Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10939 |
| ensemblid | ENSG00000141385.12 |
| hgncid | 315 |
| symbol | AFG3L2 |
| name | AFG3 like matrix AAA peptidase subunit 2 |
| refseq_nuc | NM_006796.3 |
| refseq_prot | NP_006787.2 |
| ensembl_nuc | ENST00000269143.8 |
| ensembl_prot | ENSP00000269143.2 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 12328944 |
| end | 12377227 |
| strand | - |
| ver | v1.2 |
| region | chr18:12328944-12377227 |
| region5000 | chr18:12323944-12382227 |
| regionname0 | AFG3L2_chr18_12328944_12377227 |
| regionname5000 | AFG3L2_chr18_12323944_12382227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 797 | 373 | 90 | 78 | 155 | 14 | 34 | 113 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | MAHRC others(792): Show |
chr18 | 12323944 | 12382227 |
| a0002 | 0/0 | 797 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | MAHRC others(792): Show |
chr18 | 12323944 | 12382227 |
| a0003 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | MAHRC others(792): Show |
chr18 | 12323944 | 12382227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2391 | 186 | 36 | 44 | 70 | 11 | 24 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0001c0002 | 1/0 | 2391 | 155 | 30 | 32 | 81 | 3 | 8 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0001c0003 | 0/0 | 2391 | 30 | 24 | 2 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0001c0005 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0001c0007 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0002c0004 | 0/0 | 2391 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 | ||
| a0003c0006 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | ATGGC others(2386): Show |
chr18 | 12323944 | 12382227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3160 | 174 | 27 | 42 | 69 | 11 | 24 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0001t0002 | 0/0 | 3160 | 4 | 4 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0001t0004 | 0/0 | 3160 | 4 | 2 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0001t0006 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0001t0007 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0001t0009 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0002t0001 | 1/0 | 3160 | 9 | 6 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0002t0002 | 0/0 | 3160 | 65 | 17 | 9 | 34 | 1 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0002t0003 | 0/0 | 3160 | 81 | 7 | 23 | 45 | 2 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0001 | 0/0 | 3160 | 4 | 1 | 0 | 3 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0002 | 0/0 | 3160 | 15 | 15 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0003 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0004 | 0/0 | 3160 | 5 | 5 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0005 | 0/0 | 3160 | 4 | 2 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0003t0008 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0005t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0001c0007t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0002c0004t0001 | 0/0 | 3160 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| a0003c0006t0002 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | GAGAG others(3155): Show |
chr18 | 12323944 | 12382227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0005g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0002c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0003c0006t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0039 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0188 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0286 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0310 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0284 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0271 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0313 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0302 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0304 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01167 | hp2 | a0001 | c0003 | t0005 | g0018 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0303 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0276 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01169 | hp2 | a0001 | c0003 | t0005 | g0018 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0292 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0278 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0287 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0269 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0270 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0279 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0019 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0085 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0322 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0077 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0076 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0332 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0291 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0309 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0289 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0307 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0336 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0301 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0080 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0326 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0280 | EAS | CDX | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0107 | EAS | CDX | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0298 | EAS | CDX | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0308 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0331 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0057 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0079 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02683 | hp1 | a0001 | c0007 | t0001 | g0199 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0100 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0328 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0325 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0058 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0329 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0094 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0068 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0017 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0096 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0060 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0081 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02976 | hp1 | a0001 | c0003 | t0004 | g0061 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0324 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0087 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0084 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0086 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0319 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0089 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0083 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0297 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0015 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03492 | hp1 | a0002 | c0004 | t0001 | g0015 