Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9669 |
| ensemblid | ENSG00000158417.12 |
| hgncid | 30793 |
| symbol | EIF5B |
| name | eukaryotic translation initiation factor 5B |
| refseq_nuc | NM_015904.4 |
| refseq_prot | NP_056988.3 |
| ensembl_nuc | ENST00000289371.11 |
| ensembl_prot | ENSP00000289371.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 99337389 |
| end | 99401326 |
| strand | + |
| ver | v1.2 |
| region | chr2:99337389-99401326 |
| region5000 | chr2:99332389-99406326 |
| regionname0 | EIF5B_chr2_99337389_99401326 |
| regionname5000 | EIF5B_chr2_99332389_99406326 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1220 | 229 | 64 | 58 | 75 | 9 | 23 | 62 | EIF5B_chr2_99332389_99406326 | EIF5B | MGKKQ others(1215): Show |
chr2 | 99332389 | 99406326 |
| a0002 | 1/1 | 1220 | 110 | 17 | 16 | 63 | 1 | 11 | 46 | EIF5B_chr2_99332389_99406326 | EIF5B | MGKKQ others(1215): Show |
chr2 | 99332389 | 99406326 |
| a0003 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | MGKKQ others(1215): Show |
chr2 | 99332389 | 99406326 |
| a0004 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | MGKKQ others(1215): Show |
chr2 | 99332389 | 99406326 |
| a0005 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | MGKKQ others(1215): Show |
chr2 | 99332389 | 99406326 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3660 | 94 | 12 | 25 | 51 | 2 | 4 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0003 | 0/0 | 3660 | 79 | 40 | 7 | 19 | 2 | 11 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0004 | 0/0 | 3660 | 44 | 8 | 22 | 3 | 4 | 7 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0005 | 0/0 | 3660 | 6 | 0 | 4 | 1 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0006 | 0/0 | 3660 | 3 | 2 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0009 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0011 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0001c0012 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0002c0001 | 1/1 | 3660 | 108 | 16 | 16 | 63 | 1 | 10 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0002c0007 | 0/0 | 3660 | 2 | 1 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0003c0013 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0004c0008 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 | ||
| a0005c0010 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ATGGG others(3655): Show |
chr2 | 99332389 | 99406326 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 5741 | 40 | 5 | 7 | 24 | 1 | 3 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0002t0003 | 0/0 | 5737 | 46 | 6 | 17 | 21 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5732): Show |
chr2 | 99332389 | 99406326 |
| a0001c0002t0007 | 0/0 | 5737 | 6 | 0 | 0 | 6 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5732): Show |
chr2 | 99332389 | 99406326 |
| a0001c0002t0015 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5732): Show |
chr2 | 99332389 | 99406326 |
| a0001c0002t0022 | 0/0 | 5741 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0001 | 0/0 | 5741 | 21 | 10 | 5 | 5 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0002 | 0/0 | 5741 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0004 | 0/0 | 5741 | 34 | 13 | 2 | 9 | 2 | 8 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0008 | 0/0 | 5741 | 5 | 0 | 0 | 5 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0009 | 0/0 | 5725 | 5 | 5 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5720): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0010 | 0/0 | 5741 | 3 | 3 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0011 | 0/0 | 5757 | 2 | 0 | 0 | 0 | 0 | 2 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5752): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0012 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5684): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0013 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5740): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0016 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0020 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0003t0023 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACT others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0004t0001 | 0/0 | 5741 | 36 | 1 | 22 | 3 | 4 | 6 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0004t0006 | 0/0 | 5745 | 7 | 7 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5740): Show |
chr2 | 99332389 | 99406326 |
| a0001c0004t0014 | 0/0 | 5741 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0005t0002 | 0/0 | 5741 | 6 | 0 | 4 | 1 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0006t0004 | 0/0 | 5741 | 3 | 2 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0009t0001 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0001c0011t0021 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5740): Show |
chr2 | 99332389 | 99406326 |
| a0001c0012t0002 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0001t0002 | 1/1 | 5741 | 75 | 16 | 11 | 37 | 1 | 8 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0001t0005 | 0/0 | 5741 | 30 | 0 | 5 | 24 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0001t0017 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0001t0018 | 0/0 | 5741 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0001t0019 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0002c0007t0005 | 0/0 | 5741 | 2 | 1 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0003c0013t0004 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0004c0008t0001 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5736): Show |
chr2 | 99332389 | 99406326 |
| a0005c0010t0003 | 0/0 | 5737 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | ACACC others(5732): Show |
chr2 | 99332389 | 99406326 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0001 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0002t0022g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0008g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0011g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0011g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0020g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0003t0023g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0002 | 0/0 | 6 | 1 | 3 | 0 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0006g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0004t0014g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0005t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0005t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0005t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0005t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0006t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0006t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0006t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0009t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0011t0021g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0001c0012t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0017g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0018g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0001t0019g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0007t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0002c0007t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0003c0013t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0004c0008t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| a0005c0010t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0025 | EUR | GBR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0168 | EUR | GBR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00280 | hp1 | a0001 | c0003 | t0004 | g0055 | EUR | FIN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0089 | EUR | FIN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00408 | hp1 | a0002 | c0001 | t0002 | g0249 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00423 | hp1 | a0002 | c0001 | t0002 | g0240 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00438 | hp1 | a0002 | c0001 | t0002 | g0208 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00438 | hp2 | a0002 | c0001 | t0005 | g0225 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00544 | hp1 | a0002 | c0001 | t0005 | g0220 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0082 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00558 | hp1 | a0002 | c0001 | t0005 | g0192 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00558 | hp2 | a0002 | c0001 | t0002 | g0255 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0156 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00639 | hp2 | a0002 | c0001 | t0002 | g0259 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0103 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0166 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00738 | hp2 | a0002 | c0001 | t0002 | g0250 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0092 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0088 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0024 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01071 | hp1 | a0001 | c0005 | t0002 | g0024 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01099 | hp1 | a0002 | c0001 | t0002 | g0242 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0079 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0102 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0039 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0085 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01175 | hp1 | a0002 | c0001 | t0002 | g0261 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0097 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01192 | hp1 | a0002 | c0001 | t0005 | g0222 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0203 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0100 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01256 | hp2 | a0002 | c0001 | t0005 | g0266 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01258 | hp2 | a0002 | c0001 | t0005 | g0267 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01261 | hp2 | a0002 | c0001 | t0002 | g0212 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01346 | hp1 | a0001 | c0002 | t0022 | g0142 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01346 | hp2 | a0002 | c0001 | t0002 | g0260 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01358 | hp1 | a0001 | c0005 | t0002 | g0289 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01358 | hp2 | a0001 | c0003 | t0004 | g0023 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0072 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0163 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0287 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0206 | EUR | IBS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01516 | hp2 | a0001 | c0006 | t0004 | g0045 | EUR | IBS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01884 | hp1 | a0002 | c0001 | t0002 | g0202 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01891 | hp1 | a0001 | c0003 | t0013 | g0036 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01891 | hp2 | a0001 | c0003 | t0004 | g0285 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01934 | hp2 | a0002 | c0001 | t0002 | g0022 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0101 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0236 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0253 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01978 | hp2 | a0001 | c0004 | t0001 | g0086 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01981 | hp2 | a0002 | c0001 | t0005 | g0223 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0078 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02004 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02027 | hp1 | a0001 | c0003 | t0004 | g0057 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02027 | hp2 | a0002 | c0001 | t0005 | g0272 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02040 | hp1 | a0002 | c0001 | t0005 | g0275 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02055 | hp2 | a0001 | c0011 | t0021 | g0295 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02080 | hp2 | a0001 | c0002 | t0007 | g0177 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02083 | hp2 | a0002 | c0001 | t0005 | g0020 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02132 | hp1 | a0002 | c0001 | t0002 | g0263 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02132 | hp2 | a0002 | c0001 | t0005 | g0216 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0060 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02135 | hp2 | a0002 | c0001 | t0002 | g0280 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02145 | hp1 | a0001 | c0006 | t0004 | g0063 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02145 | hp2 | a0002 | c0001 | t0002 | g0262 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02165 | hp1 | a0001 | c0009 | t0001 | g0151 | EAS | CDX | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02165 | hp2 | a0002 | c0001 | t0002 | g0205 | EAS | CDX | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02257 | hp1 | a0001 | c0003 | t0012 | g0073 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02257 | hp2 | a0001 | c0003 | t0004 | g0010 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02258 | hp1 | a0001 | c0012 | t0002 | g0269 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0002 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0158 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02273 | hp2 | a0002 | c0001 | t0002 | g0022 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02280 | hp1 | a0001 | c0004 | t0006 | g0108 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0296 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0104 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02523 | hp1 | a0002 | c0001 | t0017 | g0186 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0234 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02572 | hp1 | a0002 | c0001 | t0002 | g0273 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0124 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02615 | hp1 | a0001 | c0006 | t0004 | g0046 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0011 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0282 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02647 | hp2 | a0002 | c0001 | t0002 | g0185 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02683 | hp2 | a0001 | c0003 | t0004 | g0048 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02698 | hp1 | a0002 | c0001 | t0002 | g0243 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0093 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02717 | hp2 | a0002 | c0001 | t0002 | g0200 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0012 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0094 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02735 | hp2 | a0002 | c0001 | t0002 | g0204 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02738 | hp1 | a0002 | c0001 | t0002 | g0252 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02809 | hp2 | a0001 | c0003 | t0010 | g0027 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0010 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02818 | hp2 | a0001 | c0003 | t0009 | g0032 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02886 | hp1 | a0002 | c0001 | t0002 | g0277 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02886 | hp2 | a0001 | c0003 | t0023 | g0040 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02895 | hp2 | a0001 | c0003 | t0010 | g0026 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02896 | hp1 | a0001 | c0003 | t0009 | g0030 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02897 | hp1 | a0001 | c0003 | t0009 | g0031 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02922 | hp1 | a0001 | c0004 | t0006 | g0105 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0283 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02965 | hp1 | a0002 | c0001 | t0002 | g0274 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0037 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02976 | hp1 | a0001 | c0003 | t0010 | g0028 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02976 | hp2 | a0002 | c0001 | t0002 | g0226 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03017 | hp1 | a0001 | c0003 | t0004 | g0056 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03017 | hp2 | a0002 | c0001 | t0018 | g0227 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0123 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03098 | hp1 | a0003 | c0013 | t0004 | g0286 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03098 | hp2 | a0001 | c0004 | t0006 | g0106 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0284 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03130 | hp2 | a0001 | c0004 | t0006 | g0006 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03209 | hp2 | a0002 | c0001 | t0002 | g0198 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03239 | hp1 | a0001 | c0004 | t0014 | g0096 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03239 | hp2 | a0001 | c0003 | t0004 | g0038 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0122 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03486 | hp1 | a0001 | c0003 | t0012 | g0074 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03486 | hp2 | a0002 | c0001 | t0002 | g0268 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03490 | hp1 | a0001 | c0003 | t0004 | g0052 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03490 | hp2 | a0002 | c0001 | t0005 | g0217 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03491 | hp1 | a0002 | c0001 | t0002 | g0244 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03491 | hp2 | a0001 | c0003 | t0011 | g0064 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03516 | hp1 | a0002 | c0001 | t0002 | g0199 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03516 | hp2 | a0001 | c0003 | t0016 | g0118 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03540 | hp1 | a0002 | c0001 | t0002 | g0201 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0050 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03669 | hp1 | a0001 | c0003 | t0004 | g0049 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0114 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0091 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03688 | hp2 | a0002 | c0001 | t0002 | g0292 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0095 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03710 | hp2 | a0002 | c0001 | t0002 | g0209 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0084 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03927 | hp1 | a0002 | c0001 | t0002 | g0278 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03927 | hp2 | a0001 | c0005 | t0002 | g0288 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04115 | hp1 | a0002 | c0001 | t0002 | g0228 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04115 | hp2 | a0001 | c0003 | t0004 | g0041 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0053 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04199 | hp1 | a0002 | c0007 | t0005 | g0221 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0066 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18522 | hp1 | a0001 | c0004 | t0006 | g0107 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | CHB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18612 | hp2 | a0002 | c0001 | t0002 | g0246 | EAS | CHB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18906 | hp2 | a0001 | c0003 | t0009 | g0033 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18939 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18939 | hp2 | a0002 | c0001 | t0005 | g0224 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18940 | hp2 | a0002 | c0001 | t0002 | g0197 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18941 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18941 | hp2 | a0001 | c0002 | t0007 | g0178 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18944 | hp1 | a0002 | c0001 | t0002 | g0239 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18944 | hp2 | a0002 | c0001 | t0005 | g0189 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18945 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18947 | hp1 | a0002 | c0001 | t0005 | g0196 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18948 | hp1 | a0002 | c0001 | t0005 | g0188 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18949 | hp1 | a0002 | c0001 | t0002 | g0218 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18949 | hp2 | a0004 | c0008 | t0001 | g0144 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18950 | hp1 | a0005 | c0010 | t0003 | g0154 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18950 | hp2 | a0002 | c0001 | t0005 | g0019 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18951 | hp1 | a0002 | c0001 | t0002 | g0251 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18952 | hp2 | a0002 | c0001 | t0005 | g0019 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18954 | hp2 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18956 | hp1 | a0002 | c0001 | t0002 | g0254 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18957 | hp2 | a0002 | c0001 | t0002 | g0231 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18962 | hp2 | a0002 | c0001 | t0002 | g0237 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18964 | hp2 | a0002 | c0001 | t0002 | g0294 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18966 | hp2 | a0002 | c0001 | t0002 | g0232 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18971 | hp1 | a0001 | c0003 | t0004 | g0059 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18971 | hp2 | a0002 | c0001 | t0002 | g0214 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18972 | hp1 | a0002 | c0001 | t0005 | g0213 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18972 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18978 | hp1 | a0002 | c0001 | t0005 | g0187 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18978 | hp2 | a0001 | c0003 | t0004 | g0044 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18979 | hp1 | a0001 | c0003 | t0004 | g0061 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18979 | hp2 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18983 | hp2 | a0002 | c0001 | t0002 | g0279 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0229 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18986 | hp2 | a0001 | c0002 | t0007 | g0171 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18987 | hp2 | a0002 | c0001 | t0005 | g0021 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18988 | hp2 | a0002 | c0001 | t0005 | g0195 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18989 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18990 | hp2 | a0002 | c0001 | t0005 | g0194 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18991 | hp1 | a0002 | c0001 | t0005 | g0270 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18992 | hp2 | a0002 | c0001 | t0002 | g0207 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18993 | hp1 | a0002 | c0001 | t0002 | g0238 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18994 | hp1 | a0002 | c0001 | t0005 | g0215 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18994 | hp2 | a0002 | c0001 | t0002 | g0190 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0281 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18998 | hp1 | a0002 | c0001 | t0002 | g0184 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0043 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19002 | hp2 | a0002 | c0001 | t0005 | g0021 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19005 | hp2 | a0002 | c0001 | t0005 | g0020 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19006 | hp1 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19010 | hp1 | a0002 | c0001 | t0002 | g0257 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19010 | hp2 | a0001 | c0002 | t0007 | g0179 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19030 | hp1 | a0001 | c0003 | t0004 | g0051 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19030 | hp2 | a0001 | c0002 | t0015 | g0131 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19043 | hp2 | a0001 | c0004 | t0006 | g0006 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19058 | hp1 | a0001 | c0003 | t0004 | g0062 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19058 | hp2 | a0002 | c0001 | t0002 | g0258 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19064 | hp1 | a0002 | c0001 | t0002 | g0233 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0245 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19072 | hp2 | a0002 | c0001 | t0002 | g0271 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19080 | hp1 | a0002 | c0001 | t0002 | g0256 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19081 | hp1 | a0002 | c0001 | t0005 | g0191 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19083 | hp2 | a0002 | c0001 | t0002 | g0276 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19084 | hp2 | a0001 | c0005 | t0002 | g0290 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19086 | hp1 | a0001 | c0003 | t0008 | g0083 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19086 | hp2 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19088 | hp1 | a0002 | c0001 | t0005 | g0193 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19088 | hp2 | a0001 | c0002 | t0007 | g0180 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19090 | hp1 | a0001 | c0002 | t0007 | g0176 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19090 | hp2 | a0002 | c0001 | t0002 | g0235 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19091 | hp1 | a0001 | c0003 | t0004 | g0042 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19091 | hp2 | a0002 | c0001 | t0019 | g0219 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19240 | hp1 | a0002 | c0001 | t0002 | g0211 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0129 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20129 | hp1 | a0002 | c0001 | t0002 | g0291 | AFR | ASW | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20129 | hp2 | a0001 | c0004 | t0006 | g0006 | AFR | ASW | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0002 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0099 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20805 | hp2 | a0001 | c0003 | t0004 | g0058 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | GIH | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| NA20905 | hp2 | a0001 | c0003 | t0011 | g0065 | SAS | GIH | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0076 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG01123 | hp2 | a0002 | c0001 | t0005 | g0183 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02109 | hp1 | a0002 | c0001 | t0002 | g0210 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02109 | hp2 | a0001 | c0003 | t0013 | g0035 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02486 | hp1 | a0002 | c0007 | t0005 | g0265 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG02486 | hp2 | a0001 | c0003 | t0004 | g0012 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03471 | hp1 | a0001 | c0003 | t0009 | g0034 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG03471 | hp2 | a0001 | c0003 | t0020 | g0293 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG06807 | hp1 | a0002 | c0001 | t0002 | g0264 | AFR | USA | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | USA | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0002 | g0230 | REF | REF | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0002 | g0054 | REF | REF | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99369403 | A | G | 1 | a0003 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1399A>G | p.Met467Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/24 | 1565/5741 | 1399/3663 | 467/1220 | chr2 | 99369403 | |||
| chr2:99376359 | A | C | 4 | a0001 a0003 a0004 others(1): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
missense_variant | MODERATE | c.1565A>C | p.Lys522Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/24 | 1731/5741 | 1565/3663 | 522/1220 | chr2 | 99376359 | |||
| chr2:99382168 | G | A | 1 | a0004 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.2071G>A | p.Glu691Lys | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/24 | 2237/5741 | 2071/3663 | 691/1220 | chr2 | 99382168 | |||
| chr2:99389826 | A | G | 1 | a0005 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2380A>G | p.Ile794Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/24 | 2546/5741 | 2380/3663 | 794/1220 | chr2 | 99389826 | |||
| chr2:99389827 | T | C | 1 | a0005 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2381T>C | p.Ile794Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/24 | 2547/5741 | 2381/3663 | 794/1220 | chr2 | 99389827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99360350 | G | A | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.150G>A | p.Lys50Lys | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 2/24 | 316/5741 | 150/3663 | 50/1220 | chr2 | 99360350 | |||
| chr2:99361585 | G | A | 4 | a0001c0002 a0001c0009 a0004c0008 others(1): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
synonymous_variant | LOW | c.684G>A | p.Val228Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/24 | 850/5741 | 684/3663 | 228/1220 | chr2 | 99361585 | |||
| chr2:99364348 | G | T | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.1215G>T | p.Gly405Gly | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/24 | 1381/5741 | 1215/3663 | 405/1220 | chr2 | 99364348 | |||
| chr2:99364399 | T | C | 1 | a0001c0006 | 3 | HG01516.hp2 HG02145.hp1 HG02615.hp1 |
synonymous_variant | LOW | c.1266T>C | p.Thr422Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/24 | 1432/5741 | 1266/3663 | 422/1220 | chr2 | 99364399 | |||
| chr2:99379054 | C | T | 1 | a0001c0004 | 44 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(41): Show |
synonymous_variant | LOW | c.1878C>T | p.Thr626Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 11/24 | 2044/5741 | 1878/3663 | 626/1220 | chr2 | 99379054 | |||
| chr2:99379341 | T | C | 11 | a0001c0002 a0001c0003 a0001c0004 others(8): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
synonymous_variant | LOW | c.1974T>C | p.Asp658Asp | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/24 | 2140/5741 | 1974/3663 | 658/1220 | chr2 | 99379341 | |||
| chr2:99390381 | C | T | 1 | a0001c0009 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.2566C>T | p.Leu856Leu | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/24 | 2732/5741 | 2566/3663 | 856/1220 | chr2 | 99390381 | |||
| chr2:99394347 | A | G | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.2961A>G | p.Thr987Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 19/24 | 3127/5741 | 2961/3663 | 987/1220 | chr2 | 99394347 | |||
| chr2:99394350 | G | A | 1 | a0001c0011 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2964G>A | p.Leu988Leu | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 19/24 | 3130/5741 | 2964/3663 | 988/1220 | chr2 | 99394350 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99337393 | C | T | 1 | a0001c0003t0023 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-162C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 162 | chr2 | 99337393 | ||||||
| chr2:99337496 | C | G | 1 | a0001c0011t0021 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 59 | chr2 | 99337496 | ||||||
| chr2:99337496 | C | T | 1 | a0001c0002t0022 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 59 | chr2 | 99337496 | ||||||
| chr2:99399603 | G | T | 1 | a0001c0003t0010 | 3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 189 | chr2 | 99399603 | ||||||
| chr2:99400024 | A | G | 1 | a0001c0003t0020 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 610 | chr2 | 99400024 | ||||||
| chr2:99400044 | T | TAAAG | 2 | a0001c0003t0013 a0001c0011t0021 |
3 | HG01891.hp1 HG02055.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*634_*637dupGAAA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 638 | INFO_REALIGN_3_PRIME | chr2 | 99400044 | |||||
| chr2:99400155 | T | TATCA | 1 | a0001c0004t0006 | 7 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*745dupATCA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 746 | INFO_REALIGN_3_PRIME | chr2 | 99400155 | |||||
| chr2:99400191 | CAGTAGAG others(45): Show |
C | 1 | a0001c0003t0012 | 2 | HG02257.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830_*881delAGTAGA others(46): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 830 | INFO_REALIGN_3_PRIME | chr2 | 99400191 | |||||
| chr2:99400209 | ATTAATCT others(9): Show |
A | 1 | a0001c0002t0001 | 4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*815_*830delATCTTG others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 815 | INFO_REALIGN_3_PRIME | chr2 | 99400209 | |||||
| chr2:99400250 | G | C | 18 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0007 others(15): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*836G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 836 | chr2 | 99400250 | ||||||
| chr2:99400261 | A | ATTAATCT others(9): Show |
1 | a0001c0003t0011 | 2 | HG03491.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*866_*881dupAATCTT others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 882 | INFO_REALIGN_3_PRIME | chr2 | 99400261 | |||||
| chr2:99400261 | ATTAATCT others(9): Show |
A | 1 | a0001c0003t0009 | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*866_*881delAATCTT others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 866 | INFO_REALIGN_3_PRIME | chr2 | 99400261 | |||||
| chr2:99400386 | G | A | 6 | a0001c0003t0004 a0001c0003t0011 a0001c0003t0023 others(3): Show |
42 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*972G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 972 | chr2 | 99400386 | ||||||
| chr2:99400407 | T | A | 1 | a0001c0004t0014 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 993 | chr2 | 99400407 | ||||||
| chr2:99400611 | A | C | 5 | a0001c0003t0008 a0002c0001t0005 a0002c0001t0017 others(2): Show |
39 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1197 | chr2 | 99400611 | ||||||
| chr2:99400718 | T | A | 1 | a0002c0001t0018 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1304T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1304 | chr2 | 99400718 | ||||||
| chr2:99400812 | C | T | 1 | a0001c0003t0016 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1398 | chr2 | 99400812 | ||||||
| chr2:99400820 | G | A | 1 | a0002c0001t0019 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1406 | chr2 | 99400820 | ||||||
| chr2:99401051 | ATAAT | A | 4 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0015 others(1): Show |
54 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1641_*1644delTTAA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1641 | INFO_REALIGN_3_PRIME | chr2 | 99401051 | |||||
| chr2:99401082 | G | A | 1 | a0001c0002t0007 | 6 | HG02080.hp2 NA18941.hp2 NA18986.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1668G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1668 | chr2 | 99401082 | ||||||
| chr2:99401210 | T | C | 1 | a0001c0002t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1796 | chr2 | 99401210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99337721 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+132A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337721 | |||||||
| chr2:99337727 | C | T | 1 | a0001c0011t0021g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.35+138C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337727 | |||||||
| chr2:99337789 | C | G | 1 | a0002c0001t0002g0294 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.35+200C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337789 | |||||||
| chr2:99337809 | C | T | 1 | a0001c0003t0020g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.35+220C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337809 | |||||||
| chr2:99337813 | C | CT | 116 | a0001c0003t0004g0023 a0001c0003t0004g0282 a0001c0003t0004g0283 others(113): Show |
122 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.35+224_35+225insT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337813 | |||||||
| chr2:99337878 | A | T | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.35+289A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337878 | |||||||
| chr2:99337926 | C | T | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+337C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337926 | |||||||
| chr2:99337979 | A | G | 33 | a0001c0002t0001g0169 a0001c0002t0003g0001 a0001c0002t0003g0005 others(30): Show |
48 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.35+390A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337979 | |||||||
| chr2:99338004 | T | C | 1 | a0001c0004t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.35+415T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338004 | |||||||
| chr2:99338052 | G | A | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+463G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338052 | |||||||
| chr2:99338141 | C | T | 1 | a0002c0001t0002g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.35+552C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338141 | |||||||
| chr2:99338145 | A | G | 59 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(56): Show |
73 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.35+556A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338145 | |||||||
| chr2:99338163 | C | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+574C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338163 | |||||||
