Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8662 |
| ensemblid | ENSG00000106263.19 |
| hgncid | 3280 |
| symbol | EIF3B |
| name | eukaryotic translation initiation factor 3 subunit B |
| refseq_nuc | NM_001037283.2 |
| refseq_prot | NP_001032360.1 |
| ensembl_nuc | ENST00000360876.9 |
| ensembl_prot | ENSP00000354125.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 2354827 |
| end | 2380745 |
| strand | + |
| ver | v1.2 |
| region | chr7:2354827-2380745 |
| region5000 | chr7:2349827-2385745 |
| regionname0 | EIF3B_chr7_2354827_2380745 |
| regionname5000 | EIF3B_chr7_2349827_2385745 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 814 | 232 | 44 | 49 | 102 | 8 | 28 | 70 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0002 | 1/0 | 814 | 117 | 40 | 24 | 35 | 6 | 11 | 27 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0003 | 0/0 | 814 | 16 | 1 | 7 | 8 | 0 | 0 | 7 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0004 | 0/0 | 814 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0005 | 0/0 | 814 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0006 | 0/0 | 814 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0007 | 0/0 | 814 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0008 | 0/0 | 814 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0009 | 0/0 | 814 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0010 | 0/0 | 814 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0011 | 0/0 | 814 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0012 | 0/0 | 814 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0013 | 0/0 | 814 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0014 | 0/0 | 814 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| a0015 | 0/0 | 814 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | MQDAE others(809): Show |
chr7 | 2349827 | 2385745 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2442 | 149 | 26 | 36 | 65 | 8 | 13 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0003 | 0/0 | 2442 | 65 | 4 | 10 | 36 | 0 | 15 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0005 | 0/0 | 2442 | 6 | 5 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0008 | 0/0 | 2442 | 2 | 1 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0009 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0010 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0011 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0014 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0015 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0016 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0001c0017 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0002c0002 | 1/0 | 2442 | 117 | 40 | 24 | 35 | 6 | 11 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0003c0004 | 0/0 | 2442 | 16 | 1 | 7 | 8 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0004c0006 | 0/0 | 2442 | 5 | 5 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0005c0007 | 0/0 | 2442 | 3 | 0 | 0 | 0 | 0 | 3 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0006c0012 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0007c0021 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0008c0025 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0009c0020 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0010c0019 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0011c0013 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0012c0023 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0013c0022 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0014c0018 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 | ||
| a0015c0024 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGCA others(2437): Show |
chr7 | 2349827 | 2385745 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3096 | 133 | 20 | 33 | 60 | 7 | 13 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0002 | 0/0 | 3096 | 3 | 3 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0003 | 0/0 | 3097 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3092): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0004 | 0/0 | 3096 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0005 | 0/0 | 3096 | 3 | 2 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0007 | 0/0 | 3096 | 2 | 0 | 1 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0009 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0011 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0012 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0001t0014 | 0/1 | 3096 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0003t0001 | 0/0 | 3096 | 62 | 4 | 10 | 34 | 0 | 14 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0003t0003 | 0/0 | 3097 | 2 | 0 | 0 | 1 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3092): Show |
chr7 | 2349827 | 2385745 |
| a0001c0003t0013 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3115): Show |
chr7 | 2349827 | 2385745 |
| a0001c0005t0001 | 0/0 | 3096 | 6 | 5 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0008t0001 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0008t0002 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0009t0001 | 0/0 | 3096 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0010t0001 | 0/0 | 3096 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0011t0001 | 0/0 | 3096 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0014t0001 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0015t0002 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0016t0010 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0001c0017t0001 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0002c0002t0001 | 1/0 | 3096 | 114 | 39 | 22 | 35 | 6 | 11 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0002c0002t0006 | 0/0 | 3096 | 2 | 1 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0002c0002t0016 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0003c0004t0001 | 0/0 | 3096 | 15 | 1 | 6 | 8 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0003c0004t0003 | 0/0 | 3097 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3092): Show |
chr7 | 2349827 | 2385745 |
| a0004c0006t0001 | 0/0 | 3096 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0004c0006t0008 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0005c0007t0001 | 0/0 | 3096 | 3 | 0 | 0 | 0 | 0 | 3 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0006c0012t0001 | 0/0 | 3096 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0007c0021t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0008c0025t0001 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0009c0020t0001 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0010c0019t0001 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0011c0013t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0012c0023t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0013c0022t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0014c0018t0001 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| a0015c0024t0015 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | ATGGC others(3091): Show |
chr7 | 2349827 | 2385745 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 5 | 7 | 0 | 2 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0001t0014g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0008 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0003t0013g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0005t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0008t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0008t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0009t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0010t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0011t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0011t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0014t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0015t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0016t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0001c0017t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0002c0002t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0003c0004t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0004c0006t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0004c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0004c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0004c0006t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0005c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0005c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0005c0007t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0006c0012t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0006c0012t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0007c0021t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0008c0025t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0009c0020t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0010c0019t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0011c0013t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0012c0023t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0013c0022t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0014c0018t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| a0015c0024t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0284 | EUR | GBR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0001 | EUR | GBR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00609 | hp2 | a0007 | c0021 | t0001 | g0035 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00639 | hp1 | a0002 | c0002 | t0006 | g0248 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00673 | hp1 | a0001 | c0003 | t0013 | g0179 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0131 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01175 | hp2 | a0008 | c0025 | t0001 | g0279 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01192 | hp1 | a0001 | c0008 | t0002 | g0278 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0027 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01255 | hp1 | a0002 | c0002 | t0016 | g0160 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0013 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0233 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0241 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | IBS | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0138 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01928 | hp1 | a0003 | c0004 | t0001 | g0083 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01943 | hp2 | a0003 | c0004 | t0001 | g0013 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01952 | hp1 | a0003 | c0004 | t0003 | g0013 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01975 | hp2 | a0003 | c0004 | t0001 | g0089 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01978 | hp2 | a0009 | c0020 | t0001 | g0249 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0286 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0262 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02132 | hp2 | a0001 | c0001 | t0012 | g0096 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0136 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | CDX | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0113 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02258 | hp2 | a0004 | c0006 | t0001 | g0029 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02273 | hp1 | a0001 | c0014 | t0001 | g0020 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02280 | hp2 | a0004 | c0006 | t0001 | g0029 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02293 | hp1 | a0003 | c0004 | t0001 | g0112 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02293 | hp2 | a0003 | c0004 | t0001 | g0002 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02523 | hp2 | a0003 | c0004 | t0001 | g0072 | EAS | KHV | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0135 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0153 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0143 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02630 | hp2 | a0004 | c0006 | t0001 | g0044 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02818 | hp1 | a0001 | c0011 | t0001 | g0189 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0027 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02895 | hp1 | a0001 | c0010 | t0001 | g0021 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02895 | hp2 | a0001 | c0009 | t0001 | g0166 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02970 | hp1 | a0001 | c0017 | t0001 | g0194 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02970 | hp2 | a0002 | c0002 | t0006 | g0243 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02976 | hp2 | a0004 | c0006 | t0008 | g0163 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03098 | hp2 | a0006 | c0012 | t0001 | g0200 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03209 | hp2 | a0001 | c0008 | t0001 | g0277 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03225 | hp1 | a0001 | c0011 | t0001 | g0190 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0137 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0169 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0170 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03516 | hp2 | a0001 | c0015 | t0002 | g0139 | AFR | ESN | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03540 | hp2 | a0004 | c0006 | t0001 | g0045 | AFR | GWD | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0145 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03688 | hp2 | a0005 | c0007 | t0001 | g0075 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0180 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0234 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0172 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0186 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0171 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0188 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04184 | hp2 | a0005 | c0007 | t0001 | g0084 | SAS | BEB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG04228 | hp2 | a0005 | c0007 | t0001 | g0073 | SAS | STU | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18522 | hp1 | a0001 | c0009 | t0001 | g0151 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | CHB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18906 | hp2 | a0010 | c0019 | t0001 | g0196 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18942 | hp2 | a0003 | c0004 | t0001 | g0071 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18947 | hp2 | a0001 | c0016 | t0010 | g0285 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18977 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0063 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18979 | hp2 | a0011 | c0013 | t0001 | g0025 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19003 | hp1 | a0012 | c0023 | t0001 | g0191 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0098 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19006 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19009 | hp1 | a0013 | c0022 | t0001 | g0231 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19010 | hp1 | a0014 | c0018 | t0001 | g0003 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0273 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19063 | hp2 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19065 | hp1 | a0003 | c0004 | t0001 | g0099 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | YRI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20129 | hp1 | a0001 | c0010 | t0001 | g0021 | AFR | ASW | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ASW | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0230 | EUR | TSI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0281 | EUR | TSI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0289 | EUR | TSI | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | GIH | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | ACB | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG03471 | hp2 | a0006 | c0012 | t0001 | g0199 | AFR | MSL | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0271 | AFR | USA | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | USA | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA18955 | hp2 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | USA | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| NA21309 | hp2 | a0015 | c0024 | t0015 | g0185 | AFR | LWK | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0118 | REF | REF | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0250 | REF | REF | EIF3B_chr7_2349827_2385745 | EIF3B | chr7 | 2349827 | 2385745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2354973 | G | A | 1 | a0011 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.52G>A | p.Glu18Lys | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 147/3096 | 52/2445 | 18/814 | chr7 | 2354973 | |||
| chr7:2354989 | A | T | 1 | a0008 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.68A>T | p.Gln23Leu | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 163/3096 | 68/2445 | 23/814 | chr7 | 2354989 | |||
| chr7:2355073 | C | T | 1 | a0015 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.152C>T | p.Ser51Phe | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 247/3096 | 152/2445 | 51/814 | chr7 | 2355073 | |||
| chr7:2355111 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
missense_variant | MODERATE | c.190T>C | p.Ser64Pro | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 285/3096 | 190/2445 | 64/814 | chr7 | 2355111 | |||
| chr7:2355133 | C | T | 1 | a0012 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.212C>T | p.Ala71Val | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 307/3096 | 212/2445 | 71/814 | chr7 | 2355133 | |||
| chr7:2355160 | C | A | 1 | a0004 | 5 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.239C>A | p.Pro80Gln | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 334/3096 | 239/2445 | 80/814 | chr7 | 2355160 | |||
| chr7:2355299 | G | C | 1 | a0006 | 2 | HG03098.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.378G>C | p.Glu126Asp | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 473/3096 | 378/2445 | 126/814 | chr7 | 2355299 | |||
| chr7:2355373 | C | T | 1 | a0005 | 3 | HG03688.hp2 HG04184.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.452C>T | p.Pro151Leu | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 547/3096 | 452/2445 | 151/814 | chr7 | 2355373 | |||
| chr7:2355391 | A | G | 1 | a0010 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.470A>G | p.Glu157Gly | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 565/3096 | 470/2445 | 157/814 | chr7 | 2355391 | |||
| chr7:2355408 | G | C | 1 | a0003 | 16 | HG01261.hp2 HG01928.hp1 HG01943.hp2 others(13): Show |
missense_variant | MODERATE | c.487G>C | p.Val163Leu | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 582/3096 | 487/2445 | 163/814 | chr7 | 2355408 | |||
| chr7:2360766 | G | T | 1 | a0013 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.556G>T | p.Val186Leu | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/19 | 651/3096 | 556/2445 | 186/814 | chr7 | 2360766 | |||
| chr7:2363084 | G | T | 1 | a0014 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.827G>T | p.Ser276Ile | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/19 | 922/3096 | 827/2445 | 276/814 | chr7 | 2363084 | |||
| chr7:2375430 | C | T | 1 | a0007 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1931C>T | p.Thr644Met | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/19 | 2026/3096 | 1931/2445 | 644/814 | chr7 | 2375430 | |||
| chr7:2377047 | C | G | 1 | a0009 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2126C>G | p.Pro709Arg | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/19 | 2221/3096 | 2126/2445 | 709/814 | chr7 | 2377047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2354993 | G | A | 1 | a0001c0008 | 2 | HG01192.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.72G>A | p.Pro24Pro | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 167/3096 | 72/2445 | 24/814 | chr7 | 2354993 | |||
| chr7:2355356 | C | T | 3 | a0001c0003 a0004c0006 a0015c0024 |
71 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
synonymous_variant | LOW | c.435C>T | p.Asn145Asn | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 530/3096 | 435/2445 | 145/814 | chr7 | 2355356 | |||
| chr7:2360759 | C | T | 1 | a0001c0011 | 2 | HG02818.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.549C>T | p.Ile183Ile | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/19 | 644/3096 | 549/2445 | 183/814 | chr7 | 2360759 | |||
| chr7:2362663 | C | T | 1 | a0001c0010 | 2 | HG02895.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.711C>T | p.Tyr237Tyr | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/19 | 806/3096 | 711/2445 | 237/814 | chr7 | 2362663 | |||
| chr7:2362753 | G | A | 1 | a0001c0014 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.801G>A | p.Thr267Thr | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/19 | 896/3096 | 801/2445 | 267/814 | chr7 | 2362753 | |||
| chr7:2364500 | T | C | 2 | a0001c0005 a0001c0015 |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.1128T>C | p.Val376Val | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/19 | 1223/3096 | 1128/2445 | 376/814 | chr7 | 2364500 | |||
| chr7:2366317 | G | A | 1 | a0001c0016 | 1 | NA18947.hp2 | splice_region_variant&synonymous_variant | LOW | c.1158G>A | p.Arg386Arg | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 7/19 | 1253/3096 | 1158/2445 | 386/814 | chr7 | 2366317 | |||
| chr7:2372728 | C | T | 2 | a0001c0005 a0001c0015 |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.1743C>T | p.His581His | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/19 | 1838/3096 | 1743/2445 | 581/814 | chr7 | 2372728 | |||
| chr7:2372740 | G | A | 1 | a0001c0017 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1755G>A | p.Pro585Pro | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/19 | 1850/3096 | 1755/2445 | 585/814 | chr7 | 2372740 | |||
| chr7:2374601 | G | A | 1 | a0001c0009 | 2 | HG02895.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1884G>A | p.Leu628Leu | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/19 | 1979/3096 | 1884/2445 | 628/814 | chr7 | 2374601 | |||
| chr7:2375443 | C | T | 2 | a0001c0005 a0010c0019 |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.1944C>T | p.Ile648Ile | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/19 | 2039/3096 | 1944/2445 | 648/814 | chr7 | 2375443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2354869 | A | C | 1 | a0002c0002t0016 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 53 | chr7 | 2354869 | ||||||
| chr7:2354900 | G | A | 1 | a0004c0006t0008 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 22 | chr7 | 2354900 | ||||||
| chr7:2354901 | C | A | 1 | a0004c0006t0008 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/19 | 21 | chr7 | 2354901 | ||||||
| chr7:2380208 | C | T | 1 | a0015c0024t0015 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 711 | chr7 | 2380208 | ||||||
| chr7:2380225 | T | TC | 3 | a0001c0001t0003 a0001c0003t0003 a0003c0004t0003 |
4 | HG01109.hp1 HG01952.hp1 HG03927.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*39dupC | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 732 | INFO_REALIGN_3_PRIME | chr7 | 2380225 | |||||
| chr7:2380236 | G | A | 1 | a0001c0001t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 739 | chr7 | 2380236 | ||||||
| chr7:2380472 | G | A | 1 | a0002c0002t0006 | 2 | HG00639.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 975 | chr7 | 2380472 | ||||||
| chr7:2380493 | G | GGCGTTGG others(17): Show |
1 | a0001c0003t0013 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305_*328dupGCGTTG others(18): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1021 | INFO_REALIGN_3_PRIME | chr7 | 2380493 | |||||
| chr7:2380519 | G | A | 1 | a0001c0016t0010 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1022 | chr7 | 2380519 | ||||||
| chr7:2380541 | G | T | 1 | a0001c0001t0007 | 2 | HG00140.hp2 HG00733.hp1 |
3_prime_UTR_variant | MODIFIER | c.*352G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1044 | chr7 | 2380541 | ||||||
| chr7:2380551 | A | G | 1 | a0001c0001t0005 | 3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*362A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1054 | chr7 | 2380551 | ||||||
| chr7:2380557 | C | T | 1 | a0001c0001t0001 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1060 | chr7 | 2380557 | ||||||
| chr7:2380575 | G | T | 3 | a0001c0001t0002 a0001c0008t0002 a0001c0015t0002 |
5 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*386G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1078 | chr7 | 2380575 | ||||||
| chr7:2380648 | G | A | 1 | a0001c0001t0011 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1151 | chr7 | 2380648 | ||||||
| chr7:2380651 | A | G | 1 | a0001c0001t0012 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1154 | chr7 | 2380651 | ||||||
| chr7:2380656 | G | A | 1 | a0001c0001t0004 | 3 | HG00621.hp1 NA18997.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*467G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 19/19 | 1159 | chr7 | 2380656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2355610 | CCCCTTTT others(11): Show |
C | 2 | a0004c0006t0001g0044 a0004c0006t0001g0045 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.499+191_499+208del others(18): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355610 | |||||||
| chr7:2355662 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.499+242G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355662 | |||||||
| chr7:2355690 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.499+270G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355690 | |||||||
| chr7:2355805 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.499+385C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355805 | |||||||
| chr7:2355833 | A | G | 1 | a0001c0001t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.499+413A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355833 | |||||||
| chr7:2355874 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.499+454T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355874 | |||||||
| chr7:2355888 | C | T | 1 | a0002c0002t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.499+468C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355888 | |||||||
| chr7:2355900 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.499+480C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355900 | |||||||
| chr7:2355965 | C | T | 1 | a0001c0003t0001g0286 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.499+545C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355965 | |||||||
| chr7:2355979 | CTA | C | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+562_499+563del others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2355979 | ||||||
| chr7:2355999 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG00735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.499+579C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2355999 | |||||||
