Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51386 |
| ensemblid | ENSG00000100129.18 |
| hgncid | 18138 |
| symbol | EIF3L |
| name | eukaryotic translation initiation factor 3 subunit L |
| refseq_nuc | NM_016091.4 |
| refseq_prot | NP_057175.1 |
| ensembl_nuc | ENST00000652021.1 |
| ensembl_prot | ENSP00000499067.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 37849419 |
| end | 37889407 |
| strand | + |
| ver | v1.2 |
| region | chr22:37849419-37889407 |
| region5000 | chr22:37844419-37894407 |
| regionname0 | EIF3L_chr22_37849419_37889407 |
| regionname5000 | EIF3L_chr22_37844419_37894407 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 564 | 317 | 84 | 62 | 117 | 14 | 38 | 94 | EIF3L_chr22_37844419_37894407 | EIF3L | MSYPA others(559): Show |
chr22 | 37844419 | 37894407 |
| a0002 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | MSYPA others(559): Show |
chr22 | 37844419 | 37894407 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1692 | 161 | 28 | 33 | 69 | 9 | 20 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0001c0002 | 0/0 | 1692 | 125 | 46 | 27 | 35 | 4 | 13 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0001c0003 | 0/0 | 1692 | 28 | 9 | 2 | 12 | 0 | 5 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0001c0005 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0001c0006 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0001c0007 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 | ||
| a0002c0004 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | ATGTC others(1687): Show |
chr22 | 37844419 | 37894407 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2669 | 156 | 24 | 33 | 69 | 8 | 20 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0001t0002 | 0/0 | 2669 | 4 | 4 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0001t0006 | 0/0 | 2659 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2654): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0001 | 0/0 | 2669 | 120 | 43 | 26 | 34 | 4 | 13 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0003 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0004 | 0/0 | 2669 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0005 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0007 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0002t0008 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0003t0001 | 0/0 | 2669 | 28 | 9 | 2 | 12 | 0 | 5 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0005t0001 | 0/0 | 2669 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0006t0001 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0001c0007t0001 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| a0002c0004t0001 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | CTTTC others(2664): Show |
chr22 | 37844419 | 37894407 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0002t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0006t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0001c0007t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0225 | EUR | FIN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0202 | EUR | FIN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0288 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0198 | EUR | IBS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0074 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02145 | hp1 | a0001 | c0002 | t0008 | g0294 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0001 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0017 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0283 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ESN | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0204 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0031 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | STU | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | YRI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19003 | hp2 | a0001 | c0007 | t0001 | g0138 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | LWK | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | LWK | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | YRI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0289 | EUR | TSI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0226 | EUR | TSI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20805 | hp1 | a0001 | c0005 | t0001 | g0002 | EUR | TSI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | GIH | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | CLM | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0231 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | ACB | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | USA | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | USA | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | USA | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0234 | REF | REF | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0216 | REF | REF | EIF3L_chr22_37844419_37894407 | EIF3L | chr22 | 37844419 | 37894407 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37875845 | T | G | 1 | a0002 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.911T>G | p.Met304Arg | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/13 | 942/2669 | 911/1695 | 304/564 | chr22 | 37875845 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37849473 | T | C | 1 | a0002c0004 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.24T>C | p.Tyr8Tyr | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/13 | 55/2669 | 24/1695 | 8/564 | chr22 | 37849473 | |||
| chr22:37850041 | C | T | 1 | a0001c0007 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.60C>T | p.Pro20Pro | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/13 | 91/2669 | 60/1695 | 20/564 | chr22 | 37850041 | |||
| chr22:37855622 | C | G | 1 | a0001c0003 | 28 | HG00609.hp2 HG01081.hp1 HG01496.hp1 others(25): Show |
synonymous_variant | LOW | c.351C>G | p.Ala117Ala | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/13 | 382/2669 | 351/1695 | 117/564 | chr22 | 37855622 | |||
| chr22:37870307 | A | G | 1 | a0001c0006 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.711A>G | p.Lys237Lys | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/13 | 742/2669 | 711/1695 | 237/564 | chr22 | 37870307 | |||
| chr22:37870343 | C | T | 1 | a0001c0005 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.747C>T | p.Ser249Ser | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/13 | 778/2669 | 747/1695 | 249/564 | chr22 | 37870343 | |||
| chr22:37877742 | T | C | 3 | a0001c0002 a0001c0003 a0001c0005 |
154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
synonymous_variant | LOW | c.1146T>C | p.Ile382Ile | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/13 | 1177/2669 | 1146/1695 | 382/564 | chr22 | 37877742 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37888829 | G | A | 1 | a0001c0002t0003 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 365 | chr22 | 37888829 | ||||||
| chr22:37888858 | G | C | 1 | a0001c0002t0004 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 394 | chr22 | 37888858 | ||||||
| chr22:37889019 | G | A | 1 | a0001c0002t0005 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 555 | chr22 | 37889019 | ||||||
| chr22:37889144 | G | T | 1 | a0001c0002t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 680 | chr22 | 37889144 | ||||||
| chr22:37889159 | C | T | 1 | a0001c0002t0007 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*695C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 695 | chr22 | 37889159 | ||||||
| chr22:37889226 | T | C | 1 | a0001c0001t0002 | 4 | HG01884.hp1 HG02486.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*762T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 762 | chr22 | 37889226 | ||||||
| chr22:37889290 | ATCTGCCC others(3): Show |
A | 1 | a0001c0001t0006 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833_*842delCATCTC others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 833 | INFO_REALIGN_3_PRIME | chr22 | 37889290 | |||||
| chr22:37889293 | T | C | 7 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(4): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*829T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 13/13 | 829 | chr22 | 37889293 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37849493 | C | G | 1 | a0001c0002t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.33+11C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849493 | |||||||
| chr22:37849603 | G | T | 1 | a0001c0001t0002g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+121G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849603 | |||||||
| chr22:37849629 | C | G | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33+147C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849629 | |||||||
| chr22:37849635 | C | G | 1 | a0001c0002t0008g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.33+153C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849635 | |||||||
| chr22:37849838 | A | G | 1 | a0001c0003t0001g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.34-177A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849838 | |||||||
| chr22:37849862 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.34-153C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849862 | |||||||
| chr22:37849931 | C | A | 1 | a0001c0002t0005g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.34-84C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37849931 | |||||||
| chr22:37850000 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.34-15T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 1/12 | chr22 | 37850000 | |||||||
| chr22:37850070 | C | A | 1 | a0001c0002t0001g0019 | 1 | HG02148.hp2 | splice_region_variant&intron_variant | LOW | c.82+7C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850070 | |||||||
| chr22:37850090 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
5 | NA18941.hp1 NA18942.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+27G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850090 | |||||||
| chr22:37850106 | G | C | 1 | a0001c0002t0001g0023 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.82+43G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850106 | |||||||
| chr22:37850190 | T | A | 1 | a0001c0002t0001g0024 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.82+127T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850190 | |||||||
| chr22:37850403 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.82+340G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850403 | |||||||
| chr22:37850498 | A | G | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82+435A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850498 | |||||||
| chr22:37850500 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.82+437C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850500 | |||||||
| chr22:37850511 | A | T | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82+448A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850511 | |||||||
| chr22:37850518 | T | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82+455T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850518 | |||||||
| chr22:37850586 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82+523G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850586 | |||||||
| chr22:37850644 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.82+581A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850644 | |||||||
| chr22:37850730 | G | C | 17 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(14): Show |
17 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.83-550G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850730 | |||||||
| chr22:37850978 | C | A | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.83-302C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850978 | |||||||
| chr22:37850978 | C | T | 1 | a0001c0001t0006g0289 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.83-302C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37850978 | |||||||
