Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56478 |
| ensemblid | ENSG00000184708.18 |
| hgncid | 16687 |
| symbol | EIF4ENIF1 |
| name | eukaryotic translation initiation factor 4E nuclear import factor 1 |
| refseq_nuc | NM_019843.4 |
| refseq_prot | NP_062817.2 |
| ensembl_nuc | ENST00000330125.10 |
| ensembl_prot | ENSP00000328103.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 31439367 |
| end | 31489842 |
| strand | - |
| ver | v1.2 |
| region | chr22:31439367-31489842 |
| region5000 | chr22:31434367-31494842 |
| regionname0 | EIF4ENIF1_chr22_31439367_31489842 |
| regionname5000 | EIF4ENIF1_chr22_31434367_31494842 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 985 | 361 | 78 | 70 | 160 | 14 | 37 | 129 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| a0002 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| a0003 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| a0004 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| a0005 | 0/0 | 985 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| a0006 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | MDRRS others(980): Show |
chr22 | 31434367 | 31494842 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2955 | 212 | 39 | 54 | 98 | 9 | 11 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0002 | 0/1 | 2955 | 68 | 2 | 2 | 53 | 1 | 9 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0003 | 0/0 | 2955 | 60 | 24 | 14 | 3 | 4 | 15 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0004 | 0/0 | 2955 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0005 | 0/0 | 2955 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0006 | 0/0 | 2955 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0007 | 0/0 | 2955 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0010 | 0/0 | 2955 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0013 | 0/0 | 2955 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0001c0014 | 0/0 | 2955 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0002c0015 | 0/0 | 2955 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0003c0009 | 0/0 | 2955 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0004c0011 | 0/0 | 2955 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0005c0008 | 0/0 | 2955 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 | ||
| a0006c0012 | 0/0 | 2955 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | ATGGA others(2950): Show |
chr22 | 31434367 | 31494842 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3647 | 190 | 36 | 50 | 86 | 6 | 11 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0001t0002 | 0/0 | 3647 | 18 | 3 | 3 | 12 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0001t0003 | 0/0 | 3647 | 3 | 0 | 1 | 0 | 2 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0001t0005 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0002t0001 | 0/1 | 3647 | 68 | 2 | 2 | 53 | 1 | 9 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0003t0001 | 0/0 | 3647 | 58 | 23 | 13 | 3 | 4 | 15 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0003t0004 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0003t0006 | 0/0 | 3647 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0004t0001 | 0/0 | 3647 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0005t0001 | 0/0 | 3647 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0006t0001 | 0/0 | 3647 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0007t0001 | 0/0 | 3647 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0010t0001 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0013t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0001c0014t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0002c0015t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0003c0009t0001 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0004c0011t0001 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0005c0008t0001 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| a0006c0012t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | AGTTA others(3642): Show |
chr22 | 31434367 | 31494842 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0006g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0007t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0013t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0014t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0002c0015t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0003c0009t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0004c0011t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0005c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0006c0012t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0230 | EUR | GBR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0290 | EUR | GBR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0236 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0293 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0291 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0335 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0326 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0315 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0283 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0332 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0140 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0286 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01358 | hp2 | a0001 | c0003 | t0006 | g0357 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0289 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0287 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0355 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0308 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02027 | hp1 | a0002 | c0015 | t0001 | g0350 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0313 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0322 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02572 | hp1 | a0003 | c0009 | t0001 | g0147 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0328 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0314 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0330 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0340 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0149 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0285 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0343 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0344 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0316 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0273 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0319 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0356 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03130 | hp2 | a0004 | c0011 | t0001 | g0260 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0321 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0209 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0333 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0267 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0345 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0148 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0342 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0317 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0331 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0336 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0327 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03831 | hp2 | a0005 | c0008 | t0001 | g0102 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0347 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0349 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03927 | hp2 | a0001 | c0010 | t0001 | g0082 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0288 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0318 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04204 | hp2 | a0001 | c0007 | t0001 | g0113 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | CHB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18949 | hp1 | a0001 | c0006 | t0001 | g0201 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18954 | hp2 | a0001 | c0014 | t0001 | g0118 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0339 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18988 | hp1 | a0001 | c0006 | t0001 | g0227 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18992 | hp1 | a0001 | c0006 | t0001 | g0143 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18995 | hp2 | a0006 | c0012 | t0001 | g0039 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0294 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19057 | hp2 | a0001 | c0006 | t0001 | g0176 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19084 | hp1 | a0001 | c0013 | t0001 | g0164 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0116 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0298 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0325 | EUR | TSI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0240 | EUR | TSI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0115 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0320 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0338 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0112 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0307 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0297 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0008 | REF | REF | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0106 | REF | REF | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31441992 | G | A | 1 | a0006 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.2333C>T | p.Thr778Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/19 | 2509/3647 | 2333/2958 | 778/985 | chr22 | 31441992 | |||
| chr22:31447561 | C | T | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1853G>A | p.Ser618Asn | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/19 | 2029/3647 | 1853/2958 | 618/985 | chr22 | 31447561 | |||
| chr22:31454251 | C | T | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1405G>A | p.Val469Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/19 | 1581/3647 | 1405/2958 | 469/985 | chr22 | 31454251 | |||
| chr22:31471917 | C | T | 1 | a0005 | 1 | HG03831.hp2 | missense_variant&splice_region_variant | MODERATE | c.97G>A | p.Glu33Lys | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/19 | 273/3647 | 97/2958 | 33/985 | chr22 | 31471917 | |||
| chr22:31488654 | G | A | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.65C>T | p.Pro22Leu | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/19 | 241/3647 | 65/2958 | 22/985 | chr22 | 31488654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31440813 | G | A | 1 | a0001c0007 | 2 | HG02965.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.2607C>T | p.Ile869Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/19 | 2783/3647 | 2607/2958 | 869/985 | chr22 | 31440813 | |||
| chr22:31442099 | G | A | 2 | a0001c0003 a0002c0015 |
61 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(58): Show |
synonymous_variant | LOW | c.2226C>T | p.Ser742Ser | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/19 | 2402/3647 | 2226/2958 | 742/985 | chr22 | 31442099 | |||
| chr22:31447503 | A | C | 1 | a0001c0006 | 4 | NA18949.hp1 NA18988.hp1 NA18992.hp1 others(1): Show |
synonymous_variant | LOW | c.1911T>G | p.Ala637Ala | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/19 | 2087/3647 | 1911/2958 | 637/985 | chr22 | 31447503 | |||
| chr22:31454252 | G | A | 1 | a0001c0004 | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
synonymous_variant | LOW | c.1404C>T | p.Ala468Ala | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/19 | 1580/3647 | 1404/2958 | 468/985 | chr22 | 31454252 | |||
| chr22:31455260 | A | C | 2 | a0001c0005 a0003c0009 |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.1155T>G | p.Pro385Pro | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/19 | 1331/3647 | 1155/2958 | 385/985 | chr22 | 31455260 | |||
| chr22:31463798 | G | T | 3 | a0001c0005 a0001c0010 a0003c0009 |
6 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
synonymous_variant | LOW | c.468C>A | p.Gly156Gly | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 644/3647 | 468/2958 | 156/985 | chr22 | 31463798 | |||
| chr22:31463873 | A | G | 2 | a0001c0002 a0001c0014 |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
synonymous_variant | LOW | c.393T>C | p.Val131Val | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 569/3647 | 393/2958 | 131/985 | chr22 | 31463873 | |||
| chr22:31463894 | G | A | 1 | a0001c0013 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.372C>T | p.Gly124Gly | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 548/3647 | 372/2958 | 124/985 | chr22 | 31463894 | |||
| chr22:31488647 | G | C | 1 | a0001c0014 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.72C>G | p.Ser24Ser | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/19 | 248/3647 | 72/2958 | 24/985 | chr22 | 31488647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31439520 | T | C | 1 | a0001c0003t0004 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 360 | chr22 | 31439520 | ||||||
| chr22:31439692 | T | G | 1 | a0001c0001t0005 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 188 | chr22 | 31439692 | ||||||
| chr22:31439732 | T | C | 1 | a0001c0001t0003 | 3 | HG00140.hp1 HG00639.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 148 | chr22 | 31439732 | ||||||
| chr22:31439745 | A | G | 1 | a0001c0001t0002 | 18 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*135T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 135 | chr22 | 31439745 | ||||||
| chr22:31489708 | G | A | 1 | a0001c0003t0006 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/19 | 990 | chr22 | 31489708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31440265 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2717-144T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440265 | |||||||
| chr22:31440392 | G | T | 335 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(332): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.2717-271C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440392 | |||||||
| chr22:31440460 | C | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716+244G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440460 | |||||||
| chr22:31440500 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(117): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2716+204A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440500 | |||||||
| chr22:31440612 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2716+92T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440612 | |||||||
| chr22:31441147 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0175 |
2 | HG02132.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2552-279G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441147 | |||||||
| chr22:31441148 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2552-280C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441148 | |||||||
| chr22:31441208 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2552-340C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441208 | |||||||
| chr22:31441240 | G | A | 2 | a0001c0002t0001g0071 a0001c0002t0001g0090 |
2 | HG02056.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2552-372C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441240 | |||||||
| chr22:31441294 | T | C | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2552-426A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441294 | |||||||
| chr22:31441341 | C | T | 13 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(10): Show |
13 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2551+433G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441341 | |||||||
| chr22:31441406 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2551+368C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441406 | |||||||
| chr22:31441467 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2551+307C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441467 | |||||||
| chr22:31441473 | G | C | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2551+301C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441473 | |||||||
| chr22:31441514 | A | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0053 a0001c0002t0001g0065 |
3 | HG00544.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2551+260T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441514 | |||||||
| chr22:31441550 | G | GA | 97 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0036 others(94): Show |
98 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.2551+223dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAA | 12 | a0001c0001t0001g0208 a0001c0001t0001g0299 a0001c0001t0001g0312 others(9): Show |
12 | HG02083.hp1 HG02145.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2551+222_2551+223d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAA | 8 | a0001c0001t0002g0263 a0001c0001t0002g0266 a0001c0001t0002g0270 others(5): Show |
8 | HG00408.hp2 HG01934.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.2551+219_2551+223d others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAA | 6 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0272 others(3): Show |
6 | HG00609.hp1 HG01346.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2551+218_2551+223d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(6): Show |
1 | a0001c0001t0001g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2551+211_2551+223d others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(13): Show |
1 | a0001c0001t0002g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2551+204_2551+223d others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(14): Show |
1 | a0001c0001t0002g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2551+203_2551+223d others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(15): Show |
1 | a0001c0001t0001g0120 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2551+202_2551+223d others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(17): Show |
1 | a0001c0001t0002g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2551+223_2551+224i others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | G | GAAAAAAA others(23): Show |
1 | a0001c0001t0001g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2551+223_2551+224i others(32): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441550 | GA | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0207 a0001c0001t0001g0211 others(7): Show |
12 | HG00323.hp1 HG02109.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2551+223delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | |||||||
| chr22:31441551 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2551+223T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441551 | |||||||
| chr22:31441572 | AAG | A | 8 | a0001c0003t0001g0307 a0001c0003t0001g0319 a0001c0003t0001g0323 others(5): Show |