| chr7:2356089 | G | T | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.499+669G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356089 | |||||||
| chr7:2356249 | C | T | 4 | a0002c0002t0001g0018 a0002c0002t0001g0043 a0002c0002t0001g0283 others(1): Show |
7 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+829C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356249 | |||||||
| chr7:2356351 | G | A | 3 | a0001c0003t0001g0140 a0001c0003t0001g0141 a0001c0003t0001g0142 |
3 | HG01081.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.499+931G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356351 | |||||||
| chr7:2356383 | CG | C | 5 | a0002c0002t0001g0017 a0002c0002t0001g0280 a0002c0002t0001g0281 others(2): Show |
7 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+966delG | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356383 | ||||||
| chr7:2356407 | C | T | 2 | a0001c0008t0001g0277 a0001c0008t0002g0278 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.499+987C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356407 | |||||||
| chr7:2356417 | C | T | 1 | a0002c0002t0001g0276 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.499+997C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356417 | |||||||
| chr7:2356419 | G | A | 3 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0145 |
3 | HG00642.hp1 HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.499+999G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356419 | |||||||
| chr7:2356458 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+1038C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356458 | |||||||
| chr7:2356493 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.499+1073C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356493 | |||||||
| chr7:2356541 | T | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.499+1121T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356541 | |||||||
| chr7:2356565 | T | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.499+1145T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356565 | |||||||
| chr7:2356580 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.499+1160G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356580 | |||||||
| chr7:2356602 | C | CA | 65 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(62): Show |
79 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.499+1198dupA | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356602 | ||||||
| chr7:2356602 | C | CAA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
22 | HG00423.hp1 HG00597.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.499+1197_499+1198d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356602 | ||||||
| chr7:2356613 | AAAAAAG | A | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1205_499+1210d others(8): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356613 | ||||||
| chr7:2356615 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0270 |
2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.499+1195A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356615 | |||||||
| chr7:2356619 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.499+1199G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356619 | |||||||
| chr7:2356620 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
9 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.499+1200A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356620 | |||||||
| chr7:2356621 | AAAAG | A | 6 | a0001c0001t0001g0195 a0001c0017t0001g0194 a0002c0002t0001g0192 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+1205_499+1208d others(6): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356621 | ||||||
| chr7:2356837 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499+1417C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356837 | |||||||
| chr7:2356850 | A | T | 2 | a0001c0011t0001g0189 a0001c0011t0001g0190 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.499+1430A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356850 | |||||||
| chr7:2356853 | C | CTT | 4 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
7 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+1442_499+1443d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2356853 | ||||||
| chr7:2356865 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.499+1445A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2356865 | |||||||
| chr7:2357003 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.499+1583A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357003 | |||||||
| chr7:2357054 | G | A | 1 | a0004c0006t0008g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.499+1634G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357054 | |||||||
| chr7:2357114 | C | G | 2 | a0004c0006t0001g0044 a0004c0006t0001g0045 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.499+1694C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357114 | |||||||
| chr7:2357136 | T | A | 1 | a0001c0001t0001g0256 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.499+1716T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357136 | |||||||
| chr7:2357252 | C | T | 1 | a0002c0002t0001g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.499+1832C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357252 | |||||||
| chr7:2357397 | C | T | 1 | a0001c0003t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.499+1977C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357397 | |||||||
| chr7:2357443 | G | C | 8 | a0002c0002t0001g0009 a0002c0002t0001g0031 a0002c0002t0001g0155 others(5): Show |
12 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+2023G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357443 | |||||||
| chr7:2357458 | C | G | 2 | a0004c0006t0001g0044 a0004c0006t0001g0045 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.499+2038C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357458 | |||||||
| chr7:2357535 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.499+2115G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357535 | |||||||
| chr7:2357991 | A | G | 2 | a0001c0008t0001g0277 a0001c0008t0002g0278 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.499+2571A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2357991 | |||||||
| chr7:2358015 | CT | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.499+2604delT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2358015 | ||||||
| chr7:2358151 | A | G | 2 | a0001c0003t0001g0141 a0001c0003t0001g0142 |
2 | HG01081.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.500-2559A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2358151 | |||||||
| chr7:2358272 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.500-2438T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2358272 | |||||||
| chr7:2358303 | C | T | 1 | a0002c0002t0001g0254 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.500-2407C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2358303 | |||||||
| chr7:2358473 | T | C | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.500-2237T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2358473 | |||||||
| chr7:2358504 | GC | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.500-2205delC | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2358504 | |||||||
| chr7:2359016 | C | G | 1 | a0001c0001t0007g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.500-1694C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359016 | |||||||
| chr7:2359041 | A | AGACCCTG others(314): Show |
1 | a0001c0001t0001g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.500-1655_500-1654i others(323): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2359041 | ||||||
| chr7:2359045 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG00741.hp1 HG01123.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1665C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359045 | |||||||
| chr7:2359373 | G | T | 30 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0030 others(27): Show |
38 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.500-1337G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359373 | |||||||
| chr7:2359462 | C | T | 7 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0158 others(4): Show |
11 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.500-1248C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359462 | |||||||
| chr7:2359526 | C | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.500-1184C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359526 | |||||||
| chr7:2359544 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.500-1166C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359544 | |||||||
| chr7:2359635 | A | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01361.hp1 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.500-1075A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359635 | |||||||
| chr7:2359640 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.500-1070C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359640 | |||||||
| chr7:2359655 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.500-1055G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359655 | |||||||
| chr7:2359655 | G | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
9 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.500-1055G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359655 | |||||||
| chr7:2359850 | G | C | 6 | a0002c0002t0001g0010 a0002c0002t0001g0018 a0002c0002t0001g0043 others(3): Show |
12 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-860G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359850 | |||||||
| chr7:2359859 | G | A | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02258.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.500-851G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2359859 | |||||||
| chr7:2360011 | C | T | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-699C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360011 | |||||||
| chr7:2360103 | G | A | 3 | a0003c0004t0001g0023 a0003c0004t0001g0071 a0003c0004t0001g0072 |
4 | HG02523.hp2 NA18942.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-607G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360103 | |||||||
| chr7:2360170 | A | ACTCGAGA others(5): Show |
1 | a0001c0003t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.500-539_500-528dup others(12): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2360170 | ||||||
| chr7:2360223 | C | T | 5 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(2): Show |
5 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-487C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360223 | |||||||
| chr7:2360340 | A | G | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.500-370A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360340 | |||||||
| chr7:2360344 | C | G | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-366C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360344 | |||||||
| chr7:2360527 | TC | T | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-181delC | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 2360527 | ||||||
| chr7:2360671 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.500-39T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 1/18 | chr7 | 2360671 | |||||||
| chr7:2361015 | G | A | 2 | a0001c0011t0001g0189 a0001c0011t0001g0190 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.692+113G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361015 | |||||||
| chr7:2361031 | C | T | 4 | a0001c0005t0001g0027 a0001c0005t0001g0136 a0001c0005t0001g0137 others(1): Show |
5 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.692+129C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361031 | |||||||
| chr7:2361102 | T | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0195 a0001c0001t0001g0256 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+200T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361102 | |||||||
| chr7:2361178 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.692+276G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361178 | |||||||
| chr7:2361180 | C | T | 1 | a0001c0003t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.692+278C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361180 | |||||||
| chr7:2361331 | C | T | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.692+429C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361331 | |||||||
| chr7:2361349 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.692+447G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361349 | |||||||
| chr7:2361617 | C | T | 37 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0030 others(34): Show |
46 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.692+715C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361617 | |||||||
| chr7:2361670 | C | T | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.692+768C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361670 | |||||||
| chr7:2361671 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.692+769G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361671 | |||||||
| chr7:2361674 | C | T | 1 | a0001c0003t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.692+772C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361674 | |||||||
| chr7:2361728 | T | C | 1 | a0002c0002t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.692+826T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361728 | |||||||
| chr7:2361869 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.693-776C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361869 | |||||||
| chr7:2361934 | G | A | 37 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0030 others(34): Show |
46 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.693-711G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2361934 | |||||||
| chr7:2361952 | C | CTTATTTA others(1): Show |
37 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0030 others(34): Show |
46 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.693-675_693-668dup others(8): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 2361952 | ||||||
| chr7:2361952 | C | CTTATTTA others(5): Show |
9 | a0001c0001t0005g0028 a0001c0001t0005g0149 a0001c0003t0001g0143 others(6): Show |
11 | HG00642.hp1 HG01099.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.693-679_693-668dup others(12): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 2361952 | ||||||
| chr7:2361952 | CTTATTTA others(5): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0165 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.693-679_693-668del others(12): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 2361952 | ||||||
| chr7:2362022 | C | G | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.693-623C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362022 | |||||||
| chr7:2362299 | T | C | 11 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0201 others(8): Show |
13 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.693-346T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362299 | |||||||
| chr7:2362319 | T | G | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-326T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362319 | |||||||
| chr7:2362326 | G | A | 8 | a0002c0002t0001g0036 a0002c0002t0001g0215 a0002c0002t0001g0216 others(5): Show |
9 | NA18950.hp1 NA18974.hp2 NA18983.hp2 others(6): Show |
intron_variant | MODIFIER | c.693-319G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362326 | |||||||
| chr7:2362331 | A | G | 1 | a0002c0002t0001g0015 | 3 | HG02109.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.693-314A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362331 | |||||||
| chr7:2362434 | C | T | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.693-211C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362434 | |||||||
| chr7:2362518 | G | A | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-127G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362518 | |||||||
| chr7:2362565 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.693-80G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 2/18 | chr7 | 2362565 | |||||||
| chr7:2362796 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.812+32C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/18 | chr7 | 2362796 | |||||||
| chr7:2362819 | G | A | 1 | a0002c0002t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.812+55G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/18 | chr7 | 2362819 | |||||||
| chr7:2362824 | C | T | 1 | a0015c0024t0015g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.812+60C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/18 | chr7 | 2362824 | |||||||
| chr7:2363041 | G | A | 2 | a0001c0001t0001g0195 a0001c0017t0001g0194 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.813-29G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 3/18 | chr7 | 2363041 | |||||||
| chr7:2363188 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.870+61C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363188 | |||||||
| chr7:2363198 | A | G | 3 | a0002c0002t0001g0040 a0002c0002t0001g0252 a0002c0002t0001g0253 |
4 | HG02622.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+71A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363198 | |||||||
| chr7:2363375 | CTTGAGCC others(7): Show |
C | 37 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0030 others(34): Show |
46 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.871-237_871-224del others(14): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 2363375 | ||||||
| chr7:2363428 | G | A | 44 | a0001c0001t0001g0047 a0001c0001t0001g0256 a0001c0001t0001g0270 others(41): Show |
53 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.871-204G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363428 | |||||||
| chr7:2363493 | G | A | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(1): Show |
4 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-139G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363493 | |||||||
| chr7:2363552 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.871-80A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363552 | |||||||
| chr7:2363561 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.871-71A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363561 | |||||||
| chr7:2363605 | G | T | 2 | a0006c0012t0001g0199 a0006c0012t0001g0200 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.871-27G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | chr7 | 2363605 | |||||||
| chr7:2363619 | C | CTT | 4 | a0001c0001t0001g0011 a0001c0001t0001g0275 a0001c0001t0001g0287 others(1): Show |
7 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-11_871-10dupTT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 2363619 | ||||||
| chr7:2363886 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.999+126C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2363886 | |||||||
| chr7:2364058 | G | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(1): Show |
4 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+298G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364058 | |||||||
| chr7:2364071 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1000-301C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364071 | |||||||
| chr7:2364078 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0275 a0001c0001t0001g0287 others(1): Show |
7 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-294G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364078 | |||||||
| chr7:2364147 | C | T | 2 | a0001c0009t0001g0151 a0001c0009t0001g0166 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1000-225C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364147 | |||||||
| chr7:2364186 | T | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0275 a0001c0001t0001g0287 others(1): Show |
7 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-186T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364186 | |||||||
| chr7:2364276 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0132 |
6 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-96T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364276 | |||||||
| chr7:2364367 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.1000-5T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 5/18 | chr7 | 2364367 | |||||||
| chr7:2364622 | A | G | 1 | a0001c0003t0001g0268 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1157+93A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364622 | |||||||
| chr7:2364634 | C | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1157+105C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364634 | |||||||
| chr7:2364635 | G | A | 1 | a0005c0007t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1157+106G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364635 | |||||||
| chr7:2364696 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1157+167C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364696 | |||||||
| chr7:2364820 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1157+291G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364820 | |||||||
| chr7:2364865 | T | G | 1 | a0008c0025t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1157+336T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364865 | |||||||
| chr7:2364904 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1157+375C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364904 | |||||||
| chr7:2364937 | C | G | 1 | a0001c0003t0001g0184 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1157+408C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364937 | |||||||
| chr7:2364959 | A | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1157+430A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2364959 | |||||||
| chr7:2365022 | G | A | 112 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(109): Show |
140 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1157+493G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365022 | |||||||
| chr7:2365092 | G | A | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1157+563G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365092 | |||||||
| chr7:2365249 | C | T | 1 | a0002c0002t0001g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1157+720C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365249 | |||||||
| chr7:2365267 | C | T | 1 | a0001c0003t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1157+738C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365267 | |||||||
| chr7:2365277 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG00423.hp1 HG00597.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1157+748C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365277 | |||||||
| chr7:2365278 | G | A | 1 | a0001c0003t0001g0258 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1157+749G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365278 | |||||||
| chr7:2365317 | A | C | 119 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(116): Show |
148 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.1157+788A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365317 | |||||||
| chr7:2365334 | C | G | 1 | a0001c0003t0001g0042 | 2 | NA18954.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1157+805C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365334 | |||||||
| chr7:2365367 | A | T | 2 | a0004c0006t0001g0044 a0004c0006t0001g0045 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1157+838A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365367 | |||||||
| chr7:2365370 | G | A | 1 | a0012c0023t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1157+841G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365370 | |||||||
| chr7:2365385 | C | T | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1157+856C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365385 | |||||||
| chr7:2365393 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1157+864A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365393 | |||||||
| chr7:2365492 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1158-825G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365492 | |||||||
| chr7:2365625 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1158-692G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365625 | |||||||
| chr7:2365647 | G | GT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
8 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158-663dupT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365647 | ||||||
| chr7:2365655 | G | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1158-662G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365655 | |||||||
| chr7:2365663 | GTTTGTTT others(6): Show |
G | 2 | a0001c0005t0001g0135 a0002c0002t0001g0220 |
2 | HG02572.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1158-646_1158-634d others(15): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365663 | ||||||
| chr7:2365667 | G | GT | 3 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0008t0002g0278 |
3 | HG01192.hp1 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1158-647dupT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365667 | ||||||
| chr7:2365667 | GTTTGTTT others(7): Show |
G | 113 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(110): Show |
142 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1158-646_1158-633d others(16): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365667 | ||||||
| chr7:2365667 | GTTTGTTT others(8): Show |
G | 2 | a0002c0002t0001g0247 a0002c0002t0001g0254 |
2 | HG03491.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1158-646_1158-632d others(17): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365667 | ||||||
| chr7:2365669 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1158-648T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365669 | |||||||
| chr7:2365671 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1158-646G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365671 | |||||||
| chr7:2365671 | GTTTGTTT others(7): Show |
G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0001g0256 |
3 | HG02723.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1158-642_1158-629d others(16): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365671 | ||||||
| chr7:2365674 | T | G | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1158-643T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365674 | |||||||
| chr7:2365675 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1158-642G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365675 | |||||||
| chr7:2365676 | T | TG | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158-641_1158-640i others(3): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365676 | |||||||
| chr7:2365680 | G | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0117 a0001c0001t0001g0119 |