| chr2:99338173 | GT | G | 254 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(251): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.35+593delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338173 | ||||||
| chr2:99338272 | C | A | 110 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(107): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.35+683C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338272 | |||||||
| chr2:99338584 | G | A | 11 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(8): Show |
12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.35+995G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338584 | |||||||
| chr2:99338604 | T | C | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+1015T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338604 | |||||||
| chr2:99338652 | A | G | 1 | a0002c0001t0002g0281 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.35+1063A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338652 | |||||||
| chr2:99338922 | G | GTGTA | 96 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(93): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | G | GTGTATA | 5 | a0002c0001t0002g0273 a0002c0001t0002g0274 a0002c0001t0002g0276 others(2): Show |
5 | HG02040.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | G | GTGTATAT others(1): Show |
3 | a0002c0001t0002g0278 a0002c0001t0002g0279 a0002c0001t0002g0280 |
3 | HG02135.hp2 HG03927.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | G | GTGTATAT others(17): Show |
3 | a0001c0005t0002g0287 a0001c0005t0002g0288 a0001c0005t0002g0289 |
3 | HG01358.hp1 HG01496.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(24): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | G | GTGTATAT others(19): Show |
1 | a0001c0005t0002g0024 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(26): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | G | GTGTATAT others(23): Show |
1 | a0001c0005t0002g0290 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.35+1334_35+1335ins others(30): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338922 | GTA | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+1348_35+1349del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | ||||||
| chr2:99338929 | T | TATATATA others(43): Show |
1 | a0001c0004t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.35+1347_35+1348ins others(50): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338929 | ||||||
| chr2:99338937 | T | C | 7 | a0001c0004t0001g0078 a0001c0005t0002g0024 a0001c0005t0002g0287 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.35+1348T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338937 | |||||||
| chr2:99338965 | AAT | A | 111 | a0001c0003t0001g0077 a0001c0005t0002g0024 a0001c0005t0002g0287 others(108): Show |
116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.35+1388_35+1389del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338965 | ||||||
| chr2:99338971 | T | C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+1382T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338971 | |||||||
| chr2:99338975 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35+1386T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338975 | |||||||
| chr2:99338981 | A | T | 1 | a0002c0001t0005g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.35+1392A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338981 | |||||||
| chr2:99338989 | C | T | 1 | a0002c0001t0005g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.35+1400C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338989 | |||||||
| chr2:99338993 | A | AATATATA others(21): Show |
1 | a0001c0005t0002g0290 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.35+1417_35+1418ins others(28): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | ||||||
| chr2:99338993 | A | AATATATA others(23): Show |
2 | a0001c0005t0002g0287 a0001c0005t0002g0288 |
2 | HG01496.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(30): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | ||||||
| chr2:99338993 | A | AATATATA others(29): Show |
2 | a0001c0005t0002g0024 a0001c0005t0002g0289 |
3 | HG01070.hp2 HG01071.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(36): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | ||||||
| chr2:99338993 | A | AATATATA others(15): Show |
97 | a0002c0001t0002g0022 a0002c0001t0002g0185 a0002c0001t0002g0190 others(94): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.35+1415_35+1416ins others(22): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | ||||||
| chr2:99338993 | A | AATATATA others(17): Show |
4 | a0001c0012t0002g0269 a0002c0001t0002g0268 a0002c0001t0002g0271 others(1): Show |
4 | HG02258.hp1 HG03486.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+1415_35+1416ins others(24): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | ||||||
| chr2:99339005 | C | T | 3 | a0002c0001t0002g0184 a0002c0001t0005g0266 a0002c0001t0005g0267 |
3 | HG01256.hp2 HG01258.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.35+1416C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339005 | |||||||
| chr2:99339006 | A | ACAAATAT others(14): Show |
1 | a0002c0001t0002g0184 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.35+1417_35+1418ins others(21): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339006 | |||||||
| chr2:99339006 | A | ACAAATAT others(16): Show |
2 | a0002c0001t0005g0266 a0002c0001t0005g0267 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(23): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339006 | |||||||
| chr2:99339007 | T | A | 1 | a0002c0001t0002g0184 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.35+1418T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339007 | |||||||
| chr2:99339016 | T | C | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+1427T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339016 | |||||||
| chr2:99339057 | A | G | 1 | a0001c0003t0001g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.35+1468A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339057 | |||||||
| chr2:99339205 | G | T | 1 | a0002c0007t0005g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.35+1616G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339205 | |||||||
| chr2:99339208 | A | G | 1 | a0001c0002t0003g0182 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.35+1619A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339208 | |||||||
| chr2:99339235 | A | G | 3 | a0001c0003t0004g0066 a0001c0003t0011g0064 a0001c0003t0011g0065 |
3 | HG03491.hp2 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.35+1646A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339235 | |||||||
| chr2:99339692 | T | C | 1 | a0001c0004t0001g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.35+2103T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339692 | |||||||
| chr2:99339744 | T | G | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+2155T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339744 | |||||||
| chr2:99339782 | C | G | 1 | a0001c0011t0021g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.35+2193C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339782 | |||||||
| chr2:99339842 | G | A | 1 | a0002c0001t0002g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.35+2253G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339842 | |||||||
| chr2:99339886 | T | C | 3 | a0001c0003t0009g0030 a0001c0003t0009g0031 a0001c0003t0009g0032 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.35+2297T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339886 | |||||||
| chr2:99339911 | T | TTTG | 3 | a0001c0002t0001g0014 a0001c0002t0001g0120 a0001c0002t0001g0121 |
4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+2343_35+2345dup others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99339911 | ||||||
| chr2:99340175 | G | A | 13 | a0002c0001t0002g0190 a0002c0001t0005g0019 a0002c0001t0005g0187 others(10): Show |
14 | HG00558.hp1 HG02027.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.35+2586G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340175 | |||||||
| chr2:99340323 | A | T | 12 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(9): Show |
13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.35+2734A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340323 | |||||||
| chr2:99340373 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+2784A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340373 | |||||||
| chr2:99340413 | G | T | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+2824G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340413 | |||||||
| chr2:99340452 | A | G | 14 | a0001c0002t0003g0018 a0001c0002t0003g0170 a0001c0002t0003g0172 others(11): Show |
15 | HG02080.hp2 HG04184.hp2 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+2863A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340452 | |||||||
| chr2:99340520 | G | T | 1 | a0001c0002t0001g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.35+2931G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340520 | |||||||
| chr2:99340809 | A | G | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+3220A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340809 | |||||||
| chr2:99340833 | G | T | 1 | a0002c0001t0002g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+3244G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340833 | |||||||
| chr2:99340840 | A | G | 110 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(107): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.35+3251A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340840 | |||||||
| chr2:99340855 | C | T | 1 | a0002c0001t0002g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.35+3266C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340855 | |||||||
| chr2:99340950 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35+3361G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340950 | |||||||
| chr2:99341112 | G | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+3523G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341112 | |||||||
| chr2:99341490 | G | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+3901G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341490 | |||||||
| chr2:99341501 | A | G | 1 | a0001c0002t0001g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.35+3912A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341501 | |||||||
| chr2:99341758 | A | C | 1 | a0002c0001t0002g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.35+4169A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341758 | |||||||
| chr2:99341763 | G | T | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.35+4174G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341763 | |||||||
| chr2:99341814 | G | A | 1 | a0002c0001t0002g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+4225G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341814 | |||||||
| chr2:99342233 | C | CT | 6 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.35+4655dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99342233 | ||||||
| chr2:99342363 | G | C | 1 | a0001c0003t0004g0282 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.35+4774G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342363 | |||||||
| chr2:99342560 | G | A | 3 | a0001c0004t0001g0080 a0001c0004t0001g0081 a0001c0004t0001g0082 |
3 | HG00544.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.35+4971G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342560 | |||||||
| chr2:99342627 | CT | C | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+5042delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99342627 | ||||||
| chr2:99342759 | G | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+5170G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342759 | |||||||
| chr2:99342785 | C | T | 1 | a0001c0003t0001g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.35+5196C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342785 | |||||||
| chr2:99342872 | G | A | 1 | a0002c0001t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.35+5283G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342872 | |||||||
| chr2:99343007 | C | G | 1 | a0001c0002t0003g0168 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.35+5418C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343007 | |||||||
| chr2:99343202 | C | T | 3 | a0002c0001t0002g0259 a0002c0001t0002g0260 a0002c0001t0002g0261 |
3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.35+5613C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343202 | |||||||
| chr2:99343246 | G | A | 4 | a0001c0002t0003g0122 a0001c0002t0003g0123 a0001c0002t0003g0124 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+5657G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343246 | |||||||
| chr2:99343348 | T | C | 1 | a0001c0003t0004g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.35+5759T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343348 | |||||||
| chr2:99343382 | A | C | 110 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(107): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.35+5793A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343382 | |||||||
| chr2:99343490 | G | T | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.35+5901G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343490 | |||||||
| chr2:99343540 | G | A | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.35+5951G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343540 | |||||||
| chr2:99343849 | A | G | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6260A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343849 | |||||||
| chr2:99343925 | C | CT | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+6347dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99343925 | ||||||
| chr2:99343957 | C | T | 1 | a0002c0001t0002g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+6368C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343957 | |||||||
| chr2:99344012 | G | A | 1 | a0002c0001t0002g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.35+6423G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344012 | |||||||
| chr2:99344076 | G | A | 2 | a0001c0003t0008g0003 a0001c0003t0008g0083 |
5 | NA18939.hp1 NA18941.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+6487G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344076 | |||||||
| chr2:99344100 | T | A | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6511T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344100 | |||||||
| chr2:99344123 | G | A | 4 | a0001c0003t0009g0030 a0001c0003t0009g0031 a0001c0003t0009g0032 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+6534G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344123 | |||||||
| chr2:99344142 | G | A | 2 | a0002c0001t0005g0272 a0002c0001t0017g0186 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.35+6553G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344142 | |||||||
| chr2:99344166 | C | T | 4 | a0002c0001t0002g0255 a0002c0001t0002g0256 a0002c0001t0002g0257 others(1): Show |
4 | HG00558.hp2 NA19010.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6577C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344166 | |||||||
| chr2:99344233 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.35+6644A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344233 | |||||||
| chr2:99344348 | G | A | 1 | a0002c0001t0002g0197 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.35+6759G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344348 | |||||||
| chr2:99344404 | T | TTTG | 17 | a0001c0002t0001g0014 a0001c0002t0001g0120 a0001c0002t0001g0121 others(14): Show |
18 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.35+6845_35+6847dup others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344404 | ||||||
| chr2:99344404 | T | TTTGTTG | 29 | a0001c0004t0001g0002 a0001c0004t0001g0004 a0001c0004t0001g0025 others(26): Show |
37 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.35+6842_35+6847dup others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344404 | ||||||
| chr2:99344442 | GT | G | 104 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0185 others(101): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.35+6865delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344442 | ||||||
| chr2:99344467 | C | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+6878C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344467 | |||||||
| chr2:99344561 | G | A | 6 | a0001c0004t0001g0084 a0001c0005t0002g0024 a0001c0005t0002g0287 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.35+6972G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344561 | |||||||
| chr2:99344597 | C | T | 6 | a0001c0002t0003g0005 a0001c0002t0003g0163 a0001c0002t0003g0164 others(3): Show |
9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.35+7008C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344597 | |||||||
| chr2:99344894 | C | A | 11 | a0002c0001t0002g0203 a0002c0001t0002g0204 a0002c0001t0002g0205 others(8): Show |
11 | HG00438.hp1 HG00558.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.35+7305C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344894 | |||||||
| chr2:99345043 | G | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.35+7454G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345043 | |||||||
| chr2:99345068 | A | G | 1 | a0001c0002t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.35+7479A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345068 | |||||||
| chr2:99345182 | G | A | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+7593G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345182 | |||||||
| chr2:99345307 | C | T | 1 | a0001c0009t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.35+7718C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345307 | |||||||
| chr2:99345422 | G | A | 1 | a0002c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.35+7833G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345422 | |||||||
| chr2:99345438 | C | G | 1 | a0001c0004t0001g0104 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.35+7849C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345438 | |||||||
| chr2:99345445 | T | C | 4 | a0001c0003t0001g0067 a0001c0003t0001g0068 a0001c0003t0001g0069 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+7856T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345445 | |||||||
| chr2:99345611 | A | AAT | 51 | a0001c0004t0001g0085 a0001c0004t0001g0086 a0001c0004t0001g0087 others(48): Show |
54 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.35+8022_35+8023ins others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | |||||||
| chr2:99345611 | A | AT | 89 | a0001c0002t0001g0126 a0001c0002t0003g0163 a0001c0002t0003g0170 others(86): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.35+8022_35+8023ins others(1): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | |||||||
| chr2:99345611 | A | T | 111 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(108): Show |