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0099 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0272 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0173 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0281 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0082 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0299 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0288 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0312 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0311 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0273 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0295 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0274 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0300 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0264 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0090 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0017 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19065 | hp2 | a0003 | c0006 | t0002 | g0106 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0335 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0285 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0078 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0340 | AFR | ASW | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | ASW | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0268 | EUR | TSI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0330 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0305 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0088 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0314 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0317 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA21309 | hp2 | a0001 | c0003 | t0004 | g0064 | AFR | LWK | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0141 | REF | REF | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0238 | REF | REF | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12329764 | T | C | 1 | a0002 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.2195A>G | p.Glu732Gly | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 17/17 | 2340/3160 | 2195/2394 | 732/797 | chr18 | 12329764 | |||
| chr18:12358858 | G | A | 1 | a0003 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.838C>T | p.Arg280Trp | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/17 | 983/3160 | 838/2394 | 280/797 | chr18 | 12358858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12348286 | T | C | 5 | a0001c0001 a0001c0003 a0001c0005 others(2): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
synonymous_variant | LOW | c.1650A>G | p.Glu550Glu | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/17 | 1795/3160 | 1650/2394 | 550/797 | chr18 | 12348286 | |||
| chr18:12351343 | C | T | 4 | a0001c0001 a0001c0005 a0001c0007 others(1): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
synonymous_variant | LOW | c.1389G>A | p.Leu463Leu | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 11/17 | 1534/3160 | 1389/2394 | 463/797 | chr18 | 12351343 | |||
| chr18:12358796 | C | T | 1 | a0001c0005 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.900G>A | p.Lys300Lys | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/17 | 1045/3160 | 900/2394 | 300/797 | chr18 | 12358796 | |||
| chr18:12367019 | G | A | 1 | a0001c0007 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.498C>T | p.Ser166Ser | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/17 | 643/3160 | 498/2394 | 166/797 | chr18 | 12367019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12329254 | G | A | 2 | a0001c0003t0005 a0001c0003t0008 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 17/17 | 311 | chr18 | 12329254 | ||||||
| chr18:12329456 | T | G | 2 | a0001c0001t0006 a0001c0001t0007 |
3 | HG02055.hp1 HG03579.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*109A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 17/17 | 109 | chr18 | 12329456 | ||||||
| chr18:12329537 | C | G | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0003 others(5): Show |
172 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 17/17 | 28 | chr18 | 12329537 | ||||||
| chr18:12329563 | C | T | 2 | a0001c0003t0005 a0001c0003t0008 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 17/17 | 2 | chr18 | 12329563 | ||||||
| chr18:12377098 | C | T | 1 | a0001c0001t0009 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/17 | 16 | chr18 | 12377098 | ||||||
| chr18:12377178 | C | G | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(4): Show |
95 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-96G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/17 | 96 | chr18 | 12377178 | ||||||
| chr18:12377219 | C | G | 1 | a0001c0001t0007 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/17 | 137 | chr18 | 12377219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12329925 | G | A | 69 | a0001c0002t0002g0049 a0001c0002t0002g0096 a0001c0002t0002g0097 others(66): Show |
76 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2176-142C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12329925 | |||||||
| chr18:12330017 | CAATG | C | 4 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-238_2176-235d others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330017 | |||||||
| chr18:12330021 | G | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-238C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330021 | |||||||
| chr18:12330041 | G | A | 1 | a0001c0002t0002g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2176-258C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330041 | |||||||
| chr18:12330056 | C | T | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-273G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330056 | |||||||
| chr18:12330084 | T | C | 1 | a0001c0002t0003g0314 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2176-301A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330084 | |||||||
| chr18:12330092 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(167): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.2176-309A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330092 | |||||||
| chr18:12330168 | TGCAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2176-396_2176-386d others(13): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330168 | |||||||
| chr18:12330199 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-416C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330199 | |||||||
| chr18:12330304 | C | T | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-521G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330304 | |||||||
| chr18:12330334 | C | CA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(157): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2176-552dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330334 | |||||||
| chr18:12330334 | C | CAA | 6 | a0001c0001t0001g0178 a0001c0001t0001g0221 a0001c0001t0001g0229 others(3): Show |
6 | HG01952.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-553_2176-552d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330334 | |||||||
| chr18:12330338 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(163): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.2176-555G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330338 | |||||||