3 | NA18978.hp1 NA19006.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1158-637G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365680 | |||||||
| chr7:2365680 | GT | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1158-623delT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 2365680 | ||||||
| chr7:2365681 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0117 |
2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1158-636T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365681 | |||||||
| chr7:2365682 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1158-635T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365682 | |||||||
| chr7:2365685 | T | G | 4 | a0001c0003t0001g0143 a0001c0003t0001g0171 a0001c0003t0003g0172 others(1): Show |
4 | HG02602.hp2 HG03927.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-632T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365685 | |||||||
| chr7:2365686 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1158-631T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365686 | |||||||
| chr7:2365710 | G | C | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1158-607G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365710 | |||||||
| chr7:2365850 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1158-467A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365850 | |||||||
| chr7:2365914 | G | C | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1158-403G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2365914 | |||||||
| chr7:2366021 | G | A | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1158-296G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2366021 | |||||||
| chr7:2366048 | A | G | 4 | a0002c0002t0001g0018 a0002c0002t0001g0043 a0002c0002t0001g0283 others(1): Show |
7 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-269A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2366048 | |||||||
| chr7:2366194 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1158-123G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2366194 | |||||||
| chr7:2366250 | C | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1158-67C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 6/18 | chr7 | 2366250 | |||||||
| chr7:2366642 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1356+51C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 8/18 | chr7 | 2366642 | |||||||
| chr7:2366786 | C | T | 1 | a0009c0020t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1356+195C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 8/18 | chr7 | 2366786 | |||||||
| chr7:2366871 | C | T | 9 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0005t0001g0027 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357-128C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 8/18 | chr7 | 2366871 | |||||||
| chr7:2366945 | T | A | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1357-54T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 8/18 | chr7 | 2366945 | |||||||
| chr7:2367060 | C | T | 1 | a0002c0002t0006g0248 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1403+15C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367060 | |||||||
| chr7:2367083 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1403+38A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367083 | |||||||
| chr7:2367102 | C | CA | 11 | a0001c0001t0005g0149 a0001c0003t0001g0144 a0001c0003t0001g0171 others(8): Show |
12 | HG00642.hp1 HG01099.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1403+74dupA | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367102 | ||||||
| chr7:2367102 | CA | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1403+74delA | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367102 | ||||||
| chr7:2367114 | A | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1403+69A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367114 | |||||||
| chr7:2367200 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1403+155G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367200 | |||||||
| chr7:2367206 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1403+161G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367206 | |||||||
| chr7:2367290 | G | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1403+245G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367290 | |||||||
| chr7:2367332 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1403+287C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367332 | |||||||
| chr7:2367369 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1403+324C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367369 | |||||||
| chr7:2367395 | C | G | 1 | a0001c0005t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1403+350C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367395 | |||||||
| chr7:2367430 | G | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1403+385G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367430 | |||||||
| chr7:2367430 | G | C | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1403+385G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367430 | |||||||
| chr7:2367460 | C | T | 1 | a0001c0005t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1403+415C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367460 | |||||||
| chr7:2367472 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1403+427G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367472 | |||||||
| chr7:2367532 | C | T | 1 | a0001c0017t0001g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1403+487C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367532 | |||||||
| chr7:2367594 | C | T | 1 | a0003c0004t0001g0114 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1403+549C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367594 | |||||||
| chr7:2367595 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1403+550G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367595 | |||||||
| chr7:2367635 | A | G | 4 | a0003c0004t0001g0013 a0003c0004t0001g0112 a0003c0004t0001g0113 others(1): Show |
5 | HG01261.hp2 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403+590A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367635 | |||||||
| chr7:2367701 | C | G | 1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1403+656C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367701 | |||||||
| chr7:2367755 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0270 |
2 | HG01496.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1403+710A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367755 | |||||||
| chr7:2367760 | G | T | 1 | a0001c0017t0001g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1403+715G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367760 | |||||||
| chr7:2367801 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1403+756C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367801 | |||||||
| chr7:2367804 | T | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1403+759T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367804 | |||||||
| chr7:2367824 | A | ATTTTTTT others(4): Show |
1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1403+779_1403+780i others(13): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367824 | |||||||
| chr7:2367824 | AATTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0274 |
4 | HG01243.hp1 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403+780_1403+789d others(12): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367824 | |||||||
| chr7:2367825 | A | AT | 11 | a0001c0001t0001g0061 a0001c0003t0001g0008 a0001c0003t0001g0030 others(8): Show |
11 | HG01109.hp2 HG01981.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1403+814dupT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0097 others(3): Show |
6 | HG00558.hp1 HG02698.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403+812_1403+814d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(19): Show |
28 | HG00673.hp2 HG01256.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.1403+811_1403+814d others(6): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTTT | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
30 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1403+810_1403+814d others(7): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTTTT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0050 others(7): Show |
12 | HG00423.hp1 HG01255.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1403+809_1403+814d others(8): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0119 |
2 | NA19062.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1403+804_1403+814d others(13): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0055 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1403+803_1403+814d others(14): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0288 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1403+800_1403+814d others(17): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | A | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(1): Show |
4 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403+780A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367825 | |||||||
| chr7:2367825 | AT | A | 23 | a0001c0003t0001g0006 a0001c0003t0001g0140 a0001c0003t0001g0141 others(20): Show |
24 | HG00544.hp2 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1403+814delT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATT | A | 42 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0133 others(39): Show |
48 | HG00609.hp1 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.1403+813_1403+814d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTT | A | 50 | a0001c0001t0005g0028 a0001c0008t0001g0277 a0001c0017t0001g0194 others(47): Show |
61 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1403+812_1403+814d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTT | A | 13 | a0001c0001t0001g0047 a0001c0001t0001g0074 a0001c0001t0001g0270 others(10): Show |
13 | HG00639.hp1 HG01070.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1403+811_1403+814d others(6): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTT | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0001g0256 others(5): Show |
9 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403+810_1403+814d others(7): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0086 others(6): Show |
9 | HG00558.hp2 HG01433.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403+806_1403+814d others(11): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(3): Show |
A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1403+805_1403+814d others(12): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0003g0001 others(1): Show |
4 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403+804_1403+814d others(13): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1403+803_1403+814d others(14): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(8): Show |
A | 2 | a0002c0002t0001g0221 a0002c0002t0001g0226 |
2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1403+800_1403+814d others(17): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367825 | ATTTTTTT others(15): Show |
A | 3 | a0001c0001t0001g0195 a0001c0011t0001g0189 a0001c0011t0001g0190 |
3 | HG02818.hp1 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1403+793_1403+814d others(24): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 2367825 | ||||||
| chr7:2367828 | T | A | 3 | a0001c0003t0001g0187 a0001c0003t0001g0271 a0002c0002t0001g0203 |
3 | HG02615.hp1 HG06807.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1403+783T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367828 | |||||||
| chr7:2367831 | T | A | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1403+786T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367831 | |||||||
| chr7:2367959 | T | C | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1403+914T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2367959 | |||||||
| chr7:2368030 | A | T | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1403+985A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368030 | |||||||
| chr7:2368054 | G | C | 7 | a0002c0002t0001g0040 a0002c0002t0001g0224 a0002c0002t0001g0225 others(4): Show |
8 | HG02622.hp2 HG02647.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1403+1009G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368054 | |||||||
| chr7:2368131 | A | C | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1403+1086A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368131 | |||||||
| chr7:2368516 | T | C | 1 | a0003c0004t0001g0114 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1404-956T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368516 | |||||||
| chr7:2368559 | C | T | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1404-913C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368559 | |||||||
| chr7:2368579 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(1): Show |
4 | HG01192.hp1 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1404-893C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368579 | |||||||
| chr7:2368706 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1404-766A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368706 | |||||||
| chr7:2368800 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1404-672G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368800 | |||||||
| chr7:2368844 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 |
3 | HG02572.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1404-628C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368844 | |||||||
| chr7:2368989 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1404-483T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2368989 | |||||||
| chr7:2369182 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1404-290C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2369182 | |||||||
| chr7:2369379 | C | T | 2 | a0001c0005t0001g0135 a0001c0015t0002g0139 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1404-93C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2369379 | |||||||
| chr7:2369400 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1404-72C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2369400 | |||||||
| chr7:2369425 | G | A | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1404-47G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 9/18 | chr7 | 2369425 | |||||||
| chr7:2369765 | A | AT | 11 | a0001c0003t0001g0008 a0001c0003t0001g0152 a0001c0003t0001g0153 others(8): Show |
14 | HG00423.hp2 HG00733.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+113dupT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | AT | A | 11 | a0001c0001t0001g0275 a0001c0001t0002g0150 a0001c0003t0001g0169 others(8): Show |
12 | HG01192.hp1 HG02004.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1614+113delT | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATT | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0002c0002t0001g0155 others(1): Show |
7 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1614+112_1614+113d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTT | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(23): Show |
28 | HG00544.hp2 HG01106.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1614+111_1614+113d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTT | A | 95 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0074 others(92): Show |
122 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1614+110_1614+113d others(6): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTTT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1614+109_1614+113d others(7): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTTTT | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0119 others(2): Show |
6 | HG02809.hp2 HG03516.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1614+108_1614+113d others(8): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTTTTT | A | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614+107_1614+113d others(9): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTTTTT others(7): Show |
A | 1 | a0002c0002t0001g0227 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1614+100_1614+113d others(16): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369765 | ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1614+96_1614+113de others(19): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 2369765 | ||||||
| chr7:2369797 | A | G | 5 | a0002c0002t0001g0040 a0002c0002t0001g0226 a0002c0002t0001g0252 others(2): Show |
6 | HG02622.hp2 HG02965.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+115A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2369797 | |||||||
| chr7:2370130 | T | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0123 |
2 | HG00438.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1614+448T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370130 | |||||||
| chr7:2370242 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1614+560C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370242 | |||||||
| chr7:2370449 | C | G | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1614+767C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370449 | |||||||
| chr7:2370516 | A | G | 103 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(100): Show |
130 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1614+834A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370516 | |||||||
| chr7:2370633 | T | G | 1 | a0001c0003t0001g0264 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1614+951T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370633 | |||||||
| chr7:2370661 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1614+979C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370661 | |||||||
| chr7:2370802 | A | G | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0005t0001g0027 others(5): Show |
9 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1615-975A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370802 | |||||||
| chr7:2370846 | C | T | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-931C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370846 | |||||||
| chr7:2370847 | G | A | 114 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(111): Show |
142 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1615-930G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370847 | |||||||
| chr7:2370890 | C | T | 7 | a0001c0001t0001g0164 a0001c0001t0001g0195 a0001c0001t0009g0273 others(4): Show |
7 | HG02559.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-887C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370890 | |||||||
| chr7:2370906 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-871G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370906 | |||||||
| chr7:2370920 | A | G | 3 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 |
3 | HG02257.hp2 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1615-857A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370920 | |||||||
| chr7:2370929 | G | A | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1615-848G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370929 | |||||||
| chr7:2370932 | G | T | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1615-845G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370932 | |||||||
| chr7:2370935 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1615-842T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370935 | |||||||
| chr7:2370945 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1615-832C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370945 | |||||||
| chr7:2370946 | C | G | 1 | a0001c0003t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1615-831C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2370946 | |||||||
| chr7:2371017 | T | C | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-760T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371017 | |||||||
| chr7:2371018 | G | C | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-759G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371018 | |||||||
| chr7:2371020 | A | G | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-757A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371020 | |||||||
| chr7:2371041 | C | T | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-736C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371041 | |||||||
| chr7:2371042 | A | G | 117 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(114): Show |
146 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.1615-735A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371042 | |||||||
| chr7:2371133 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0082 |
2 | HG03942.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1615-644G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371133 | |||||||
| chr7:2371144 | G | T | 1 | a0002c0002t0006g0248 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1615-633G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371144 | |||||||
| chr7:2371260 | G | A | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1615-517G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371260 | |||||||
| chr7:2371326 | A | G | 2 | a0001c0009t0001g0151 a0001c0009t0001g0166 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-451A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371326 | |||||||
| chr7:2371390 | C | A | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1615-387C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371390 | |||||||
| chr7:2371486 | C | G | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1615-291C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371486 | |||||||
| chr7:2371527 | C | G | 2 | a0002c0002t0006g0243 a0002c0002t0006g0248 |
2 | HG00639.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1615-250C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371527 | |||||||
| chr7:2371592 | C | T | 1 | a0002c0002t0001g0043 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1615-185C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371592 | |||||||
| chr7:2371604 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1615-173A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371604 | |||||||
| chr7:2371608 | T | G | 6 | a0002c0002t0001g0009 a0002c0002t0001g0031 a0002c0002t0001g0155 others(3): Show |
10 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1615-169T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371608 | |||||||
| chr7:2371693 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1615-84A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 10/18 | chr7 | 2371693 | |||||||
| chr7:2371980 | A | C | 1 | a0002c0002t0016g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1687+131A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2371980 | |||||||
| chr7:2372009 | C | T | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1687+160C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372009 | |||||||
| chr7:2372050 | A | T | 103 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(100): Show |
130 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1687+201A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372050 | |||||||
| chr7:2372085 | T | C | 2 | a0001c0001t0001g0074 a0001c0016t0010g0285 |
2 | NA18947.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1687+236T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372085 | |||||||
| chr7:2372133 | G | A | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1687+284G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372133 | |||||||
| chr7:2372397 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1688-276G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372397 | |||||||
| chr7:2372442 | C | T | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1688-231C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372442 | |||||||
| chr7:2372450 | G | A | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1688-223G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372450 | |||||||
| chr7:2372464 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1688-209G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 11/18 | chr7 | 2372464 | |||||||
| chr7:2372827 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1810+32T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372827 | |||||||
| chr7:2372858 | C | T | 109 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(106): Show |
137 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.1810+63C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372858 | |||||||
| chr7:2372866 | T | G | 1 | a0002c0002t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1810+71T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372866 | |||||||
| chr7:2372913 | C | A | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1810+118C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372913 | |||||||
| chr7:2372931 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1810+136C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372931 | |||||||
| chr7:2372969 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1810+174G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2372969 | |||||||
| chr7:2373003 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1810+208A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373003 | |||||||
| chr7:2373012 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1810+217G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373012 | |||||||
| chr7:2373139 | C | T | 1 | a0001c0003t0013g0179 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1810+344C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373139 | |||||||
| chr7:2373166 | G | A | 2 | a0004c0006t0001g0044 a0004c0006t0001g0045 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1810+371G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373166 | |||||||
| chr7:2373171 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG01255.hp2 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1810+376G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373171 | |||||||
| chr7:2373287 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1810+492C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373287 | |||||||
| chr7:2373357 | C | T | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1810+562C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373357 | |||||||
| chr7:2373399 | G | A | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1810+604G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373399 | |||||||
| chr7:2373500 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1810+705T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373500 | |||||||
| chr7:2373623 | T | C | 120 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(117): Show |
149 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.1810+828T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373623 | |||||||
| chr7:2373687 | G | T | 2 | a0001c0009t0001g0151 a0001c0009t0001g0166 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1811-841G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373687 | |||||||