| chr22:37851024 | C | T | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-256C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 2/12 | chr22 | 37851024 | |||||||
| chr22:37851689 | G | A | 14 | a0001c0003t0001g0005 a0001c0003t0001g0043 a0001c0003t0001g0044 others(11): Show |
15 | HG00609.hp2 HG01496.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.293+199G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851689 | |||||||
| chr22:37851705 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.293+215G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851705 | |||||||
| chr22:37851735 | G | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293+245G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851735 | |||||||
| chr22:37851751 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.293+261C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851751 | |||||||
| chr22:37851783 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(54): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.293+293A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851783 | |||||||
| chr22:37851847 | T | C | 3 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0058 |
4 | HG00544.hp1 NA18942.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+357T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851847 | |||||||
| chr22:37851978 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02145.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.293+488A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37851978 | |||||||
| chr22:37852028 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.293+538T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852028 | |||||||
| chr22:37852099 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.293+609C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852099 | |||||||
| chr22:37852169 | A | G | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+679A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852169 | |||||||
| chr22:37852216 | T | C | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+726T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852216 | |||||||
| chr22:37852263 | G | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(21): Show |
27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.293+773G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852263 | |||||||
| chr22:37852373 | C | G | 1 | a0001c0002t0001g0072 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293+883C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852373 | |||||||
| chr22:37852375 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.293+885A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852375 | |||||||
| chr22:37852452 | G | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+962G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852452 | |||||||
| chr22:37852460 | T | C | 1 | a0001c0002t0001g0073 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.293+970T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852460 | |||||||
| chr22:37852757 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293+1267C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852757 | |||||||
| chr22:37852853 | T | TAAG | 63 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(60): Show |
67 | HG00609.hp2 HG01081.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.293+1363_293+1364i others(5): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852853 | |||||||
| chr22:37852904 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+1414C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852904 | |||||||
| chr22:37852982 | T | C | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.293+1492T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852982 | |||||||
| chr22:37852988 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.293+1498G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37852988 | |||||||
| chr22:37853340 | G | C | 2 | a0001c0002t0001g0282 a0001c0002t0008g0294 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.293+1850G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37853340 | |||||||
| chr22:37853898 | T | C | 20 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(17): Show |
23 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-1667T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37853898 | |||||||
| chr22:37854043 | C | T | 2 | a0001c0002t0001g0282 a0001c0002t0008g0294 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.294-1522C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854043 | |||||||
| chr22:37854517 | G | A | 1 | a0002c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.294-1048G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854517 | |||||||
| chr22:37854553 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-1012C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854553 | |||||||
| chr22:37854562 | G | GCTCCAAG others(12): Show |
1 | a0001c0002t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.294-999_294-981dup others(19): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 37854562 | ||||||
| chr22:37854577 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.294-988C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854577 | |||||||
| chr22:37854686 | G | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.294-879G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854686 | |||||||
| chr22:37854721 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.294-844C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854721 | |||||||
| chr22:37854876 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.294-689A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37854876 | |||||||
| chr22:37854987 | TA | T | 7 | a0001c0001t0001g0232 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
7 | HG02486.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.294-574delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr22 | 37854987 | ||||||
| chr22:37855146 | C | G | 10 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(7): Show |
10 | HG02056.hp2 NA18979.hp2 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-419C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37855146 | |||||||
| chr22:37855372 | A | G | 3 | a0001c0002t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.294-193A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37855372 | |||||||
| chr22:37855495 | T | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0291 a0001c0002t0001g0075 |
3 | HG01255.hp1 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.294-70T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 3/12 | chr22 | 37855495 | |||||||
| chr22:37855679 | T | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.373+35T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37855679 | |||||||
| chr22:37855680 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.373+36G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37855680 | |||||||
| chr22:37856048 | AT | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(159): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.373+408delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37856048 | ||||||
| chr22:37856052 | T | A | 1 | a0001c0002t0008g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.373+408T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856052 | |||||||
| chr22:37856067 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.373+423A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856067 | |||||||
| chr22:37856183 | TCTC | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+542_373+544del others(3): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37856183 | ||||||
| chr22:37856366 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.373+722C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856366 | |||||||
| chr22:37856571 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.373+927G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856571 | |||||||
| chr22:37856669 | A | C | 1 | a0001c0003t0001g0054 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.373+1025A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856669 | |||||||
| chr22:37856670 | C | A | 1 | a0001c0003t0001g0054 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.373+1026C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856670 | |||||||
| chr22:37856738 | G | T | 1 | a0001c0002t0001g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.373+1094G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856738 | |||||||
| chr22:37856830 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.373+1186G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856830 | |||||||
| chr22:37856844 | CA | C | 8 | a0001c0001t0001g0157 a0001c0002t0001g0283 a0001c0002t0001g0284 others(5): Show |
8 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.373+1213delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37856844 | ||||||
| chr22:37856913 | T | C | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.373+1269T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37856913 | |||||||
| chr22:37857106 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.373+1462A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857106 | |||||||
| chr22:37857143 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.373+1499C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857143 | |||||||
| chr22:37857169 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.374-1510G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857169 | |||||||
| chr22:37857363 | G | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(21): Show |
27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.374-1316G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857363 | |||||||
| chr22:37857369 | C | CA | 140 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(137): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.374-1287dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37857369 | ||||||
| chr22:37857369 | C | CAA | 94 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.374-1288_374-1287d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37857369 | ||||||
| chr22:37857410 | A | G | 3 | a0001c0002t0001g0024 a0001c0002t0001g0188 a0001c0002t0001g0228 |
3 | NA18997.hp1 NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.374-1269A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857410 | |||||||
| chr22:37857778 | C | G | 5 | a0001c0002t0001g0282 a0001c0002t0001g0295 a0001c0002t0001g0296 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-901C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857778 | |||||||
| chr22:37857821 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.374-858A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857821 | |||||||
| chr22:37857851 | T | C | 6 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0061 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-828T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857851 | |||||||
| chr22:37857899 | G | A | 2 | a0001c0002t0001g0282 a0001c0002t0008g0294 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.374-780G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857899 | |||||||
| chr22:37857989 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.374-690G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37857989 | |||||||
| chr22:37858019 | T | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0042 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.374-660T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858019 | |||||||
| chr22:37858049 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.374-630G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858049 | |||||||
| chr22:37858109 | G | A | 20 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(17): Show |
23 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.374-570G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858109 | |||||||