8 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2551+200_2551+201d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441572 | |||||||
| chr22:31442265 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2207-147G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442265 | |||||||
| chr22:31442480 | T | C | 1 | a0001c0002t0001g0020 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2207-362A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442480 | |||||||
| chr22:31442483 | G | A | 23 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(20): Show |
23 | HG00408.hp2 HG00609.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.2207-365C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442483 | |||||||
| chr22:31442532 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(117): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2207-414G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442532 | |||||||
| chr22:31442597 | T | G | 1 | a0001c0005t0001g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2206+365A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442597 | |||||||
| chr22:31442695 | A | T | 1 | a0001c0002t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2206+267T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442695 | |||||||
| chr22:31442778 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2206+184A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442778 | |||||||
| chr22:31442831 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2206+131C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442831 | |||||||
| chr22:31442896 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2206+66G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442896 | |||||||
| chr22:31443165 | T | C | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2074-71A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443165 | |||||||
| chr22:31443205 | T | C | 1 | a0001c0007t0001g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2074-111A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443205 | |||||||
| chr22:31443258 | G | A | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2074-164C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443258 | |||||||
| chr22:31443314 | G | A | 1 | a0001c0003t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2074-220C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443314 | |||||||
| chr22:31443419 | T | TCTGCAAA others(2): Show |
24 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2074-326_2074-325i others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443419 | |||||||
| chr22:31443419 | T | TCTGCGAA others(2): Show |
311 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(308): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2074-326_2074-325i others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443419 | |||||||
| chr22:31443474 | C | T | 2 | a0001c0007t0001g0113 a0001c0007t0001g0356 |
2 | HG02965.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2074-380G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443474 | |||||||
| chr22:31443654 | T | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0207 others(5): Show |
8 | HG02148.hp1 NA18947.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2074-560A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443654 | |||||||
| chr22:31443742 | AT | A | 7 | a0001c0001t0001g0134 a0001c0001t0002g0275 a0001c0005t0001g0145 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2074-649delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443742 | |||||||
| chr22:31443806 | C | CT | 182 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(179): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.2074-713dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443806 | |||||||
| chr22:31443806 | CT | C | 8 | a0001c0001t0001g0059 a0001c0001t0002g0272 a0001c0004t0001g0001 others(5): Show |
10 | HG00609.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2074-713delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443806 | |||||||
| chr22:31443964 | T | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(73): Show |
79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.2073+642A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443964 | |||||||
| chr22:31444049 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2073+557G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444049 | |||||||
| chr22:31444109 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0208 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2073+497A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444109 | |||||||
| chr22:31444393 | A | G | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2073+213T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444393 | |||||||
| chr22:31444488 | G | C | 21 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(18): Show |
21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.2073+118C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444488 | |||||||
| chr22:31444707 | TATC | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1989-20_1989-18del others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444707 | |||||||
| chr22:31444762 | A | C | 1 | a0001c0002t0001g0020 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1989-72T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444762 | |||||||
| chr22:31444834 | T | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1989-144A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444834 | |||||||
| chr22:31445054 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0142 others(23): Show |
28 | HG00408.hp1 HG00423.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1989-364A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445054 | |||||||
| chr22:31445063 | A | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989-373T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445063 | |||||||
| chr22:31445105 | A | G | 68 | a0001c0001t0001g0282 a0001c0002t0001g0004 a0001c0002t0001g0007 others(65): Show |
69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1989-415T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445105 | |||||||
| chr22:31445301 | GAATC | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(112): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1989-615_1989-612d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445301 | |||||||
| chr22:31445763 | T | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(148): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1989-1073A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445763 | |||||||
| chr22:31445839 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1989-1149A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445839 | |||||||
| chr22:31445953 | G | GC | 81 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1989-1264dupG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | |||||||
| chr22:31445953 | G | GCC | 41 | a0001c0001t0001g0119 a0001c0001t0001g0139 a0001c0001t0001g0173 others(38): Show |
41 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1989-1265_1989-126 others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | |||||||
| chr22:31445953 | G | GCCC | 48 | a0001c0001t0001g0282 a0001c0001t0002g0265 a0001c0001t0002g0266 others(45): Show |
49 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1989-1266_1989-126 others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | |||||||
| chr22:31445963 | C | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1989-1273G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445963 | |||||||
| chr22:31446027 | T | G | 6 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989-1337A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446027 | |||||||
| chr22:31446104 | C | T | 60 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(57): Show |
63 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1988+1322G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446104 | |||||||
| chr22:31446137 | T | A | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1988+1289A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446137 | |||||||
| chr22:31446144 | G | C | 1 | a0001c0014t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1988+1282C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446144 | |||||||
| chr22:31446174 | A | C | 1 | a0001c0002t0001g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1988+1252T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446174 | |||||||
| chr22:31446192 | T | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1988+1234A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446192 | |||||||
| chr22:31446251 | C | T | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1988+1175G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446251 | |||||||
| chr22:31446285 | C | CAAAAAA | 6 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0203 others(3): Show |
6 | HG00323.hp1 HG01070.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1988+1135_1988+114 others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446285 | C | CAAAAAAA | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(212): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1988+1134_1988+114 others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446285 | C | CAAAAAAA others(1): Show |
55 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
55 | HG00408.hp2 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1988+1133_1988+114 others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446285 | C | CAAAAAAA others(2): Show |
57 | a0001c0001t0001g0013 a0001c0001t0001g0262 a0001c0002t0001g0004 others(54): Show |
58 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1988+1132_1988+114 others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446285 | C | CAAAAAAA others(3): Show |
5 | a0001c0002t0001g0027 a0001c0002t0001g0048 a0001c0002t0001g0084 others(2): Show |
5 | HG02083.hp1 HG03710.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+1131_1988+114 others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446285 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1988+1130_1988+114 others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | |||||||
| chr22:31446417 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1988+1009C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446417 | |||||||
| chr22:31446568 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1988+858G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446568 | |||||||
| chr22:31447060 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1988+366C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31447060 | |||||||
| chr22:31447392 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1988+34C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31447392 | |||||||
| chr22:31447581 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1849-16C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 13/18 | chr22 | 31447581 | |||||||
| chr22:31447947 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+206T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 13/18 | chr22 | 31447947 | |||||||
| chr22:31448237 | C | T | 2 | a0001c0003t0001g0025 a0001c0003t0001g0314 |
2 | HG02602.hp2 HG03239.hp2 |
splice_region_variant&intron_variant | LOW | c.1769-5G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448237 | |||||||
| chr22:31448256 | G | A | 1 | a0001c0003t0001g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1769-24C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448256 | |||||||
| chr22:31448284 | G | A | 3 | a0001c0002t0001g0004 a0001c0002t0001g0033 a0001c0002t0001g0084 |
4 | HG00280.hp2 HG01106.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769-52C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448284 | |||||||
| chr22:31448307 | A | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(305): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1769-75T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448307 | |||||||
| chr22:31448387 | A | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(73): Show |
79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1769-155T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448387 | |||||||
| chr22:31448776 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1769-544A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448776 | |||||||
| chr22:31448838 | A | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1768+510T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448838 | |||||||
| chr22:31448860 | CT | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1768+487delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448860 | |||||||
| chr22:31449158 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1768+190C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449158 | |||||||
| chr22:31449163 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1768+185T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449163 | |||||||
| chr22:31449167 | C | T | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768+181G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449167 | |||||||
| chr22:31449734 | C | CT | 84 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(81): Show |
88 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1585-204dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449734 | |||||||
| chr22:31449756 | A | T | 1 | a0001c0002t0001g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1585-225T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449756 | |||||||
| chr22:31449815 | C | T | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585-284G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449815 | |||||||
| chr22:31449834 | G | A | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1585-303C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449834 | |||||||
| chr22:31450093 | C | CT | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(72): Show |
78 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.1584+195dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31450093 | |||||||
| chr22:31450120 | C | T | 1 | a0001c0003t0001g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1584+169G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31450120 | |||||||
| chr22:31450463 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0133 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1513-103A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450463 | |||||||
| chr22:31450469 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01243.hp1 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1513-109T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450469 | |||||||
| chr22:31450719 | G | GAC | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1513-361_1513-360d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | |||||||
| chr22:31450719 | GAC | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(202): Show |
210 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1513-361_1513-360d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | |||||||
| chr22:31450719 | GACAC | G | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1513-363_1513-360d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | |||||||
| chr22:31450723 | C | G | 2 | a0001c0003t0001g0125 a0001c0003t0001g0292 |
2 | HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1513-363G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450723 | |||||||
| chr22:31450740 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1513-380T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450740 | |||||||
| chr22:31450740 | ACT | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1513-382_1513-381d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450740 | |||||||
| chr22:31450753 | CACATACA others(5): Show |
C | 1 | a0001c0003t0001g0330 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1513-405_1513-394d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450753 | |||||||
| chr22:31450757 | TACATATA others(19): Show |
T | 1 | a0001c0002t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1513-423_1513-398d others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450757 | |||||||
| chr22:31450763 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1513-403A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450763 | |||||||
| chr22:31450797 | TACATAC | T | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1513-443_1513-438d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450797 | |||||||
| chr22:31450801 | TACACATA others(7): Show |
T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0007t0001g0113 |
3 | HG01934.hp2 HG02293.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1513-455_1513-442d others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450801 | |||||||
| chr22:31450831 | CAT | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(73): Show |
79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1513-473_1513-472d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450831 | |||||||
| chr22:31450833 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-473A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450833 | |||||||
| chr22:31450842 | AC | A | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-483delG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450842 | |||||||
| chr22:31450844 | T | TAC | 49 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0097 others(46): Show |
51 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1513-486_1513-485d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACAC | 37 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0092 others(34): Show |
38 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1513-488_1513-485d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACAC | 21 | a0001c0001t0001g0034 a0001c0001t0001g0091 a0001c0001t0001g0093 others(18): Show |
21 | HG00423.hp1 HG00741.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1513-490_1513-485d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACACA others(1): Show |
36 | a0001c0001t0001g0011 a0001c0001t0001g0054 a0001c0001t0001g0094 others(33): Show |
36 | HG00423.hp2 HG00735.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1513-492_1513-485d others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACACA others(3): Show |
17 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0132 others(14): Show |
17 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1513-494_1513-485d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0142 a0001c0001t0001g0195 others(1): Show |
4 | HG01169.hp2 HG01978.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-496_1513-485d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1513-498_1513-485d others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | T | TACACACA others(9): Show |
3 | a0001c0001t0001g0183 a0001c0001t0001g0224 a0001c0001t0002g0264 |