| chr18:12330338 | C | CA | 5 | a0001c0001t0001g0112 a0001c0001t0001g0171 a0001c0001t0001g0200 others(2): Show |
5 | HG00741.hp2 HG01069.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-556dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330338 | |||||||
| chr18:12330504 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2176-721C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330504 | |||||||
| chr18:12330569 | G | A | 158 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(155): Show |
172 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.2176-786C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330569 | |||||||
| chr18:12330740 | T | C | 65 | a0001c0002t0002g0049 a0001c0002t0003g0002 a0001c0002t0003g0003 others(62): Show |
72 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2176-957A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330740 | |||||||
| chr18:12330780 | C | CA | 15 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0231 others(12): Show |
15 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-998dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330780 | |||||||
| chr18:12331067 | C | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(335): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2176-1284G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331067 | |||||||
| chr18:12331094 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0211 a0001c0001t0001g0240 others(1): Show |
6 | HG02257.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-1311T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331094 | |||||||
| chr18:12331145 | C | T | 1 | a0001c0002t0002g0037 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2176-1362G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331145 | |||||||
| chr18:12331241 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2176-1458G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331241 | |||||||
| chr18:12331427 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0130 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2176-1644A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331427 | |||||||
| chr18:12331502 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(293): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2176-1719A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331502 | |||||||
| chr18:12331535 | G | A | 1 | a0003c0006t0002g0106 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2176-1752C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331535 | |||||||
| chr18:12331540 | C | T | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2176-1757G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331540 | |||||||
| chr18:12331591 | C | G | 6 | a0001c0002t0002g0008 a0001c0002t0002g0068 a0001c0002t0002g0069 others(3): Show |
7 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-1808G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331591 | |||||||
| chr18:12331771 | G | A | 1 | a0001c0002t0003g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2176-1988C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331771 | |||||||
| chr18:12331804 | AATAAATA others(13): Show |
A | 1 | a0001c0003t0001g0333 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2176-2041_2176-202 others(24): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331804 | |||||||
| chr18:12331804 | AATAAATA others(15): Show |
A | 2 | a0001c0003t0001g0334 a0001c0003t0001g0335 |
2 | NA18964.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-2043_2176-202 others(26): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331804 | |||||||
| chr18:12331808 | A | AATATATA others(3): Show |
2 | a0001c0002t0001g0320 a0001c0002t0001g0321 |
2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2176-2035_2176-202 others(14): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(17): Show |
A | 1 | a0001c0003t0004g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2176-2049_2176-202 others(28): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(23): Show |
A | 1 | a0001c0002t0002g0053 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2176-2055_2176-202 others(34): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(25): Show |
A | 7 | a0001c0002t0002g0047 a0001c0003t0002g0077 a0001c0003t0002g0090 others(4): Show |
9 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2176-2057_2176-202 others(36): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(27): Show |
A | 149 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(146): Show |
161 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.2176-2059_2176-202 others(38): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(29): Show |
A | 1 | a0001c0002t0003g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2176-2061_2176-202 others(40): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331808 | AATATATA others(35): Show |
A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(166): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2176-2067_2176-202 others(46): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331808 | |||||||
| chr18:12331812 | T | A | 1 | a0001c0003t0001g0317 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2176-2029A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331812 | |||||||
| chr18:12331819 | ATATATAT others(34): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2176-2077_2176-203 others(45): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331819 | |||||||
| chr18:12331820 | T | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-2037A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331820 | |||||||
| chr18:12331836 | T | A | 1 | a0001c0003t0004g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2176-2053A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331836 | |||||||
| chr18:12331860 | T | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-2077A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331860 | |||||||
| chr18:12331921 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0155 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2176-2138C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12331921 | |||||||
| chr18:12332123 | A | AT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(139): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2176-2341dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332123 | |||||||
| chr18:12332123 | A | ATT | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(124): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2176-2342_2176-234 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332123 | |||||||
| chr18:12332123 | A | ATTT | 6 | a0001c0001t0001g0161 a0001c0001t0001g0242 a0001c0002t0002g0006 others(3): Show |
7 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-2343_2176-234 others(7): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332123 | |||||||
| chr18:12332123 | AT | A | 6 | a0001c0002t0002g0096 a0001c0002t0002g0098 a0001c0002t0002g0099 others(3): Show |
6 | HG02451.hp1 HG02717.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-2341delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332123 | |||||||
| chr18:12332603 | GA | G | 6 | a0001c0002t0002g0008 a0001c0002t0002g0068 a0001c0002t0002g0069 others(3): Show |
7 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-2821delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332603 | |||||||