| chr22:37858219 | C | CT | 41 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0001t0001g0082 others(38): Show |
43 | HG00099.hp1 HG00609.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.374-435dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37858219 | ||||||
| chr22:37858219 | C | CTT | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.374-436_374-435dup others(2): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37858219 | ||||||
| chr22:37858219 | C | CTTT | 17 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0101 others(14): Show |
17 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.374-437_374-435dup others(3): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37858219 | ||||||
| chr22:37858219 | CT | C | 15 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0169 others(12): Show |
15 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.374-435delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37858219 | ||||||
| chr22:37858219 | CTTTTTTT others(3): Show |
C | 8 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0105 others(5): Show |
8 | HG01123.hp1 HG01261.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-444_374-435del others(10): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr22 | 37858219 | ||||||
| chr22:37858258 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.374-421C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858258 | |||||||
| chr22:37858274 | C | A | 4 | a0001c0003t0001g0043 a0001c0003t0001g0045 a0001c0003t0001g0046 others(1): Show |
4 | NA18953.hp1 NA18956.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-405C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858274 | |||||||
| chr22:37858279 | G | A | 1 | a0001c0002t0001g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.374-400G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858279 | |||||||
| chr22:37858587 | A | C | 12 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(9): Show |
12 | HG00609.hp2 NA18945.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.374-92A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 4/12 | chr22 | 37858587 | |||||||
| chr22:37858762 | T | G | 2 | a0001c0003t0001g0044 a0001c0003t0001g0051 |
2 | NA18945.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.435+22T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37858762 | |||||||
| chr22:37858880 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
5 | HG00099.hp1 HG02148.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+140G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37858880 | |||||||
| chr22:37859052 | C | T | 1 | a0001c0003t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.435+312C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859052 | |||||||
| chr22:37859113 | C | A | 1 | a0001c0002t0001g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.435+373C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859113 | |||||||
| chr22:37859192 | A | G | 29 | a0001c0001t0001g0232 a0001c0003t0001g0005 a0001c0003t0001g0026 others(26): Show |
30 | HG00609.hp2 HG01081.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.435+452A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859192 | |||||||
| chr22:37859203 | C | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.435+463C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859203 | |||||||
| chr22:37859318 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.435+578A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859318 | |||||||
| chr22:37859374 | C | CTTTTTTT | 6 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0286 others(3): Show |
6 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+649_435+655dup others(7): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0001g0258 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+648_435+655dup others(8): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(2): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(49): Show |
56 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.435+647_435+655dup others(9): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(3): Show |
27 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(24): Show |
28 | HG00558.hp1 HG00609.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.435+646_435+655dup others(10): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0142 a0001c0001t0001g0244 a0001c0001t0001g0246 others(14): Show |
17 | HG00408.hp2 HG01192.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.435+645_435+655dup others(11): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(5): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0248 others(9): Show |
12 | HG00323.hp2 HG00621.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.435+644_435+655dup others(12): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG00544.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+643_435+655dup others(13): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | C | CTTTTTTT others(7): Show |
3 | a0001c0002t0001g0078 a0001c0002t0003g0108 a0001c0003t0001g0032 |
3 | HG02970.hp2 HG04228.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.435+642_435+655dup others(14): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | CT | C | 16 | a0001c0001t0001g0092 a0001c0001t0001g0104 a0001c0001t0001g0127 others(13): Show |
19 | HG00738.hp1 HG00738.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.435+655delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859374 | CTT | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.435+654_435+655del others(2): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37859374 | ||||||
| chr22:37859466 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+726C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859466 | |||||||
| chr22:37859655 | G | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(21): Show |
27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.435+915G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859655 | |||||||
| chr22:37859833 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.435+1093G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859833 | |||||||
| chr22:37859854 | C | G | 12 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(9): Show |
12 | HG00609.hp2 NA18945.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+1114C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859854 | |||||||
| chr22:37859966 | C | T | 1 | a0001c0002t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.435+1226C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859966 | |||||||
| chr22:37859980 | C | T | 12 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(9): Show |
12 | HG00609.hp2 NA18945.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+1240C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859980 | |||||||
| chr22:37859982 | A | T | 12 | a0001c0003t0001g0043 a0001c0003t0001g0044 a0001c0003t0001g0045 others(9): Show |
12 | HG00609.hp2 NA18945.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+1242A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37859982 | |||||||
| chr22:37860031 | C | T | 3 | a0001c0002t0001g0173 a0001c0002t0001g0187 a0001c0002t0001g0194 |
3 | NA18969.hp1 NA18994.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.435+1291C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860031 | |||||||
| chr22:37860208 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.435+1468A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860208 | |||||||
| chr22:37860298 | T | TA | 8 | a0001c0002t0001g0019 a0001c0002t0001g0174 a0001c0002t0001g0197 others(5): Show |
8 | HG01123.hp2 HG01175.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+1559dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37860298 | ||||||
| chr22:37860299 | A | T | 1 | a0001c0002t0001g0196 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.435+1559A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860299 | |||||||
| chr22:37860442 | T | C | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.435+1702T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860442 | |||||||
| chr22:37860476 | G | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1736G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860476 | |||||||
| chr22:37860530 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435+1790G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860530 | |||||||
| chr22:37860620 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.435+1880G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37860620 | |||||||
| chr22:37861092 | A | G | 2 | a0001c0001t0001g0232 a0001c0006t0001g0231 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.436-1877A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861092 | |||||||
| chr22:37861250 | C | T | 20 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(17): Show |
23 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.436-1719C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861250 | |||||||
| chr22:37861512 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.436-1457C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861512 | |||||||
| chr22:37861553 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
7 | HG02132.hp2 NA18747.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1416G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861553 | |||||||
| chr22:37861567 | C | G | 1 | a0001c0002t0005g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.436-1402C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861567 | |||||||
| chr22:37861671 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.436-1298G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861671 | |||||||
| chr22:37861683 | C | CA | 30 | a0001c0001t0001g0232 a0001c0002t0001g0175 a0001c0002t0001g0282 others(27): Show |
31 | HG00609.hp2 HG01081.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.436-1272dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr22 | 37861683 | ||||||
| chr22:37861870 | G | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.436-1099G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861870 | |||||||
| chr22:37861886 | G | C | 1 | a0001c0002t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.436-1083G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861886 | |||||||
| chr22:37861948 | A | G | 25 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(22): Show |
28 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.436-1021A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37861948 | |||||||
| chr22:37862396 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.436-573C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37862396 | |||||||
| chr22:37862422 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(197): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.436-547G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37862422 | |||||||
| chr22:37862803 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(159): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.436-166T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37862803 | |||||||
| chr22:37862846 | T | G | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-123T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37862846 | |||||||
| chr22:37862864 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.436-105A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 5/12 | chr22 | 37862864 | |||||||
| chr22:37863103 | CT | C | 39 | a0001c0001t0001g0022 a0001c0001t0001g0153 a0001c0001t0001g0154 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.505+83delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr22 | 37863103 | ||||||
| chr22:37863474 | G | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+129G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863474 | |||||||
| chr22:37863504 | G | A | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.579+159G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863504 | |||||||
