0003g0073 a0001c0002t0003g0080 |
3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.18+5499G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923596 | |||||||
| chr4:98923611 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+5484G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923611 | |||||||
| chr4:98923683 | T | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+5412A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923683 | |||||||
| chr4:98923816 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+5279T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923816 | |||||||
| chr4:98924077 | G | GT | 3 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0003t0001g0159 |
3 | HG02615.hp2 HG03516.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.18+5017dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924077 | |||||||
| chr4:98924081 | A | AT | 18 | a0001c0001t0001g0071 a0001c0001t0001g0240 a0001c0001t0003g0087 others(15): Show |
19 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.18+5013dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | |||||||
| chr4:98924081 | A | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
76 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+5014T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | |||||||
| chr4:98924081 | AT | A | 10 | a0001c0001t0001g0249 a0001c0001t0002g0001 a0001c0001t0004g0167 others(7): Show |
10 | HG01168.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+5013delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | |||||||
| chr4:98924156 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0069 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+4939G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924156 | |||||||
| chr4:98924235 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+4860G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924235 | |||||||
| chr4:98924270 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+4825C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924270 | |||||||
| chr4:98924322 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+4773G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924322 | |||||||
| chr4:98924428 | G | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+4667C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924428 | |||||||
| chr4:98924593 | G | GT | 16 | a0001c0001t0003g0087 a0001c0002t0003g0007 a0001c0002t0003g0072 others(13): Show |
17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+4501dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924593 | |||||||
| chr4:98924594 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+4501A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924594 | |||||||
| chr4:98924813 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+4282C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924813 | |||||||
| chr4:98924847 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.18+4248C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924847 | |||||||
| chr4:98924955 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.18+4140C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924955 | |||||||
| chr4:98924964 | C | T | 43 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(40): Show |
60 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.18+4131G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924964 | |||||||
| chr4:98924965 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4130C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924965 | |||||||
| chr4:98924981 | G | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+4114C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924981 | |||||||
| chr4:98925023 | T | G | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+4072A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925023 | |||||||
| chr4:98925169 | A | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3926T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925169 | |||||||
| chr4:98925326 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.18+3769A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925326 | |||||||
| chr4:98925420 | G | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG01070.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3675C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925420 | |||||||
| chr4:98925527 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+3568T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925527 | |||||||
| chr4:98925543 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+3552G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925543 | |||||||
| chr4:98925618 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0106 |
4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+3477T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925618 | |||||||
| chr4:98925679 | A | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+3416T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925679 | |||||||
| chr4:98925793 | T | C | 3 | a0001c0002t0003g0079 a0001c0002t0003g0084 a0001c0002t0003g0085 |
3 | HG01081.hp1 HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.18+3302A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925793 | |||||||
| chr4:98925811 | G | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+3284C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925811 | |||||||
| chr4:98925921 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+3174A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925921 | |||||||
| chr4:98925922 | TGA | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+3171_18+3172del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925922 | |||||||
| chr4:98926011 | T | TAAAAATT others(321): Show |
1 | a0001c0001t0001g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+3083_18+3084ins others(328): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926011 | |||||||
| chr4:98926089 | C | G | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+3006G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926089 | |||||||
| chr4:98926110 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.18+2985C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926110 | |||||||
| chr4:98926172 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+2923G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926172 | |||||||
| chr4:98926630 | A | C | 8 | a0001c0001t0004g0167 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+2465T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926630 | |||||||
| chr4:98926690 | A | G | 1 | a0001c0002t0003g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.18+2405T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926690 | |||||||
| chr4:98926725 | C | T | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(23): Show |
26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+2370G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926725 | |||||||
| chr4:98926801 | G | A | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+2294C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926801 | |||||||
| chr4:98926955 | C | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+2140G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926955 | |||||||
| chr4:98927163 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+1932A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927163 | |||||||
| chr4:98927288 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18+1807C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927288 | |||||||
| chr4:98927327 | G | A | 4 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0001t0004g0181 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+1768C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927327 | |||||||
| chr4:98927472 | ATGG | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(60): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+1620_18+1622del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927472 | |||||||
| chr4:98927528 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+1567G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927528 | |||||||
| chr4:98927550 | A | G | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.18+1545T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927550 | |||||||
| chr4:98927600 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.18+1495T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927600 | |||||||
| chr4:98927654 | C | CA | 30 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0231 others(27): Show |
30 | HG00438.hp2 HG01168.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+1440dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | C | CAA | 13 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(10): Show |
13 | HG00423.hp2 HG00735.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+1439_18+1440dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAA | C | 6 | a0001c0002t0003g0080 a0001c0002t0003g0083 a0001c0002t0003g0084 others(3): Show |
6 | HG00733.hp2 HG01358.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+1438_18+1440del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAA | C | 18 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(15): Show |
18 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.18+1437_18+1440del others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAA | C | 17 | a0001c0001t0001g0071 a0001c0001t0001g0168 a0001c0001t0001g0169 others(14): Show |
17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+1436_18+1440del others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAAA | C | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(22): Show |
25 | HG01346.hp2 HG02074.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+1435_18+1440del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAAAA | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
123 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+1434_18+1440del others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01074.hp1 HG01261.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+1433_18+1440del others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG01081.hp2 HG01123.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+1429_18+1440del others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927654 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0005g0193 others(1): Show |
4 | HG01943.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+1428_18+1440del others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | |||||||
| chr4:98927836 | C | A | 6 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(3): Show |
6 | HG00423.hp2 HG02129.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+1259G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927836 | |||||||
| chr4:98928143 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG04115.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.18+952A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928143 | |||||||
| chr4:98928519 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+576G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928519 | |||||||
| chr4:98928520 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+575C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928520 | |||||||
| chr4:98928532 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+563C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928532 | |||||||
| chr4:98928533 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+562G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928533 | |||||||
| chr4:98928612 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+483C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928612 | |||||||
| chr4:98928640 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+455C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928640 | |||||||
| chr4:98928671 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+424C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928671 | |||||||
| chr4:98928673 | T | A | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+422A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928673 | |||||||
| chr4:98928676 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+419G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928676 | |||||||
| chr4:98928680 | T | A | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+415A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928680 | |||||||
| chr4:98928684 | T | A | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+411A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928684 | |||||||
| chr4:98928694 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+401C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928694 | |||||||
| chr4:98928703 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+392C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928703 | |||||||
| chr4:98928713 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+382G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928713 | |||||||
| chr4:98928719 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+376C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928719 | |||||||
| chr4:98928721 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+374C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928721 | |||||||
| chr4:98928773 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+322G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928773 | |||||||
| chr4:98928779 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
103 | HG00558.hp2 HG00733.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.18+316A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928779 | |||||||
| chr4:98928975 | A | G | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.18+120T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928975 |