| chr18:12332681 | TA | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(100): Show |
115 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2176-2899delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332681 | |||||||
| chr18:12332682 | A | T | 7 | a0001c0001t0001g0243 a0001c0002t0003g0266 a0001c0002t0003g0280 others(4): Show |
7 | HG00558.hp1 HG00597.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-2899T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332682 | |||||||
| chr18:12332683 | TA | T | 33 | a0001c0001t0001g0118 a0001c0001t0001g0142 a0001c0001t0001g0153 others(30): Show |
35 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.2176-2901delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332683 | |||||||
| chr18:12332684 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(298): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.2176-2901T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332684 | |||||||
| chr18:12332697 | A | C | 3 | a0001c0002t0002g0097 a0001c0002t0002g0098 a0001c0002t0002g0099 |
3 | HG01167.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2176-2914T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332697 | |||||||
| chr18:12332745 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0232 |
2 | HG00280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2176-2962G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332745 | |||||||
| chr18:12332835 | T | TAC | 54 | a0001c0002t0002g0049 a0001c0002t0003g0002 a0001c0002t0003g0003 others(51): Show |
61 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.2176-3054_2176-305 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332835 | |||||||
| chr18:12332835 | T | TACAC | 4 | a0001c0002t0003g0188 a0001c0002t0003g0273 a0001c0002t0003g0274 others(1): Show |
4 | HG00140.hp1 HG01993.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-3056_2176-305 others(8): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332835 | |||||||
| chr18:12332835 | TAC | T | 197 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2176-3054_2176-305 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332835 | |||||||
| chr18:12332866 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(168): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2176-3083C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332866 | |||||||
| chr18:12332867 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(168): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2176-3084C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332867 | |||||||
| chr18:12332874 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2176-3091G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332874 | |||||||
| chr18:12332907 | A | AAATATAT others(30): Show |
127 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2176-3125_2176-312 others(41): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332907 | |||||||
| chr18:12332907 | A | AAATATAT others(67): Show |
10 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0250 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2176-3125_2176-312 others(78): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332907 | |||||||
| chr18:12332916 | T | TTATATAT others(23): Show |
1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-3134_2176-313 others(34): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332916 | |||||||
| chr18:12332926 | C | T | 15 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2176-3143G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332926 | |||||||
| chr18:12332932 | C | CTATATAA others(37): Show |
4 | a0001c0001t0001g0221 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG01952.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-3150_2176-314 others(48): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332932 | |||||||
| chr18:12332940 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(269): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.2176-3157G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332940 | |||||||
| chr18:12332945 | A | AATATATA others(25): Show |
4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0163 others(1): Show |
4 | HG00544.hp2 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-3163_2176-316 others(36): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332945 | |||||||
| chr18:12332945 | A | T | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2176-3162T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332945 | |||||||
| chr18:12332951 | T | TATAA | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-3169_2176-316 others(8): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332951 | |||||||
| chr18:12332951 | T | TATTA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(22): Show |
32 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2176-3169_2176-316 others(8): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332951 | |||||||
| chr18:12332952 | T | C | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-3169A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332952 | |||||||
| chr18:12332957 | A | AACATATA others(2): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(21): Show |
31 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.2176-3175_2176-317 others(13): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332957 | |||||||
| chr18:12332957 | A | ATAACATA others(4): Show |
1 | a0001c0001t0001g0122 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2176-3175_2176-317 others(15): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332957 | |||||||
| chr18:12332958 | C | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(23): Show |
33 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.2176-3175G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332958 | |||||||
| chr18:12332958 | C | CTA | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-3177_2176-317 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332958 | |||||||
| chr18:12332962 | AAT | A | 72 | a0001c0001t0001g0111 a0001c0002t0002g0049 a0001c0002t0002g0096 others(69): Show |
79 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2176-3181_2176-318 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332962 | |||||||
| chr18:12332969 | T | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(26): Show |
36 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2176-3186A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332969 | |||||||
| chr18:12332981 | A | ACTATAAT others(4): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(26): Show |
36 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2176-3199_2176-319 others(15): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332981 | |||||||
| chr18:12332982 | A | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(26): Show |
36 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2176-3199T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332982 | |||||||
| chr18:12332997 | TTATA | T | 69 | a0001c0002t0002g0049 a0001c0002t0002g0096 a0001c0002t0002g0097 others(66): Show |
76 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2176-3218_2176-321 others(8): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332997 | |||||||
| chr18:12333042 | TCTATTAT others(26): Show |
T | 129 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(126): Show |