| chr7:2373694 | G | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1811-834G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373694 | |||||||
| chr7:2373729 | A | G | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1811-799A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373729 | |||||||
| chr7:2373733 | GCACCTTG others(7): Show |
G | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1811-792_1811-779d others(16): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 2373733 | ||||||
| chr7:2373766 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1811-762C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373766 | |||||||
| chr7:2373803 | C | T | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1811-725C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373803 | |||||||
| chr7:2373920 | A | G | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1811-608A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373920 | |||||||
| chr7:2373960 | A | T | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1811-568A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373960 | |||||||
| chr7:2373973 | C | A | 7 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(4): Show |
8 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1811-555C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2373973 | |||||||
| chr7:2374012 | G | C | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1811-516G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374012 | |||||||
| chr7:2374077 | C | T | 1 | a0001c0003t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1811-451C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374077 | |||||||
| chr7:2374192 | T | A | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1811-336T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374192 | |||||||
| chr7:2374313 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1811-215C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374313 | |||||||
| chr7:2374429 | C | G | 1 | a0001c0001t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1811-99C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374429 | |||||||
| chr7:2374506 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1811-22C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374506 | |||||||
| chr7:2374507 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1811-21A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 12/18 | chr7 | 2374507 | |||||||
| chr7:2374637 | C | T | 3 | a0001c0001t0001g0195 a0001c0011t0001g0189 a0001c0011t0001g0190 |
3 | HG02818.hp1 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1889+31C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374637 | |||||||
| chr7:2374656 | G | A | 1 | a0001c0003t0013g0179 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1889+50G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374656 | |||||||
| chr7:2374730 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1889+124A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374730 | |||||||
| chr7:2374852 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1889+246T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374852 | |||||||
| chr7:2374915 | C | A | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1889+309C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374915 | |||||||
| chr7:2374917 | G | C | 1 | a0002c0002t0001g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1889+311G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374917 | |||||||
| chr7:2374919 | G | A | 2 | a0002c0002t0006g0243 a0002c0002t0006g0248 |
2 | HG00639.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1889+313G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374919 | |||||||
| chr7:2374932 | G | A | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1889+326G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374932 | |||||||
| chr7:2374952 | T | C | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1889+346T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2374952 | |||||||
| chr7:2375032 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1890-357C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375032 | |||||||
| chr7:2375122 | C | T | 103 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(100): Show |
130 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1890-267C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375122 | |||||||
| chr7:2375190 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1890-199A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375190 | |||||||
| chr7:2375217 | A | G | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1890-172A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375217 | |||||||
| chr7:2375224 | A | G | 1 | a0001c0003t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1890-165A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375224 | |||||||
| chr7:2375313 | C | T | 1 | a0005c0007t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1890-76C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 13/18 | chr7 | 2375313 | |||||||
| chr7:2375632 | CCT | C | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2028+108_2028+109d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 2375632 | ||||||
| chr7:2375665 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2028+138A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375665 | |||||||
| chr7:2375736 | G | T | 1 | a0002c0002t0001g0209 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2028+209G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375736 | |||||||
| chr7:2375741 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2028+214G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375741 | |||||||
| chr7:2375775 | C | A | 1 | a0006c0012t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028+248C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375775 | |||||||
| chr7:2375789 | T | C | 7 | a0001c0001t0001g0059 a0002c0002t0001g0009 a0002c0002t0001g0031 others(4): Show |
11 | HG01167.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2028+262T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375789 | |||||||
| chr7:2375893 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01516.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2028+366C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375893 | |||||||
| chr7:2375894 | GCGTTACC others(7): Show |
G | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2028+371_2028+384d others(16): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 2375894 | ||||||
| chr7:2375960 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2028+433A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2375960 | |||||||
| chr7:2376011 | T | C | 1 | a0002c0002t0001g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2028+484T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376011 | |||||||
| chr7:2376032 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0122 |
2 | HG01515.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2028+505C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376032 | |||||||
| chr7:2376056 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028+529C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376056 | |||||||
| chr7:2376136 | T | C | 111 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
139 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.2028+609T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376136 | |||||||
| chr7:2376162 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2028+635T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376162 | |||||||
| chr7:2376165 | T | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(5): Show |
11 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2028+638T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376165 | |||||||
| chr7:2376199 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2028+672T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376199 | |||||||
| chr7:2376250 | T | G | 1 | a0002c0002t0001g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2029-700T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376250 | |||||||
| chr7:2376270 | A | G | 113 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(110): Show |
141 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.2029-680A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376270 | |||||||
| chr7:2376313 | A | G | 103 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(100): Show |
130 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.2029-637A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376313 | |||||||
| chr7:2376332 | TA | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2029-598delA | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 2376332 | ||||||
| chr7:2376332 | TAA | T | 17 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0081 others(14): Show |
20 | HG00558.hp2 HG01081.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.2029-599_2029-598d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | 2376332 | ||||||
| chr7:2376378 | C | A | 1 | a0001c0003t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2029-572C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376378 | |||||||
| chr7:2376482 | G | A | 1 | a0001c0003t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2029-468G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376482 | |||||||
| chr7:2376568 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.2029-382C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376568 | |||||||
| chr7:2376611 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2029-339G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376611 | |||||||
| chr7:2376699 | G | T | 1 | a0002c0002t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2029-251G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376699 | |||||||
| chr7:2376747 | C | T | 2 | a0001c0001t0001g0061 a0002c0002t0001g0252 |
2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2029-203C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376747 | |||||||
| chr7:2376751 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2029-199C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376751 | |||||||
| chr7:2376859 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2029-91C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 14/18 | chr7 | 2376859 | |||||||
| chr7:2377118 | A | T | 1 | a0002c0002t0001g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2154+43A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377118 | |||||||
| chr7:2377176 | A | T | 7 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0158 others(4): Show |
11 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2154+101A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377176 | |||||||
| chr7:2377187 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.2154+112A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377187 | |||||||
| chr7:2377189 | A | G | 1 | a0002c0002t0001g0222 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2154+114A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377189 | |||||||
| chr7:2377409 | G | C | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2154+334G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377409 | |||||||
| chr7:2377437 | C | T | 1 | a0002c0002t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2154+362C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377437 | |||||||
| chr7:2377453 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2154+378C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377453 | |||||||
| chr7:2377465 | GATGGAGG others(566): Show |
G | 6 | a0001c0001t0005g0028 a0001c0001t0005g0149 a0001c0003t0001g0176 others(3): Show |
7 | HG01099.hp2 HG01175.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+434_2155-608d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377465 | ||||||
| chr7:2377467 | TGGAGGAA others(57): Show |
T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 others(15): Show |
26 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.2154+434_2154+497d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377467 | ||||||
| chr7:2377477 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2154+402A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377477 | |||||||
| chr7:2377484 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG00621.hp1 HG01243.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+409A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377484 | |||||||
| chr7:2377484 | ACGAGCGC others(185): Show |
A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2154+434_2154+625d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377484 | ||||||
| chr7:2377490 | G | GCTCCTGG others(313): Show |
1 | a0001c0003t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2154+433_2154+434i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377490 | ||||||
| chr7:2377490 | G | T | 4 | a0001c0001t0004g0005 a0001c0001t0004g0095 a0001c0001t0004g0290 others(1): Show |
4 | HG00621.hp1 NA18997.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+415G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377490 | |||||||
| chr7:2377490 | GCTCCTGG others(502): Show |
G | 10 | a0002c0002t0001g0017 a0002c0002t0001g0157 a0002c0002t0001g0214 others(7): Show |
12 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2154+434_2155-672d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377490 | ||||||
| chr7:2377493 | C | CCTGGGAT others(57): Show |
2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2154+455_2154+456i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377493 | ||||||
| chr7:2377499 | ATGCTGTG others(56): Show |
A | 3 | a0001c0009t0001g0151 a0001c0009t0001g0166 a0012c0023t0001g0191 |
3 | HG02895.hp2 NA18522.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2154+425_2154+487d others(65): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377499 | |||||||
| chr7:2377500 | T | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+425T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377500 | |||||||
| chr7:2377500 | T | TGCTGTGT others(953): Show |
1 | a0001c0005t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2154+455_2154+456i others(962): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377500 | ||||||
| chr7:2377500 | T | TGCTGTGT others(1273): Show |
1 | a0001c0005t0001g0136 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2154+455_2154+456i others(1282): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377500 | ||||||
| chr7:2377500 | T | TGCTGTGT others(761): Show |
1 | a0001c0005t0001g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2154+455_2154+456i others(770): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377500 | ||||||
| chr7:2377501 | G | T | 3 | a0001c0001t0004g0005 a0001c0001t0004g0095 a0001c0001t0004g0290 |
3 | HG00621.hp1 NA18997.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2154+426G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377501 | |||||||
| chr7:2377503 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
10 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+428T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377503 | |||||||
| chr7:2377503 | T | TGTGTTCT others(57): Show |
1 | a0001c0001t0001g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2154+433_2154+434i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377503 | ||||||
| chr7:2377503 | T | TGTGTTCT others(441): Show |
1 | a0001c0001t0001g0001 | 2 | HG00438.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2154+433_2154+434i others(450): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377503 | ||||||
| chr7:2377503 | T | TGTGTTCT others(185): Show |
1 | a0001c0003t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2154+433_2154+434i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377503 | ||||||
| chr7:2377503 | T | TGTGTTCT others(569): Show |
1 | a0001c0001t0001g0125 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2154+433_2154+434i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377503 | ||||||
| chr7:2377503 | TGTGTTGT others(121): Show |
T | 2 | a0002c0002t0001g0212 a0002c0002t0001g0223 |
2 | HG02258.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2154+434_2154+561d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377503 | ||||||
| chr7:2377509 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0124 others(82): Show |
100 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.2154+434G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377509 | |||||||
| chr7:2377509 | G | GTGTGAAT others(377): Show |
1 | a0001c0003t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2154+455_2154+456i others(386): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377509 | ||||||
| chr7:2377509 | GTGTGAAT others(502): Show |
G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+456_2155-650d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377509 | ||||||
| chr7:2377531 | A | AGGAGGAA others(569): Show |
1 | a0003c0004t0001g0023 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2154+472_2154+473i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(57): Show |
2 | a0001c0001t0001g0002 a0001c0001t0009g0273 |
2 | NA18999.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2154+472_2154+473i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(1785): Show |
1 | a0001c0001t0001g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2154+472_2154+473i others(1794): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(1849): Show |
1 | a0001c0001t0001g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2154+472_2154+473i others(1858): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(377): Show |
1 | a0001c0001t0001g0001 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2154+472_2154+473i others(386): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(505): Show |
1 | a0001c0003t0001g0007 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2154+472_2154+473i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(1785): Show |
1 | a0001c0001t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2154+472_2154+473i others(1794): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(953): Show |
1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2154+472_2154+473i others(962): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | AGGAGGAA others(889): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0102 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2154+472_2154+473i others(898): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0059 others(86): Show |
105 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.2154+456A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377531 | |||||||
| chr7:2377531 | AGGAGGAA others(57): Show |
A | 2 | a0001c0001t0001g0164 a0001c0017t0001g0194 |
2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2154+473_2154+536d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377531 | AGGAGGAA others(185): Show |
A | 1 | a0001c0003t0001g0006 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2154+473_2154+664d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377531 | ||||||
| chr7:2377543 | C | T | 1 | a0001c0003t0001g0006 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2154+468C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377543 | |||||||
| chr7:2377547 | C | CGCGAGCT others(1013): Show |
1 | a0001c0003t0001g0007 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2154+472_2154+473i others(1022): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377547 | |||||||
| chr7:2377548 | A | ACGAGCGC others(243): Show |
1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2154+488_2154+489i others(252): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377548 | ||||||
| chr7:2377548 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2154+473A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377548 | |||||||
| chr7:2377548 | ACGAGCGC others(121): Show |
A | 2 | a0001c0003t0001g0173 a0001c0003t0001g0177 |
2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2154+543_2154+670d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377548 | ||||||
| chr7:2377548 | ACGAGCGC others(185): Show |
A | 6 | a0001c0003t0001g0006 a0001c0003t0001g0153 a0001c0003t0001g0171 others(3): Show |
7 | HG00733.hp2 HG02602.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+617_2155-806d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377548 | ||||||
| chr7:2377554 | G | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0124 others(74): Show |
92 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2154+479G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377554 | |||||||
| chr7:2377554 | GCTCCTGG others(249): Show |
G | 1 | a0001c0003t0001g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2154+489_2154+744d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377554 | ||||||
| chr7:2377557 | C | CCTGGGAA others(441): Show |
1 | a0001c0001t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2154+488_2154+489i others(450): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377557 | ||||||
| chr7:2377557 | C | CCTGGGAA others(57): Show |
1 | a0002c0002t0001g0210 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2154+488_2154+489i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377557 | ||||||
| chr7:2377557 | C | T | 4 | a0004c0006t0001g0029 a0004c0006t0001g0044 a0004c0006t0001g0045 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+482C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377557 | |||||||
| chr7:2377564 | T | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0124 others(78): Show |
96 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.2154+489T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377564 | |||||||
| chr7:2377564 | TG | T | 3 | a0001c0009t0001g0151 a0001c0009t0001g0166 a0012c0023t0001g0191 |
3 | HG02895.hp2 NA18522.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2154+490delG | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377564 | |||||||
| chr7:2377565 | G | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0124 others(78): Show |
96 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.2154+490G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377565 | |||||||
| chr7:2377567 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0124 others(84): Show |
102 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.2154+492T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377567 | |||||||
| chr7:2377567 | T | TGTGTTCT others(1529): Show |
1 | a0001c0001t0001g0024 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2154+542_2154+543i others(1538): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTCT others(633): Show |
1 | a0003c0004t0001g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2154+542_2154+543i others(642): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTCT others(953): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2154+583_2154+584i others(962): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTCT others(505): Show |
1 | a0001c0003t0001g0042 | 2 | NA18954.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2154+583_2154+584i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTCT others(889): Show |
1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(898): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTCT others(889): Show |
1 | a0003c0004t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2154+537_2154+538i others(898): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTGT others(121): Show |
1 | a0001c0005t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2154+497_2154+498i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377567 | T | TGTGTTGT others(118): Show |
1 | a0001c0001t0001g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2154+497_2154+498i others(127): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377567 | ||||||
| chr7:2377573 | C | CTGTGAAT others(313): Show |
1 | a0001c0001t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2154+542_2154+543i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377573 | ||||||
| chr7:2377573 | C | G | 9 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0150 others(6): Show |
10 | HG01192.hp1 HG01192.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+498C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377573 | |||||||
| chr7:2377587 | G | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0146 a0001c0001t0001g0256 others(1): Show |
4 | HG01496.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+512G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377587 | |||||||
| chr7:2377595 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0195 a0001c0001t0002g0150 others(4): Show |
7 | HG01433.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+520T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377595 | |||||||
| chr7:2377595 | T | TGGAGGAA others(185): Show |
1 | a0001c0003t0003g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2154+553_2154+554i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377595 | ||||||
| chr7:2377606 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0146 a0001c0001t0001g0165 others(2): Show |
5 | HG01496.hp1 HG02723.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+531G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377606 | |||||||
| chr7:2377612 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0002g0150 a0001c0003t0003g0172 others(2): Show |
5 | HG01891.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+537G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377612 | |||||||
| chr7:2377613 | C | T | 3 | a0003c0004t0001g0071 a0005c0007t0001g0075 a0005c0007t0001g0084 |
3 | HG03688.hp2 HG04184.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2154+538C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377613 | |||||||
| chr7:2377618 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(18): Show |
23 | HG00639.hp2 HG01891.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.2154+543T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377618 | |||||||
| chr7:2377618 | T | TCTCCTGG others(505): Show |
1 | a0001c0001t0003g0001 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377618 | ||||||
| chr7:2377618 | T | TCTCCTGG others(761): Show |
1 | a0001c0003t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(770): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377618 | ||||||
| chr7:2377618 | T | TCTCCTGG others(377): Show |
1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(386): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377618 | ||||||
| chr7:2377618 | TCTCCTGG others(57): Show |
T | 1 | a0002c0002t0001g0032 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2154+553_2154+616d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377618 | ||||||
| chr7:2377621 | C | CCTGGGAA others(121): Show |
3 | a0001c0001t0001g0109 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG02071.hp1 NA18967.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2154+583_2154+584i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(1785): Show |