| chr22:37863539 | T | G | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.579+194T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863539 | |||||||
| chr22:37863614 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.579+269A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863614 | |||||||
| chr22:37863630 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.579+285C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863630 | |||||||
| chr22:37863688 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.579+343G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863688 | |||||||
| chr22:37863777 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.579+432A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863777 | |||||||
| chr22:37863841 | A | G | 25 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(22): Show |
28 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+496A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37863841 | |||||||
| chr22:37864059 | A | G | 25 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(22): Show |
28 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+714A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864059 | |||||||
| chr22:37864304 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.579+959C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864304 | |||||||
| chr22:37864497 | G | A | 1 | a0001c0002t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.579+1152G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864497 | |||||||
| chr22:37864540 | C | CT | 8 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0061 others(5): Show |
8 | HG01255.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+1210dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37864540 | ||||||
| chr22:37864540 | CT | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(201): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.579+1210delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37864540 | ||||||
| chr22:37864564 | A | C | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.579+1219A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864564 | |||||||
| chr22:37864600 | A | G | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.579+1255A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864600 | |||||||
| chr22:37864635 | T | C | 1 | a0001c0002t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.579+1290T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864635 | |||||||
| chr22:37864689 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+1344C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864689 | |||||||
| chr22:37864729 | G | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1384G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864729 | |||||||
| chr22:37864758 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1413C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864758 | |||||||
| chr22:37864778 | A | G | 1 | a0001c0002t0001g0105 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.579+1433A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864778 | |||||||
| chr22:37864823 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.579+1478G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37864823 | |||||||
| chr22:37865000 | C | T | 25 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(22): Show |
28 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+1655C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865000 | |||||||
| chr22:37865192 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0261 |
2 | HG01433.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+1847G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865192 | |||||||
| chr22:37865446 | G | A | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+2101G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865446 | |||||||
| chr22:37865584 | T | A | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.579+2239T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865584 | |||||||
| chr22:37865817 | T | A | 1 | a0002c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.579+2472T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865817 | |||||||
| chr22:37865886 | C | A | 1 | a0001c0002t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.579+2541C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37865886 | |||||||
| chr22:37866110 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.579+2765A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866110 | |||||||
| chr22:37866404 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.579+3059A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866404 | |||||||
| chr22:37866437 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.579+3092G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866437 | |||||||
| chr22:37866440 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.579+3095C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866440 | |||||||
| chr22:37866454 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.579+3109T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866454 | |||||||
| chr22:37866523 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.579+3178G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866523 | |||||||
| chr22:37866555 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.579+3210G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866555 | |||||||
| chr22:37866761 | G | T | 6 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0061 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-3415G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866761 | |||||||
| chr22:37866833 | A | G | 3 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0038 |
3 | HG02559.hp2 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.580-3343A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866833 | |||||||
| chr22:37866884 | G | T | 1 | a0001c0002t0001g0185 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.580-3292G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866884 | |||||||
| chr22:37866972 | T | C | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.580-3204T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866972 | |||||||
| chr22:37866992 | A | G | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-3184A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37866992 | |||||||
| chr22:37867191 | C | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.580-2985C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867191 | |||||||
| chr22:37867381 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0101 others(3): Show |
7 | HG00621.hp1 HG02056.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-2795G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867381 | |||||||
| chr22:37867397 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.580-2779G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867397 | |||||||
| chr22:37867563 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.580-2613G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867563 | |||||||
| chr22:37867656 | CA | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(218): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.580-2501delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37867656 | ||||||
| chr22:37867726 | A | G | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.580-2450A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867726 | |||||||
| chr22:37867782 | G | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2394G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867782 | |||||||
| chr22:37867816 | A | G | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.580-2360A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867816 | |||||||
| chr22:37867844 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.580-2332A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867844 | |||||||
| chr22:37867870 | G | C | 22 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(19): Show |
25 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-2306G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867870 | |||||||
| chr22:37867946 | C | T | 1 | a0001c0002t0005g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.580-2230C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37867946 | |||||||
| chr22:37867954 | C | CA | 9 | a0001c0001t0001g0086 a0001c0001t0001g0277 a0001c0002t0001g0039 others(6): Show |
9 | HG01099.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-2206dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37867954 | ||||||
| chr22:37868020 | A | G | 2 | a0001c0002t0001g0282 a0001c0002t0008g0294 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.580-2156A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868020 | |||||||
| chr22:37868044 | T | C | 2 | a0001c0002t0001g0176 a0001c0002t0001g0226 |
2 | HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.580-2132T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868044 | |||||||
| chr22:37868052 | C | A | 3 | a0001c0002t0001g0177 a0001c0002t0001g0178 a0001c0002t0001g0179 |
3 | HG03834.hp2 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.580-2124C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868052 | |||||||
| chr22:37868083 | A | T | 36 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(33): Show |
39 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.580-2093A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868083 | |||||||
| chr22:37868110 | A | AT | 18 | a0001c0001t0001g0230 a0001c0002t0001g0015 a0001c0002t0001g0171 others(15): Show |
19 | HG00408.hp1 HG00735.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-2044dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868110 | ||||||
| chr22:37868110 | A | ATTTTTTT others(3): Show |
2 | a0001c0002t0001g0295 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.580-2053_580-2044d others(12): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868110 | ||||||
| chr22:37868110 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0001g0296 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.580-2054_580-2044d others(13): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868110 | ||||||
| chr22:37868110 | AT | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0080 others(28): Show |
31 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.580-2044delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868110 | ||||||
| chr22:37868110 | ATT | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(169): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.580-2045_580-2044d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868110 | ||||||
| chr22:37868247 | T | G | 20 | a0001c0001t0001g0230 a0001c0002t0001g0001 a0001c0002t0001g0007 others(17): Show |
23 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.580-1929T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868247 | |||||||
| chr22:37868280 | A | AT | 19 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0112 others(16): Show |
19 | HG01099.hp1 HG01123.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-1880dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868280 | ||||||
| chr22:37868280 | AT | A | 10 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(7): Show |
13 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-1880delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868280 | ||||||
| chr22:37868455 | CT | C | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-1712delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868455 | ||||||
| chr22:37868634 | C | CT | 14 | a0001c0001t0001g0249 a0001c0002t0001g0006 a0001c0002t0001g0057 others(11): Show |
15 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-1517dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
8 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-1518_580-1517d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTT | 5 | a0001c0001t0001g0004 a0001c0001t0002g0262 a0001c0001t0002g0298 others(2): Show |