3 | NA18949.hp2 NA18955.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1513-500_1513-485d others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TAC | T | 24 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0310 others(21): Show |
25 | HG00544.hp1 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1513-486_1513-485d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACAC | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0126 others(20): Show |
23 | HG00673.hp1 HG01081.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1513-488_1513-485d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACAC | T | 18 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0152 others(15): Show |
18 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1513-490_1513-485d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(1): Show |
T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0150 others(34): Show |
40 | HG00280.hp2 HG00673.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1513-492_1513-485d others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(3): Show |
T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0044 a0001c0004t0001g0112 |
3 | HG02071.hp2 HG03471.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1513-494_1513-485d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513-496_1513-485d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0059 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1513-500_1513-485d others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(11): Show |
T | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1513-502_1513-485d others(20): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1513-506_1513-485d others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450844 | TACACACA others(17): Show |
T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-508_1513-485d others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | |||||||
| chr22:31450846 | CACACACA others(2): Show |
C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02717.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-495_1513-487d others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450846 | |||||||
| chr22:31450846 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-497_1513-487d others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450846 | |||||||
| chr22:31450852 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0346 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1513-492G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450852 | |||||||
| chr22:31450854 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0256 |
2 | HG00738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1513-494G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450854 | |||||||
| chr22:31450856 | C | T | 4 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02717.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-496G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450856 | |||||||
| chr22:31450858 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-498G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450858 | |||||||
| chr22:31450864 | C | G | 1 | a0001c0002t0001g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1513-504G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450864 | |||||||
| chr22:31450884 | CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0007t0001g0113 |
3 | HG02109.hp2 HG02630.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1513-536_1513-525d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450884 | |||||||
| chr22:31450886 | CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0120 a0001c0007t0001g0356 |
2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1513-536_1513-527d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450886 | |||||||
| chr22:31450895 | A | ACACAC | 3 | a0001c0001t0001g0225 a0001c0001t0001g0241 a0001c0003t0001g0338 |
3 | HG00735.hp2 HG02135.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1513-536_1513-535i others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450895 | |||||||
| chr22:31450896 | A | C | 22 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0222 others(19): Show |
22 | HG00408.hp2 HG00609.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1513-536T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450896 | |||||||
| chr22:31450898 | A | C | 4 | a0001c0001t0002g0263 a0001c0001t0002g0270 a0001c0001t0002g0281 others(1): Show |
4 | HG01346.hp1 HG02895.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1513-538T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450898 | |||||||
| chr22:31451083 | G | A | 3 | a0001c0003t0001g0125 a0001c0003t0001g0291 a0001c0003t0001g0292 |
3 | HG00741.hp1 HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1513-723C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451083 | |||||||
| chr22:31451275 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1513-915A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451275 | |||||||
| chr22:31451337 | G | C | 2 | a0001c0003t0001g0326 a0001c0003t0001g0335 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1513-977C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451337 | |||||||
| chr22:31451383 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1513-1023G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451383 | |||||||
| chr22:31451440 | AT | A | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0248 others(3): Show |
6 | HG01169.hp1 HG02055.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1513-1081delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451440 | |||||||
| chr22:31451569 | C | T | 1 | a0001c0003t0001g0345 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1513-1209G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451569 | |||||||
| chr22:31451661 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1513-1301A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451661 | |||||||
| chr22:31451664 | C | CT | 9 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0001g0190 others(6): Show |
9 | HG02145.hp2 HG02965.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-1305dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451664 | |||||||
| chr22:31451664 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1513-1304G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451664 | |||||||
| chr22:31451665 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-1305A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451665 | |||||||
| chr22:31451864 | C | G | 67 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0014 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1513-1504G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451864 | |||||||
| chr22:31451926 | A | C | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-1566T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451926 | |||||||
| chr22:31452077 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1513-1717C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452077 | |||||||
| chr22:31452165 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-1805A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452165 | |||||||
| chr22:31452231 | T | G | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1513-1871A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452231 | |||||||
| chr22:31452385 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1512+1759T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452385 | |||||||
| chr22:31452578 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0139 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1512+1566G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452578 | |||||||
| chr22:31452639 | C | G | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1512+1505G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452639 | |||||||
| chr22:31452739 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+1405C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452739 | |||||||
| chr22:31452805 | G | T | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1339C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452805 | |||||||
| chr22:31452806 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+1338C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452806 | |||||||
| chr22:31452958 | A | G | 67 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0014 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1512+1186T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452958 | |||||||
| chr22:31453036 | G | GA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1512+1107dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453036 | |||||||
| chr22:31453044 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1100C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453044 | |||||||
| chr22:31453045 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1099T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453045 | |||||||
| chr22:31453165 | T | C | 1 | a0001c0003t0001g0267 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1512+979A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453165 | |||||||
| chr22:31453278 | CCTAACTT others(4): Show |
C | 1 | a0001c0003t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1512+855_1512+865d others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453278 | |||||||
| chr22:31453291 | C | A | 1 | a0001c0003t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1512+853G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453291 | |||||||
| chr22:31453376 | C | CT | 7 | a0001c0001t0001g0054 a0001c0001t0001g0173 a0001c0001t0001g0190 others(4): Show |
7 | HG02040.hp2 HG03209.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512+767dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453376 | |||||||
| chr22:31453444 | G | A | 1 | a0001c0002t0001g0018 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1512+700C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453444 | |||||||
| chr22:31453489 | C | T | 3 | a0001c0003t0001g0003 a0001c0003t0001g0297 a0001c0003t0001g0298 |
5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1512+655G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453489 | |||||||
| chr22:31453557 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1512+587C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453557 | |||||||
| chr22:31453652 | C | T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(17): Show |
20 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1512+492G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453652 | |||||||
| chr22:31453984 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1512+160T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453984 | |||||||
| chr22:31454078 | T | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+66A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31454078 | |||||||
| chr22:31454137 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02717.hp1 | splice_region_variant&intron_variant | LOW | c.1512+7A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31454137 | |||||||
| chr22:31454447 | T | G | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-71A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454447 | |||||||
| chr22:31454621 | A | G | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-245T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454621 | |||||||
| chr22:31454673 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0124 a0001c0001t0001g0138 |
3 | HG01496.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1280-297A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454673 | |||||||
| chr22:31454727 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-351T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454727 | |||||||
| chr22:31454731 | T | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-355A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454731 | |||||||
| chr22:31454745 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1280-369C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454745 | |||||||
| chr22:31454775 | G | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+361C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454775 | |||||||
| chr22:31454784 | T | C | 1 | a0001c0003t0001g0336 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1279+352A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454784 | |||||||
| chr22:31454832 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1279+304C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454832 | |||||||
| chr22:31454905 | A | AC | 114 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(111): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1279+230dupG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454905 | |||||||
| chr22:31455076 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0002g0281 a0001c0001t0002g0337 |
3 | HG01346.hp1 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1279+60G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31455076 | |||||||
| chr22:31455362 | G | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1100-47C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455362 | |||||||
| chr22:31455382 | T | A | 3 | a0001c0003t0001g0267 a0001c0003t0001g0294 a0001c0003t0006g0357 |
3 | HG01358.hp2 HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1100-67A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455382 | |||||||
| chr22:31455395 | CT | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0091 others(54): Show |
59 | HG00408.hp1 HG00423.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1100-81delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455395 | |||||||
| chr22:31455399 | T | C | 5 | a0001c0003t0001g0328 a0001c0005t0001g0145 a0001c0005t0001g0146 others(2): Show |
5 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-84A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455399 | |||||||
| chr22:31455400 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0188 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1100-85A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455400 | |||||||
| chr22:31455467 | C | T | 68 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(65): Show |
71 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1100-152G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455467 | |||||||
| chr22:31455502 | G | A | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1100-187C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455502 | |||||||
| chr22:31455608 | C | A | 9 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099+244G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455608 | |||||||
| chr22:31456091 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-104G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456091 | |||||||
| chr22:31456223 | C | CT | 18 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(15): Show |
18 | HG00609.hp1 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.964-237dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456223 | |||||||
| chr22:31456223 | CT | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.964-237delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456223 | |||||||
| chr22:31456254 | C | T | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-267G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456254 | |||||||
| chr22:31456263 | A | G | 3 | a0001c0001t0001g0135 a0001c0006t0001g0143 a0001c0006t0001g0176 |
3 | HG02738.hp2 NA18992.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.964-276T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456263 | |||||||
| chr22:31456264 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964-277G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456264 | |||||||
| chr22:31456285 | A | G | 2 | a0001c0003t0001g0022 a0001c0003t0001g0331 |
2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964-298T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456285 | |||||||
| chr22:31456287 | G | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0331 |
2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964-300C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456287 | |||||||
| chr22:31456309 | C | T | 1 | a0001c0002t0001g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.964-322G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456309 | |||||||
| chr22:31456325 | A | G | 5 | a0001c0003t0001g0125 a0001c0003t0001g0285 a0001c0003t0001g0287 others(2): Show |
5 | HG00741.hp1 HG01361.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-338T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456325 | |||||||
| chr22:31456336 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.964-349C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456336 | |||||||
| chr22:31456368 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.964-381G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456368 | |||||||
| chr22:31456372 | T | C | 31 | a0001c0001t0001g0120 a0001c0001t0001g0128 a0001c0001t0001g0129 others(28): Show |
31 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.964-385A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456372 | |||||||
| chr22:31456373 | G | A | 1 | a0001c0002t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-386C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456373 | |||||||
| chr22:31456379 | A | G | 1 | a0001c0002t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.964-392T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456379 | |||||||
| chr22:31456380 | C | T | 24 | a0001c0001t0001g0231 a0001c0001t0002g0263 a0001c0001t0002g0264 others(21): Show |
26 | HG00408.hp2 HG00609.hp1 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.964-393G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456380 | |||||||
| chr22:31456381 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0064 |
2 | HG03654.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.964-394C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456381 | |||||||
| chr22:31456382 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-395G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456382 | |||||||
| chr22:31456421 | T | C | 193 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0034 others(190): Show |
199 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.964-434A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456421 | |||||||
| chr22:31456424 | C | T | 1 | a0001c0003t0001g0313 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.964-437G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456424 | |||||||
| chr22:31456425 | G | A | 3 | a0001c0001t0001g0010 a0001c0002t0001g0055 a0001c0002t0001g0056 |
3 | HG00609.hp2 HG02074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.964-438C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456425 | |||||||
| chr22:31456430 | A | G | 3 | a0001c0002t0001g0063 a0001c0003t0001g0286 a0001c0003t0001g0290 |