140 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.2176-3292_2176-326 others(37): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333042 | |||||||
| chr18:12333046 | T | TTATATAA others(1): Show |
4 | a0001c0001t0001g0149 a0001c0001t0001g0191 a0001c0001t0001g0252 others(1): Show |
4 | HG00099.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-3264_2176-326 others(12): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333046 | |||||||
| chr18:12333052 | AATAGATT others(18): Show |
A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(164): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2176-3294_2176-327 others(29): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333052 | |||||||
| chr18:12333056 | GATTATAA others(29): Show |
G | 10 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(7): Show |
11 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2176-3309_2176-327 others(40): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333056 | |||||||
| chr18:12333079 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(164): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2176-3296A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333079 | |||||||
| chr18:12333079 | T | TATAATAG others(50): Show |
1 | a0001c0001t0001g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2176-3297_2176-329 others(61): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333079 | |||||||
| chr18:12333124 | TTA | T | 13 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0149 others(10): Show |
13 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-3343_2176-334 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333124 | |||||||
| chr18:12333127 | TATATATA | T | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-3351_2176-334 others(11): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333127 | |||||||
| chr18:12333164 | TATA | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(247): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2176-3384_2176-338 others(7): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333164 | |||||||
| chr18:12333179 | T | C | 4 | a0001c0001t0004g0101 a0001c0003t0001g0333 a0001c0003t0001g0334 others(1): Show |
4 | NA18964.hp1 NA19030.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-3396A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333179 | |||||||
| chr18:12333193 | TATATA | T | 13 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-3415_2176-341 others(9): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333193 | |||||||
| chr18:12333198 | A | T | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2176-3415T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333198 | |||||||
| chr18:12333266 | T | TTATAAAT others(17): Show |
1 | a0001c0003t0004g0058 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2176-3507_2176-348 others(28): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333266 | |||||||
| chr18:12333362 | A | T | 4 | a0001c0002t0003g0336 a0001c0002t0003g0337 a0001c0002t0003g0340 others(1): Show |
4 | HG00438.hp2 HG02129.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-3579T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333362 | |||||||
| chr18:12333364 | A | T | 71 | a0001c0002t0002g0049 a0001c0002t0002g0096 a0001c0002t0002g0097 others(68): Show |
78 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2176-3581T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333364 | |||||||
| chr18:12333368 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2176-3585A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333368 | |||||||
| chr18:12333369 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(168): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2176-3586A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333369 | |||||||
| chr18:12333370 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2176-3587A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333370 | |||||||
| chr18:12333394 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2176-3611C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333394 | |||||||
| chr18:12333419 | G | T | 71 | a0001c0002t0002g0049 a0001c0002t0002g0096 a0001c0002t0002g0097 others(68): Show |
78 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2176-3636C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333419 | |||||||
| chr18:12333687 | C | T | 54 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(51): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2175+3654G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333687 | |||||||
| chr18:12333787 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2175+3554C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333787 | |||||||
| chr18:12333802 | G | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+3539C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333802 | |||||||
| chr18:12333959 | T | C | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175+3382A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333959 | |||||||
| chr18:12334060 | T | A | 1 | a0001c0002t0003g0299 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2175+3281A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334060 | |||||||
| chr18:12334061 | GT | G | 69 | a0001c0002t0002g0049 a0001c0002t0002g0096 a0001c0002t0002g0097 others(66): Show |
76 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2175+3279delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334061 | |||||||
| chr18:12334143 | C | T | 16 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(13): Show |
18 | HG00423.hp2 HG01099.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.2175+3198G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334143 | |||||||
| chr18:12334204 | C | G | 4 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+3137G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334204 | |||||||
| chr18:12334368 | G | A | 64 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2175+2973C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334368 | |||||||
| chr18:12334410 | G | C | 64 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2175+2931C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334410 | |||||||
| chr18:12334561 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2175+2780G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334561 | |||||||
| chr18:12334698 | G | A | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2175+2643C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334698 | |||||||
| chr18:12334703 | C | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(325): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2175+2638G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334703 | |||||||
| chr18:12334777 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2175+2564G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334777 | |||||||
| chr18:12334964 | C | T | 22 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(19): Show |
24 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.2175+2377G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334964 | |||||||
| chr18:12334965 | G | A | 5 | a0001c0002t0002g0096 a0001c0002t0002g0097 a0001c0002t0002g0098 others(2): Show |
5 | HG01167.hp1 HG02717.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2175+2376C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334965 | |||||||