1 | a0001c0003t0001g0264 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(1794): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(1209): Show |
1 | a0001c0001t0001g0003 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(1218): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(57): Show |
1 | a0001c0001t0001g0001 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(505): Show |
1 | a0001c0003t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(57): Show |
1 | a0001c0001t0001g0134 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAA others(121): Show |
1 | a0001c0003t0001g0260 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2154+554_2154+555i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | CCTGGGAT others(569): Show |
1 | a0001c0003t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2154+552_2154+553i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377621 | ||||||
| chr7:2377621 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0059 others(78): Show |
97 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.2154+546C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377621 | |||||||
| chr7:2377628 | A | AGCCGTGT others(54): Show |
1 | a0001c0003t0001g0030 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2154+553_2154+554i others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377628 | |||||||
| chr7:2377628 | A | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0003t0003g0172 others(7): Show |
12 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2154+553A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377628 | |||||||
| chr7:2377629 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0003t0001g0030 others(9): Show |
14 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2154+554T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377629 | |||||||
| chr7:2377629 | T | TCCGTGTT others(313): Show |
1 | a0001c0001t0001g0024 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377629 | ||||||
| chr7:2377629 | T | TCCGTGTT others(57): Show |
6 | a0003c0004t0001g0001 a0003c0004t0001g0002 a0003c0004t0001g0013 others(3): Show |
7 | HG01261.hp2 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+561_2154+562i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377629 | ||||||
| chr7:2377629 | TCCGTGTT others(310): Show |
T | 22 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0001g0035 others(19): Show |
26 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2154+584_2155-714d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377629 | ||||||
| chr7:2377631 | C | CGTGTTCT others(761): Show |
1 | a0001c0001t0004g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2154+583_2154+584i others(770): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | C | CGTGTTCT others(569): Show |
1 | a0004c0006t0001g0045 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | C | CGTGTTGT others(57): Show |
1 | a0003c0004t0001g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2154+561_2154+562i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0003t0003g0172 others(5): Show |
10 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2154+556C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377631 | |||||||
| chr7:2377631 | CGTGTTCT others(57): Show |
C | 1 | a0001c0003t0001g0174 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2154+584_2154+647d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | CGTGTTCT others(121): Show |
C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0001g0256 others(1): Show |
4 | HG02723.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+584_2154+711d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | CGTGTTCT others(374): Show |
C | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2154+584_2155-650d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377631 | CGTGTTCT others(438): Show |
C | 9 | a0001c0001t0001g0047 a0001c0001t0001g0270 a0001c0016t0010g0285 others(6): Show |
10 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2154+584_2155-586d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377631 | ||||||
| chr7:2377637 | C | CTGTGAAT others(633): Show |
1 | a0001c0001t0007g0001 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2154+583_2154+584i others(642): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377637 | ||||||
| chr7:2377637 | C | G | 10 | a0001c0001t0001g0092 a0001c0003t0001g0142 a0001c0005t0001g0027 others(7): Show |
11 | HG01192.hp2 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154+562C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377637 | |||||||
| chr7:2377659 | A | AGGAGGAA others(953): Show |
1 | a0001c0003t0001g0007 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(962): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377659 | ||||||
| chr7:2377659 | A | AGGAGGAA others(1145): Show |
1 | a0001c0003t0001g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(1154): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377659 | ||||||
| chr7:2377659 | A | AGGAGGAA others(697): Show |
1 | a0001c0003t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(706): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377659 | ||||||
| chr7:2377659 | A | AGGAGGAA others(441): Show |
1 | a0001c0003t0001g0267 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(450): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377659 | ||||||
| chr7:2377659 | A | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
240 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.2154+584A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377659 | |||||||
| chr7:2377671 | C | A | 2 | a0001c0003t0001g0142 a0001c0003t0001g0143 |
2 | HG02602.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2154+596C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377671 | |||||||
| chr7:2377675 | C | CGCGAGCT others(2165): Show |
1 | a0001c0001t0004g0095 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2154+606_2154+607i others(2174): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377675 | ||||||
| chr7:2377676 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0077 others(8): Show |
13 | HG01081.hp2 HG01256.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.2154+601G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377676 | |||||||
| chr7:2377676 | G | GCGAGCGC others(121): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0093 |
2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2154+616_2154+617i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377676 | ||||||
| chr7:2377676 | G | GCGAGCGC others(371): Show |
1 | a0001c0003t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2154+616_2154+617i others(380): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377676 | ||||||
| chr7:2377676 | G | GCGAGCTC others(3001): Show |
1 | a0001c0001t0001g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(3010): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377676 | ||||||
| chr7:2377677 | C | T | 1 | a0001c0003t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2154+602C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377677 | |||||||
| chr7:2377681 | C | CTCTTCTG others(439): Show |
1 | a0013c0022t0001g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2154+606_2154+607i others(448): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377681 | |||||||
| chr7:2377682 | G | A | 2 | a0001c0003t0001g0142 a0001c0003t0003g0041 |
2 | NA19000.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2154+607G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377682 | |||||||
| chr7:2377682 | G | GCTCCTGG others(118): Show |
3 | a0001c0003t0001g0154 a0001c0003t0001g0169 a0001c0003t0001g0170 |
3 | HG03017.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2154+616_2154+617i others(127): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377682 | ||||||
| chr7:2377682 | G | GCTCCTGG others(185): Show |
1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2154+616_2154+617i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377682 | ||||||
| chr7:2377682 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
113 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.2154+607G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377682 | |||||||
| chr7:2377682 | GCTCCTGG others(438): Show |
G | 1 | a0001c0001t0002g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2154+617_2155-553d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377682 | ||||||
| chr7:2377685 | C | CCTGGGAA others(54): Show |
4 | a0001c0003t0001g0030 a0001c0003t0001g0167 a0001c0003t0001g0187 others(1): Show |
4 | HG00544.hp1 HG02615.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+616_2154+617i others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377685 | ||||||
| chr7:2377685 | C | CCTGGGAA others(633): Show |
1 | a0001c0001t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2154+616_2154+617i others(642): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377685 | ||||||
| chr7:2377685 | C | G | 1 | a0001c0003t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2154+610C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377685 | |||||||
| chr7:2377685 | C | T | 67 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(64): Show |
85 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2154+610C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377685 | |||||||
| chr7:2377686 | C | G | 1 | a0001c0005t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2154+611C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377686 | |||||||
| chr7:2377691 | ATGCTGTG others(245): Show |
A | 5 | a0002c0002t0001g0201 a0002c0002t0001g0224 a0002c0002t0001g0276 others(2): Show |
5 | HG00639.hp1 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+617_2155-746d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377691 | |||||||
| chr7:2377691 | ATGCTGTG others(373): Show |
A | 22 | a0001c0001t0001g0059 a0002c0002t0001g0009 a0002c0002t0001g0014 others(19): Show |
31 | HG01167.hp2 HG01168.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.2154+617_2155-618d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377691 | |||||||
| chr7:2377692 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
118 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2154+617T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377692 | |||||||
| chr7:2377693 | G | GCCGTGTT others(441): Show |
1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(450): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(57): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0085 |
2 | NA18964.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2154+619_2154+620i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(2418): Show |
1 | a0001c0003t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(2427): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(761): Show |
1 | a0001c0001t0007g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(770): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(569): Show |
1 | a0001c0001t0001g0004 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2154+619_2154+620i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(185): Show |
1 | a0001c0001t0001g0081 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(313): Show |
1 | a0001c0001t0001g0094 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(313): Show |
1 | a0001c0001t0001g0107 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2154+619_2154+620i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(697): Show |
1 | a0001c0001t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2154+619_2154+620i others(706): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(633): Show |
1 | a0001c0001t0001g0022 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2154+619_2154+620i others(642): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | GCCGTGTT others(249): Show |
1 | a0001c0011t0001g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2154+619_2154+620i others(258): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377693 | ||||||
| chr7:2377693 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
85 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2154+618G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377693 | |||||||
| chr7:2377695 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
128 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.2154+620T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377695 | |||||||
| chr7:2377695 | T | TGTGTTCT others(569): Show |
1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2154+647_2154+648i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(121): Show |
1 | a0001c0001t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2154+664_2154+665i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(825): Show |
1 | a0001c0001t0001g0001 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2154+734_2154+735i others(834): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(57): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0090 others(1): Show |
4 | HG01928.hp2 HG03710.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+670_2154+671i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(121): Show |
1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2154+670_2154+671i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(1017): Show |
1 | a0003c0004t0001g0023 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2154+670_2154+671i others(1026): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(185): Show |
1 | a0001c0001t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2154+670_2154+671i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(185): Show |
1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2154+670_2154+671i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(1593): Show |
1 | a0003c0004t0001g0112 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2154+670_2154+671i others(1602): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | T | TGTGTTCT others(249): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0102 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2154+665_2154+666i others(258): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377695 | TGTGTTCT others(246): Show |
T | 1 | a0001c0001t0012g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2154+671_2155-691d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377695 | ||||||
| chr7:2377701 | C | G | 13 | a0001c0003t0001g0008 a0001c0003t0001g0142 a0001c0003t0001g0168 others(10): Show |
15 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2154+626C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377701 | |||||||
| chr7:2377715 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0164 |
2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2154+640G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377715 | |||||||
| chr7:2377721 | CATG | C | 5 | a0001c0003t0001g0008 a0001c0003t0001g0184 a0001c0003t0013g0179 others(2): Show |
5 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+647_2154+649d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377721 | |||||||
| chr7:2377723 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(18): Show |
24 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.2154+648T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377723 | |||||||
| chr7:2377723 | T | TGGAGGAA others(755): Show |
1 | a0001c0003t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2155-425_2155-424i others(764): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377723 | ||||||
| chr7:2377723 | T | TGGAGGAA others(819): Show |
1 | a0001c0003t0001g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2155-522_2155-521i others(828): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377723 | ||||||
| chr7:2377723 | T | TGGAGGAA others(505): Show |
1 | a0001c0001t0001g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2154+670_2154+671i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377723 | ||||||
| chr7:2377723 | T | TGGAGGAA others(249): Show |
1 | a0001c0001t0001g0001 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2154+670_2154+671i others(258): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377723 | ||||||
| chr7:2377734 | G | A | 1 | a0001c0003t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2154+659G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377734 | |||||||
| chr7:2377735 | C | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0184 a0001c0003t0013g0179 others(2): Show |
5 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+660C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377735 | |||||||
| chr7:2377740 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
22 | HG01167.hp1 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2154+665G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377740 | |||||||
| chr7:2377741 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0003t0001g0261 |
4 | HG00735.hp1 HG01069.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154+666C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377741 | |||||||
| chr7:2377745 | C | CTCTTCTG others(119): Show |
2 | a0006c0012t0001g0199 a0006c0012t0001g0200 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2154+670_2154+671i others(128): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377745 | |||||||
| chr7:2377746 | G | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0184 a0001c0003t0013g0179 others(2): Show |
5 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+671G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377746 | |||||||
| chr7:2377746 | G | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
133 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.2154+671G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377746 | |||||||
| chr7:2377746 | GCTCCTGG others(374): Show |
G | 1 | a0001c0001t0002g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2154+681_2155-553d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377746 | ||||||
| chr7:2377747 | C | T | 1 | a0001c0003t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2154+672C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377747 | |||||||
| chr7:2377749 | C | CCTGGGAA others(877): Show |
1 | a0001c0001t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2154+680_2154+681i others(886): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377749 | ||||||
| chr7:2377749 | C | CCTGGGAT others(313): Show |
1 | a0004c0006t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2154+683_2154+684i others(322): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377749 | ||||||
| chr7:2377749 | C | G | 5 | a0001c0003t0001g0008 a0001c0003t0001g0184 a0001c0003t0013g0179 others(2): Show |
5 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+674C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377749 | |||||||
| chr7:2377749 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0061 others(29): Show |
41 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2154+674C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377749 | |||||||
| chr7:2377755 | ATGCTGTG others(181): Show |
A | 1 | a0001c0003t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2154+681_2155-746d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377755 | |||||||
| chr7:2377756 | T | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2154+681T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377756 | |||||||
| chr7:2377757 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.2154+682G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377757 | |||||||
| chr7:2377759 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2154+684T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377759 | |||||||
| chr7:2377759 | T | TGTGTTCT others(3577): Show |
1 | a0001c0001t0001g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2154+734_2154+735i others(3586): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377759 | ||||||
| chr7:2377759 | T | TGTGTTCT others(1581): Show |
1 | a0001c0001t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2155-681_2155-680i others(1590): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377759 | ||||||
| chr7:2377759 | T | TGTGTTCT others(1209): Show |
1 | a0001c0001t0001g0134 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2154+744_2154+745i others(1218): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377759 | ||||||
| chr7:2377759 | TGTGTTCT others(182): Show |
T | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2154+745_2155-681d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377759 | ||||||
| chr7:2377765 | C | G | 12 | a0001c0001t0001g0164 a0001c0003t0001g0030 a0001c0003t0001g0141 others(9): Show |
12 | HG01081.hp2 HG01106.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2154+690C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377765 | |||||||
| chr7:2377779 | G | C | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2154+704G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377779 | |||||||
| chr7:2377779 | G | GGGTGTCA others(441): Show |
1 | a0001c0001t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2154+711_2154+712i others(450): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377779 | ||||||
| chr7:2377779 | G | GGGTGTCA others(101): Show |
1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2154+734_2154+735i others(110): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377779 | ||||||
| chr7:2377779 | G | T | 2 | a0001c0003t0001g0142 a0001c0003t0001g0263 |
2 | NA19011.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2154+704G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377779 | |||||||
| chr7:2377787 | T | A | 5 | a0001c0001t0001g0004 a0001c0001t0004g0290 a0001c0003t0001g0008 others(2): Show |
7 | HG00735.hp1 HG01069.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+712T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377787 | |||||||
| chr7:2377798 | G | A | 2 | a0001c0003t0001g0142 a0001c0008t0002g0278 |
2 | HG01192.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2154+723G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377798 | |||||||
| chr7:2377799 | C | A | 2 | a0001c0003t0001g0141 a0001c0003t0003g0172 |
2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2154+724C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377799 | |||||||
| chr7:2377804 | G | A | 8 | a0001c0001t0001g0003 a0001c0003t0001g0030 a0002c0002t0001g0010 others(5): Show |
12 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.2154+729G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377804 | |||||||
| chr7:2377805 | C | T | 3 | a0001c0001t0004g0290 a0001c0009t0001g0166 a0003c0004t0001g0071 |
3 | HG02895.hp2 NA18942.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.2154+730C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377805 | |||||||
| chr7:2377810 | T | A | 2 | a0001c0003t0001g0141 a0001c0003t0003g0172 |
2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2154+735T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377810 | |||||||
| chr7:2377810 | T | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(21): Show |
30 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2154+735T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377810 | |||||||
| chr7:2377810 | T | TCTCCTGG others(249): Show |
1 | a0001c0001t0001g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2154+775_2154+776i others(258): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377810 | ||||||
| chr7:2377811 | C | T | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2154+736C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377811 | |||||||
| chr7:2377813 | C | CCTGGGAA others(121): Show |
1 | a0005c0007t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2154+775_2154+776i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377813 | ||||||
| chr7:2377813 | C | CCTGGGAA others(754): Show |
1 | a0001c0001t0001g0049 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2154+775_2154+776i others(763): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377813 | ||||||
| chr7:2377813 | C | CCTGGGAA others(121): Show |
1 | a0001c0005t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2154+775_2154+776i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377813 | ||||||
| chr7:2377813 | C | G | 2 | a0001c0003t0001g0141 a0001c0003t0003g0172 |
2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2154+738C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377813 | |||||||
| chr7:2377813 | C | T | 36 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 others(33): Show |
43 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2154+738C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377813 | |||||||
| chr7:2377813 | CCTGGGAA others(118): Show |
C | 1 | a0001c0003t0013g0179 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2154+745_2155-745d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377813 | ||||||
| chr7:2377820 | A | AGCCGTGT others(54): Show |
1 | a0001c0003t0001g0008 | 2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2154+745_2154+746i others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377820 | |||||||
| chr7:2377820 | A | T | 14 | a0001c0003t0001g0008 a0001c0003t0001g0030 a0001c0003t0001g0141 others(11): Show |
14 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.2154+745A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377820 | |||||||
| chr7:2377821 | T | G | 17 | a0001c0001t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(14): Show |
19 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2154+746T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377821 | |||||||
| chr7:2377821 | TCCGTGTT others(118): Show |
T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0164 a0001c0009t0001g0151 others(2): Show |
5 | HG00609.hp1 HG02559.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+776_2155-714d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377821 | ||||||
| chr7:2377823 | C | CGTGTTCT others(54): Show |
1 | a0001c0003t0001g0175 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2154+774_2154+775i others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377823 | ||||||
| chr7:2377823 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0030 a0001c0003t0001g0141 others(8): Show |
11 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2154+748C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377823 | |||||||
| chr7:2377823 | CGTGTTCT others(182): Show |
C | 1 | a0002c0002t0001g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2154+776_2155-650d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377823 | ||||||
| chr7:2377823 | CGTGTTCT others(246): Show |
C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0133 others(6): Show |
11 | HG01109.hp2 HG02572.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154+776_2155-586d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377823 | ||||||
| chr7:2377829 | C | CTGTGAAT others(121): Show |