139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.35+8022A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | |||||||
| chr2:99345696 | G | C | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.35+8107G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345696 | |||||||
| chr2:99345780 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.35+8191A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345780 | |||||||
| chr2:99345787 | A | T | 3 | a0001c0003t0013g0035 a0001c0003t0013g0036 a0001c0011t0021g0295 |
3 | HG01891.hp1 HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.35+8198A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345787 | |||||||
| chr2:99345918 | T | C | 4 | a0001c0003t0009g0030 a0001c0003t0009g0031 a0001c0003t0009g0032 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+8329T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345918 | |||||||
| chr2:99345943 | C | CA | 135 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(132): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.35+8370dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99345943 | ||||||
| chr2:99345943 | CA | C | 105 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(102): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.35+8370delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99345943 | ||||||
| chr2:99345991 | G | T | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.35+8402G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345991 | |||||||
| chr2:99346024 | C | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+8435C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346024 | |||||||
| chr2:99346048 | A | G | 1 | a0002c0001t0002g0254 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.35+8459A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346048 | |||||||
| chr2:99346109 | T | C | 2 | a0002c0001t0002g0212 a0002c0001t0002g0226 |
2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.35+8520T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346109 | |||||||
| chr2:99346119 | A | C | 3 | a0001c0003t0010g0026 a0001c0003t0010g0027 a0001c0003t0010g0028 |
3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.35+8530A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346119 | |||||||
| chr2:99346140 | T | G | 2 | a0001c0003t0001g0013 a0001c0003t0001g0071 |
3 | HG00642.hp2 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.35+8551T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346140 | |||||||
| chr2:99346338 | T | A | 1 | a0001c0003t0004g0010 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.35+8749T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346338 | |||||||
| chr2:99346407 | A | G | 1 | a0002c0001t0002g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.35+8818A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346407 | |||||||
| chr2:99346589 | C | CT | 111 | a0001c0003t0004g0060 a0001c0003t0004g0061 a0001c0003t0004g0062 others(108): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.35+9027dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346589 | C | CTT | 21 | a0001c0004t0001g0081 a0001c0004t0001g0087 a0001c0004t0001g0102 others(18): Show |
22 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.35+9026_35+9027dup others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346589 | CT | C | 87 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(84): Show |
114 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.35+9027delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346589 | CTT | C | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+9026_35+9027del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346589 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+9017_35+9027del others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346589 | CTTTTTTT others(10): Show |
C | 1 | a0002c0001t0002g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+9011_35+9027del others(17): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | ||||||
| chr2:99346689 | G | A | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+9100G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346689 | |||||||
| chr2:99346892 | G | T | 1 | a0002c0001t0002g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.35+9303G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346892 | |||||||
| chr2:99347268 | A | G | 1 | a0001c0003t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.35+9679A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347268 | |||||||
| chr2:99347505 | G | GT | 7 | a0001c0002t0003g0181 a0001c0005t0002g0024 a0001c0005t0002g0287 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.35+9930dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347505 | ||||||
| chr2:99347505 | GT | G | 10 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0120 others(7): Show |
12 | HG02630.hp2 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.35+9930delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347505 | ||||||
| chr2:99347577 | A | G | 2 | a0001c0002t0007g0179 a0001c0002t0007g0180 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.35+9988A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347577 | |||||||
| chr2:99347712 | T | C | 2 | a0001c0003t0010g0026 a0001c0003t0010g0027 |
2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.35+10123T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347712 | |||||||
| chr2:99347821 | G | A | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+10232G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347821 | |||||||
| chr2:99347953 | T | TAG | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+10368_35+10369d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347953 | ||||||
| chr2:99348076 | G | A | 1 | a0001c0004t0001g0089 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.35+10487G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348076 | |||||||
| chr2:99348399 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.35+10810G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348399 | |||||||
| chr2:99348777 | A | T | 11 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(8): Show |
12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.35+11188A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348777 | |||||||
| chr2:99349001 | T | G | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.36-11235T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349001 | |||||||
| chr2:99349017 | T | C | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-11219T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349017 | |||||||
| chr2:99349206 | G | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-11030G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349206 | |||||||
| chr2:99349334 | T | C | 12 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0110 others(9): Show |
15 | HG00609.hp2 HG02148.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.36-10902T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349334 | |||||||
| chr2:99349732 | G | A | 1 | a0005c0010t0003g0154 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.36-10504G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349732 | |||||||
| chr2:99349822 | G | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-10414G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349822 | |||||||
| chr2:99349963 | A | G | 1 | a0001c0004t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.36-10273A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349963 | |||||||
| chr2:99350061 | G | A | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-10175G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350061 | |||||||
| chr2:99350096 | T | C | 1 | a0001c0003t0004g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.36-10140T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350096 | |||||||
| chr2:99350129 | T | C | 3 | a0001c0002t0003g0018 a0001c0002t0003g0172 a0001c0002t0003g0181 |
4 | NA18940.hp1 NA18995.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-10107T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350129 | |||||||
| chr2:99350272 | A | G | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-9964A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350272 | |||||||
| chr2:99350368 | G | A | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.36-9868G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350368 | |||||||
| chr2:99350396 | TC | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-9834delC | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99350396 | ||||||
| chr2:99350653 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.36-9583A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350653 | |||||||
| chr2:99351050 | G | A | 2 | a0002c0001t0005g0266 a0002c0001t0005g0267 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.36-9186G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351050 | |||||||
| chr2:99351068 | T | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-9168T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351068 | |||||||
| chr2:99351189 | A | G | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-9047A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351189 | |||||||
| chr2:99351250 | T | C | 1 | a0002c0001t0017g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.36-8986T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351250 | |||||||
| chr2:99351264 | G | C | 1 | a0001c0002t0003g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8972G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351264 | |||||||
| chr2:99351265 | T | A | 1 | a0001c0002t0003g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8971T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351265 | |||||||
| chr2:99351271 | C | A | 1 | a0001c0002t0003g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8965C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351271 | |||||||
| chr2:99351273 | T | G | 1 | a0001c0002t0003g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8963T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351273 | |||||||
| chr2:99351274 | G | T | 1 | a0001c0002t0003g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8962G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351274 | |||||||
| chr2:99351284 | T | C | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-8952T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351284 | |||||||
| chr2:99351336 | A | G | 1 | a0001c0003t0004g0059 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.36-8900A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351336 | |||||||
| chr2:99351467 | A | G | 1 | a0002c0001t0002g0250 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.36-8769A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351467 | |||||||
| chr2:99351599 | G | A | 3 | a0001c0004t0001g0080 a0001c0004t0001g0081 a0001c0004t0001g0082 |
3 | HG00544.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.36-8637G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351599 | |||||||
| chr2:99351644 | C | T | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-8592C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351644 | |||||||
| chr2:99351687 | G | GT | 68 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(65): Show |
91 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.36-8539dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99351687 | ||||||
| chr2:99351694 | T | TG | 4 | a0001c0002t0003g0122 a0001c0002t0003g0123 a0001c0002t0003g0124 others(1): Show |
4 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-8542_36-8541ins others(1): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351694 | |||||||
| chr2:99351792 | G | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-8444G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351792 | |||||||
| chr2:99351811 | C | T | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-8425C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351811 | |||||||
| chr2:99351819 | T | C | 1 | a0001c0003t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.36-8417T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351819 | |||||||
| chr2:99351867 | T | C | 6 | a0002c0001t0002g0210 a0002c0001t0002g0211 a0002c0001t0002g0212 others(3): Show |
6 | HG01261.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-8369T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351867 | |||||||
| chr2:99351951 | C | T | 1 | a0001c0003t0004g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.36-8285C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351951 | |||||||
| chr2:99352048 | C | A | 1 | a0002c0001t0002g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.36-8188C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352048 | |||||||
| chr2:99352128 | T | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-8108T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352128 | |||||||
| chr2:99352152 | T | C | 4 | a0001c0003t0001g0067 a0001c0003t0001g0068 a0001c0003t0001g0069 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-8084T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352152 | |||||||
| chr2:99352364 | T | A | 1 | a0001c0003t0023g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.36-7872T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352364 | |||||||
| chr2:99352525 | C | CT | 17 | a0001c0002t0001g0145 a0001c0002t0003g0124 a0001c0002t0003g0161 others(14): Show |
18 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.36-7695dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99352525 | ||||||
| chr2:99352632 | G | A | 256 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(253): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.36-7604G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352632 | |||||||
| chr2:99352716 | A | C | 6 | a0001c0003t0004g0023 a0001c0003t0004g0282 a0001c0003t0004g0283 others(3): Show |
7 | HG01358.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.36-7520A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352716 | |||||||
| chr2:99352978 | A | G | 4 | a0002c0001t0005g0020 a0002c0001t0005g0021 a0002c0001t0005g0220 others(1): Show |
6 | HG00544.hp1 HG02083.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-7258A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352978 | |||||||
| chr2:99353005 | C | CTTTTT | 8 | a0002c0001t0002g0205 a0002c0001t0002g0212 a0002c0001t0002g0226 others(5): Show |
8 | HG01261.hp2 HG02145.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.36-7208_36-7204dup others(5): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTT | 16 | a0002c0001t0002g0204 a0002c0001t0002g0206 a0002c0001t0002g0207 others(13): Show |
16 | HG00639.hp2 HG01516.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-7209_36-7204dup others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT | 23 | a0002c0001t0002g0022 a0002c0001t0002g0197 a0002c0001t0002g0198 others(20): Show |
24 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-7210_36-7204dup others(7): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT others(1): Show |
16 | a0002c0001t0002g0185 a0002c0001t0002g0190 a0002c0001t0002g0202 others(13): Show |
18 | HG01099.hp1 HG01884.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.36-7211_36-7204dup others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT others(2): Show |
20 | a0002c0001t0002g0184 a0002c0001t0002g0244 a0002c0001t0002g0245 others(17): Show |
21 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-7212_36-7204dup others(9): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT others(3): Show |
5 | a0002c0001t0002g0199 a0002c0001t0002g0249 a0002c0001t0005g0183 others(2): Show |
5 | HG00408.hp1 HG00438.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-7213_36-7204dup others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT others(4): Show |
5 | a0002c0001t0002g0200 a0002c0001t0002g0218 a0002c0001t0005g0223 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-7214_36-7204dup others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | CTTTTTTT others(6): Show |
1 | a0002c0001t0002g0281 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.36-7216_36-7204dup others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | C | T | 1 | a0002c0001t0005g0196 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.36-7231C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353005 | |||||||
| chr2:99353005 | CT | C | 18 | a0001c0003t0004g0011 a0001c0003t0004g0012 a0001c0003t0004g0023 others(15): Show |
21 | HG01168.hp1 HG01358.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-7204delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTT | C | 9 | a0001c0003t0001g0029 a0001c0003t0004g0041 a0001c0003t0010g0026 others(6): Show |
9 | HG01243.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.36-7205_36-7204del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTT | C | 33 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(30): Show |
39 | HG00609.hp2 HG00642.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.36-7206_36-7204del others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTTT | C | 25 | a0001c0004t0001g0002 a0001c0004t0001g0004 a0001c0004t0001g0025 others(22): Show |
33 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.36-7207_36-7204del others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTTTTTT | C | 70 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(67): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.36-7210_36-7204del others(7): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTTTTTT others(1): Show |
C | 8 | a0001c0002t0001g0128 a0001c0002t0003g0155 a0001c0002t0003g0156 others(5): Show |
8 | HG00639.hp1 HG02040.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.36-7211_36-7204del others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTTTTTT others(4): Show |
C | 1 | a0002c0001t0002g0232 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.36-7214_36-7204del others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353005 | CTTTTTTT others(6): Show |
C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-7216_36-7204del others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | ||||||
| chr2:99353009 | T | C | 1 | a0001c0003t0004g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.36-7227T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353009 | |||||||
| chr2:99353150 | G | A | 1 | a0001c0003t0011g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.36-7086G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353150 | |||||||
| chr2:99353215 | A | C | 3 | a0001c0003t0010g0026 a0001c0003t0010g0027 a0001c0003t0010g0028 |
3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.36-7021A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353215 | |||||||
| chr2:99353371 | A | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-6865A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353371 | |||||||