3 | HG00140.hp2 HG01257.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.964-443T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456430 | |||||||
| chr22:31456434 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964-447T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456434 | |||||||
| chr22:31456438 | T | G | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.964-451A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456438 | |||||||
| chr22:31456439 | G | C | 129 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
133 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(130): Show |
intron_variant | MODIFIER | c.964-452C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456439 | |||||||
| chr22:31456441 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(106): Show |
111 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.964-454A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456441 | |||||||
| chr22:31456444 | C | T | 2 | a0001c0001t0001g0210 a0006c0012t0001g0039 |
2 | NA18995.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.964-457G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456444 | |||||||
| chr22:31456445 | G | C | 7 | a0001c0001t0002g0268 a0001c0001t0002g0279 a0001c0002t0001g0004 others(4): Show |
8 | HG00280.hp2 HG01891.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-458C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456445 | |||||||
| chr22:31456458 | T | C | 3 | a0001c0002t0001g0024 a0001c0002t0001g0030 a0001c0002t0001g0042 |
3 | NA18948.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.964-471A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456458 | |||||||
| chr22:31456465 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0279 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.964-478G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456465 | |||||||
| chr22:31456500 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0054 others(120): Show |
127 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.964-513T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456500 | |||||||
| chr22:31456503 | A | G | 119 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0059 others(116): Show |
123 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.964-516T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456503 | |||||||
| chr22:31456512 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.964-525G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456512 | |||||||
| chr22:31456513 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0282 a0001c0001t0002g0270 others(1): Show |
5 | HG02965.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-526T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456513 | |||||||
| chr22:31456515 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0282 a0001c0002t0001g0062 |
4 | HG02965.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-528T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456515 | |||||||
| chr22:31456618 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-631C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456618 | |||||||
| chr22:31456649 | G | A | 331 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(328): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.964-662C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456649 | |||||||
| chr22:31456717 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.964-730T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456717 | |||||||
| chr22:31456718 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.964-731G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456718 | |||||||
| chr22:31456721 | T | C | 1 | a0001c0005t0001g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.964-734A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456721 | |||||||
| chr22:31457022 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.964-1035A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457022 | |||||||
| chr22:31457033 | T | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0134 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.964-1046A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457033 | |||||||
| chr22:31457104 | A | T | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-1117T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457104 | |||||||
| chr22:31457126 | T | G | 21 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(18): Show |
21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-1139A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457126 | |||||||
| chr22:31457239 | T | C | 67 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0014 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.963+1236A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457239 | |||||||
| chr22:31457291 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+1184C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457291 | |||||||
| chr22:31457385 | A | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(113): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.963+1090T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457385 | |||||||
| chr22:31457455 | C | G | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+1020G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457455 | |||||||
| chr22:31457498 | G | A | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+977C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457498 | |||||||
| chr22:31457532 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.963+943A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457532 | |||||||
| chr22:31457533 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.963+942G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457533 | |||||||
| chr22:31457836 | G | A | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.963+639C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457836 | |||||||
| chr22:31457867 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.963+608G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457867 | |||||||
| chr22:31457877 | A | G | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+598T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457877 | |||||||
| chr22:31457905 | A | G | 1 | a0001c0003t0001g0349 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.963+570T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457905 | |||||||
| chr22:31458223 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(162): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.963+252T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458223 | |||||||
| chr22:31458227 | C | CA | 72 | a0001c0001t0001g0093 a0001c0001t0001g0203 a0001c0001t0001g0261 others(69): Show |
73 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+247dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458227 | |||||||
| chr22:31458244 | C | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(131): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.963+231G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458244 | |||||||
| chr22:31458298 | C | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+177G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458298 | |||||||
| chr22:31458384 | A | G | 72 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(69): Show |
75 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.963+91T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458384 | |||||||
| chr22:31458412 | C | T | 1 | a0001c0003t0001g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.963+63G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458412 | |||||||
| chr22:31458448 | AT | A | 334 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(331): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+26delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458448 | |||||||
| chr22:31458860 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(218): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.788-210A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458860 | |||||||
| chr22:31458918 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-268C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458918 | |||||||
| chr22:31458925 | C | CT | 14 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(11): Show |
14 | HG00738.hp2 HG01993.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-276dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | |||||||
| chr22:31458925 | CT | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(143): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.788-276delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | |||||||
| chr22:31458925 | CTT | C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0244 a0001c0001t0001g0257 others(3): Show |
6 | HG00423.hp2 HG02055.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.788-277_788-276del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | |||||||
| chr22:31459031 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-381C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459031 | |||||||
| chr22:31459076 | C | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0331 |
2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.788-426G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459076 | |||||||
| chr22:31459252 | AT | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-603delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459252 | |||||||
| chr22:31459262 | T | A | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-612A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459262 | |||||||
| chr22:31459334 | T | C | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.788-684A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459334 | |||||||
| chr22:31459383 | A | G | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-733T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459383 | |||||||
| chr22:31459453 | G | C | 1 | a0001c0003t0001g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.788-803C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459453 | |||||||
| chr22:31459489 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(218): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.788-839A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459489 | |||||||
| chr22:31459501 | T | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.788-851A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459501 | |||||||
| chr22:31459577 | T | TG | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-928_788-927ins others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459577 | |||||||
| chr22:31459578 | A | G | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-928T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459578 | |||||||
| chr22:31459591 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.788-941A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459591 | |||||||
| chr22:31459603 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-953T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459603 | |||||||
| chr22:31459752 | A | ATGTTTTT others(3): Show |
309 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(306): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.788-1112_788-1103d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459752 | |||||||
| chr22:31459791 | A | G | 3 | a0001c0002t0001g0024 a0001c0002t0001g0030 a0001c0002t0001g0042 |
3 | NA18948.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.788-1141T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459791 | |||||||
| chr22:31459853 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-1203C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459853 | |||||||
| chr22:31459968 | T | C | 92 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.788-1318A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459968 | |||||||
| chr22:31460135 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-1485T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460135 | |||||||
| chr22:31460177 | G | C | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-1527C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460177 | |||||||
| chr22:31460275 | T | C | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-1625A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460275 | |||||||
| chr22:31460372 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.788-1722C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460372 | |||||||
| chr22:31460392 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-1742C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460392 | |||||||
| chr22:31460517 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.788-1867G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460517 | |||||||
| chr22:31460854 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.787+2078C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460854 | |||||||
| chr22:31460879 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.787+2053T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460879 | |||||||
| chr22:31460945 | A | AAAAC | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.787+1983_787+1986d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460945 | |||||||
| chr22:31461072 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.787+1860C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461072 | |||||||
| chr22:31461104 | A | G | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.787+1828T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461104 | |||||||
| chr22:31461108 | T | G | 1 | a0001c0002t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.787+1824A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461108 | |||||||
| chr22:31461323 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+1609A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461323 | |||||||
| chr22:31461448 | G | GT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0200 a0001c0001t0002g0264 others(3): Show |
6 | HG01106.hp1 HG01361.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+1483dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461448 | |||||||
| chr22:31461723 | G | A | 2 | a0001c0003t0001g0267 a0001c0003t0006g0357 |
2 | HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.787+1209C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461723 | |||||||
| chr22:31461744 | T | C | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.787+1188A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461744 | |||||||
| chr22:31461897 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0064 |
2 | NA18950.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.787+1035G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461897 | |||||||
| chr22:31461913 | T | C | 2 | a0001c0007t0001g0113 a0001c0007t0001g0356 |
2 | HG02965.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.787+1019A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461913 | |||||||
| chr22:31461935 | T | C | 1 | a0001c0005t0001g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.787+997A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461935 | |||||||
| chr22:31461948 | AC | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(112): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.787+983delG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461948 | |||||||
| chr22:31461963 | A | T | 1 | a0001c0002t0001g0018 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.787+969T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461963 | |||||||
| chr22:31462043 | C | T | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.787+889G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462043 | |||||||
| chr22:31462107 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0191 |
2 | NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.787+825T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462107 | |||||||
| chr22:31462206 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.787+726C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462206 | |||||||
| chr22:31462375 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787+557G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462375 | |||||||
| chr22:31462400 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.787+532C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462400 | |||||||
| chr22:31462484 | C | CA | 210 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(207): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.787+447dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462484 | |||||||
| chr22:31462484 | C | CAA | 17 | a0001c0001t0001g0121 a0001c0001t0001g0282 a0001c0001t0002g0264 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+446_787+447dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462484 | |||||||
| chr22:31462753 | T | A | 1 | a0001c0001t0002g0280 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.787+179A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462753 | |||||||
| chr22:31463149 | A | G | 2 | a0001c0002t0001g0087 a0001c0002t0001g0090 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.586-16T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463149 | |||||||
| chr22:31463160 | A | G | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.586-27T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463160 | |||||||
| chr22:31463195 | A | G | 4 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0293 others(1): Show |
4 | HG00323.hp2 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-62T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463195 | |||||||
| chr22:31463439 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585+242C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463439 | |||||||
| chr22:31463525 | A | G | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+156T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463525 | |||||||
| chr22:31463600 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.585+81G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463600 | |||||||
| chr22:31463651 | T | TA | 134 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0059 others(131): Show |
137 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.585+29dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463651 | |||||||
| chr22:31463651 | TA | T | 17 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG01070.hp1 HG01070.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.585+29delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463651 | |||||||
| chr22:31464186 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0133 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.299-219C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464186 | |||||||
| chr22:31464258 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.299-291G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464258 | |||||||
| chr22:31464292 | G | C | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-325C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464292 | |||||||