1 | a0009c0020t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2154+775_2154+776i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377829 | ||||||
| chr7:2377829 | C | G | 7 | a0001c0001t0002g0150 a0001c0003t0001g0141 a0001c0003t0001g0142 others(4): Show |
7 | HG01081.hp2 HG01192.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.2154+754C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377829 | |||||||
| chr7:2377843 | G | C | 1 | a0001c0003t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2154+768G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377843 | |||||||
| chr7:2377843 | G | T | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2154+768G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377843 | |||||||
| chr7:2377851 | A | AGGAGGAA others(1017): Show |
1 | a0001c0001t0001g0001 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2154+793_2154+794i others(1026): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377851 | ||||||
| chr7:2377851 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2154+776A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377851 | |||||||
| chr7:2377862 | G | A | 2 | a0001c0003t0001g0141 a0001c0008t0002g0278 |
2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2154+787G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377862 | |||||||
| chr7:2377863 | C | A | 1 | a0002c0002t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2154+788C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377863 | |||||||
| chr7:2377868 | G | A | 7 | a0001c0001t0001g0085 a0001c0003t0001g0008 a0001c0003t0001g0030 others(4): Show |
7 | HG00423.hp2 HG00544.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+793G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377868 | |||||||
| chr7:2377869 | C | T | 2 | a0001c0001t0001g0004 a0001c0003t0001g0007 |
2 | HG01123.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.2154+794C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377869 | |||||||
| chr7:2377874 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2154+799G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377874 | |||||||
| chr7:2377874 | G | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
117 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2154+799G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377874 | |||||||
| chr7:2377875 | C | T | 1 | a0001c0003t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2154+800C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377875 | |||||||
| chr7:2377877 | C | G | 1 | a0002c0002t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2154+802C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377877 | |||||||
| chr7:2377877 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0287 a0001c0001t0001g0288 others(11): Show |
16 | HG00642.hp2 HG01123.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+802C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377877 | |||||||
| chr7:2377877 | CCTGGGAA others(54): Show |
C | 4 | a0001c0003t0001g0008 a0002c0002t0001g0010 a0002c0002t0001g0018 others(1): Show |
8 | HG00738.hp2 HG01099.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-805_2155-745d others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377877 | ||||||
| chr7:2377884 | A | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(34): Show |
40 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.2155-805A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377884 | |||||||
| chr7:2377884 | AGCCGTGT others(54): Show |
A | 7 | a0002c0002t0001g0016 a0002c0002t0001g0032 a0002c0002t0001g0038 others(4): Show |
9 | HG00642.hp2 HG01496.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2155-796_2155-736d others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377884 | ||||||
| chr7:2377885 | G | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
142 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2155-804G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377885 | |||||||
| chr7:2377887 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(34): Show |
40 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.2155-802C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377887 | |||||||
| chr7:2377887 | CGTGTTGT others(118): Show |
C | 1 | a0002c0002t0001g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2155-796_2155-672d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377887 | ||||||
| chr7:2377893 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.2155-796G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377893 | |||||||
| chr7:2377907 | G | C | 1 | a0002c0002t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2155-782G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377907 | |||||||
| chr7:2377907 | G | T | 1 | a0001c0003t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2155-782G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377907 | |||||||
| chr7:2377913 | C | CAAG | 19 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(16): Show |
19 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.2155-776_2155-775i others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CAAGGAGG others(124): Show |
1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(133): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CAAGGAGG others(316): Show |
1 | a0001c0001t0001g0024 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(325): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CAAGGAGG others(60): Show |
1 | a0001c0005t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(69): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CAAGGAGG others(60): Show |
1 | a0001c0001t0001g0001 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(69): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATG | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2155-776_2155-775i others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(508): Show |
1 | a0001c0001t0003g0001 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(517): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(60): Show |
1 | a0001c0001t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(69): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(764): Show |
1 | a0005c0007t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(773): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(60): Show |
4 | a0001c0001t0001g0076 a0001c0001t0001g0097 a0001c0001t0001g0117 others(1): Show |
4 | HG00558.hp1 HG00621.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-776_2155-775i others(69): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(828): Show |
1 | a0001c0001t0001g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(837): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(188): Show |
1 | a0001c0003t0001g0007 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(197): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(188): Show |
1 | a0001c0003t0001g0007 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(197): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(252): Show |
1 | a0001c0001t0001g0005 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1084): Show |
1 | a0001c0003t0001g0266 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1093): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(252): Show |
1 | a0001c0001t0001g0092 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1916): Show |
1 | a0001c0001t0001g0001 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1925): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(124): Show |
1 | a0003c0004t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(133): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(188): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0129 |
2 | HG02486.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2155-776_2155-775i others(197): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1340): Show |
1 | a0001c0001t0001g0066 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1349): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1084): Show |
1 | a0003c0004t0001g0013 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1093): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(252): Show |
1 | a0001c0001t0001g0291 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(2364): Show |
1 | a0001c0001t0001g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(2373): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(316): Show |
1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(325): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(188): Show |
1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(197): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(252): Show |
1 | a0001c0003t0001g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(252): Show |
1 | a0001c0001t0001g0081 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(636): Show |
1 | a0001c0001t0001g0048 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(645): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1020): Show |
1 | a0001c0014t0001g0020 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1029): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1404): Show |
1 | a0003c0004t0003g0013 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1413): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1020): Show |
1 | a0001c0001t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1029): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(1468): Show |
1 | a0001c0003t0001g0258 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2155-776_2155-775i others(1477): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | C | CATGGAGG others(828): Show |
1 | a0001c0005t0001g0136 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2155-776_2155-775i others(837): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377913 | |||||||
| chr7:2377913 | CGAGGAAG others(249): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0165 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2155-765_2155-510d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377913 | ||||||
| chr7:2377923 | G | A | 2 | a0001c0003t0001g0141 a0002c0002t0001g0236 |
2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2155-766G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377923 | |||||||
| chr7:2377924 | A | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2155-765A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377924 | |||||||
| chr7:2377928 | C | CGAGCGTT others(53): Show |
1 | a0002c0002t0001g0236 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2155-760_2155-759i others(62): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377928 | ||||||
| chr7:2377929 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0052 others(6): Show |
10 | HG00099.hp1 HG00544.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.2155-760G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377929 | |||||||
| chr7:2377930 | C | T | 3 | a0001c0003t0001g0263 a0001c0003t0001g0264 a0001c0003t0001g0268 |
3 | NA18960.hp2 NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2155-759C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377930 | |||||||
| chr7:2377934 | C | T | 1 | a0001c0003t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2155-755C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377934 | |||||||
| chr7:2377935 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2155-754A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377935 | |||||||
| chr7:2377935 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(61): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2155-754A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377935 | |||||||
| chr7:2377936 | C | T | 2 | a0001c0001t0001g0004 a0001c0003t0001g0187 |
2 | HG01123.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2155-753C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377936 | |||||||
| chr7:2377938 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.2155-751G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377938 | |||||||
| chr7:2377938 | G | GCTGGGAT others(117): Show |
1 | a0001c0001t0001g0049 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(126): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377938 | ||||||
| chr7:2377938 | G | T | 13 | a0001c0001t0001g0024 a0001c0003t0001g0263 a0001c0003t0001g0264 others(10): Show |
13 | HG00099.hp2 HG01192.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2155-751G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377938 | |||||||
| chr7:2377938 | GCTGGGAT others(434): Show |
G | 5 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0002c0002t0001g0192 others(2): Show |
5 | HG02809.hp2 HG03516.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2155-741_2155-301d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377938 | ||||||
| chr7:2377943 | G | A | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-746G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377943 | |||||||
| chr7:2377945 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
110 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2155-744T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377945 | |||||||
| chr7:2377945 | T | TGCTGTGT others(117): Show |
1 | a0006c0012t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(126): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377945 | ||||||
| chr7:2377945 | T | TGCTGTGT others(949): Show |
1 | a0006c0012t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(958): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377945 | ||||||
| chr7:2377945 | T | TGCTGTGT others(752): Show |
1 | a0001c0003t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2155-742_2155-741i others(761): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377945 | ||||||
| chr7:2377945 | TG | T | 7 | a0001c0003t0001g0178 a0002c0002t0001g0201 a0002c0002t0001g0224 others(4): Show |
7 | HG00639.hp1 HG01975.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155-743delG | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377945 | |||||||
| chr7:2377946 | G | GCCGTGTT others(121): Show |
1 | a0001c0003t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2155-714_2155-713i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(1593): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0053 |
3 | HG01255.hp2 HG01256.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2155-742_2155-741i others(1602): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(2169): Show |
1 | a0001c0001t0001g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(2178): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(1593): Show |
1 | a0001c0001t0001g0067 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2155-742_2155-741i others(1602): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(825): Show |
1 | a0001c0001t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(834): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(2937): Show |
1 | a0011c0013t0001g0025 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2155-742_2155-741i others(2946): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(3129): Show |
1 | a0001c0001t0001g0025 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2155-742_2155-741i others(3138): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | GCTGTGTT others(185): Show |
1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2155-742_2155-741i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377946 | ||||||
| chr7:2377946 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
112 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2155-743G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377946 | |||||||
| chr7:2377948 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
96 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2155-741C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377948 | |||||||
| chr7:2377954 | C | G | 32 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0065 others(29): Show |
38 | HG00423.hp1 HG00738.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.2155-735C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377954 | |||||||
| chr7:2377968 | G | C | 12 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0154 others(9): Show |
13 | HG01978.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2155-721G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377968 | |||||||
| chr7:2377976 | T | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0066 a0001c0001t0001g0103 others(14): Show |
17 | HG00423.hp2 HG00621.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.2155-713T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377976 | |||||||
| chr7:2377976 | T | TGGAGGAA others(57): Show |
1 | a0001c0003t0001g0264 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2155-696_2155-695i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377976 | ||||||
| chr7:2377987 | G | A | 14 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0142 others(11): Show |
15 | HG01978.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2155-702G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377987 | |||||||
| chr7:2377990 | GGC | G | 11 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0142 others(8): Show |
12 | HG01978.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2155-695_2155-694d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377990 | ||||||
| chr7:2377990 | GGCGCGAG others(248): Show |
G | 1 | a0004c0006t0008g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2155-695_2155-441d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377990 | ||||||
| chr7:2377992 | C | CGAGCGTT others(53): Show |
1 | a0001c0003t0001g0154 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2155-696_2155-695i others(62): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377992 | ||||||
| chr7:2377993 | G | A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0009g0273 others(8): Show |
11 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.2155-696G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377993 | |||||||
| chr7:2377994 | C | T | 2 | a0001c0001t0001g0164 a0005c0007t0001g0075 |
2 | HG02559.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2155-695C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377994 | |||||||
| chr7:2377998 | C | T | 3 | a0002c0002t0001g0236 a0006c0012t0001g0199 a0006c0012t0001g0200 |
3 | HG01243.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2155-691C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377998 | |||||||
| chr7:2377999 | T | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
114 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2155-690T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2377999 | |||||||
| chr7:2377999 | T | TCTTCTGG others(57): Show |
1 | a0001c0005t0001g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2155-688_2155-687i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377999 | ||||||
| chr7:2377999 | TCTCCTGG others(57): Show |
T | 2 | a0001c0003t0001g0171 a0001c0003t0001g0183 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2155-632_2155-569d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2377999 | ||||||
| chr7:2378000 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0008t0001g0277 others(6): Show |
10 | HG01978.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2155-689C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378000 | |||||||
| chr7:2378002 | C | CCTGGGAT others(121): Show |
1 | a0004c0006t0001g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2155-633_2155-632i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378002 | ||||||
| chr7:2378002 | C | G | 3 | a0002c0002t0001g0236 a0006c0012t0001g0199 a0006c0012t0001g0200 |
3 | HG01243.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2155-687C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378002 | |||||||
| chr7:2378002 | C | T | 47 | a0001c0001t0001g0164 a0002c0002t0001g0010 a0002c0002t0001g0016 others(44): Show |
59 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.2155-687C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378002 | |||||||
| chr7:2378008 | ATGCTGTG others(56): Show |
A | 1 | a0002c0002t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2155-680_2155-618d others(65): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378008 | |||||||
| chr7:2378009 | T | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2155-680T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378009 | |||||||
| chr7:2378010 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2155-679G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378010 | |||||||
| chr7:2378012 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.2155-677T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378012 | |||||||
| chr7:2378012 | T | TGTGTTCT others(569): Show |
1 | a0003c0004t0001g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2155-633_2155-632i others(578): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378012 | ||||||
| chr7:2378012 | T | TGTGTTCT others(505): Show |
1 | a0003c0004t0001g0001 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2155-633_2155-632i others(514): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378012 | ||||||
| chr7:2378012 | T | TGTGTTCT others(697): Show |
1 | a0001c0001t0001g0020 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2155-633_2155-632i others(706): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378012 | ||||||
| chr7:2378018 | C | G | 28 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0062 others(25): Show |
30 | HG01081.hp2 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2155-671C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378018 | |||||||
| chr7:2378032 | G | T | 8 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0142 others(5): Show |
9 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2155-657G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378032 | |||||||
| chr7:2378040 | T | A | 12 | a0001c0001t0001g0062 a0001c0001t0001g0087 a0001c0001t0001g0106 others(9): Show |
12 | HG01081.hp2 HG01243.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-649T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378040 | |||||||
| chr7:2378040 | T | TGGAGGAA others(57): Show |
1 | a0001c0005t0001g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2155-633_2155-632i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378040 | ||||||
| chr7:2378051 | G | A | 8 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0142 others(5): Show |
9 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2155-638G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378051 | |||||||
| chr7:2378052 | C | A | 2 | a0002c0002t0001g0207 a0015c0024t0015g0185 |
2 | HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-637C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378052 | |||||||
| chr7:2378055 | GCA | G | 8 | a0001c0001t0001g0256 a0001c0003t0001g0140 a0001c0003t0001g0142 others(5): Show |
9 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2155-632_2155-631d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378055 | ||||||
| chr7:2378057 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2155-632A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378057 | |||||||
| chr7:2378058 | C | T | 1 | a0001c0009t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2155-631C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378058 | |||||||
| chr7:2378059 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2155-630G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378059 | |||||||
| chr7:2378062 | C | T | 5 | a0001c0003t0001g0141 a0001c0005t0001g0135 a0002c0002t0001g0236 others(2): Show |
5 | HG01081.hp2 HG01243.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-627C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378062 | |||||||
| chr7:2378063 | G | A | 2 | a0002c0002t0001g0207 a0015c0024t0015g0185 |
2 | HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-626G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378063 | |||||||
| chr7:2378063 | G | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0022 others(91): Show |
117 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2155-626G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378063 | |||||||
| chr7:2378063 | GCTCCTGG others(57): Show |
G | 1 | a0001c0008t0002g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2155-616_2155-553d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378063 | ||||||
| chr7:2378066 | C | G | 7 | a0001c0003t0001g0141 a0001c0005t0001g0135 a0002c0002t0001g0207 others(4): Show |
7 | HG01081.hp2 HG01243.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-623C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378066 | |||||||
| chr7:2378066 | C | T | 43 | a0001c0001t0001g0100 a0001c0009t0001g0151 a0002c0002t0001g0010 others(40): Show |
56 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2155-623C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378066 | |||||||
| chr7:2378073 | T | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(109): Show |
139 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2155-616T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378073 | |||||||
| chr7:2378073 | TG | T | 23 | a0001c0001t0001g0059 a0002c0002t0001g0009 a0002c0002t0001g0014 others(20): Show |
32 | HG01167.hp2 HG01168.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.2155-615delG | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378073 | |||||||
| chr7:2378074 | G | C | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-615G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378074 | |||||||
| chr7:2378074 | G | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
124 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2155-615G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378074 | |||||||
| chr7:2378076 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(122): Show |
161 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2155-613T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378076 | |||||||
| chr7:2378076 | T | TGTGTTCT others(889): Show |
1 | a0001c0001t0009g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2155-569_2155-568i others(898): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | T | TGTGTTCT others(57): Show |
2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2155-585_2155-522d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | T | TGTGTTGT others(1401): Show |
1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2155-608_2155-607i others(1410): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | T | TGTGTTGT others(185): Show |
1 | a0001c0001t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2155-608_2155-607i others(194): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | T | TGTGTTGT others(1593): Show |
1 | a0001c0001t0001g0068 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2155-608_2155-607i others(1602): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | T | TGTGTTGT others(633): Show |
1 | a0001c0003t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2155-608_2155-607i others(642): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378076 | TGTGTTCT others(121): Show |