| chr2:99353564 | T | C | 1 | a0002c0001t0002g0254 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.36-6672T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353564 | |||||||
| chr2:99353653 | G | A | 6 | a0001c0003t0004g0010 a0001c0003t0004g0047 a0001c0003t0023g0040 others(3): Show |
7 | HG01516.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.36-6583G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353653 | |||||||
| chr2:99353707 | C | T | 1 | a0002c0001t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.36-6529C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353707 | |||||||
| chr2:99354337 | G | C | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.36-5899G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354337 | |||||||
| chr2:99354403 | A | G | 1 | a0001c0002t0001g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.36-5833A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354403 | |||||||
| chr2:99354685 | G | C | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-5551G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354685 | |||||||
| chr2:99354796 | CT | C | 40 | a0001c0002t0001g0145 a0001c0002t0001g0147 a0001c0003t0001g0071 others(37): Show |
44 | HG01109.hp2 HG01358.hp2 HG01516.hp2 others(41): Show |
intron_variant | MODIFIER | c.36-5416delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | ||||||
| chr2:99354796 | CTT | C | 95 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(92): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.36-5417_36-5416del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | ||||||
| chr2:99354796 | CTTT | C | 45 | a0001c0002t0001g0149 a0001c0002t0003g0001 a0001c0002t0003g0005 others(42): Show |
61 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.36-5418_36-5416del others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | ||||||
| chr2:99354796 | CTTTT | C | 107 | a0001c0002t0003g0155 a0001c0002t0003g0166 a0001c0003t0001g0117 others(104): Show |
111 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.36-5419_36-5416del others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | ||||||
| chr2:99354826 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-5410A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354826 | |||||||
| chr2:99354851 | G | A | 1 | a0002c0001t0002g0256 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.36-5385G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354851 | |||||||
| chr2:99355138 | T | A | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.36-5098T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355138 | |||||||
| chr2:99355271 | C | A | 1 | a0002c0001t0002g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.36-4965C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355271 | |||||||
| chr2:99355391 | A | G | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.36-4845A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355391 | |||||||
| chr2:99355413 | T | C | 1 | a0002c0001t0005g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.36-4823T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355413 | |||||||
| chr2:99355492 | T | TTTTTACA others(18): Show |
4 | a0002c0001t0002g0232 a0002c0001t0002g0238 a0002c0001t0002g0263 others(1): Show |
4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4744_36-4743ins others(25): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355492 | |||||||
| chr2:99355493 | A | C | 4 | a0002c0001t0002g0232 a0002c0001t0002g0238 a0002c0001t0002g0263 others(1): Show |
4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4743A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355493 | |||||||
| chr2:99355495 | G | T | 4 | a0002c0001t0002g0232 a0002c0001t0002g0238 a0002c0001t0002g0263 others(1): Show |
4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4741G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355495 | |||||||
| chr2:99355496 | T | A | 4 | a0002c0001t0002g0232 a0002c0001t0002g0238 a0002c0001t0002g0263 others(1): Show |
4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4740T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355496 | |||||||
| chr2:99355593 | G | T | 12 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(9): Show |
13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.36-4643G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355593 | |||||||
| chr2:99355610 | G | GT | 49 | a0001c0002t0001g0150 a0001c0002t0015g0131 a0001c0003t0001g0077 others(46): Show |
62 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.36-4606dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99355610 | ||||||
| chr2:99355610 | GT | G | 157 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(154): Show |
182 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.36-4606delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99355610 | ||||||
| chr2:99355883 | G | A | 1 | a0001c0003t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.36-4353G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355883 | |||||||
| chr2:99355892 | C | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-4344C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355892 | |||||||
| chr2:99355907 | C | A | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-4329C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355907 | |||||||
| chr2:99355928 | T | A | 2 | a0001c0002t0001g0132 a0001c0002t0001g0153 |
2 | NA18988.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.36-4308T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355928 | |||||||
| chr2:99356149 | A | G | 1 | a0001c0003t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.36-4087A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356149 | |||||||
| chr2:99356227 | G | A | 1 | a0001c0011t0021g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.36-4009G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356227 | |||||||
| chr2:99356519 | G | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-3717G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356519 | |||||||
| chr2:99356725 | T | A | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-3511T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356725 | |||||||
| chr2:99356836 | C | G | 8 | a0001c0004t0001g0004 a0001c0004t0001g0078 a0001c0004t0001g0086 others(5): Show |
11 | HG01070.hp1 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.36-3400C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356836 | |||||||
| chr2:99356986 | G | A | 3 | a0002c0001t0002g0231 a0002c0001t0002g0233 a0002c0001t0002g0254 |
3 | NA18956.hp1 NA18957.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.36-3250G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356986 | |||||||
| chr2:99357284 | G | T | 2 | a0001c0002t0001g0143 a0001c0002t0001g0150 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.36-2952G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357284 | |||||||
| chr2:99357322 | G | A | 3 | a0002c0001t0002g0199 a0002c0001t0002g0200 a0002c0001t0002g0273 |
3 | HG02572.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.36-2914G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357322 | |||||||
| chr2:99357334 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.36-2902G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357334 | |||||||
| chr2:99357377 | G | A | 1 | a0001c0002t0003g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.36-2859G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357377 | |||||||
| chr2:99357492 | G | A | 1 | a0001c0003t0001g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.36-2744G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357492 | |||||||
| chr2:99357637 | C | G | 1 | a0001c0004t0001g0088 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.36-2599C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357637 | |||||||
| chr2:99357645 | T | C | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-2591T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357645 | |||||||
| chr2:99357702 | T | C | 3 | a0001c0006t0004g0045 a0001c0006t0004g0046 a0001c0006t0004g0063 |
3 | HG01516.hp2 HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.36-2534T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357702 | |||||||
| chr2:99357706 | A | G | 1 | a0001c0012t0002g0269 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36-2530A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357706 | |||||||
| chr2:99358010 | G | A | 46 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0110 others(43): Show |
59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.36-2226G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358010 | |||||||
| chr2:99358144 | A | G | 1 | a0001c0004t0001g0088 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.36-2092A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358144 | |||||||
| chr2:99358180 | C | T | 1 | a0001c0002t0001g0141 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.36-2056C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358180 | |||||||
| chr2:99358256 | G | A | 1 | a0001c0005t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.36-1980G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358256 | |||||||
| chr2:99358450 | C | T | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-1786C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358450 | |||||||
| chr2:99358587 | T | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-1649T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358587 | |||||||
| chr2:99359084 | C | T | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.36-1152C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359084 | |||||||
| chr2:99359166 | G | A | 4 | a0002c0001t0005g0189 a0002c0001t0005g0192 a0002c0001t0005g0193 others(1): Show |
4 | HG00558.hp1 NA18944.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-1070G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359166 | |||||||
| chr2:99359206 | C | CA | 110 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(107): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.36-1017dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99359206 | ||||||
| chr2:99359206 | CA | C | 11 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(8): Show |
12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.36-1017delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99359206 | ||||||
| chr2:99359261 | C | T | 3 | a0002c0001t0002g0259 a0002c0001t0002g0260 a0002c0001t0002g0261 |
3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.36-975C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359261 | |||||||
| chr2:99359262 | G | A | 34 | a0001c0004t0001g0002 a0001c0004t0001g0004 a0001c0004t0001g0025 others(31): Show |
44 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.36-974G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359262 | |||||||
| chr2:99359407 | C | A | 35 | a0002c0001t0002g0190 a0002c0001t0002g0214 a0002c0001t0002g0274 others(32): Show |
38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.36-829C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359407 | |||||||
| chr2:99359747 | G | C | 3 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0175 |
3 | HG04184.hp2 NA18957.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.36-489G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359747 | |||||||
| chr2:99359828 | C | A | 145 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(142): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.36-408C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359828 | |||||||
| chr2:99359879 | G | A | 10 | a0001c0002t0001g0017 a0001c0002t0001g0133 a0001c0002t0001g0134 others(7): Show |
11 | HG02080.hp1 HG02818.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.36-357G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359879 | |||||||
| chr2:99360101 | A | G | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-135A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99360101 | |||||||
| chr2:99360559 | A | T | 3 | a0001c0003t0010g0026 a0001c0003t0010g0027 a0001c0003t0010g0028 |
3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.246+10A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360559 | |||||||
| chr2:99360699 | TAGGAATG others(3): Show |
T | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.246+154_246+163del others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 99360699 | ||||||
| chr2:99360733 | G | A | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+184G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360733 | |||||||
| chr2:99360758 | T | A | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.246+209T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360758 | |||||||
| chr2:99360879 | C | A | 8 | a0001c0002t0001g0007 a0001c0002t0001g0136 a0001c0002t0001g0137 others(5): Show |
10 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-269C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360879 | |||||||
| chr2:99361014 | T | C | 1 | a0002c0001t0018g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.247-134T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99361014 | |||||||
| chr2:99361032 | T | C | 1 | a0001c0002t0003g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247-116T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99361032 | |||||||
| chr2:99362073 | A | AT | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+261dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 99362073 | ||||||
| chr2:99362205 | C | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+385C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362205 | |||||||
| chr2:99362313 | A | C | 2 | a0002c0001t0002g0251 a0002c0001t0002g0276 |
2 | NA18951.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.919+493A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362313 | |||||||
| chr2:99362487 | T | A | 46 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0110 others(43): Show |
59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.919+667T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362487 | |||||||
| chr2:99362551 | T | C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+731T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362551 | |||||||
| chr2:99362555 | C | T | 1 | a0002c0001t0005g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.919+735C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362555 | |||||||
| chr2:99362697 | T | C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+877T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362697 | |||||||
| chr2:99362744 | T | C | 1 | a0001c0002t0001g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920-901T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362744 | |||||||
| chr2:99362822 | G | A | 1 | a0001c0003t0004g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-823G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362822 | |||||||
| chr2:99362902 | G | A | 2 | a0001c0004t0001g0025 a0001c0004t0001g0103 |
2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.920-743G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362902 | |||||||
| chr2:99362925 | A | G | 1 | a0002c0001t0002g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.920-720A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362925 | |||||||
| chr2:99363038 | T | C | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.920-607T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363038 | |||||||
| chr2:99363199 | C | G | 3 | a0002c0001t0002g0237 a0002c0001t0002g0271 a0002c0001t0002g0294 |
3 | NA18962.hp2 NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.920-446C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363199 | |||||||
| chr2:99363210 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.920-435A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363210 | |||||||
| chr2:99363363 | T | G | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-282T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363363 | |||||||
| chr2:99363489 | A | G | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.920-156A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363489 | |||||||
| chr2:99363625 | G | T | 1 | a0002c0001t0002g0276 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.920-20G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363625 | |||||||
| chr2:99364759 | A | G | 2 | a0002c0001t0002g0243 a0002c0001t0002g0250 |
2 | HG00738.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1288+338A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364759 | |||||||
| chr2:99364760 | T | C | 4 | a0002c0001t0002g0234 a0002c0001t0002g0235 a0002c0001t0002g0239 others(1): Show |
4 | HG01978.hp1 HG02523.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+339T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364760 | |||||||
| chr2:99364879 | AT | A | 116 | a0001c0002t0001g0016 a0001c0002t0001g0145 a0001c0002t0001g0149 others(113): Show |
121 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1288+467delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99364879 | ||||||
| chr2:99364989 | T | A | 2 | a0001c0004t0001g0025 a0001c0004t0001g0103 |
2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1288+568T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364989 | |||||||
| chr2:99365174 | T | A | 1 | a0001c0004t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1288+753T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365174 | |||||||
| chr2:99365207 | G | T | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1288+786G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365207 | |||||||
| chr2:99365269 | T | C | 1 | a0001c0003t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1288+848T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365269 | |||||||
| chr2:99365399 | A | G | 257 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1288+978A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365399 | |||||||
| chr2:99365469 | G | A | 1 | a0001c0003t0004g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1288+1048G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365469 | |||||||
| chr2:99365543 | T | C | 1 | a0002c0001t0002g0214 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1288+1122T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365543 | |||||||
| chr2:99365589 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1288+1168C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365589 | |||||||
| chr2:99365716 | T | TCAAAATC others(94): Show |
3 | a0001c0002t0001g0016 a0001c0002t0001g0138 a0001c0002t0001g0145 |
4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1296_1288+129 others(105): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99365716 | ||||||
| chr2:99365719 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0138 a0001c0002t0001g0145 |
4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1298C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365719 | |||||||
| chr2:99365720 | T | G | 3 | a0001c0002t0001g0016 a0001c0002t0001g0138 a0001c0002t0001g0145 |