| chr22:31464336 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(113): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.299-369T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464336 | |||||||
| chr22:31464496 | GGTGAAAC others(1591): Show |
G | 2 | a0001c0003t0001g0318 a0001c0003t0001g0336 |
2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2081_299-530de others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464496 | |||||||
| chr22:31464555 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.299-588C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464555 | |||||||
| chr22:31464597 | G | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-630C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464597 | |||||||
| chr22:31464636 | G | A | 1 | a0001c0007t0001g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299-669C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464636 | |||||||
| chr22:31464650 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.299-683A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464650 | |||||||
| chr22:31464655 | A | G | 303 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(300): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.299-688T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464655 | |||||||
| chr22:31464675 | C | CA | 12 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG00408.hp2 HG01123.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-709dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAA | 8 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0002g0268 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-713_299-709dup others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAA | 21 | a0001c0001t0002g0269 a0001c0002t0001g0004 a0001c0002t0001g0015 others(18): Show |
22 | HG00280.hp2 HG00673.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-714_299-709dup others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAAA | 7 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0040 others(4): Show |
7 | HG01358.hp2 HG02074.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-715_299-709dup others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-718_299-709dup others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAAA others(4): Show |
2 | a0001c0003t0001g0328 a0001c0003t0004g0317 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.299-719_299-709dup others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAAA others(5): Show |
2 | a0001c0003t0001g0338 a0001c0003t0001g0340 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.299-720_299-709dup others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | C | CAAAAAAA others(6): Show |
1 | a0001c0003t0001g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-721_299-709dup others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0183 a0001c0001t0001g0187 others(6): Show |
9 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-718_299-709del others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0215 |
2 | NA18940.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.299-719_299-709del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | CAAAAAAA others(5): Show |
C | 46 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0036 others(43): Show |
46 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-720_299-709del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464675 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0196 |
2 | HG01515.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.299-721_299-709del others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | |||||||
| chr22:31464689 | A | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0234 |
2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-722T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | |||||||
| chr22:31464689 | AAAAAAAA others(5): Show |
A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0142 a0001c0001t0001g0144 others(30): Show |
33 | HG00408.hp1 HG00423.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.299-734_299-723del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | |||||||
| chr22:31464689 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0002 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.299-736_299-723del others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | |||||||
| chr22:31464690 | AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0165 others(4): Show |
7 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-736_299-724del others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464690 | |||||||
| chr22:31464691 | A | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0001g0234 |
3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-724T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464691 | |||||||
| chr22:31464691 | AAAAAAAA others(5): Show |
A | 12 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(9): Show |
12 | NA18953.hp2 NA18971.hp1 NA18972.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-736_299-725del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464691 | |||||||
| chr22:31464693 | A | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0001g0234 |
3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-726T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464693 | |||||||
| chr22:31464695 | A | ATATATAT others(6): Show |
1 | a0001c0003t0001g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.299-729_299-728ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464695 | |||||||
| chr22:31464695 | A | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0231 a0001c0001t0001g0234 |
3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-728T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464695 | |||||||
| chr22:31464697 | A | T | 12 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0220 others(9): Show |
12 | HG00544.hp2 HG00639.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-730T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464697 | |||||||
| chr22:31464699 | A | AAAAAAAA others(40): Show |
1 | a0001c0001t0001g0311 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(47): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(31): Show |
3 | a0001c0003t0001g0286 a0001c0003t0001g0290 a0001c0003t0001g0322 |
3 | HG00140.hp2 HG01257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(47): Show |
1 | a0001c0001t0001g0309 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(54): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(14): Show |
1 | a0001c0004t0001g0001 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(21): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(22): Show |
1 | a0006c0012t0001g0039 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0304 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(30): Show |
1 | a0002c0015t0001g0350 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(37): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(36): Show |
1 | a0001c0003t0001g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(43): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(9): Show |
1 | a0001c0004t0001g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(27): Show |
1 | a0001c0003t0001g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(34): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0299 a0001c0001t0001g0310 |
2 | NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(35): Show |
3 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0003t0001g0327 |
3 | HG03831.hp1 NA18989.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(42): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(15): Show |
2 | a0001c0003t0001g0251 a0001c0004t0001g0115 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0285 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0313 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0305 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(8): Show |
1 | a0001c0003t0001g0314 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(19): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(14): Show |
1 | a0001c0004t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(21): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0054 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(26): Show |
1 | a0001c0003t0001g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(33): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(28): Show |
2 | a0001c0003t0001g0052 a0001c0003t0001g0355 |
2 | HG01515.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(45): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(7): Show |
2 | a0001c0003t0001g0333 a0004c0011t0001g0260 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0059 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(25): Show |
1 | a0001c0003t0001g0291 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(32): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0348 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0329 a0001c0003t0001g0345 |
2 | HG03516.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(10): Show |
1 | a0001c0003t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0075 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(31): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(28): Show |
2 | a0001c0003t0001g0006 a0001c0003t0001g0331 |
2 | HG01081.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(30): Show |
1 | a0001c0003t0001g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(37): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0123 a0001c0004t0001g0001 |
2 | HG01516.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0003 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(21): Show |
1 | a0001c0003t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0060 a0001c0003t0001g0315 |
2 | HG01081.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(39): Show |
1 | a0001c0003t0001g0022 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(46): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(4): Show |
1 | a0001c0003t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(6): Show |
2 | a0001c0003t0001g0308 a0001c0003t0001g0332 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0122 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(27): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(24): Show |
1 | a0001c0003t0001g0293 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(31): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(28): Show |
1 | a0001c0003t0001g0289 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(5): Show |
3 | a0001c0003t0001g0307 a0001c0003t0001g0319 a0001c0003t0001g0323 |
3 | HG02895.hp2 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(7): Show |
1 | a0001c0003t0001g0342 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(11): Show |
1 | a0001c0004t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(20): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(17): Show |
1 | a0001c0003t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0330 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAA others(27): Show |
1 | a0001c0003t0001g0283 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(34): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAT | 7 | a0001c0001t0001g0120 a0001c0001t0001g0210 a0001c0002t0001g0021 others(4): Show |
7 | HG02074.hp1 HG06807.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-733_299-732ins others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAT others(4): Show |
1 | a0001c0002t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAT others(16): Show |
2 | a0001c0001t0001g0324 a0001c0003t0001g0298 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAT others(18): Show |
1 | a0001c0003t0001g0003 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(25): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAAT others(22): Show |
2 | a0001c0003t0001g0326 a0001c0003t0001g0335 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAAT | 6 | a0001c0001t0001g0152 a0001c0001t0001g0208 a0001c0002t0001g0047 others(3): Show |
6 | HG00609.hp2 HG02132.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-733_299-732ins others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAATA others(7): Show |
2 | a0001c0001t0001g0248 a0001c0001t0001g0250 |
2 | HG02717.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAAATA others(11): Show |
2 | a0001c0004t0001g0001 a0001c0004t0001g0117 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAATAT others(6): Show |
1 | a0001c0002t0001g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAAATAT others(12): Show |
1 | a0001c0002t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(19): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAAATATA others(15): Show |
2 | a0001c0003t0001g0006 a0001c0003t0001g0343 |
2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | AAATATAT others(10): Show |
1 | a0001c0003t0001g0292 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0256 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464699 | A | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0029 others(34): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-732T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | |||||||
| chr22:31464700 | AT | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0108 others(4): Show |
7 | HG01243.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-734delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464700 | |||||||
| chr22:31464701 | T | A | 49 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0104 others(46): Show |
49 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.299-734A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464701 | |||||||
| chr22:31464703 | T | A | 30 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(27): Show |
30 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.299-736A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464703 | |||||||
| chr22:31464703 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0189 |
2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.299-736A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464703 | |||||||
| chr22:31464705 | T | A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0124 a0001c0001t0001g0127 others(14): Show |
17 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-738A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464705 | |||||||
| chr22:31464707 | T | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.299-740A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464707 | |||||||
| chr22:31464713 | T | A | 1 | a0001c0001t0002g0278 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.299-746A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464713 | |||||||
| chr22:31464725 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299-758A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464725 | |||||||
| chr22:31464726 | A | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(236): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.299-759T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464726 | |||||||
| chr22:31464955 | C | T | 22 | a0001c0001t0001g0111 a0001c0001t0001g0124 a0001c0001t0001g0126 others(19): Show |
22 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-988G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464955 | |||||||
| chr22:31464997 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-1030A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464997 | |||||||
| chr22:31465075 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1108C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465075 | |||||||
| chr22:31465086 | G | C | 1 | a0001c0003t0001g0327 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-1119C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465086 | |||||||
| chr22:31465153 | G | A | 2 | a0001c0001t0001g0155 a0001c0002t0001g0037 |
2 | NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.299-1186C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465153 | |||||||
| chr22:31465217 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.299-1250C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465217 | |||||||
| chr22:31465224 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.299-1257C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465224 | |||||||
| chr22:31465323 | C | CA | 58 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0100 others(55): Show |
58 | HG00609.hp1 HG01106.hp2 HG01346.hp1 others(55): Show |
intron_variant | MODIFIER | c.299-1357dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465323 | |||||||
| chr22:31465341 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1374T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465341 | |||||||
| chr22:31465373 | G | T | 1 | a0001c0001t0002g0266 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.299-1406C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465373 | |||||||
| chr22:31465380 | C | T | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-1413G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465380 | |||||||
| chr22:31465407 | G | A | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1440C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465407 | |||||||
| chr22:31465532 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1565C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465532 | |||||||
| chr22:31465577 | C | T | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-1610G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465577 | |||||||
| chr22:31465860 | G | A | 67 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0014 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.299-1893C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465860 | |||||||
| chr22:31465964 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(228): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.299-1997T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465964 | |||||||
| chr22:31465966 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-1999T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465966 | |||||||
| chr22:31466058 | C | G | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-2091G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466058 | |||||||
| chr22:31466118 | A | C | 2 | a0001c0003t0001g0318 a0001c0003t0001g0336 |
2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2057T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466118 | |||||||
| chr22:31466129 | G | A | 2 | a0001c0003t0001g0318 a0001c0003t0001g0336 |
2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2046C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466129 | |||||||
| chr22:31466178 | T | C | 1 | a0001c0002t0001g0050 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.298+1997A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466178 | |||||||
| chr22:31466200 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.298+1975C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466200 | |||||||