6 | HG01884.hp1 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-1520_580-1517d others(6): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTT | 62 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.580-1521_580-1517d others(7): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0092 others(17): Show |
21 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.580-1522_580-1517d others(8): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT | 8 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0001g0142 others(5): Show |
8 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-1523_580-1517d others(9): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0248 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.580-1526_580-1517d others(12): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0002t0001g0147 others(1): Show |
4 | HG01123.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1527_580-1517d others(13): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(5): Show |
4 | a0001c0002t0001g0042 a0001c0002t0001g0105 a0001c0002t0001g0106 others(1): Show |
4 | HG01261.hp1 HG03139.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1528_580-1517d others(14): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0001g0039 a0001c0002t0001g0107 |
2 | HG02257.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.580-1529_580-1517d others(15): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0246 a0001c0002t0001g0078 |
2 | HG01993.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.580-1530_580-1517d others(16): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(8): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0252 others(4): Show |
9 | HG00323.hp2 HG00738.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1531_580-1517d others(17): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0255 a0001c0001t0001g0278 |
3 | HG00741.hp1 HG01361.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.580-1532_580-1517d others(18): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0257 a0001c0001t0001g0270 others(1): Show |
4 | HG01074.hp1 HG01255.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1533_580-1517d others(19): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0251 a0001c0001t0001g0268 |
3 | HG01081.hp2 HG01106.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.580-1534_580-1517d others(20): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0242 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.580-1535_580-1517d others(21): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.580-1536_580-1517d others(22): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0264 a0001c0001t0001g0277 |
2 | HG01099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.580-1538_580-1517d others(24): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.580-1539_580-1517d others(25): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0281 a0001c0001t0001g0291 a0001c0002t0001g0077 |
3 | HG02145.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-1540_580-1517d others(26): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0135 others(1): Show |
4 | HG02647.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1541_580-1517d others(27): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.580-1517_580-1516i others(28): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.580-1517_580-1516i others(29): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0233 a0001c0001t0001g0247 a0001c0001t0001g0266 |
3 | HG01346.hp2 HG01517.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.580-1517_580-1516i others(30): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(22): Show |
1 | a0001c0002t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.580-1517_580-1516i others(31): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0002g0267 |
3 | HG01175.hp2 HG02922.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.580-1517_580-1516i others(32): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(24): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01192.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.580-1517_580-1516i others(33): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0290 |
2 | HG02717.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.580-1517_580-1516i others(34): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.580-1517_580-1516i others(38): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0006g0289 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.580-1517_580-1516i others(39): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | C | CTTTTTTT others(39): Show |
1 | a0001c0001t0001g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.580-1517_580-1516i others(48): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CT | C | 12 | a0001c0001t0001g0025 a0001c0002t0001g0173 a0001c0002t0001g0190 others(9): Show |
12 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-1517delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CTTT | C | 8 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(5): Show |
11 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-1519_580-1517d others(5): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CTTTT | C | 11 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0060 others(8): Show |
11 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-1520_580-1517d others(6): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CTTTTT | C | 7 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0282 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1521_580-1517d others(7): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0001g0197 a0001c0002t0001g0227 |
2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.580-1527_580-1517d others(13): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868634 | CTTTTTTT others(5): Show |
C | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.580-1528_580-1517d others(14): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr22 | 37868634 | ||||||
| chr22:37868665 | G | A | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-1511G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37868665 | |||||||
| chr22:37869028 | G | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1148G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869028 | |||||||
| chr22:37869261 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.580-915G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869261 | |||||||
| chr22:37869610 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.580-566G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869610 | |||||||
| chr22:37869648 | C | T | 6 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0061 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-528C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869648 | |||||||
| chr22:37869831 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.580-345G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869831 | |||||||
| chr22:37869855 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.580-321G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869855 | |||||||
| chr22:37869997 | A | C | 1 | a0001c0002t0001g0218 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.580-179A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37869997 | |||||||
| chr22:37870026 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.580-150T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37870026 | |||||||
| chr22:37870091 | G | A | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.580-85G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37870091 | |||||||
| chr22:37870101 | G | A | 1 | a0001c0002t0001g0192 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.580-75G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 7/12 | chr22 | 37870101 | |||||||
| chr22:37870369 | C | G | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.751+22C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870369 | |||||||
| chr22:37870371 | G | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+24G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870371 | |||||||
| chr22:37870481 | G | T | 1 | a0001c0002t0005g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.751+134G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870481 | |||||||
| chr22:37870710 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.751+363C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870710 | |||||||
| chr22:37870710 | CT | C | 8 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(5): Show |
11 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.751+372delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37870710 | ||||||
| chr22:37870750 | C | T | 1 | a0001c0002t0005g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.751+403C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870750 | |||||||
| chr22:37870895 | C | T | 1 | a0002c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.751+548C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870895 | |||||||
| chr22:37870899 | A | G | 2 | a0001c0002t0001g0282 a0001c0002t0008g0294 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.751+552A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37870899 | |||||||
| chr22:37871081 | T | C | 1 | a0001c0002t0001g0217 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.751+734T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871081 | |||||||
| chr22:37871083 | A | G | 35 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(32): Show |
38 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.751+736A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871083 | |||||||
| chr22:37871127 | GA | G | 34 | a0001c0001t0001g0165 a0001c0002t0001g0001 a0001c0002t0001g0007 others(31): Show |
37 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.751+791delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37871127 | ||||||
| chr22:37871205 | C | T | 4 | a0001c0002t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 others(1): Show |
4 | HG01884.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+858C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871205 | |||||||
| chr22:37871297 | T | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0001g0271 |
3 | HG01192.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.751+950T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871297 | |||||||
| chr22:37871404 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.751+1057C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871404 | |||||||
| chr22:37871439 | G | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(225): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.751+1092G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871439 | |||||||
| chr22:37871499 | AC | A | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.751+1153delC | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871499 | |||||||
| chr22:37871612 | T | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(225): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.751+1265T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871612 | |||||||
| chr22:37871615 | C | T | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+1268C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871615 | |||||||
| chr22:37871691 | A | C | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.751+1344A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871691 | |||||||
| chr22:37871728 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.751+1381G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871728 | |||||||
| chr22:37871826 | A | G | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.751+1479A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871826 | |||||||
| chr22:37871868 | CG | C | 3 | a0001c0002t0001g0204 a0001c0002t0001g0215 a0001c0002t0005g0017 |
3 | HG03041.hp1 HG03831.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.751+1525delG | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37871868 | ||||||