4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1299T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365720 | |||||||
| chr2:99365721 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0138 a0001c0002t0001g0145 |
4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1300C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365721 | |||||||
| chr2:99365738 | G | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1288+1317G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365738 | |||||||
| chr2:99365848 | C | A | 1 | a0001c0003t0001g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1288+1427C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365848 | |||||||
| chr2:99365883 | A | G | 1 | a0002c0001t0002g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1288+1462A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365883 | |||||||
| chr2:99365964 | T | C | 1 | a0002c0001t0002g0204 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1288+1543T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365964 | |||||||
| chr2:99366002 | A | G | 1 | a0001c0003t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1288+1581A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366002 | |||||||
| chr2:99366044 | G | A | 1 | a0001c0002t0003g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1288+1623G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366044 | |||||||
| chr2:99366088 | T | TAC | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1288+1679_1288+168 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99366088 | ||||||
| chr2:99366088 | TAC | T | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1288+1679_1288+168 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99366088 | ||||||
| chr2:99366210 | C | T | 1 | a0001c0003t0020g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1288+1789C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366210 | |||||||
| chr2:99366267 | T | C | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1288+1846T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366267 | |||||||
| chr2:99366311 | A | G | 4 | a0001c0003t0004g0042 a0001c0003t0004g0043 a0001c0003t0004g0044 others(1): Show |
4 | NA18978.hp2 NA18998.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+1890A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366311 | |||||||
| chr2:99366342 | C | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1288+1921C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366342 | |||||||
| chr2:99366510 | C | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-1983C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366510 | |||||||
| chr2:99366522 | A | G | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-1971A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366522 | |||||||
| chr2:99366542 | G | T | 288 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(285): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.1289-1951G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366542 | |||||||
| chr2:99366729 | G | A | 1 | a0001c0002t0001g0138 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1289-1764G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366729 | |||||||
| chr2:99367368 | C | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1289-1125C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367368 | |||||||
| chr2:99367431 | C | CT | 244 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(241): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.1289-1049dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99367431 | ||||||
| chr2:99367431 | C | CTT | 12 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(9): Show |
13 | HG00642.hp2 HG01123.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-1050_1289-104 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99367431 | ||||||
| chr2:99367512 | C | T | 1 | a0001c0003t0004g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1289-981C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367512 | |||||||
| chr2:99367546 | C | T | 2 | a0002c0007t0005g0221 a0002c0007t0005g0265 |
2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1289-947C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367546 | |||||||
| chr2:99367577 | T | C | 1 | a0002c0001t0002g0207 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1289-916T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367577 | |||||||
| chr2:99367715 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1289-778A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367715 | |||||||
| chr2:99367734 | C | T | 12 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(9): Show |
13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-759C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367734 | |||||||
| chr2:99367735 | G | A | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1289-758G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367735 | |||||||
| chr2:99367746 | C | T | 1 | a0001c0002t0003g0168 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1289-747C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367746 | |||||||
| chr2:99367905 | G | C | 1 | a0001c0004t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1289-588G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367905 | |||||||
| chr2:99368271 | T | C | 1 | a0001c0002t0001g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1289-222T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368271 | |||||||
| chr2:99368414 | A | G | 1 | a0002c0001t0018g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1289-79A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368414 | |||||||
| chr2:99368430 | A | G | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-63A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368430 | |||||||
| chr2:99368689 | C | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387+98C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368689 | |||||||
| chr2:99368710 | T | C | 1 | a0002c0001t0005g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1387+119T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368710 | |||||||
| chr2:99368817 | A | G | 1 | a0001c0005t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1387+226A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368817 | |||||||
| chr2:99369027 | C | T | 1 | a0001c0003t0001g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1388-365C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369027 | |||||||
| chr2:99369048 | G | A | 1 | a0002c0001t0002g0247 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1388-344G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369048 | |||||||
| chr2:99369071 | A | G | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1388-321A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369071 | |||||||
| chr2:99369282 | A | T | 1 | a0001c0003t0004g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1388-110A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369282 | |||||||
| chr2:99369295 | G | T | 1 | a0001c0002t0001g0141 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1388-97G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369295 | |||||||
| chr2:99369308 | T | G | 1 | a0001c0003t0001g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1388-84T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369308 | |||||||
| chr2:99369580 | C | A | 1 | a0001c0002t0001g0145 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1477+99C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99369580 | |||||||
| chr2:99369642 | A | G | 2 | a0002c0001t0002g0212 a0002c0001t0002g0226 |
2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1477+161A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99369642 | |||||||
| chr2:99370020 | A | G | 9 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0112 others(6): Show |
12 | HG00609.hp2 HG02148.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477+539A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370020 | |||||||
| chr2:99370128 | T | C | 2 | a0001c0002t0001g0016 a0001c0002t0001g0145 |
3 | HG00609.hp1 NA18956.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1477+647T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370128 | |||||||
| chr2:99370164 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1477+683A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370164 | |||||||
| chr2:99370181 | T | C | 105 | a0001c0012t0002g0269 a0002c0001t0002g0022 a0002c0001t0002g0184 others(102): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1477+700T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370181 | |||||||
| chr2:99370469 | T | C | 58 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(55): Show |
72 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1477+988T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370469 | |||||||
| chr2:99370966 | A | G | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-690A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370966 | |||||||
| chr2:99370980 | G | T | 1 | a0001c0002t0001g0145 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1478-676G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370980 | |||||||
| chr2:99371215 | G | A | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1478-441G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371215 | |||||||
| chr2:99371290 | A | C | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1478-366A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371290 | |||||||
| chr2:99371362 | T | C | 1 | a0002c0001t0002g0205 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1478-294T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371362 | |||||||
| chr2:99371373 | A | G | 2 | a0001c0004t0001g0025 a0001c0004t0001g0103 |
2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1478-283A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371373 | |||||||
| chr2:99371413 | G | A | 1 | a0001c0003t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1478-243G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371413 | |||||||
| chr2:99371443 | A | G | 1 | a0001c0003t0001g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1478-213A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371443 | |||||||
| chr2:99371445 | G | A | 6 | a0002c0001t0002g0190 a0002c0001t0005g0187 a0002c0001t0005g0188 others(3): Show |
6 | NA18947.hp1 NA18948.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-211G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371445 | |||||||
| chr2:99371466 | C | T | 1 | a0001c0004t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1478-190C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371466 | |||||||
| chr2:99371488 | CA | C | 144 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(141): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1478-151delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 99371488 | ||||||
| chr2:99371543 | A | C | 1 | a0002c0001t0005g0220 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1478-113A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371543 | |||||||
| chr2:99371559 | C | T | 1 | a0002c0001t0005g0191 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1478-97C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371559 | |||||||
| chr2:99371990 | CA | C | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1552+264delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99371990 | ||||||
| chr2:99372192 | C | G | 1 | a0002c0001t0002g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1552+462C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372192 | |||||||
| chr2:99372408 | G | A | 1 | a0001c0011t0021g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1552+678G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372408 | |||||||
| chr2:99372482 | G | T | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1552+752G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372482 | |||||||
| chr2:99372585 | G | A | 3 | a0001c0002t0001g0014 a0001c0002t0001g0120 a0001c0002t0001g0121 |
4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552+855G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372585 | |||||||
| chr2:99372708 | A | T | 6 | a0001c0002t0003g0005 a0001c0002t0003g0163 a0001c0002t0003g0164 others(3): Show |
9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1552+978A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372708 | |||||||
| chr2:99372774 | G | T | 1 | a0001c0002t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1552+1044G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372774 | |||||||
| chr2:99372875 | C | T | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1552+1145C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372875 | |||||||
| chr2:99372885 | T | A | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1552+1155T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372885 | |||||||
| chr2:99372899 | T | G | 1 | a0001c0004t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1552+1169T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372899 | |||||||
| chr2:99372996 | C | A | 2 | a0002c0001t0005g0224 a0002c0001t0005g0270 |
2 | NA18939.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1552+1266C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372996 | |||||||
| chr2:99373055 | T | G | 3 | a0001c0002t0001g0016 a0001c0002t0001g0138 a0001c0002t0001g0145 |
4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552+1325T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373055 | |||||||
| chr2:99373101 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1552+1371A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373101 | |||||||
| chr2:99373330 | C | G | 1 | a0002c0001t0002g0258 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1552+1600C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373330 | |||||||
| chr2:99373380 | G | C | 2 | a0002c0001t0002g0255 a0002c0001t0002g0256 |
2 | HG00558.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1552+1650G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373380 | |||||||
| chr2:99373386 | G | A | 1 | a0001c0002t0003g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1552+1656G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373386 | |||||||
| chr2:99373482 | C | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552+1752C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373482 | |||||||
| chr2:99373483 | G | T | 1 | a0001c0003t0001g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1552+1753G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373483 | |||||||
| chr2:99373707 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1552+1977T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373707 | |||||||
| chr2:99373790 | A | G | 1 | a0001c0003t0004g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1552+2060A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373790 | |||||||
| chr2:99373852 | G | T | 2 | a0001c0003t0001g0110 a0001c0003t0001g0111 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1552+2122G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373852 | |||||||
| chr2:99373861 | C | T | 151 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(148): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1552+2131C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373861 | |||||||
| chr2:99373912 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1552+2182A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373912 | |||||||
| chr2:99374063 | C | T | 6 | a0001c0002t0003g0005 a0001c0002t0003g0163 a0001c0002t0003g0164 others(3): Show |
9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553-2284C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374063 | |||||||
| chr2:99374107 | G | A | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1553-2240G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374107 | |||||||
| chr2:99374268 | G | A | 1 | a0002c0001t0005g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1553-2079G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374268 | |||||||
| chr2:99374288 | TA | T | 75 | a0001c0002t0001g0169 a0001c0002t0003g0001 a0001c0002t0003g0005 others(72): Show |
94 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1553-2037delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99374288 | ||||||
| chr2:99374288 | TAA | T | 120 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(117): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1553-2038_1553-203 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99374288 | ||||||
| chr2:99374719 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-1628A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374719 | |||||||
| chr2:99374777 | A | G | 1 | a0002c0001t0018g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-1570A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374777 | |||||||
| chr2:99375018 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-1329A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375018 | |||||||
| chr2:99375076 | A | C | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1553-1271A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375076 | |||||||
| chr2:99375117 | CTG | C | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1553-1229_1553-122 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375117 | |||||||
| chr2:99375205 | C | T | 30 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0015 others(27): Show |
37 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1553-1142C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375205 | |||||||
| chr2:99375415 | G | A | 1 | a0002c0001t0005g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1553-932G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375415 | |||||||
| chr2:99375459 | C | T | 80 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(77): Show |
103 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1553-888C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375459 | |||||||
| chr2:99375469 | G | A | 1 | a0002c0001t0018g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-878G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375469 | |||||||
| chr2:99375478 | A | G | 4 | a0001c0003t0001g0013 a0001c0003t0001g0071 a0001c0003t0012g0073 others(1): Show |
5 | HG00642.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553-869A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375478 | |||||||
| chr2:99375523 | C | G | 1 | a0001c0004t0001g0102 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1553-824C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375523 | |||||||
| chr2:99375724 | T | C | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1553-623T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375724 | |||||||
| chr2:99375754 | C | G | 1 | a0001c0002t0003g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1553-593C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375754 | |||||||
| chr2:99376109 | C | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-238C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376109 | |||||||