| chr22:31466241 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+1934A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466241 | |||||||
| chr22:31466290 | A | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1885T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466290 | |||||||
| chr22:31466319 | G | A | 2 | a0001c0003t0001g0349 a0001c0010t0001g0082 |
2 | HG03927.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.298+1856C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466319 | |||||||
| chr22:31466351 | T | C | 4 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
4 | NA18612.hp2 NA18942.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1824A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466351 | |||||||
| chr22:31466368 | G | A | 3 | a0001c0003t0001g0319 a0001c0003t0001g0320 a0001c0003t0001g0323 |
3 | HG02486.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.298+1807C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466368 | |||||||
| chr22:31466415 | TG | T | 337 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.298+1759delC | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466415 | |||||||
| chr22:31466443 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298+1732C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466443 | |||||||
| chr22:31466524 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.298+1651C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466524 | |||||||
| chr22:31466642 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.298+1533A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466642 | |||||||
| chr22:31466713 | G | A | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1462C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466713 | |||||||
| chr22:31466983 | T | C | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1192A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466983 | |||||||
| chr22:31467036 | A | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(113): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.298+1139T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467036 | |||||||
| chr22:31467049 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.298+1126T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467049 | |||||||
| chr22:31467111 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.298+1064G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467111 | |||||||
| chr22:31467118 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.298+1057C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467118 | |||||||
| chr22:31467139 | T | C | 67 | a0001c0002t0001g0004 a0001c0002t0001g0007 a0001c0002t0001g0014 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.298+1036A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467139 | |||||||
| chr22:31467277 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298+898A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467277 | |||||||
| chr22:31467568 | T | C | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+607A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467568 | |||||||
| chr22:31467576 | G | C | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+599C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467576 | |||||||
| chr22:31467641 | G | A | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+534C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467641 | |||||||
| chr22:31467720 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.298+455C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467720 | |||||||
| chr22:31467764 | GA | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+410delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467764 | |||||||
| chr22:31467802 | C | A | 1 | a0001c0002t0001g0063 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.298+373G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467802 | |||||||
| chr22:31467803 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0284 |
3 | HG01516.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.298+372T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467803 | |||||||
| chr22:31467810 | A | C | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.298+365T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467810 | |||||||
| chr22:31467931 | C | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0033 |
3 | HG00280.hp2 HG01106.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.298+244G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467931 | |||||||
| chr22:31468007 | G | A | 1 | a0001c0002t0001g0014 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+168C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31468007 | |||||||
| chr22:31468127 | C | G | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+48G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31468127 | |||||||
| chr22:31468415 | G | T | 18 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(15): Show |
18 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.171-113C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468415 | |||||||
| chr22:31468433 | C | T | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.171-131G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468433 | |||||||
| chr22:31468703 | A | G | 1 | a0001c0002t0001g0020 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.171-401T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468703 | |||||||
| chr22:31468890 | A | G | 1 | a0001c0003t0001g0315 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171-588T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468890 | |||||||
| chr22:31469546 | G | A | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.171-1244C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469546 | |||||||
| chr22:31469554 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.171-1252A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469554 | |||||||
| chr22:31469648 | A | G | 1 | a0001c0003t0001g0315 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171-1346T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469648 | |||||||
| chr22:31469672 | C | T | 1 | a0001c0014t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.171-1370G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469672 | |||||||
| chr22:31469689 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1387T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469689 | |||||||
| chr22:31469697 | T | C | 71 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(68): Show |
72 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.171-1395A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469697 | |||||||
| chr22:31469755 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.171-1453A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469755 | |||||||
| chr22:31470022 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.171-1720C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470022 | |||||||
| chr22:31470121 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.170+1723C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470121 | |||||||
| chr22:31470146 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 |
3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.170+1698T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470146 | |||||||
| chr22:31470161 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.170+1683G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470161 | |||||||
| chr22:31470164 | C | CA | 36 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0034 others(33): Show |
36 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.170+1679dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470164 | |||||||
| chr22:31470164 | CA | C | 75 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0107 others(72): Show |
78 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.170+1679delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470164 | |||||||
| chr22:31470180 | A | G | 70 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(67): Show |
71 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.170+1664T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470180 | |||||||
| chr22:31470181 | A | G | 70 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(67): Show |
73 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.170+1663T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470181 | |||||||
| chr22:31470250 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.170+1594C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470250 | |||||||
| chr22:31470290 | G | GT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+1553dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470290 | |||||||
| chr22:31470341 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+1503G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470341 | |||||||
| chr22:31470372 | C | T | 15 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(12): Show |
15 | HG02040.hp2 HG02602.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.170+1472G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470372 | |||||||
| chr22:31470374 | G | A | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0002g0279 |
3 | HG01891.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.170+1470C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470374 | |||||||
| chr22:31470421 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.170+1423A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470421 | |||||||
| chr22:31470511 | C | T | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(7): Show |
10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1333G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470511 | |||||||
| chr22:31470629 | A | AT | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+1214dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470629 | |||||||
| chr22:31470685 | C | CT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0067 others(74): Show |
79 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.170+1158dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | |||||||
| chr22:31470685 | C | CTT | 8 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0206 others(5): Show |
10 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1157_170+1158d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | |||||||
| chr22:31470685 | CT | C | 13 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
13 | HG01516.hp1 HG01517.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.170+1158delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | |||||||
| chr22:31470778 | G | A | 1 | a0001c0007t0001g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.170+1066C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470778 | |||||||
| chr22:31470795 | G | A | 71 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(68): Show |
72 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.170+1049C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470795 | |||||||
| chr22:31470812 | A | C | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+1032T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470812 | |||||||
| chr22:31470882 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+962C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470882 | |||||||
| chr22:31471008 | G | C | 1 | a0001c0003t0001g0285 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.170+836C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471008 | |||||||
| chr22:31471013 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.170+831C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471013 | |||||||
| chr22:31471053 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+791T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471053 | |||||||
| chr22:31471128 | T | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0003t0001g0125 |
3 | HG01257.hp1 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.170+716A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471128 | |||||||
| chr22:31471129 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0003t0001g0125 |
3 | HG01257.hp1 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.170+715A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471129 | |||||||
| chr22:31471217 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.170+627C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471217 | |||||||
| chr22:31471317 | C | CTT | 71 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0060 others(68): Show |
72 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.170+525_170+526dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471317 | |||||||
| chr22:31471397 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.170+447G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471397 | |||||||
| chr22:31471460 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+384C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471460 | |||||||
| chr22:31471717 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+127G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471717 | |||||||
| chr22:31471777 | T | C | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.170+67A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471777 | |||||||
| chr22:31471930 | G | A | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-13C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31471930 | |||||||
| chr22:31472041 | G | C | 1 | a0003c0009t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-124C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472041 | |||||||
| chr22:31472057 | G | C | 1 | a0001c0004t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97-140C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472057 | |||||||
| chr22:31472069 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-152A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472069 | |||||||
| chr22:31472123 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-206A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472123 | |||||||
| chr22:31472125 | C | T | 1 | a0001c0003t0001g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.97-208G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472125 | |||||||
| chr22:31472168 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-251C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472168 | |||||||
| chr22:31472237 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.97-320A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472237 | |||||||
| chr22:31472269 | GA | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-353delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472269 | |||||||
| chr22:31472270 | A | AT | 78 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(75): Show |
80 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.97-354dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | |||||||
| chr22:31472270 | A | ATT | 19 | a0001c0001t0001g0009 a0001c0001t0001g0124 a0001c0001t0001g0127 others(16): Show |
19 | HG01257.hp1 HG01258.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-355_97-354dupAA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | |||||||
| chr22:31472270 | A | ATTT | 6 | a0001c0001t0001g0111 a0001c0001t0001g0126 a0001c0001t0001g0139 others(3): Show |
6 | HG01496.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-356_97-354dupAA others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | |||||||
| chr22:31472308 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.97-391C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472308 | |||||||
| chr22:31472433 | T | G | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.97-516A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472433 | |||||||
| chr22:31472441 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-524C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472441 | |||||||
| chr22:31472564 | G | A | 2 | a0001c0003t0001g0307 a0001c0003t0001g0308 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-647C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472564 | |||||||
| chr22:31472596 | G | T | 1 | a0001c0010t0001g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.97-679C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472596 | |||||||
| chr22:31472684 | T | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-767A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472684 | |||||||
| chr22:31472779 | C | T | 21 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(18): Show |
21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.97-862G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472779 | |||||||
| chr22:31472780 | G | C | 1 | a0001c0006t0001g0143 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.97-863C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472780 | |||||||
| chr22:31473059 | C | T | 1 | a0003c0009t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-1142G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473059 | |||||||
| chr22:31473063 | C | CT | 31 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0119 others(28): Show |
31 | HG00408.hp2 HG00609.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-1147dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473063 | |||||||
| chr22:31473063 | CT | C | 11 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0252 others(8): Show |
11 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-1147delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473063 | |||||||
| chr22:31473075 | T | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-1158A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473075 | |||||||
| chr22:31473201 | C | T | 1 | a0001c0007t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-1284G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473201 | |||||||
| chr22:31473419 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-1502A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473419 | |||||||
| chr22:31473481 | A | C | 70 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(67): Show |
73 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.97-1564T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473481 | |||||||
| chr22:31473679 | GCT | G | 4 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(1): Show |
4 | NA18949.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-1764_97-1763del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473679 | |||||||
| chr22:31473906 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(81): Show |
86 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.97-1989A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473906 | |||||||
| chr22:31473944 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.97-2027G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473944 | |||||||
| chr22:31474008 | CCT | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2093_97-2092del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474008 | |||||||
| chr22:31474064 | C | CT | 71 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0059 others(68): Show |