| chr18:12334966 | G | C | 6 | a0001c0002t0003g0305 a0001c0002t0003g0310 a0001c0002t0003g0336 others(3): Show |
6 | HG00438.hp2 HG00639.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175+2375C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334966 | |||||||
| chr18:12334976 | C | T | 1 | a0001c0002t0001g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2175+2365G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12334976 | |||||||
| chr18:12335092 | C | G | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2175+2249G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335092 | |||||||
| chr18:12335280 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2175+2061G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335280 | |||||||
| chr18:12335337 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG00280.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2175+2004C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335337 | |||||||
| chr18:12335579 | G | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175+1762C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335579 | |||||||
| chr18:12335583 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(168): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2175+1758G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335583 | |||||||
| chr18:12335645 | G | C | 1 | a0001c0003t0001g0335 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2175+1696C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335645 | |||||||
| chr18:12335673 | C | T | 157 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(154): Show |
171 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.2175+1668G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335673 | |||||||
| chr18:12335883 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2175+1458T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335883 | |||||||
| chr18:12335937 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+1404A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12335937 | |||||||
| chr18:12336048 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(169): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2175+1293T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336048 | |||||||
| chr18:12336057 | C | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(325): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2175+1284G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336057 | |||||||
| chr18:12336094 | G | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2175+1247C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336094 | |||||||
| chr18:12336243 | T | C | 12 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2175+1098A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336243 | |||||||
| chr18:12336449 | C | A | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2175+892G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336449 | |||||||
| chr18:12336454 | C | T | 7 | a0001c0003t0002g0083 a0001c0003t0002g0084 a0001c0003t0002g0085 others(4): Show |
7 | HG01884.hp1 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+887G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336454 | |||||||
| chr18:12336466 | C | T | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2175+875G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336466 | |||||||
| chr18:12336728 | T | G | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2175+613A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336728 | |||||||
| chr18:12337014 | C | T | 4 | a0001c0002t0003g0263 a0001c0002t0003g0264 a0001c0002t0003g0343 others(1): Show |
4 | NA18977.hp1 NA18998.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+327G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12337014 | |||||||
| chr18:12337088 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2175+253G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12337088 | |||||||
| chr18:12337211 | A | T | 27 | a0001c0002t0002g0049 a0001c0002t0003g0019 a0001c0002t0003g0195 others(24): Show |
28 | HG00673.hp2 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.2175+130T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12337211 | |||||||
| chr18:12337289 | C | T | 6 | a0001c0002t0003g0305 a0001c0002t0003g0310 a0001c0002t0003g0336 others(3): Show |
6 | HG00438.hp2 HG00639.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175+52G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12337289 | |||||||
| chr18:12337676 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1981-141T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12337676 | |||||||
| chr18:12337689 | G | C | 11 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0152 others(8): Show |
11 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1981-154C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12337689 | |||||||
| chr18:12337763 | T | C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0258 |
3 | HG02886.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1981-228A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12337763 | |||||||
| chr18:12337910 | T | C | 1 | a0001c0002t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1981-375A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12337910 | |||||||
| chr18:12337919 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1981-384C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12337919 | |||||||
| chr18:12338016 | C | T | 1 | a0001c0002t0003g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1981-481G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338016 | |||||||
| chr18:12338051 | T | C | 1 | a0001c0002t0003g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1981-516A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338051 | |||||||
| chr18:12338060 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1981-525G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338060 | |||||||
| chr18:12338272 | C | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(335): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1981-737G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338272 | |||||||
| chr18:12338289 | T | C | 1 | a0001c0002t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1981-754A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338289 | |||||||
| chr18:12338471 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(168): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1981-936G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338471 | |||||||
| chr18:12338511 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1981-976G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338511 | |||||||
| chr18:12338636 | T | A | 4 | a0001c0001t0004g0101 a0001c0003t0001g0333 a0001c0003t0001g0334 others(1): Show |
4 | NA18964.hp1 NA19030.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-1101A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338636 | |||||||
| chr18:12338693 | A | G | 1 | a0001c0003t0004g0058 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1981-1158T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338693 | |||||||
| chr18:12338884 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
11 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1980+1317T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338884 | |||||||