| chr2:99376278 | A | G | 2 | a0002c0001t0002g0198 a0002c0001t0002g0201 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1553-69A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376278 | |||||||
| chr2:99376321 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-26A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376321 | |||||||
| chr2:99376681 | G | A | 1 | a0001c0003t0004g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1842+45G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376681 | |||||||
| chr2:99376697 | T | C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842+61T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376697 | |||||||
| chr2:99376713 | G | A | 35 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0023 others(32): Show |
38 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.1842+77G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376713 | |||||||
| chr2:99376754 | G | A | 1 | a0001c0012t0002g0269 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1842+118G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376754 | |||||||
| chr2:99376787 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1842+151C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376787 | |||||||
| chr2:99377013 | A | G | 1 | a0001c0002t0001g0148 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1842+377A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377013 | |||||||
| chr2:99377238 | G | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1842+602G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377238 | |||||||
| chr2:99377427 | G | A | 1 | a0002c0001t0002g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1842+791G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377427 | |||||||
| chr2:99377564 | C | T | 1 | a0001c0004t0014g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1842+928C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377564 | |||||||
| chr2:99377570 | A | G | 1 | a0002c0001t0002g0250 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1842+934A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377570 | |||||||
| chr2:99377694 | G | C | 4 | a0002c0001t0002g0184 a0002c0001t0002g0218 a0002c0001t0002g0249 others(1): Show |
4 | HG00408.hp1 NA18949.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1058G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377694 | |||||||
| chr2:99377705 | A | G | 1 | a0001c0002t0001g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1842+1069A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377705 | |||||||
| chr2:99377736 | A | G | 4 | a0001c0003t0001g0029 a0001c0003t0010g0026 a0001c0003t0010g0027 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1100A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377736 | |||||||
| chr2:99377767 | G | A | 5 | a0001c0004t0006g0006 a0001c0004t0006g0105 a0001c0004t0006g0106 others(2): Show |
7 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1842+1131G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377767 | |||||||
| chr2:99378103 | T | C | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1843-916T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378103 | |||||||
| chr2:99378450 | G | A | 1 | a0002c0001t0005g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1843-569G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378450 | |||||||
| chr2:99378497 | C | G | 151 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(148): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1843-522C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378497 | |||||||
| chr2:99378503 | A | G | 1 | a0002c0001t0002g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1843-516A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378503 | |||||||
| chr2:99378873 | T | G | 1 | a0001c0003t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1843-146T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378873 | |||||||
| chr2:99378995 | AT | A | 148 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(145): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1843-9delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr2 | 99378995 | ||||||
| chr2:99379702 | A | G | 46 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0110 others(43): Show |
59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.2061+274A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99379702 | |||||||
| chr2:99380207 | T | A | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2061+779T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99380207 | |||||||
| chr2:99380304 | A | C | 1 | a0001c0002t0001g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2061+876A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99380304 | |||||||
| chr2:99381029 | A | G | 1 | a0001c0003t0011g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2062-1130A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381029 | |||||||
| chr2:99381030 | T | C | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2062-1129T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381030 | |||||||
| chr2:99381116 | G | C | 1 | a0002c0001t0002g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2062-1043G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381116 | |||||||
| chr2:99381516 | G | GGT | 22 | a0001c0002t0001g0133 a0001c0002t0001g0147 a0001c0002t0003g0009 others(19): Show |
23 | HG00140.hp2 HG01934.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GGTGT | 50 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(47): Show |
58 | HG00408.hp2 HG00733.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GGTGTGT | 38 | a0001c0002t0001g0007 a0001c0002t0001g0014 a0001c0002t0001g0127 others(35): Show |
51 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GGTGTGTG others(1): Show |
19 | a0001c0002t0001g0119 a0001c0002t0003g0001 a0001c0002t0003g0123 others(16): Show |
19 | HG01261.hp2 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GGTGTGTG others(3): Show |
11 | a0001c0003t0001g0029 a0001c0003t0004g0042 a0001c0003t0004g0044 others(8): Show |
11 | HG00280.hp1 HG01243.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GGTGTGTG others(5): Show |
1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2062-642_2062-641i others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | ||||||
| chr2:99381516 | G | GTGTGTGT others(4): Show |
1 | a0001c0005t0002g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2062-643_2062-642i others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381516 | |||||||
| chr2:99381518 | G | GGT | 42 | a0002c0001t0002g0022 a0002c0001t0002g0184 a0002c0001t0002g0197 others(39): Show |
43 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2062-607_2062-606d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | GGTGT | 11 | a0001c0012t0002g0269 a0002c0001t0002g0199 a0002c0001t0002g0208 others(8): Show |
11 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-609_2062-606d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | GGTGTGT | 9 | a0002c0001t0002g0185 a0002c0001t0002g0198 a0002c0001t0002g0200 others(6): Show |
9 | HG01884.hp1 HG02523.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-611_2062-606d others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | GGTGTGTG others(1): Show |
23 | a0002c0001t0002g0214 a0002c0001t0002g0277 a0002c0001t0002g0292 others(20): Show |
24 | HG00558.hp1 HG01123.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-613_2062-606d others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | GGTGTGTG others(3): Show |
5 | a0002c0001t0002g0274 a0002c0001t0005g0019 a0002c0001t0005g0220 others(2): Show |
6 | HG00544.hp1 HG02965.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-615_2062-606d others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | GGTGTGTG others(5): Show |
1 | a0002c0001t0005g0213 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2062-617_2062-606d others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | ||||||
| chr2:99381518 | G | T | 192 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(189): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.2062-641G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381518 | |||||||
| chr2:99381702 | C | CT | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-454dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381702 | ||||||
| chr2:99381898 | C | G | 1 | a0002c0001t0005g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2062-261C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381898 | |||||||
| chr2:99381959 | A | AT | 7 | a0001c0002t0003g0122 a0001c0002t0003g0123 a0001c0002t0003g0124 others(4): Show |
7 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2062-193dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381959 | ||||||
| chr2:99382098 | C | T | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2062-61C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99382098 | |||||||
| chr2:99382232 | A | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.2129+6A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382232 | |||||||
| chr2:99382295 | G | C | 1 | a0001c0002t0007g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2129+69G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382295 | |||||||
| chr2:99382329 | A | G | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2129+103A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382329 | |||||||
| chr2:99382414 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2129+188C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382414 | |||||||
| chr2:99382634 | C | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2130-146C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382634 | |||||||
| chr2:99382991 | G | A | 4 | a0001c0003t0001g0067 a0001c0003t0001g0068 a0001c0003t0001g0069 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+70G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99382991 | |||||||
| chr2:99383020 | TTATTGTG others(8): Show |
T | 1 | a0001c0003t0004g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2271+113_2271+127d others(17): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383020 | ||||||
| chr2:99383035 | A | G | 1 | a0001c0004t0006g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2271+114A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383035 | |||||||
| chr2:99383054 | T | TTG | 3 | a0001c0003t0004g0049 a0001c0003t0004g0055 a0001c0003t0004g0058 |
3 | HG00280.hp1 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2271+147_2271+148d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383054 | ||||||
| chr2:99383148 | G | A | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2271+227G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383148 | |||||||
| chr2:99383299 | C | G | 1 | a0001c0004t0001g0098 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2271+378C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383299 | |||||||
| chr2:99383419 | T | C | 31 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0015 others(28): Show |
38 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.2271+498T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383419 | |||||||
| chr2:99383710 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2271+789A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383710 | |||||||
| chr2:99383775 | A | AG | 38 | a0001c0003t0002g0296 a0001c0003t0004g0010 a0001c0003t0004g0011 others(35): Show |
42 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.2271+855dupG | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383775 | ||||||
| chr2:99383836 | G | T | 1 | a0001c0002t0001g0135 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2271+915G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383836 | |||||||
| chr2:99383863 | ACT | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+947_2271+948d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383863 | ||||||
| chr2:99383980 | C | T | 1 | a0001c0003t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2271+1059C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383980 | |||||||
| chr2:99383984 | C | T | 1 | a0002c0001t0002g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2271+1063C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383984 | |||||||
| chr2:99384070 | A | G | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+1149A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384070 | |||||||
| chr2:99384114 | G | T | 1 | a0002c0001t0002g0241 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2271+1193G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384114 | |||||||
| chr2:99384154 | G | A | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2271+1233G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384154 | |||||||
| chr2:99384191 | C | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1270C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384191 | |||||||
| chr2:99384196 | C | CAAAAAAA others(3): Show |
164 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(161): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2271+1277_2271+128 others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | ||||||
| chr2:99384196 | C | CAAAAAAA others(4): Show |
23 | a0001c0002t0001g0119 a0001c0002t0001g0141 a0001c0002t0001g0153 others(20): Show |
24 | HG00609.hp2 HG00642.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2271+1276_2271+128 others(15): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | ||||||
| chr2:99384196 | C | CAAAAAAA others(5): Show |
1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2271+1286_2271+128 others(16): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | ||||||
| chr2:99384326 | C | CA | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2271+1406dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384326 | ||||||
| chr2:99384425 | G | A | 1 | a0001c0002t0003g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2271+1504G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384425 | |||||||
| chr2:99384464 | C | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2271+1543C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384464 | |||||||
| chr2:99384486 | A | C | 1 | a0001c0003t0001g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2271+1565A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384486 | |||||||
| chr2:99384614 | G | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1693G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384614 | |||||||
| chr2:99384646 | A | G | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1725A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384646 | |||||||
| chr2:99384711 | C | G | 1 | a0002c0001t0002g0252 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2271+1790C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384711 | |||||||
| chr2:99384943 | C | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2022C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384943 | |||||||
| chr2:99385140 | G | A | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2219G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385140 | |||||||
| chr2:99385173 | A | C | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2271+2252A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385173 | |||||||
| chr2:99385336 | C | T | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2415C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385336 | |||||||
| chr2:99385408 | T | C | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2271+2487T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385408 | |||||||
| chr2:99385471 | C | A | 1 | a0001c0002t0001g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2271+2550C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385471 | |||||||
| chr2:99385478 | G | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+2557G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385478 | |||||||
| chr2:99385531 | C | T | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+2610C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385531 | |||||||
| chr2:99385534 | G | A | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2271+2613G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385534 | |||||||
| chr2:99385602 | G | A | 190 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(187): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2271+2681G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385602 | |||||||
| chr2:99385655 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2271+2734A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385655 | |||||||
| chr2:99385700 | A | G | 1 | a0002c0007t0005g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2271+2779A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385700 | |||||||
| chr2:99386027 | G | A | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+3106G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386027 | |||||||
| chr2:99386143 | A | G | 3 | a0001c0002t0003g0129 a0001c0002t0003g0130 a0001c0002t0015g0131 |
3 | HG03579.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2271+3222A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386143 | |||||||
| chr2:99386312 | A | G | 1 | a0002c0001t0002g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2271+3391A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386312 | |||||||
| chr2:99386468 | C | CGT | 36 | a0001c0003t0002g0296 a0002c0001t0002g0184 a0002c0001t0002g0198 others(33): Show |
37 | HG00408.hp1 HG00558.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.2272-3215_2272-321 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386468 | C | CGTGT | 4 | a0001c0012t0002g0269 a0002c0001t0002g0252 a0002c0001t0005g0187 others(1): Show |
4 | HG02258.hp1 HG02738.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2272-3217_2272-321 others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386468 | CGTGT | C | 14 | a0001c0003t0004g0039 a0001c0003t0004g0041 a0001c0003t0004g0042 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2272-3217_2272-321 others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386468 | CGTGTGT | C | 29 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(26): Show |
33 | HG00280.hp1 HG01358.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.2272-3219_2272-321 others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386468 | CGTGTGTG others(1): Show |
C | 11 | a0001c0002t0003g0166 a0001c0002t0007g0176 a0001c0003t0002g0037 others(8): Show |
11 | HG00735.hp1 HG01106.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2272-3221_2272-321 others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386468 | CGTGTGTG others(3): Show |
C | 135 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(132): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2272-3223_2272-321 others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | ||||||
| chr2:99386521 | C | CTG | 3 | a0001c0004t0001g0084 a0001c0004t0001g0093 a0001c0004t0001g0094 |