| chr22:37871871 | G | GA | 23 | a0001c0002t0001g0024 a0001c0002t0001g0075 a0001c0002t0001g0171 others(20): Show |
23 | HG00408.hp1 HG00735.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+1524_751+1525i others(3): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871871 | |||||||
| chr22:37871872 | G | A | 107 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(104): Show |
111 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.751+1525G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871872 | |||||||
| chr22:37871872 | G | GA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0253 a0001c0002t0001g0055 others(5): Show |
8 | HG02148.hp1 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.751+1545dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37871872 | ||||||
| chr22:37871872 | GA | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.751+1545delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37871872 | ||||||
| chr22:37871874 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.751+1527A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37871874 | |||||||
| chr22:37872032 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.751+1685G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872032 | |||||||
| chr22:37872108 | A | T | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.751+1761A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872108 | |||||||
| chr22:37872276 | C | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.751+1929C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872276 | |||||||
| chr22:37872355 | C | T | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.751+2008C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872355 | |||||||
| chr22:37872395 | G | T | 19 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(16): Show |
22 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.752-1975G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872395 | |||||||
| chr22:37872397 | T | A | 19 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(16): Show |
22 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.752-1973T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872397 | |||||||
| chr22:37872562 | A | G | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.752-1808A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872562 | |||||||
| chr22:37872623 | T | G | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-1747T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872623 | |||||||
| chr22:37872669 | A | G | 1 | a0001c0002t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.752-1701A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872669 | |||||||
| chr22:37872795 | C | CT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0101 others(2): Show |
6 | HG02155.hp2 NA18955.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-1565dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37872795 | ||||||
| chr22:37872915 | G | A | 71 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(68): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.752-1455G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872915 | |||||||
| chr22:37872945 | T | A | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.752-1425T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37872945 | |||||||
| chr22:37873006 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.752-1364T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873006 | |||||||
| chr22:37873107 | G | C | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.752-1263G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873107 | |||||||
| chr22:37873228 | A | T | 1 | a0001c0001t0006g0289 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.752-1142A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873228 | |||||||
| chr22:37873231 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.752-1139C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873231 | |||||||
| chr22:37873303 | G | GT | 77 | a0001c0001t0001g0165 a0001c0001t0001g0268 a0001c0002t0001g0002 others(74): Show |
81 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.752-1054dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37873303 | ||||||
| chr22:37873303 | G | GTT | 9 | a0001c0002t0001g0023 a0001c0002t0001g0177 a0001c0002t0001g0178 others(6): Show |
9 | HG02647.hp2 HG03239.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.752-1055_752-1054d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr22 | 37873303 | ||||||
| chr22:37873373 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.752-997A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873373 | |||||||
| chr22:37873434 | G | GA | 133 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0006 others(130): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.752-936_752-935ins others(1): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873434 | |||||||
| chr22:37873459 | G | A | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.752-911G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873459 | |||||||
| chr22:37873643 | T | C | 1 | a0001c0002t0001g0170 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.752-727T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873643 | |||||||
| chr22:37873696 | C | T | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.752-674C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873696 | |||||||
| chr22:37873921 | C | A | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.752-449C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873921 | |||||||
| chr22:37873957 | A | C | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.752-413A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873957 | |||||||
| chr22:37873974 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.752-396C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37873974 | |||||||
| chr22:37874174 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.752-196A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37874174 | |||||||
| chr22:37874325 | C | G | 2 | a0001c0003t0001g0028 a0001c0003t0001g0029 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.752-45C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 8/12 | chr22 | 37874325 | |||||||
| chr22:37874561 | C | T | 7 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(4): Show |
10 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.906+37C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874561 | |||||||
| chr22:37874633 | C | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG00738.hp2 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.906+109C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874633 | |||||||
| chr22:37874698 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.906+174C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874698 | |||||||
| chr22:37874717 | C | T | 3 | a0001c0002t0001g0184 a0001c0002t0001g0196 a0001c0002t0001g0215 |
3 | NA18993.hp1 NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.906+193C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874717 | |||||||
| chr22:37874807 | C | T | 10 | a0001c0003t0001g0043 a0001c0003t0001g0045 a0001c0003t0001g0046 others(7): Show |
10 | HG00609.hp2 NA18949.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.906+283C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874807 | |||||||
| chr22:37874889 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.906+365C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874889 | |||||||
| chr22:37874895 | A | AT | 79 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0133 others(76): Show |
83 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.906+393dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 37874895 | ||||||
| chr22:37874895 | A | ATT | 8 | a0001c0001t0001g0086 a0001c0001t0001g0230 a0001c0002t0001g0174 others(5): Show |
8 | HG01123.hp2 HG01175.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+392_906+393dup others(2): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 37874895 | ||||||
| chr22:37874895 | AT | A | 13 | a0001c0001t0001g0093 a0001c0001t0001g0261 a0001c0002t0001g0055 others(10): Show |
13 | HG01081.hp1 HG01109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+393delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 37874895 | ||||||
| chr22:37874895 | ATT | A | 14 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(11): Show |
17 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.906+392_906+393del others(2): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr22 | 37874895 | ||||||
| chr22:37874965 | G | A | 19 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(16): Show |
22 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.906+441G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37874965 | |||||||
| chr22:37875022 | C | T | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+498C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875022 | |||||||
| chr22:37875225 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.907-616A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875225 | |||||||
| chr22:37875226 | A | C | 2 | a0001c0002t0001g0195 a0001c0002t0001g0213 |
2 | HG01168.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.907-615A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875226 | |||||||
| chr22:37875677 | C | G | 1 | a0001c0002t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.907-164C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875677 | |||||||
| chr22:37875707 | C | G | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-134C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875707 | |||||||
| chr22:37875722 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.907-119T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 9/12 | chr22 | 37875722 | |||||||
| chr22:37876055 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1077+44G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876055 | |||||||
| chr22:37876133 | CT | C | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+123delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876133 | |||||||
| chr22:37876205 | C | T | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+194C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876205 | |||||||
| chr22:37876216 | A | G | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077+205A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876216 | |||||||
| chr22:37876221 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1077+210C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876221 | |||||||
| chr22:37876289 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077+278C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876289 | |||||||
| chr22:37876295 | A | AT | 33 | a0001c0001t0001g0022 a0001c0001t0001g0100 a0001c0001t0001g0101 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1077+311dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 37876295 | ||||||
| chr22:37876295 | AT | A | 32 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(29): Show |
35 | HG00733.hp1 HG00741.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.1077+311delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 37876295 | ||||||
| chr22:37876295 | ATT | A | 85 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(82): Show |
89 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1077+310_1077+311d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 37876295 | ||||||
| chr22:37876390 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1077+379T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876390 | |||||||
| chr22:37876401 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
5 | NA18941.hp1 NA18942.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+390A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876401 | |||||||
| chr22:37876418 | A | C | 1 | a0001c0002t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1077+407A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876418 | |||||||