T | 1 | a0001c0001t0001g0256 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2155-607_2155-480d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378076 | ||||||
| chr7:2378078 | T | A | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-611T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378078 | |||||||
| chr7:2378082 | C | CTGTGAAT others(3150): Show |
1 | a0001c0003t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2155-586_2155-585i others(3159): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378082 | ||||||
| chr7:2378082 | C | G | 32 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0051 others(29): Show |
35 | HG00609.hp1 HG01081.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.2155-607C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378082 | |||||||
| chr7:2378096 | G | C | 2 | a0002c0002t0001g0207 a0015c0024t0015g0185 |
2 | HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-593G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378096 | |||||||
| chr7:2378104 | T | A | 13 | a0001c0001t0001g0164 a0001c0001t0001g0195 a0001c0001t0011g0098 others(10): Show |
13 | HG01978.hp2 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2155-585T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378104 | |||||||
| chr7:2378115 | G | A | 3 | a0001c0003t0001g0141 a0002c0002t0001g0207 a0015c0024t0015g0185 |
3 | HG01081.hp2 HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-574G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378115 | |||||||
| chr7:2378116 | CAGGCGCG others(118): Show |
C | 1 | a0001c0003t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2155-562_2155-438d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378116 | ||||||
| chr7:2378118 | GGC | G | 3 | a0001c0003t0001g0141 a0002c0002t0001g0207 a0015c0024t0015g0185 |
3 | HG01081.hp2 HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-567_2155-566d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378118 | ||||||
| chr7:2378120 | C | CGCGAGTG others(55): Show |
1 | a0009c0020t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2155-564_2155-563i others(64): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378120 | ||||||
| chr7:2378120 | CGCGAGCT others(242): Show |
C | 5 | a0001c0008t0001g0277 a0001c0009t0001g0166 a0002c0002t0001g0156 others(2): Show |
6 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155-562_2155-314d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378120 | ||||||
| chr7:2378122 | C | CGAGCGCT others(121): Show |
1 | a0001c0001t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2155-563_2155-562i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378122 | ||||||
| chr7:2378122 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0064 others(8): Show |
11 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2155-567C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378122 | |||||||
| chr7:2378126 | C | T | 1 | a0006c0012t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2155-563C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378126 | |||||||
| chr7:2378127 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(41): Show |
46 | HG00099.hp2 HG01081.hp2 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.2155-562T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378127 | |||||||
| chr7:2378128 | C | T | 2 | a0002c0002t0001g0207 a0015c0024t0015g0185 |
2 | HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-561C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378128 | |||||||
| chr7:2378130 | C | CCTGGGAT others(121): Show |
1 | a0001c0001t0001g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2155-553_2155-552i others(130): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378130 | ||||||
| chr7:2378130 | C | G | 1 | a0006c0012t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2155-559C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378130 | |||||||
| chr7:2378130 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0049 others(106): Show |
140 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.2155-559C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378130 | |||||||
| chr7:2378131 | C | G | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2155-558C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378131 | |||||||
| chr7:2378137 | A | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(12): Show |
17 | HG01081.hp2 HG01261.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.2155-552A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378137 | |||||||
| chr7:2378137 | ATCCGTGT others(118): Show |
A | 1 | a0001c0017t0001g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2155-551_2155-427d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378137 | |||||||
| chr7:2378138 | T | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(25): Show |
30 | HG00099.hp2 HG01081.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.2155-551T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378138 | |||||||
| chr7:2378140 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(18): Show |
22 | HG01081.hp2 HG01261.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.2155-549C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378140 | |||||||
| chr7:2378146 | C | CTGTGAAT others(1074): Show |
1 | a0001c0001t0002g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2155-522_2155-521i others(1083): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378146 | ||||||
| chr7:2378146 | C | G | 13 | a0001c0001t0001g0106 a0001c0003t0001g0140 a0001c0003t0001g0141 others(10): Show |
13 | HG00099.hp2 HG01081.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.2155-543C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378146 | |||||||
| chr7:2378160 | G | T | 2 | a0001c0003t0001g0141 a0015c0024t0015g0185 |
2 | HG01081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-529G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378160 | |||||||
| chr7:2378166 | CAAG | C | 3 | a0001c0009t0001g0151 a0002c0002t0001g0284 a0010c0019t0001g0196 |
3 | HG00099.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2155-522_2155-520d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378166 | |||||||
| chr7:2378168 | A | AGGAGGAA others(57): Show |
1 | a0001c0005t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2155-500_2155-499i others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378168 | ||||||
| chr7:2378168 | A | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.2155-521A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378168 | |||||||
| chr7:2378179 | G | A | 2 | a0001c0003t0001g0141 a0015c0024t0015g0185 |
2 | HG01081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2155-510G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378179 | |||||||
| chr7:2378180 | C | A | 3 | a0001c0001t0001g0106 a0001c0009t0001g0151 a0002c0002t0001g0284 |
3 | HG00099.hp2 NA18522.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2155-509C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378180 | |||||||
| chr7:2378181 | A | G | 1 | a0001c0001t0012g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2155-508A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378181 | |||||||
| chr7:2378185 | G | A | 2 | a0001c0003t0001g0271 a0002c0002t0001g0210 |
2 | HG01975.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2155-504G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378185 | |||||||
| chr7:2378186 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(8): Show |
14 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2155-503C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378186 | |||||||
| chr7:2378190 | C | T | 3 | a0001c0003t0001g0140 a0006c0012t0001g0199 a0006c0012t0001g0200 |
3 | HG03098.hp2 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2155-499C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378190 | |||||||
| chr7:2378191 | G | A | 2 | a0001c0009t0001g0151 a0002c0002t0001g0284 |
2 | HG00099.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-498G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378191 | |||||||
| chr7:2378191 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
71 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2155-498G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378191 | |||||||
| chr7:2378194 | C | G | 5 | a0001c0003t0001g0140 a0001c0009t0001g0151 a0002c0002t0001g0284 others(2): Show |
5 | HG00099.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-495C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378194 | |||||||
| chr7:2378194 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
16 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2155-495C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378194 | |||||||
| chr7:2378201 | A | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(27): Show |
42 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.2155-488A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378201 | |||||||
| chr7:2378202 | G | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2155-487G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378202 | |||||||
| chr7:2378204 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(35): Show |
50 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2155-485C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378204 | |||||||
| chr7:2378204 | CGTGTTGT others(178): Show |
C | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2155-458_2155-274d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378204 | ||||||
| chr7:2378210 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2155-479G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378210 | |||||||
| chr7:2378212 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2155-477G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378212 | |||||||
| chr7:2378223 | T | C | 1 | a0002c0002t0001g0242 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2155-466T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378223 | |||||||
| chr7:2378224 | G | C | 2 | a0001c0009t0001g0151 a0002c0002t0001g0284 |
2 | HG00099.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-465G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378224 | |||||||
| chr7:2378230 | C | CAAG | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
25 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.2155-459_2155-458i others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATG | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2155-459_2155-458i others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(193): Show |
1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-459_2155-458i others(202): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(124): Show |
3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0107 |
3 | NA18747.hp2 NA18955.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2155-459_2155-458i others(133): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(3196): Show |
1 | a0001c0001t0001g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2155-459_2155-458i others(3205): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(1276): Show |
1 | a0001c0003t0001g0261 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2155-459_2155-458i others(1285): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(252): Show |
1 | a0001c0003t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2155-459_2155-458i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(316): Show |
2 | a0001c0001t0007g0001 a0001c0001t0007g0131 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.2155-459_2155-458i others(325): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(508): Show |
1 | a0001c0001t0004g0095 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2155-459_2155-458i others(517): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(252): Show |
1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2155-459_2155-458i others(261): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378230 | C | CATGGAGG others(188): Show |
1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2155-459_2155-458i others(197): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378230 | |||||||
| chr7:2378240 | G | A | 3 | a0001c0003t0001g0140 a0001c0009t0001g0151 a0002c0002t0001g0284 |
3 | HG00099.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-449G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378240 | |||||||
| chr7:2378241 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2155-448A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378241 | |||||||
| chr7:2378243 | GGC | G | 3 | a0001c0003t0001g0140 a0001c0009t0001g0151 a0002c0002t0001g0284 |
3 | HG00099.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-442_2155-441d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378243 | ||||||
| chr7:2378247 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0108 others(5): Show |
12 | HG01358.hp1 HG02027.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-442C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378247 | |||||||
| chr7:2378251 | C | T | 5 | a0001c0003t0001g0142 a0001c0005t0001g0135 a0002c0002t0001g0207 others(2): Show |
5 | HG02165.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-438C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378251 | |||||||
| chr7:2378252 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2155-437A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378252 | |||||||
| chr7:2378252 | A | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(38): Show |
55 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.2155-437A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378252 | |||||||
| chr7:2378253 | C | T | 3 | a0001c0009t0001g0151 a0002c0002t0001g0284 a0004c0006t0008g0163 |
3 | HG00099.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-436C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378253 | |||||||
| chr7:2378255 | G | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.2155-434G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378255 | |||||||
| chr7:2378255 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0108 others(6): Show |
13 | HG01358.hp1 HG01975.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.2155-434G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378255 | |||||||
| chr7:2378255 | GCTGGGAT others(55): Show |
G | 1 | a0002c0002t0001g0234 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2155-404_2155-343d others(64): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378255 | ||||||
| chr7:2378255 | GCTGGGAT others(117): Show |
G | 1 | a0002c0002t0001g0276 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2155-404_2155-281d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378255 | ||||||
| chr7:2378258 | GGGATGCT others(52): Show |
G | 1 | a0001c0003t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2155-430_2155-372d others(61): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378258 | |||||||
| chr7:2378262 | T | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
93 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.2155-427T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378262 | |||||||
| chr7:2378263 | G | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(48): Show |
68 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2155-426G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378263 | |||||||
| chr7:2378265 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
88 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.2155-424T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378265 | |||||||
| chr7:2378271 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
135 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.2155-418G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378271 | |||||||
| chr7:2378285 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2155-404C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378285 | |||||||
| chr7:2378285 | C | T | 3 | a0001c0003t0001g0140 a0001c0009t0001g0151 a0002c0002t0016g0160 |
3 | HG01255.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2155-404C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378285 | |||||||
| chr7:2378285 | CGGTGTCA others(117): Show |
C | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2155-385_2155-262d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378285 | ||||||
| chr7:2378291 | CATG | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
19 | HG00735.hp1 HG01069.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2155-397_2155-395d others(5): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378291 | |||||||
| chr7:2378293 | T | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0108 others(8): Show |
15 | HG01358.hp1 HG02027.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-396T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378293 | |||||||
| chr7:2378294 | G | GGAGGAAG others(118): Show |
1 | a0001c0003t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2155-386_2155-385i others(127): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378294 | ||||||
| chr7:2378294 | G | GGAGGAAG others(246): Show |
1 | a0001c0003t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2155-386_2155-385i others(255): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378294 | ||||||
| chr7:2378298 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2155-391G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378298 | |||||||
| chr7:2378304 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.2155-385A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378304 | |||||||
| chr7:2378305 | C | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
19 | HG00735.hp1 HG01069.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2155-384C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378305 | |||||||
| chr7:2378307 | G | GGC | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2155-380_2155-379d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(184): Show |
1 | a0003c0004t0001g0071 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(193): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(504): Show |
1 | a0003c0004t0001g0099 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(513): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(504): Show |
1 | a0001c0001t0001g0062 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(513): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(568): Show |
1 | a0001c0003t0001g0007 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(577): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1208): Show |
1 | a0005c0007t0001g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1217): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(760): Show |
1 | a0001c0003t0001g0264 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(769): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1912): Show |
1 | a0003c0004t0001g0023 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1921): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(696): Show |
1 | a0001c0001t0001g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(705): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(568): Show |
1 | a0001c0014t0001g0020 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(577): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(248): Show |
5 | a0001c0001t0001g0005 a0001c0003t0001g0258 a0003c0004t0001g0001 others(2): Show |
5 | HG02293.hp1 NA18951.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2155-379_2155-378i others(257): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1848): Show |
1 | a0005c0007t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1857): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(696): Show |
2 | a0001c0001t0001g0003 a0001c0001t0003g0001 |
2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.2155-379_2155-378i others(705): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(376): Show |
2 | a0001c0001t0001g0001 a0001c0001t0011g0098 |
2 | HG00673.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2155-379_2155-378i others(385): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(504): Show |
1 | a0001c0001t0001g0003 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(513): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1592): Show |
1 | a0001c0001t0001g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1601): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(824): Show |
2 | a0001c0003t0001g0257 a0001c0003t0001g0263 |
2 | HG00558.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2155-379_2155-378i others(833): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(824): Show |
1 | a0001c0001t0001g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(833): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(760): Show |
1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(769): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(312): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0126 others(1): Show |
4 | HG01123.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.2155-379_2155-378i others(321): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(248): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0005 |
2 | HG01928.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.2155-379_2155-378i others(257): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(760): Show |
1 | a0001c0001t0001g0024 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(769): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(568): Show |
2 | a0003c0004t0001g0013 a0003c0004t0003g0013 |
2 | HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2155-379_2155-378i others(577): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(632): Show |
1 | a0001c0001t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(641): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(440): Show |
1 | a0001c0001t0001g0020 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(449): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(2168): Show |
1 | a0001c0003t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(2177): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1080): Show |
1 | a0001c0001t0001g0004 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1089): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(824): Show |
1 | a0001c0001t0001g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(833): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1272): Show |
1 | a0001c0001t0001g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1281): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(760): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0056 others(2): Show |
7 | HG01255.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2155-379_2155-378i others(769): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(888): Show |
1 | a0001c0001t0001g0001 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(897): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(632): Show |
1 | a0001c0001t0001g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(641): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1080): Show |
1 | a0001c0001t0001g0005 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1089): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(696): Show |
1 | a0001c0003t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(705): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(568): Show |
1 | a0001c0003t0001g0266 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(577): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1720): Show |
1 | a0001c0001t0001g0001 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1729): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(568): Show |
1 | a0001c0001t0001g0024 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(577): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(184): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0048 others(5): Show |
8 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.2155-379_2155-378i others(193): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGCGAG others(1528): Show |
1 | a0001c0001t0001g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(1537): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGTGAG others(120): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0078 others(9): Show |
14 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2155-379_2155-378i others(129): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGTGAG others(696): Show |
1 | a0001c0001t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2155-379_2155-378i others(705): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | G | GGCGTGAG others(312): Show |
1 | a0001c0001t0001g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2155-379_2155-378i others(321): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378307 | GGCGAGCG others(119): Show |
G | 1 | a0002c0002t0016g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2155-374_2155-249d others(2): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378307 | ||||||
| chr7:2378309 | CGAGCGTT others(53): Show |
C | 1 | a0002c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2155-378_2155-319d others(62): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378309 | ||||||
| chr7:2378311 | A | C | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-378A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378311 | |||||||
| chr7:2378313 | C | A | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-376C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378313 | |||||||
| chr7:2378313 | C | T | 5 | a0001c0003t0001g0173 a0001c0003t0001g0177 a0002c0002t0001g0201 others(2): Show |
5 | HG03098.hp2 HG03471.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2155-376C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378313 | |||||||
| chr7:2378314 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.2155-375G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378314 | |||||||
| chr7:2378314 | G | T | 1 | a0001c0003t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2155-375G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378314 | |||||||
| chr7:2378315 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2155-374T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378315 | |||||||
| chr7:2378315 | TTCCTGGG others(55): Show |
T | 33 | a0002c0002t0001g0010 a0002c0002t0001g0016 a0002c0002t0001g0018 others(30): Show |
46 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2155-342_2155-281d others(64): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378315 | ||||||
| chr7:2378316 | T | G | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-373T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378316 | |||||||
| chr7:2378317 | C | CCTGGGAA others(182): Show |
1 | a0001c0001t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(191): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(54): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0003t0001g0041 others(3): Show |