72 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.97-2148dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474064 | |||||||
| chr22:31474064 | C | CTT | 8 | a0001c0001t0001g0075 a0001c0002t0001g0019 a0001c0002t0001g0037 others(5): Show |
8 | HG00544.hp1 HG02602.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-2149_97-2148dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474064 | |||||||
| chr22:31474118 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.97-2201G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474118 | |||||||
| chr22:31474341 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97-2424C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474341 | |||||||
| chr22:31474414 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(151): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.97-2497G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474414 | |||||||
| chr22:31474487 | CT | C | 10 | a0001c0001t0001g0107 a0001c0001t0001g0185 a0001c0001t0001g0204 others(7): Show |
10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-2571delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474487 | |||||||
| chr22:31474488 | T | TA | 20 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(17): Show |
20 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-2572_97-2571ins others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474488 | |||||||
| chr22:31474603 | T | C | 3 | a0001c0003t0001g0267 a0001c0003t0001g0294 a0001c0003t0006g0357 |
3 | HG01358.hp2 HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.97-2686A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474603 | |||||||
| chr22:31474665 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-2748C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474665 | |||||||
| chr22:31474733 | C | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-2816G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474733 | |||||||
| chr22:31474746 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.97-2829G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474746 | |||||||
| chr22:31474747 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2830T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474747 | |||||||
| chr22:31475015 | A | G | 1 | a0001c0007t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-3098T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475015 | |||||||
| chr22:31475176 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-3259A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475176 | |||||||
| chr22:31475193 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97-3276C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475193 | |||||||
| chr22:31475202 | T | C | 1 | a0001c0014t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97-3285A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475202 | |||||||
| chr22:31475267 | GA | G | 126 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0121 others(123): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.97-3351delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475267 | |||||||
| chr22:31475491 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0311 |
2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.97-3574G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475491 | |||||||
| chr22:31475710 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0154 |
3 | HG02109.hp2 HG06807.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.97-3793C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475710 | |||||||
| chr22:31475721 | T | TA | 106 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0109 others(103): Show |
109 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.97-3805dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475721 | |||||||
| chr22:31475721 | TA | T | 10 | a0001c0001t0001g0204 a0001c0001t0001g0210 a0001c0001t0001g0248 others(7): Show |
10 | HG00738.hp2 HG01167.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-3805delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475721 | |||||||
| chr22:31475761 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-3844C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475761 | |||||||
| chr22:31475866 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.97-3949T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475866 | |||||||
| chr22:31476235 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.97-4318C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476235 | |||||||
| chr22:31476463 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-4546G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476463 | |||||||
| chr22:31476622 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.97-4705G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476622 | |||||||
| chr22:31476669 | T | C | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-4752A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476669 | |||||||
| chr22:31476843 | C | CA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-4927dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476843 | |||||||
| chr22:31476891 | T | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-4974A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476891 | |||||||
| chr22:31476980 | C | CA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0054 others(6): Show |
9 | HG01358.hp2 HG02040.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5064dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476980 | |||||||
| chr22:31476980 | CA | C | 16 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(13): Show |
18 | HG01516.hp1 HG01517.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-5064delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476980 | |||||||
| chr22:31476996 | A | G | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5079T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476996 | |||||||
| chr22:31477000 | G | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-5083C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477000 | |||||||
| chr22:31477001 | G | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-5084C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477001 | |||||||
| chr22:31477062 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.97-5145C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477062 | |||||||
| chr22:31477118 | C | CA | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-5202dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477118 | |||||||
| chr22:31477135 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.97-5218C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477135 | |||||||
| chr22:31477223 | G | C | 1 | a0001c0002t0001g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.97-5306C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477223 | |||||||
| chr22:31477286 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-5369C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477286 | |||||||
| chr22:31477301 | A | G | 1 | a0001c0003t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97-5384T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477301 | |||||||
| chr22:31477315 | T | C | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5398A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477315 | |||||||
| chr22:31477357 | C | CA | 95 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
96 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.97-5441dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | |||||||
| chr22:31477357 | C | CAA | 20 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0208 others(17): Show |
20 | HG00609.hp2 HG01978.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-5442_97-5441dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | |||||||
| chr22:31477357 | CA | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(13): Show |
18 | HG00738.hp2 HG01993.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-5441delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | |||||||
| chr22:31477366 | A | C | 6 | a0001c0004t0001g0001 a0001c0004t0001g0112 a0001c0004t0001g0115 others(3): Show |
8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-5449T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477366 | |||||||
| chr22:31477367 | AAAAAAAA others(10): Show |
A | 1 | a0001c0003t0001g0267 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.97-5467_97-5451del others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477367 | |||||||
| chr22:31477369 | AAAAAAC | A | 57 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.97-5458_97-5453del others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477369 | |||||||
| chr22:31477370 | AAAAAC | A | 34 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0282 others(31): Show |
36 | HG00408.hp2 HG00609.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.97-5458_97-5454del others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477370 | |||||||
| chr22:31477373 | AACAAAAA others(4): Show |
A | 1 | a0001c0003t0001g0342 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-5467_97-5457del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477373 | |||||||
| chr22:31477374 | ACAAAAAA others(3): Show |
A | 1 | a0001c0003t0001g0273 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.97-5467_97-5458del others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477374 | |||||||
| chr22:31477375 | C | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(188): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.97-5458G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477375 | |||||||
| chr22:31477384 | C | A | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.97-5467G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477384 | |||||||
| chr22:31477390 | A | G | 98 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(95): Show |
101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.97-5473T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477390 | |||||||
| chr22:31477466 | C | G | 1 | a0001c0001t0002g0271 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.97-5549G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477466 | |||||||
| chr22:31477700 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97-5783G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477700 | |||||||
| chr22:31477852 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.97-5935C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477852 | |||||||
| chr22:31478122 | T | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG01109.hp1 HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.97-6205A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478122 | |||||||
| chr22:31478288 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-6371C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478288 | |||||||
| chr22:31478295 | C | T | 1 | a0001c0003t0001g0315 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.97-6378G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478295 | |||||||
| chr22:31478356 | T | TA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-6440dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478356 | |||||||
| chr22:31478370 | G | A | 1 | a0001c0001t0002g0280 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.97-6453C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478370 | |||||||
| chr22:31478475 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.97-6558G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478475 | |||||||
| chr22:31478515 | C | CA | 193 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(190): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.97-6599dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | |||||||
| chr22:31478515 | C | CAA | 14 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0160 others(11): Show |
14 | HG01261.hp2 HG01981.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-6600_97-6599dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | |||||||
| chr22:31478515 | C | CAAA | 12 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(9): Show |
12 | HG01168.hp2 HG01496.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-6601_97-6599dup others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | |||||||
| chr22:31478515 | C | CAAAA | 81 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(78): Show |
84 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.97-6602_97-6599dup others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | |||||||
| chr22:31478515 | C | CAAAAA | 16 | a0001c0001t0001g0262 a0001c0001t0001g0296 a0001c0001t0001g0299 others(13): Show |
16 | HG01346.hp1 HG01358.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-6603_97-6599dup others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | |||||||
| chr22:31478722 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0142 others(57): Show |
62 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-6805G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478722 | |||||||
| chr22:31478778 | C | T | 71 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(68): Show |
74 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.97-6861G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478778 | |||||||
| chr22:31478808 | C | T | 7 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-6891G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478808 | |||||||
| chr22:31478820 | C | T | 7 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-6903G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478820 | |||||||
| chr22:31478835 | C | T | 2 | a0001c0001t0001g0111 a0001c0007t0001g0113 |
2 | HG02809.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.97-6918G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478835 | |||||||
| chr22:31478921 | C | T | 1 | a0001c0005t0001g0145 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97-7004G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478921 | |||||||
| chr22:31478949 | C | CA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0100 others(120): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.97-7033dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | |||||||
| chr22:31478949 | C | CAA | 9 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0211 others(6): Show |
9 | HG00323.hp1 HG00741.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-7034_97-7033dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | |||||||
| chr22:31478949 | CA | C | 7 | a0001c0001t0001g0284 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
7 | HG01516.hp2 HG02602.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7033delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | |||||||
| chr22:31479031 | AGACAGAT | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-7121_97-7115del others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479031 | |||||||
| chr22:31479237 | T | C | 1 | a0001c0002t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97-7320A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479237 | |||||||
| chr22:31479322 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0142 others(57): Show |
62 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-7405T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479322 | |||||||
| chr22:31479668 | A | G | 7 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-7751T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479668 | |||||||
| chr22:31479687 | G | GT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(4): Show |
7 | HG02056.hp1 HG02148.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7771dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | |||||||
| chr22:31479687 | GT | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0103 others(207): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.97-7771delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | |||||||
| chr22:31479687 | GTT | G | 11 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG00323.hp1 HG01515.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-7772_97-7771del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | |||||||
| chr22:31479792 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-7875G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479792 | |||||||
| chr22:31479803 | T | C | 1 | a0001c0002t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.97-7886A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479803 | |||||||
| chr22:31479890 | T | G | 3 | a0001c0003t0001g0003 a0001c0003t0001g0297 a0001c0003t0001g0298 |
5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-7973A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479890 | |||||||
| chr22:31480279 | T | C | 1 | a0001c0002t0001g0065 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.96+8344A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480279 | |||||||
| chr22:31480415 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0222 |
2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.96+8208T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480415 | |||||||
| chr22:31480458 | T | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0066 |
3 | HG03239.hp1 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.96+8165A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480458 | |||||||
| chr22:31480480 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0121 others(214): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.96+8143C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480480 | |||||||
| chr22:31480522 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.96+8101C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480522 | |||||||
| chr22:31480624 | G | T | 1 | a0001c0002t0001g0027 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.96+7999C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480624 | |||||||
| chr22:31480711 | C | A | 1 | a0001c0002t0001g0018 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.96+7912G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480711 | |||||||
| chr22:31480750 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.96+7873G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480750 | |||||||
| chr22:31480807 | G | A | 1 | a0001c0006t0001g0201 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.96+7816C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480807 | |||||||
| chr22:31481032 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.96+7591G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481032 | |||||||
| chr22:31481145 | T | C | 1 | a0001c0003t0001g0330 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+7478A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481145 | |||||||
| chr22:31481185 | CAG | C | 80 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.96+7436_96+7437del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481185 | |||||||