| chr22:37876497 | C | T | 1 | a0001c0003t0001g0048 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1077+486C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876497 | |||||||
| chr22:37876530 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1077+519C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876530 | |||||||
| chr22:37876537 | C | G | 1 | a0001c0002t0001g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1077+526C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876537 | |||||||
| chr22:37876689 | TTGA | T | 70 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(67): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1077+683_1077+685d others(5): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr22 | 37876689 | ||||||
| chr22:37876720 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1077+709C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876720 | |||||||
| chr22:37876806 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1077+795A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876806 | |||||||
| chr22:37876887 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
5 | HG00099.hp1 HG02148.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-787G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876887 | |||||||
| chr22:37876922 | C | T | 134 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0006 others(131): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1078-752C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37876922 | |||||||
| chr22:37877296 | T | G | 69 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(66): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1078-378T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37877296 | |||||||
| chr22:37877301 | C | T | 2 | a0001c0002t0001g0175 a0001c0002t0001g0211 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1078-373C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37877301 | |||||||
| chr22:37877311 | C | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1078-363C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37877311 | |||||||
| chr22:37877564 | C | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0042 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1078-110C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37877564 | |||||||
| chr22:37877584 | C | G | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1078-90C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 10/12 | chr22 | 37877584 | |||||||
| chr22:37878417 | T | TA | 28 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0087 others(25): Show |
29 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1575+265dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878417 | ||||||
| chr22:37878417 | TA | T | 101 | a0001c0001t0001g0250 a0001c0001t0001g0272 a0001c0001t0002g0267 others(98): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1575+265delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878417 | ||||||
| chr22:37878417 | TAA | T | 8 | a0001c0002t0001g0071 a0001c0002t0001g0185 a0001c0002t0001g0195 others(5): Show |
8 | HG01168.hp1 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1575+264_1575+265d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878417 | ||||||
| chr22:37878417 | TAAA | T | 12 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0060 others(9): Show |
12 | HG02145.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+263_1575+265d others(5): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878417 | ||||||
| chr22:37878417 | TAAAA | T | 8 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(5): Show |
11 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1575+262_1575+265d others(6): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878417 | ||||||
| chr22:37878441 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1575+270A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37878441 | |||||||
| chr22:37878470 | G | GT | 6 | a0001c0001t0001g0126 a0001c0002t0001g0019 a0001c0002t0001g0199 others(3): Show |
6 | HG01943.hp2 HG01952.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+309dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878470 | ||||||
| chr22:37878625 | A | G | 14 | a0001c0003t0001g0005 a0001c0003t0001g0043 a0001c0003t0001g0044 others(11): Show |
15 | HG00609.hp2 HG01496.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.1575+454A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37878625 | |||||||
| chr22:37878637 | A | AT | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1575+471dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878637 | ||||||
| chr22:37878867 | G | A | 1 | a0001c0002t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1575+696G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37878867 | |||||||
| chr22:37878905 | G | C | 4 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0037 others(1): Show |
4 | HG02559.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+734G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37878905 | |||||||
| chr22:37878946 | G | GT | 30 | a0001c0001t0001g0021 a0001c0001t0001g0086 a0001c0001t0001g0102 others(27): Show |
30 | HG00544.hp2 HG00609.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1575+794dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37878946 | ||||||
| chr22:37878983 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0137 others(1): Show |
5 | NA18956.hp2 NA18983.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+812G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37878983 | |||||||
| chr22:37879255 | C | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1575+1084C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879255 | |||||||
| chr22:37879301 | C | T | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1575+1130C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879301 | |||||||
| chr22:37879388 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1575+1217G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879388 | |||||||
| chr22:37879493 | CA | C | 10 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0140 others(7): Show |
10 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1575+1336delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37879493 | ||||||
| chr22:37879583 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1575+1412G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879583 | |||||||
| chr22:37879617 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1575+1446C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879617 | |||||||
| chr22:37879802 | C | CT | 13 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0042 others(10): Show |
13 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1575+1646dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37879802 | ||||||
| chr22:37879825 | A | C | 1 | a0001c0002t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1575+1654A>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879825 | |||||||
| chr22:37879838 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1575+1667C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879838 | |||||||
| chr22:37879903 | G | T | 1 | a0001c0002t0004g0288 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1575+1732G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879903 | |||||||
| chr22:37879948 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1575+1777C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37879948 | |||||||
| chr22:37880096 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0128 |
4 | HG02155.hp2 NA18955.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+1925C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37880096 | |||||||
| chr22:37880279 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1575+2108A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37880279 | |||||||
| chr22:37880408 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1575+2237C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37880408 | |||||||
| chr22:37880419 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1575+2248T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37880419 | |||||||
| chr22:37880782 | T | A | 1 | a0001c0002t0001g0295 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1575+2611T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37880782 | |||||||
| chr22:37881281 | C | G | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1575+3110C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881281 | |||||||
| chr22:37881485 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1575+3314C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881485 | |||||||
| chr22:37881512 | G | A | 5 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0030 others(2): Show |
5 | HG01081.hp1 HG02615.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+3341G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881512 | |||||||
| chr22:37881636 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+3465C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881636 | |||||||
| chr22:37881655 | C | T | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1575+3484C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881655 | |||||||
| chr22:37881709 | G | T | 1 | a0001c0002t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1575+3538G>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37881709 | |||||||
| chr22:37882114 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1575+3943C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882114 | |||||||
| chr22:37882299 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1575+4128C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882299 | |||||||
| chr22:37882570 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG00738.hp2 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1576-4195G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882570 | |||||||
| chr22:37882584 | C | T | 3 | a0001c0002t0001g0061 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | HG02622.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1576-4181C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882584 | |||||||
| chr22:37882600 | C | G | 2 | a0001c0002t0001g0296 a0001c0002t0001g0297 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1576-4165C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882600 | |||||||
| chr22:37882734 | G | A | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1576-4031G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882734 | |||||||
| chr22:37882743 | A | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(21): Show |
27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1576-4022A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882743 | |||||||
| chr22:37882772 | C | G | 71 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(68): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1576-3993C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882772 | |||||||
| chr22:37882773 | T | C | 71 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(68): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1576-3992T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882773 | |||||||
| chr22:37882805 | G | A | 133 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0006 others(130): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1576-3960G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882805 | |||||||
| chr22:37882808 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1576-3957C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882808 | |||||||
| chr22:37882819 | G | A | 4 | a0001c0003t0001g0049 a0001c0003t0001g0050 a0001c0003t0001g0053 others(1): Show |
4 | NA18949.hp2 NA18964.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-3946G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37882819 | |||||||
| chr22:37883126 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1576-3639A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883126 | |||||||