10 | HG01358.hp1 HG01975.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.2155-366_2155-365i others(63): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(630): Show |
1 | a0001c0003t0001g0260 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(639): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(438): Show |
1 | a0001c0001t0001g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(447): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(438): Show |
1 | a0003c0004t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(447): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(1270): Show |
1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2155-366_2155-365i others(1279): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(502): Show |
2 | a0001c0003t0001g0042 a0005c0007t0001g0084 |
3 | HG04184.hp2 NA18954.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2155-366_2155-365i others(511): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(1590): Show |
1 | a0003c0004t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(1599): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(4662): Show |
1 | a0001c0001t0004g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2155-366_2155-365i others(4671): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(1334): Show |
1 | a0001c0001t0001g0003 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2155-366_2155-365i others(1343): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(822): Show |
1 | a0001c0001t0001g0066 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2155-366_2155-365i others(831): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(438): Show |
2 | a0001c0001t0001g0109 a0001c0003t0001g0007 |
2 | NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2155-366_2155-365i others(447): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(886): Show |
1 | a0003c0004t0001g0114 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2155-366_2155-365i others(895): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAA others(1014): Show |
1 | a0001c0001t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2155-366_2155-365i others(1023): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1078): Show |
1 | a0001c0003t0001g0268 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(1087): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(2934): Show |
1 | a0001c0001t0001g0019 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(2943): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(438): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0087 |
2 | NA18964.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2155-357_2155-356i others(447): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(374): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0127 |
3 | HG01074.hp1 HG01081.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2155-357_2155-356i others(383): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(310): Show |
1 | a0001c0001t0001g0001 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2155-357_2155-356i others(319): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1334): Show |
1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(1343): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(886): Show |
1 | a0003c0004t0001g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2155-357_2155-356i others(895): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(2038): Show |
1 | a0001c0001t0004g0290 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2155-357_2155-356i others(2047): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1782): Show |
1 | a0003c0004t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(1791): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1718): Show |
1 | a0001c0001t0001g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(1727): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(246): Show |
1 | a0001c0003t0001g0007 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2155-357_2155-356i others(255): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(182): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0100 a0001c0003t0001g0265 |
5 | HG00438.hp2 HG02080.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.2155-357_2155-356i others(191): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(2614): Show |
1 | a0001c0001t0001g0054 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2155-343_2155-342i others(2623): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1398): Show |
1 | a0001c0001t0001g0052 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2155-343_2155-342i others(1407): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | CCTGGGAT others(1654): Show |
1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2155-343_2155-342i others(1663): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378317 | ||||||
| chr7:2378317 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.2155-372C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378317 | |||||||
| chr7:2378323 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2155-366A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378323 | |||||||
| chr7:2378324 | T | A | 7 | a0001c0001t0001g0116 a0001c0003t0001g0140 a0001c0003t0001g0141 others(4): Show |
7 | HG00099.hp2 HG01081.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155-365T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378324 | |||||||
| chr7:2378327 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2155-362T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378327 | |||||||
| chr7:2378333 | G | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02015.hp1 HG02071.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2155-356G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378333 | |||||||
| chr7:2378335 | G | T | 1 | a0001c0003t0001g0173 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2155-354G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378335 | |||||||
| chr7:2378347 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2155-342T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378347 | |||||||
| chr7:2378347 | T | G | 28 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0001g0090 others(25): Show |
30 | HG00099.hp2 HG00544.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2155-342T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378347 | |||||||
| chr7:2378347 | T | TGGTGTCA others(308): Show |
1 | a0001c0001t0009g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2155-304_2155-303i others(317): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378347 | ||||||
| chr7:2378347 | T | TGGTGTCA others(1011): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0102 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2155-324_2155-323i others(1020): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378347 | ||||||
| chr7:2378355 | T | A | 4 | a0001c0003t0001g0140 a0002c0002t0001g0284 a0006c0012t0001g0199 others(1): Show |
4 | HG00099.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-334T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378355 | |||||||
| chr7:2378360 | G | A | 1 | a0002c0002t0001g0201 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2155-329G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378360 | |||||||
| chr7:2378366 | A | G | 26 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0001g0090 others(23): Show |
28 | HG00099.hp2 HG00544.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.2155-323A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378366 | |||||||
| chr7:2378367 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2155-322C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378367 | |||||||
| chr7:2378369 | G | GGC | 24 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0001g0090 others(21): Show |
26 | HG00099.hp2 HG00544.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.2155-318_2155-317d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378369 | ||||||
| chr7:2378369 | G | GGCGTGAG others(120): Show |
1 | a0001c0001t0001g0092 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2155-317_2155-316i others(129): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378369 | ||||||
| chr7:2378369 | GGCGAGCG others(57): Show |
G | 48 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0060 others(45): Show |
61 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.2155-303_2155-240d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378369 | ||||||
| chr7:2378375 | C | T | 7 | a0001c0003t0001g0140 a0001c0005t0001g0027 a0001c0005t0001g0136 others(4): Show |
8 | HG00099.hp2 HG01192.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2155-314C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378375 | |||||||
| chr7:2378376 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0116 |
2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2155-313G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378376 | |||||||
| chr7:2378376 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0003t0001g0261 |
3 | NA19004.hp1 NA19055.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2155-313G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378376 | |||||||
| chr7:2378377 | C | CTCCTGGG others(628): Show |
1 | a0001c0001t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2155-304_2155-303i others(637): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378377 | ||||||
| chr7:2378377 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.2155-312C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378377 | |||||||
| chr7:2378379 | C | G | 9 | a0001c0001t0001g0092 a0001c0001t0001g0116 a0001c0003t0001g0140 others(6): Show |
10 | HG00099.hp2 HG01192.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2155-310C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378379 | |||||||
| chr7:2378386 | T | A | 23 | a0001c0003t0001g0140 a0001c0003t0001g0142 a0001c0005t0001g0027 others(20): Show |
26 | HG00099.hp2 HG00544.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2155-303T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378386 | |||||||
| chr7:2378389 | T | C | 1 | a0006c0012t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2155-300T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378389 | |||||||
| chr7:2378395 | G | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0090 a0001c0001t0001g0091 others(8): Show |
11 | HG01928.hp1 HG02015.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2155-294G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378395 | |||||||
| chr7:2378409 | G | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0092 a0001c0001t0001g0116 others(2): Show |
5 | HG02976.hp2 HG03831.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-280G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378409 | |||||||
| chr7:2378409 | G | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2155-280G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378409 | |||||||
| chr7:2378417 | T | A | 15 | a0001c0003t0001g0142 a0001c0005t0001g0027 a0001c0005t0001g0136 others(12): Show |
18 | HG00544.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2155-272T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378417 | |||||||
| chr7:2378422 | G | A | 1 | a0001c0001t0012g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2155-267G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378422 | |||||||
| chr7:2378428 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2155-261G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378428 | |||||||
| chr7:2378431 | GGC | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2155-254_2155-253d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378431 | ||||||
| chr7:2378433 | C | CACGAGCG others(1266): Show |
1 | a0001c0001t0001g0107 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2155-256_2155-255i others(1275): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378433 | |||||||
| chr7:2378433 | C | CACGAGCG others(1074): Show |
1 | a0001c0001t0001g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2155-256_2155-255i others(1083): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378433 | |||||||
| chr7:2378433 | C | CACGAGCG others(1330): Show |
1 | a0001c0001t0001g0094 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2155-256_2155-255i others(1339): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378433 | |||||||
| chr7:2378433 | C | CGAGCGTT others(115): Show |
1 | a0001c0001t0001g0049 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2155-255_2155-254i others(124): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGCGAGCG others(754): Show |
1 | a0001c0001t0004g0095 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2155-240_2155-239i others(763): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGCGAGCG others(1458): Show |
1 | a0001c0003t0001g0261 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2155-240_2155-239i others(1467): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGCGAGCT others(1458): Show |
1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2155-250_2155-249i others(1467): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGCGAGCT others(434): Show |
1 | a0001c0003t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2155-250_2155-249i others(443): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGCGAGTG others(179): Show |
1 | a0013c0022t0001g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2155-251_2155-250i others(188): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378433 | C | CGTGAGCT others(242): Show |
1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2155-255_2155-254i others(251): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378433 | ||||||
| chr7:2378439 | C | T | 14 | a0001c0003t0001g0140 a0001c0003t0001g0142 a0001c0005t0001g0027 others(11): Show |
16 | HG01168.hp2 HG01192.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2155-250C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378439 | |||||||
| chr7:2378440 | G | T | 1 | a0001c0003t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2155-249G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378440 | |||||||
| chr7:2378441 | C | T | 1 | a0004c0006t0008g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2155-248C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378441 | |||||||
| chr7:2378443 | C | G | 14 | a0001c0003t0001g0140 a0001c0003t0001g0142 a0001c0005t0001g0027 others(11): Show |
16 | HG01168.hp2 HG01192.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2155-246C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378443 | |||||||
| chr7:2378443 | CCTGGGAA others(57): Show |
C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0111 a0001c0001t0012g0096 others(1): Show |
4 | HG02132.hp2 HG03516.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-203_2155-140d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378443 | ||||||
| chr7:2378450 | A | ATCCGTGT others(628): Show |
1 | a0001c0001t0001g0090 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2155-239_2155-238i others(637): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378450 | |||||||
| chr7:2378450 | A | ATCCGTGT others(2482): Show |
1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2155-239_2155-238i others(2491): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378450 | |||||||
| chr7:2378450 | A | ATCCGTGT others(2930): Show |
1 | a0001c0001t0001g0055 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2155-239_2155-238i others(2939): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378450 | |||||||
| chr7:2378450 | A | ATCCGTGT others(1330): Show |
1 | a0001c0003t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2155-239_2155-238i others(1339): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378450 | |||||||
| chr7:2378450 | A | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2155-239A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378450 | |||||||
| chr7:2378451 | G | T | 2 | a0001c0003t0001g0178 a0003c0004t0001g0083 |
2 | HG01928.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2155-238G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378451 | |||||||
| chr7:2378453 | T | C | 4 | a0001c0003t0001g0178 a0003c0004t0001g0083 a0006c0012t0001g0200 others(1): Show |
4 | HG01928.hp1 HG03098.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-236T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378453 | |||||||
| chr7:2378459 | G | C | 2 | a0001c0003t0001g0178 a0003c0004t0001g0083 |
2 | HG01928.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2155-230G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378459 | |||||||
| chr7:2378473 | G | C | 2 | a0004c0006t0001g0029 a0004c0006t0008g0163 |
3 | HG02258.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2155-216G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378473 | |||||||
| chr7:2378481 | T | A | 121 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0059 others(118): Show |
151 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.2155-208T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378481 | |||||||
| chr7:2378486 | G | A | 2 | a0001c0005t0001g0027 a0001c0005t0001g0136 |
3 | HG01192.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2155-203G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378486 | |||||||
| chr7:2378492 | G | A | 3 | a0001c0001t0002g0148 a0004c0006t0001g0029 a0004c0006t0008g0163 |
4 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2155-197G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378492 | |||||||
| chr7:2378494 | AGG | A | 2 | a0001c0005t0001g0027 a0001c0005t0001g0136 |
3 | HG01192.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2155-194_2155-193d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378494 | |||||||
| chr7:2378495 | GGC | G | 2 | a0004c0006t0001g0029 a0004c0006t0008g0163 |
3 | HG02258.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2155-190_2155-189d others(4): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378495 | ||||||
| chr7:2378495 | GGCGCGAG others(57): Show |
G | 1 | a0001c0001t0002g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2155-190_2155-127d others(66): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378495 | ||||||
| chr7:2378497 | C | T | 2 | a0001c0005t0001g0027 a0001c0005t0001g0136 |
3 | HG01192.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2155-192C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378497 | |||||||
| chr7:2378497 | CGCGAGTG others(55): Show |
C | 1 | a0001c0003t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2155-186_2155-125d others(64): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378497 | ||||||
| chr7:2378498 | G | T | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-191G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378498 | |||||||
| chr7:2378503 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2155-186T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378503 | |||||||
| chr7:2378507 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2155-182G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378507 | |||||||
| chr7:2378514 | A | T | 4 | a0002c0002t0001g0246 a0002c0002t0001g0247 a0004c0006t0001g0029 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-175A>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378514 | |||||||
| chr7:2378515 | G | T | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2155-174G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378515 | |||||||
| chr7:2378517 | T | C | 2 | a0001c0008t0002g0278 a0003c0004t0001g0083 |
2 | HG01192.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.2155-172T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378517 | |||||||
| chr7:2378523 | G | C | 1 | a0003c0004t0001g0083 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2155-166G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378523 | |||||||
| chr7:2378536 | T | C | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2155-153T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378536 | |||||||
| chr7:2378550 | A | G | 4 | a0001c0001t0005g0028 a0001c0001t0005g0149 a0001c0005t0001g0027 others(1): Show |
6 | HG01099.hp2 HG01192.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2155-139A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378550 | |||||||
| chr7:2378556 | G | A | 2 | a0001c0005t0001g0027 a0001c0005t0001g0136 |
3 | HG01192.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2155-133G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378556 | |||||||
| chr7:2378559 | T | G | 2 | a0001c0005t0001g0027 a0001c0005t0001g0136 |
3 | HG01192.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2155-130T>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378559 | |||||||
| chr7:2378559 | T | TGCGAGCG others(55): Show |
2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2155-105_2155-104i others(64): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 2378559 | ||||||
| chr7:2378566 | G | A | 4 | a0004c0006t0001g0029 a0004c0006t0001g0044 a0004c0006t0001g0045 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-123G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378566 | |||||||
| chr7:2378579 | T | C | 1 | a0001c0003t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2155-110T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378579 | |||||||
| chr7:2378620 | A | C | 1 | a0003c0004t0001g0099 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2155-69A>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378620 | |||||||
| chr7:2378651 | T | A | 1 | a0003c0004t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2155-38T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378651 | |||||||
| chr7:2378682 | G | A | 1 | a0001c0003t0001g0260 | 1 | HG02135.hp2 | splice_region_variant&intron_variant | LOW | c.2155-7G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | chr7 | 2378682 | |||||||
| chr7:2378807 | C | T | 1 | a0002c0002t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2232+41C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2378807 | |||||||
| chr7:2378898 | A | G | 4 | a0002c0002t0001g0016 a0002c0002t0001g0037 a0002c0002t0001g0235 others(1): Show |
7 | NA18947.hp1 NA18998.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2232+132A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2378898 | |||||||
| chr7:2378931 | G | A | 2 | a0001c0001t0001g0049 a0002c0002t0001g0159 |
2 | HG01884.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2232+165G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2378931 | |||||||
| chr7:2379010 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.2233-124A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2379010 | |||||||
| chr7:2379092 | C | T | 2 | a0002c0002t0001g0232 a0002c0002t0001g0234 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2233-42C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2379092 | |||||||
| chr7:2379095 | G | T | 1 | a0002c0002t0001g0157 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2233-39G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2379095 | |||||||
| chr7:2379107 | C | A | 1 | a0001c0001t0009g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2233-27C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 16/18 | chr7 | 2379107 | |||||||
| chr7:2379284 | G | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0146 a0001c0001t0001g0165 others(3): Show |
6 | HG01496.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2341+42G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 17/18 | chr7 | 2379284 | |||||||
| chr7:2379307 | G | A | 2 | a0001c0003t0001g0173 a0001c0003t0001g0177 |
2 | NA18942.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2341+65G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 17/18 | chr7 | 2379307 | |||||||
| chr7:2379531 | G | A | 1 | a0010c0019t0001g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*14+20G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379531 | |||||||
| chr7:2379535 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*14+24T>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379535 | |||||||
| chr7:2379699 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0165 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*14+188C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379699 | |||||||
| chr7:2379718 | G | A | 5 | a0001c0015t0002g0139 a0004c0006t0001g0029 a0004c0006t0001g0044 others(2): Show |
6 | HG02258.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.*14+207G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379718 | |||||||
| chr7:2379721 | G | A | 1 | a0002c0002t0001g0037 | 2 | NA19004.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.*14+210G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379721 | |||||||
| chr7:2379721 | G | T | 2 | a0001c0001t0005g0028 a0001c0001t0005g0149 |
3 | HG01099.hp2 HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.*14+210G>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379721 | |||||||
| chr7:2379760 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.*14+249A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379760 | |||||||
| chr7:2379829 | C | T | 5 | a0001c0003t0001g0030 a0001c0003t0001g0152 a0001c0003t0001g0173 others(2): Show |
6 | HG00544.hp1 HG02004.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.*14+318C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379829 | |||||||
| chr7:2379859 | C | T | 1 | a0012c0023t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.*15-345C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379859 | |||||||
| chr7:2379880 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.*15-324G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379880 | |||||||
| chr7:2379902 | A | G | 1 | a0001c0016t0010g0285 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.*15-302A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379902 | |||||||
| chr7:2379947 | C | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*15-257C>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2379947 | |||||||
| chr7:2380034 | G | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.*15-170G>C | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380034 | |||||||
| chr7:2380058 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*15-146C>T | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380058 | |||||||
| chr7:2380174 | C | G | 6 | a0001c0005t0001g0027 a0001c0005t0001g0135 a0001c0005t0001g0136 others(3): Show |
7 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.*15-30C>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380174 | |||||||
| chr7:2380178 | T | A | 1 | a0001c0003t0001g0177 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.*15-26T>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380178 | |||||||
| chr7:2380179 | A | G | 1 | a0001c0003t0001g0177 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.*15-25A>G | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380179 | |||||||
| chr7:2380185 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18994.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.*15-19G>A | EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 18/18 | chr7 | 2380185 |