3 | HG02698.hp2 HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2272-3183_2272-318 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386521 | ||||||
| chr2:99386537 | T | G | 4 | a0001c0003t0002g0037 a0001c0011t0021g0295 a0002c0001t0002g0022 others(1): Show |
5 | HG01934.hp2 HG01975.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2272-3181T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386537 | |||||||
| chr2:99386709 | G | T | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2272-3009G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386709 | |||||||
| chr2:99386713 | G | T | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2272-3005G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386713 | |||||||
| chr2:99386715 | C | CG | 14 | a0001c0002t0001g0119 a0001c0002t0001g0135 a0001c0002t0001g0137 others(11): Show |
14 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2272-2996dupG | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386715 | ||||||
| chr2:99386741 | T | C | 1 | a0001c0003t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2272-2977T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386741 | |||||||
| chr2:99387069 | C | T | 1 | a0002c0001t0005g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2272-2649C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387069 | |||||||
| chr2:99387427 | T | C | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-2291T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387427 | |||||||
| chr2:99387458 | A | G | 1 | a0002c0001t0005g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2272-2260A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387458 | |||||||
| chr2:99387538 | A | G | 1 | a0001c0005t0002g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2272-2180A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387538 | |||||||
| chr2:99387702 | A | G | 46 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0110 others(43): Show |
59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.2272-2016A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387702 | |||||||
| chr2:99387713 | G | A | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2272-2005G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387713 | |||||||
| chr2:99388436 | G | GT | 152 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(149): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2272-1275dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99388436 | ||||||
| chr2:99388436 | G | GTT | 34 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(31): Show |
38 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.2272-1276_2272-127 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99388436 | ||||||
| chr2:99388611 | A | G | 1 | a0001c0003t0020g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2272-1107A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388611 | |||||||
| chr2:99388791 | A | T | 1 | a0002c0001t0005g0183 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2272-927A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388791 | |||||||
| chr2:99388830 | C | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2272-888C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388830 | |||||||
| chr2:99388855 | G | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-863G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388855 | |||||||
| chr2:99389103 | G | A | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2272-615G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389103 | |||||||
| chr2:99389149 | T | A | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-569T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389149 | |||||||
| chr2:99389370 | G | A | 3 | a0001c0002t0001g0014 a0001c0002t0001g0120 a0001c0002t0001g0121 |
4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-348G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389370 | |||||||
| chr2:99389411 | C | T | 146 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(143): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-307C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389411 | |||||||
| chr2:99389598 | G | GAGTA | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2272-116_2272-113d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99389598 | ||||||
| chr2:99390119 | A | G | 1 | a0001c0003t0020g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2404-100A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390119 | |||||||
| chr2:99390157 | G | T | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2404-62G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390157 | |||||||
| chr2:99390163 | C | T | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2404-56C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390163 | |||||||
| chr2:99390427 | G | GT | 151 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(148): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2586+40dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 99390427 | ||||||
| chr2:99390441 | T | A | 3 | a0001c0003t0004g0039 a0001c0012t0002g0269 a0002c0001t0002g0260 |
3 | HG01168.hp1 HG01346.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2586+40T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | chr2 | 99390441 | |||||||
| chr2:99390441 | T | TA | 35 | a0001c0003t0002g0296 a0001c0003t0004g0010 a0001c0003t0004g0011 others(32): Show |
39 | HG00280.hp1 HG01358.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.2586+45dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 99390441 | ||||||
| chr2:99390853 | A | T | 1 | a0001c0003t0001g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2748+148A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99390853 | |||||||
| chr2:99390940 | A | T | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2748+235A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99390940 | |||||||
| chr2:99391095 | T | C | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2748+390T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391095 | |||||||
| chr2:99391103 | C | T | 1 | a0001c0004t0001g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2748+398C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391103 | |||||||
| chr2:99391141 | G | A | 4 | a0001c0002t0003g0009 a0001c0002t0003g0157 a0001c0002t0003g0161 others(1): Show |
6 | HG02040.hp2 NA18612.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.2748+436G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391141 | |||||||
| chr2:99391144 | T | C | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2748+439T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391144 | |||||||
| chr2:99391353 | T | C | 1 | a0001c0011t0021g0295 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2748+648T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391353 | |||||||
| chr2:99391382 | G | C | 2 | a0001c0003t0004g0059 a0001c0003t0004g0061 |
2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2748+677G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391382 | |||||||
| chr2:99391389 | G | A | 2 | a0002c0001t0002g0262 a0002c0001t0002g0264 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2748+684G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391389 | |||||||
| chr2:99391502 | C | T | 3 | a0001c0003t0004g0010 a0001c0003t0004g0047 a0001c0003t0023g0040 |
4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2748+797C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391502 | |||||||
| chr2:99391729 | C | CT | 21 | a0001c0002t0003g0159 a0001c0002t0003g0160 a0001c0003t0001g0109 others(18): Show |
24 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2748+1043dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | ||||||
| chr2:99391729 | C | CTT | 12 | a0002c0001t0002g0184 a0002c0001t0002g0197 a0002c0001t0002g0218 others(9): Show |
12 | HG00408.hp1 NA18612.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.2748+1042_2748+104 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | ||||||
| chr2:99391729 | CT | C | 7 | a0001c0002t0001g0139 a0001c0002t0003g0122 a0001c0002t0003g0124 others(4): Show |
7 | HG00140.hp1 HG00408.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.2748+1043delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | ||||||
| chr2:99391945 | C | A | 189 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(186): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2749-1022C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391945 | |||||||
| chr2:99391956 | C | T | 1 | a0001c0003t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2749-1011C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391956 | |||||||
| chr2:99392131 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2749-836G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392131 | |||||||
| chr2:99392142 | C | G | 1 | a0002c0001t0005g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2749-825C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392142 | |||||||
| chr2:99392580 | G | A | 141 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(138): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2749-387G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392580 | |||||||
| chr2:99392668 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2749-299A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392668 | |||||||
| chr2:99392707 | G | A | 1 | a0001c0002t0003g0155 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2749-260G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392707 | |||||||
| chr2:99393291 | T | A | 1 | a0001c0006t0004g0045 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2880+193T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393291 | |||||||
| chr2:99393337 | A | G | 1 | a0002c0001t0002g0240 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2880+239A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393337 | |||||||
| chr2:99393403 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2880+305G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393403 | |||||||
| chr2:99393460 | C | T | 1 | a0002c0001t0002g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2880+362C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393460 | |||||||
| chr2:99393461 | G | A | 140 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(137): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.2880+363G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393461 | |||||||
| chr2:99393581 | T | C | 35 | a0002c0001t0002g0214 a0002c0001t0002g0274 a0002c0001t0002g0277 others(32): Show |
38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2880+483T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393581 | |||||||
| chr2:99393665 | A | C | 1 | a0001c0002t0003g0168 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2880+567A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393665 | |||||||
| chr2:99393965 | A | T | 1 | a0001c0003t0004g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2881-302A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393965 | |||||||
| chr2:99394042 | A | G | 1 | a0001c0002t0003g0166 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2881-225A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394042 | |||||||
| chr2:99394127 | C | T | 1 | a0001c0003t0013g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2881-140C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394127 | |||||||
| chr2:99394222 | A | G | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2881-45A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394222 | |||||||
| chr2:99394239 | A | G | 1 | a0002c0001t0002g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2881-28A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394239 | |||||||
| chr2:99395194 | A | C | 1 | a0001c0002t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3254+311A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395194 | |||||||
| chr2:99395209 | A | T | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3254+326A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395209 | |||||||
| chr2:99395212 | C | T | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3254+329C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395212 | |||||||
| chr2:99395251 | C | G | 191 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(188): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3254+368C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395251 | |||||||
| chr2:99395643 | G | A | 3 | a0002c0001t0002g0231 a0002c0001t0002g0233 a0002c0001t0002g0254 |
3 | NA18956.hp1 NA18957.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3254+760G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395643 | |||||||
| chr2:99395661 | T | C | 1 | a0001c0003t0004g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3254+778T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395661 | |||||||
| chr2:99395737 | T | A | 74 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(71): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3254+854T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395737 | |||||||
| chr2:99395779 | G | A | 1 | a0002c0001t0005g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3254+896G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395779 | |||||||
| chr2:99395845 | G | A | 1 | a0002c0001t0002g0240 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3255-915G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395845 | |||||||
| chr2:99395991 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3255-769G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395991 | |||||||
| chr2:99395993 | T | C | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3255-767T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395993 | |||||||
| chr2:99396050 | C | T | 188 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0014 others(185): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.3255-710C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396050 | |||||||
| chr2:99396145 | A | G | 3 | a0001c0002t0003g0159 a0001c0002t0003g0160 a0005c0010t0003g0154 |
3 | NA18950.hp1 NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3255-615A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396145 | |||||||
| chr2:99396334 | C | T | 1 | a0001c0002t0003g0172 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3255-426C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396334 | |||||||
| chr2:99396335 | G | A | 9 | a0001c0003t0001g0077 a0001c0003t0001g0109 a0001c0003t0001g0112 others(6): Show |
12 | HG00609.hp2 HG02148.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.3255-425G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396335 | |||||||
| chr2:99396338 | C | T | 2 | a0001c0003t0013g0035 a0001c0003t0013g0036 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3255-422C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396338 | |||||||
| chr2:99396366 | T | G | 2 | a0002c0001t0002g0255 a0002c0001t0002g0256 |
2 | HG00558.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3255-394T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396366 | |||||||
| chr2:99396635 | T | C | 1 | a0001c0002t0001g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3255-125T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396635 | |||||||
| chr2:99397112 | G | C | 1 | a0001c0003t0004g0058 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3393+214G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397112 | |||||||
| chr2:99397294 | CCTTT | C | 3 | a0002c0001t0002g0237 a0002c0001t0002g0271 a0002c0001t0002g0294 |
3 | NA18962.hp2 NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.3393+399_3393+402d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397294 | ||||||
| chr2:99397449 | G | A | 8 | a0002c0001t0002g0185 a0002c0001t0002g0198 a0002c0001t0002g0199 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3393+551G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397449 | |||||||
| chr2:99397487 | C | CCA | 37 | a0001c0003t0004g0010 a0001c0003t0004g0011 a0001c0003t0004g0012 others(34): Show |
41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.3393+590_3393+591d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397487 | ||||||
| chr2:99397692 | A | G | 1 | a0002c0001t0002g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3393+794A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397692 | |||||||
| chr2:99397702 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3393+804G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397702 | |||||||
| chr2:99397862 | A | G | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3394-886A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397862 | |||||||
| chr2:99397931 | G | T | 57 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(54): Show |
71 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3394-817G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397931 | |||||||
| chr2:99397931 | GT | G | 49 | a0001c0003t0002g0037 a0001c0003t0004g0010 a0001c0003t0004g0011 others(46): Show |
54 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.3394-804delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397931 | ||||||
| chr2:99397932 | T | G | 1 | a0001c0003t0016g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3394-816T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397932 | |||||||
| chr2:99398566 | T | C | 6 | a0001c0003t0002g0037 a0001c0003t0009g0030 a0001c0003t0009g0031 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3394-182T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398566 | |||||||
| chr2:99398661 | C | G | 57 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0068 others(54): Show |
71 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3394-87C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398661 | |||||||
| chr2:99398715 | C | G | 1 | a0001c0004t0001g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3394-33C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398715 | |||||||
| chr2:99398718 | C | A | 1 | a0002c0001t0002g0258 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3394-30C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398718 | |||||||
| chr2:99398928 | G | A | 1 | a0001c0004t0001g0104 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3555+19G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99398928 | |||||||
| chr2:99399031 | C | T | 1 | a0002c0001t0005g0213 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3555+122C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399031 | |||||||
| chr2:99399100 | C | T | 5 | a0001c0005t0002g0024 a0001c0005t0002g0287 a0001c0005t0002g0288 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3555+191C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399100 | |||||||
| chr2:99399176 | A | C | 2 | a0001c0003t0008g0003 a0001c0003t0008g0083 |
5 | NA18939.hp1 NA18941.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.3556-131A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399176 |