| chr22:37883219 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-3546C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883219 | |||||||
| chr22:37883296 | C | CA | 43 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0087 others(40): Show |
46 | HG00408.hp2 HG00609.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.1576-3447dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37883296 | ||||||
| chr22:37883296 | CA | C | 6 | a0001c0001t0001g0165 a0001c0002t0001g0107 a0001c0002t0001g0205 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-3447delA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37883296 | ||||||
| chr22:37883388 | T | A | 1 | a0001c0002t0001g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1576-3377T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883388 | |||||||
| chr22:37883433 | T | A | 7 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-3332T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883433 | |||||||
| chr22:37883580 | C | CA | 129 | a0001c0001t0001g0094 a0001c0002t0001g0001 a0001c0002t0001g0002 others(126): Show |
136 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1576-3174dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37883580 | ||||||
| chr22:37883829 | G | A | 1 | a0001c0002t0001g0007 | 2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1576-2936G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883829 | |||||||
| chr22:37883907 | C | G | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1576-2858C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37883907 | |||||||
| chr22:37883925 | AGAAT | A | 133 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0006 others(130): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1576-2820_1576-281 others(8): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37883925 | ||||||
| chr22:37884036 | A | T | 26 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(23): Show |
26 | HG00609.hp2 HG01081.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1576-2729A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884036 | |||||||
| chr22:37884185 | T | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0152 others(3): Show |
7 | HG00099.hp2 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-2580T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884185 | |||||||
| chr22:37884304 | C | G | 134 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0006 others(131): Show |
141 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1576-2461C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884304 | |||||||
| chr22:37884407 | A | G | 1 | a0001c0002t0001g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1576-2358A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884407 | |||||||
| chr22:37884436 | C | G | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-2329C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884436 | |||||||
| chr22:37884587 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1576-2178A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884587 | |||||||
| chr22:37884707 | C | A | 19 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(16): Show |
22 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1576-2058C>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884707 | |||||||
| chr22:37884901 | CT | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(120): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1576-1834delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884901 | CTT | C | 15 | a0001c0001t0001g0116 a0001c0001t0001g0139 a0001c0001t0001g0230 others(12): Show |
15 | HG01081.hp1 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1576-1835_1576-183 others(6): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884901 | CTTT | C | 31 | a0001c0001t0001g0277 a0001c0002t0001g0169 a0001c0002t0001g0171 others(28): Show |
32 | HG00609.hp2 HG01099.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1576-1836_1576-183 others(7): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884901 | CTTTT | C | 65 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(62): Show |
68 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1576-1837_1576-183 others(8): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884901 | CTTTTT | C | 10 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(7): Show |
10 | HG01074.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-1838_1576-183 others(9): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884901 | CTTTTTTT | C | 17 | a0001c0002t0001g0001 a0001c0002t0001g0055 a0001c0002t0001g0056 others(14): Show |
18 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1576-1840_1576-183 others(11): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37884901 | ||||||
| chr22:37884931 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1576-1834T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37884931 | |||||||
| chr22:37885026 | C | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0079 a0001c0001t0001g0150 others(6): Show |
10 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-1739C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885026 | |||||||
| chr22:37885040 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-1725T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885040 | |||||||
| chr22:37885357 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1576-1408C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885357 | |||||||
| chr22:37885377 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1576-1388T>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885377 | |||||||
| chr22:37885641 | C | CT | 6 | a0001c0001t0001g0159 a0001c0001t0001g0244 a0001c0002t0001g0107 others(3): Show |
6 | HG00408.hp2 HG01346.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-1104dupT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37885641 | ||||||
| chr22:37885641 | CT | C | 29 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0160 others(26): Show |
32 | HG00733.hp1 HG01884.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1576-1104delT | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37885641 | ||||||
| chr22:37885825 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1576-940A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885825 | |||||||
| chr22:37885887 | A | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-878A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885887 | |||||||
| chr22:37885923 | G | C | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-842G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37885923 | |||||||
| chr22:37886044 | A | T | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1576-721A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886044 | |||||||
| chr22:37886118 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
5 | NA18941.hp1 NA18942.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-647C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886118 | |||||||
| chr22:37886224 | A | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0246 a0001c0001t0001g0250 others(7): Show |
10 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1576-541A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886224 | |||||||
| chr22:37886261 | T | C | 1 | a0001c0002t0008g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1576-504T>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886261 | |||||||
| chr22:37886272 | A | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(46): Show |
52 | HG00609.hp2 HG01081.hp1 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.1576-493A>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886272 | |||||||
| chr22:37886492 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-273C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886492 | |||||||
| chr22:37886550 | C | CAA | 35 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(32): Show |
38 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1576-215_1576-214i others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886550 | |||||||
| chr22:37886551 | G | A | 5 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0030 others(2): Show |
5 | HG01081.hp1 HG02615.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1576-214G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | chr22 | 37886551 | |||||||
| chr22:37886567 | C | CA | 23 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(20): Show |
26 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1576-187dupA | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr22 | 37886567 | ||||||
| chr22:37886890 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0079 a0001c0001t0001g0150 others(6): Show |
10 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656+45C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37886890 | |||||||
| chr22:37886904 | C | T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1656+59C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37886904 | |||||||
| chr22:37886922 | T | A | 1 | a0001c0002t0001g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1656+77T>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37886922 | |||||||
| chr22:37887004 | C | G | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(18): Show |
24 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1656+159C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887004 | |||||||
| chr22:37887287 | C | T | 19 | a0001c0002t0001g0175 a0001c0002t0001g0182 a0001c0002t0001g0202 others(16): Show |
19 | HG00323.hp1 HG00609.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1656+442C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887287 | |||||||
| chr22:37887298 | C | G | 1 | a0001c0002t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1656+453C>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887298 | |||||||
| chr22:37887320 | GAA | G | 11 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(8): Show |
11 | HG01109.hp1 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1656+479_1656+480d others(4): Show |
EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr22 | 37887320 | ||||||
| chr22:37887336 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1656+491G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887336 | |||||||
| chr22:37887350 | C | T | 4 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+505C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887350 | |||||||
| chr22:37887528 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(21): Show |
27 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1656+683A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887528 | |||||||
| chr22:37887598 | A | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0015 others(67): Show |
73 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1656+753A>G | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887598 | |||||||
| chr22:37887636 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1657-790G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887636 | |||||||
| chr22:37887780 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1657-646C>T | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887780 | |||||||
| chr22:37887891 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1657-535G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37887891 | |||||||
| chr22:37888041 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1657-385G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37888041 | |||||||
| chr22:37888072 | G | A | 3 | a0001c0002t0001g0295 a0001c0002t0001g0296 a0001c0002t0001g0297 |
3 | HG02258.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1657-354G>A | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37888072 | |||||||
| chr22:37888275 | G | C | 19 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(16): Show |
22 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1657-151G>C | EIF3L | ENSG00000100129.18 | transcript | ENST00000652021.1 | protein_coding | 12/12 | chr22 | 37888275 |