| chr22:31481328 | A | AT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0111 a0001c0001t0001g0134 others(7): Show |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+7294dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481328 | |||||||
| chr22:31481328 | AT | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0121 others(203): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.96+7294delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481328 | |||||||
| chr22:31481471 | CTTAAA | C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7147_96+7151del others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481471 | |||||||
| chr22:31481518 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01928.hp1 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+7105G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481518 | |||||||
| chr22:31481771 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.96+6852C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481771 | |||||||
| chr22:31481786 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.96+6837G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481786 | |||||||
| chr22:31481798 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.96+6825T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481798 | |||||||
| chr22:31482066 | G | A | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0254 others(1): Show |
4 | HG01934.hp2 HG02293.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+6557C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482066 | |||||||
| chr22:31482165 | C | CA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0110 others(96): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.96+6457dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482165 | |||||||
| chr22:31482165 | CA | C | 6 | a0001c0001t0001g0150 a0001c0001t0002g0271 a0001c0001t0002g0272 others(3): Show |
6 | HG00609.hp1 HG01168.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+6457delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482165 | |||||||
| chr22:31482233 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.96+6390G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482233 | |||||||
| chr22:31482271 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+6352A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482271 | |||||||
| chr22:31482362 | A | G | 8 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp1 HG01261.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+6261T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482362 | |||||||
| chr22:31482419 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0004c0011t0001g0260 |
3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.96+6204G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482419 | |||||||
| chr22:31482438 | T | C | 4 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
4 | NA18612.hp2 NA18942.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+6185A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482438 | |||||||
| chr22:31482442 | C | CA | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+6180dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482442 | |||||||
| chr22:31482576 | G | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.96+6047C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482576 | |||||||
| chr22:31482595 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+6028A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482595 | |||||||
| chr22:31482673 | C | T | 1 | a0001c0002t0001g0024 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.96+5950G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482673 | |||||||
| chr22:31482691 | C | CA | 7 | a0001c0001t0001g0126 a0001c0001t0001g0139 a0001c0001t0001g0202 others(4): Show |
7 | HG02055.hp2 HG03654.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+5931dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482691 | |||||||
| chr22:31482723 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+5900C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482723 | |||||||
| chr22:31482894 | C | T | 3 | a0001c0003t0001g0003 a0001c0003t0001g0297 a0001c0003t0001g0298 |
5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+5729G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482894 | |||||||
| chr22:31483205 | C | T | 351 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(348): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.96+5418G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483205 | |||||||
| chr22:31483209 | C | CT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0091 others(120): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.96+5413dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | |||||||
| chr22:31483209 | C | CTT | 8 | a0001c0001t0001g0126 a0001c0001t0001g0139 a0001c0001t0001g0212 others(5): Show |
8 | HG01361.hp2 HG02055.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+5412_96+5413dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | |||||||
| chr22:31483209 | CT | C | 15 | a0001c0001t0001g0075 a0001c0001t0001g0252 a0001c0001t0001g0334 others(12): Show |
15 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+5413delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | |||||||
| chr22:31483255 | A | G | 80 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.96+5368T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483255 | |||||||
| chr22:31483479 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+5144T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483479 | |||||||
| chr22:31483549 | A | G | 2 | a0001c0003t0001g0267 a0001c0003t0006g0357 |
2 | HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.96+5074T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483549 | |||||||
| chr22:31483551 | C | T | 4 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(1): Show |
4 | NA18949.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+5072G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483551 | |||||||
| chr22:31483689 | G | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(332): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.96+4934C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483689 | |||||||
| chr22:31483783 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+4840G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483783 | |||||||
| chr22:31484258 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.96+4365C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484258 | |||||||
| chr22:31484447 | G | A | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+4176C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484447 | |||||||
| chr22:31484494 | A | G | 1 | a0001c0002t0001g0020 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.96+4129T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484494 | |||||||
| chr22:31484540 | TA | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0155 a0001c0001t0001g0211 others(4): Show |
7 | HG00323.hp1 HG03491.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+4082delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484540 | |||||||
| chr22:31484631 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.96+3992A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484631 | |||||||
| chr22:31484653 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+3970C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484653 | |||||||
| chr22:31484761 | GGCGGAGG others(9): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.96+3846_96+3861del others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484761 | |||||||
| chr22:31484763 | C | T | 80 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.96+3860G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484763 | |||||||
| chr22:31484884 | C | T | 2 | a0001c0001t0001g0154 a0001c0002t0001g0017 |
2 | HG03654.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.96+3739G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484884 | |||||||
| chr22:31484916 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+3707C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484916 | |||||||
| chr22:31484949 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 |
3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.96+3674A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484949 | |||||||
| chr22:31485081 | T | C | 22 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(19): Show |
22 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+3542A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485081 | |||||||
| chr22:31485183 | A | G | 73 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(70): Show |
76 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+3440T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485183 | |||||||
| chr22:31485443 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.96+3180A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485443 | |||||||
| chr22:31485717 | T | C | 15 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+2906A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485717 | |||||||
| chr22:31485736 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.96+2887C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485736 | |||||||
| chr22:31485747 | T | C | 96 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0282 others(93): Show |
99 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.96+2876A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485747 | |||||||
| chr22:31485843 | C | T | 73 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(70): Show |
76 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+2780G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485843 | |||||||
| chr22:31486007 | G | A | 1 | a0001c0007t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+2616C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486007 | |||||||
| chr22:31486008 | G | C | 1 | a0001c0007t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+2615C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486008 | |||||||
| chr22:31486030 | TGAGGTCA others(16): Show |
T | 7 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2570_96+2592del others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486030 | |||||||
| chr22:31486106 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0124 a0001c0001t0001g0138 |
3 | HG01496.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.96+2517G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486106 | |||||||
| chr22:31486195 | C | T | 80 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.96+2428G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486195 | |||||||
| chr22:31486228 | T | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0091 others(242): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.96+2395A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486228 | |||||||
| chr22:31486279 | A | T | 107 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(104): Show |
110 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.96+2344T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486279 | |||||||
| chr22:31486280 | A | T | 1 | a0001c0003t0001g0349 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.96+2343T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486280 | |||||||
| chr22:31486281 | AAAT | A | 316 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.96+2339_96+2341del others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486281 | |||||||
| chr22:31486284 | TAA | T | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
22 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+2337_96+2338del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486284 | |||||||
| chr22:31486286 | A | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(314): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.96+2337T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486286 | |||||||
| chr22:31486442 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+2181G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486442 | |||||||
| chr22:31486519 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+2104C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486519 | |||||||
| chr22:31486552 | G | A | 1 | a0001c0004t0001g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+2071C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486552 | |||||||
| chr22:31486612 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+2011G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486612 | |||||||
| chr22:31486799 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0141 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+1824C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486799 | |||||||
| chr22:31486869 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.96+1754A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486869 | |||||||
| chr22:31486878 | C | G | 1 | a0001c0003t0001g0294 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.96+1745G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486878 | |||||||
| chr22:31486920 | T | TA | 308 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(305): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.96+1702dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486920 | |||||||
| chr22:31486920 | T | TAA | 6 | a0001c0001t0001g0206 a0001c0001t0001g0247 a0001c0001t0001g0256 others(3): Show |
6 | HG00738.hp2 HG02559.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1701_96+1702dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486920 | |||||||
| chr22:31487031 | T | C | 5 | a0001c0005t0001g0145 a0001c0005t0001g0146 a0001c0005t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1592A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487031 | |||||||
| chr22:31487070 | CA | C | 15 | a0001c0001t0001g0091 a0001c0001t0001g0207 a0001c0001t0001g0284 others(12): Show |
15 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+1552delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487070 | |||||||
| chr22:31487070 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0257 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.96+1542_96+1552del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487070 | |||||||
| chr22:31487311 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+1312G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487311 | |||||||
| chr22:31487325 | A | G | 1 | a0001c0002t0001g0018 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.96+1298T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487325 | |||||||
| chr22:31487403 | A | G | 1 | a0001c0002t0001g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.96+1220T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487403 | |||||||
| chr22:31487620 | T | C | 1 | a0001c0007t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+1003A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487620 | |||||||
| chr22:31487659 | G | A | 1 | a0001c0003t0001g0340 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+964C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487659 | |||||||
| chr22:31487793 | C | CA | 27 | a0001c0001t0001g0114 a0001c0001t0001g0138 a0001c0001t0001g0139 others(24): Show |
29 | HG00738.hp2 HG01123.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+829dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | |||||||
| chr22:31487793 | CA | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0034 others(161): Show |
167 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.96+829delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | |||||||
| chr22:31487793 | CAA | C | 7 | a0001c0001t0001g0144 a0001c0005t0001g0145 a0001c0005t0001g0146 others(4): Show |
7 | HG02132.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+828_96+829delTT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | |||||||
| chr22:31487810 | A | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.96+813T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487810 | |||||||
| chr22:31487865 | C | G | 1 | a0001c0002t0001g0014 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.96+758G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487865 | |||||||
| chr22:31487982 | T | TCTTCAAA others(8): Show |
1 | a0001c0001t0001g0257 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.96+626_96+640dupTG others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487982 | |||||||
| chr22:31488047 | C | T | 80 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.96+576G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488047 | |||||||
| chr22:31488189 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.96+434T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488189 | |||||||
| chr22:31488312 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.96+311A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488312 | |||||||
| chr22:31488419 | T | C | 97 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0282 others(94): Show |
100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.96+204A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488419 | |||||||
| chr22:31488779 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-27-34C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488779 | |||||||
| chr22:31488994 | T | C | 1 | a0001c0001t0001g0351 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-27-249A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488994 | |||||||
| chr22:31488999 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(2): Show |
5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-254G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488999 | |||||||
| chr22:31488999 | C | T | 1 | a0001c0003t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-27-254G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488999 | |||||||
| chr22:31489076 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-27-331C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489076 | |||||||
| chr22:31489330 | C | T | 19 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(16): Show |
19 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28+364G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489330 | |||||||
| chr22:31489399 | G | T | 1 | a0001c0002t0001g0007 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+295C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489399 | |||||||
| chr22:31489418 | G | A | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-28+276C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489418 | |||||||
| chr22:31489509 | G | A | 1 | a0001c0003t0001g0355 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-28+185C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489509 | |||||||
| chr22:31489531 | G | A | 1 | a0001c0007t0001g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+163C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489531 | |||||||
| chr22:31489646 | CG | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0122 others(237): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-28+47delC | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489646 |