| chr18:12338922 | C | T | 4 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+1279G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338922 | |||||||
| chr18:12338977 | G | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+1224C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338977 | |||||||
| chr18:12338997 | G | C | 16 | a0001c0002t0002g0004 a0001c0002t0002g0026 a0001c0002t0002g0027 others(13): Show |
18 | HG00423.hp2 HG01099.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1980+1204C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12338997 | |||||||
| chr18:12339044 | G | A | 1 | a0001c0001t0007g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1980+1157C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339044 | |||||||
| chr18:12339089 | C | T | 2 | a0001c0002t0002g0042 a0001c0002t0002g0045 |
2 | NA19002.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1980+1112G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339089 | |||||||
| chr18:12339142 | G | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1980+1059C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339142 | |||||||
| chr18:12339236 | C | CA | 72 | a0001c0001t0001g0260 a0001c0002t0001g0320 a0001c0002t0002g0026 others(69): Show |
76 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1980+964dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339236 | |||||||
| chr18:12339236 | C | CAA | 27 | a0001c0002t0002g0034 a0001c0002t0002g0099 a0001c0002t0002g0103 others(24): Show |
30 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1980+963_1980+964d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339236 | |||||||
| chr18:12339236 | CA | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0130 others(52): Show |
57 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1980+964delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339236 | |||||||
| chr18:12339236 | CAA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(116): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1980+963_1980+964d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339236 | |||||||
| chr18:12339236 | CAAAAAAA others(6): Show |
C | 4 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+952_1980+964d others(15): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339236 | |||||||
| chr18:12339337 | G | A | 1 | a0001c0002t0003g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1980+864C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339337 | |||||||
| chr18:12339384 | C | G | 1 | a0001c0002t0003g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1980+817G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339384 | |||||||
| chr18:12339501 | G | A | 1 | a0001c0007t0001g0199 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1980+700C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339501 | |||||||
| chr18:12339552 | C | CA | 96 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0152 others(93): Show |
105 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1980+648dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339552 | |||||||
| chr18:12339552 | C | CAA | 8 | a0001c0001t0001g0260 a0001c0002t0002g0062 a0001c0002t0003g0197 others(5): Show |
8 | HG00735.hp2 HG01169.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1980+647_1980+648d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339552 | |||||||
| chr18:12339552 | CA | C | 52 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(49): Show |
56 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1980+648delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339552 | |||||||
| chr18:12339568 | C | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0342 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+633G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339568 | |||||||
| chr18:12339581 | C | G | 2 | a0001c0002t0003g0313 a0001c0002t0003g0314 |
2 | HG00735.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1980+620G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339581 | |||||||
| chr18:12339582 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1980+619C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339582 | |||||||
| chr18:12339665 | G | A | 64 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1980+536C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339665 | |||||||
| chr18:12339678 | C | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+523G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339678 | |||||||
| chr18:12339773 | T | C | 1 | a0001c0003t0002g0083 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1980+428A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339773 | |||||||
| chr18:12339848 | C | CA | 11 | a0001c0002t0001g0322 a0001c0002t0002g0032 a0001c0002t0002g0072 others(8): Show |
11 | HG01884.hp2 HG02015.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1980+352dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339848 | |||||||
| chr18:12339848 | CA | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(220): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1980+352delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339848 | |||||||
| chr18:12339968 | C | T | 65 | a0001c0002t0002g0049 a0001c0002t0003g0002 a0001c0002t0003g0003 others(62): Show |
72 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1980+233G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339968 | |||||||
| chr18:12340596 | GT | G | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(335): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1780-196delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340596 | |||||||
| chr18:12340627 | G | A | 4 | a0001c0002t0002g0027 a0001c0002t0002g0050 a0001c0002t0002g0051 others(1): Show |
4 | NA18990.hp1 NA19003.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1780-226C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340627 | |||||||
| chr18:12340814 | CG | C | 64 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1780-414delC | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340814 | |||||||
| chr18:12340919 | C | CT | 13 | a0001c0001t0004g0101 a0001c0002t0001g0338 a0001c0002t0001g0339 others(10): Show |
13 | HG00438.hp2 HG00639.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1780-519dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340919 | |||||||
| chr18:12340919 | CT | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(164): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1780-519delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340919 | |||||||
| chr18:12340937 | A | G | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1780-536T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340937 | |||||||
| chr18:12341064 | T | C | 2 | a0001c0002t0003g0265 a0001c0002t0003g0316 |
2 | NA18984.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1780-663A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341064 | |||||||
| chr18:12341167 | G | C | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1780-766C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341167 | |||||||
| chr18:12341360 | C | T | 1 | a0001c0002t0003g0279 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1780-959G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341360 | |||||||
| chr18:12341368 | A | G | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1780-967T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341368 | |||||||
| chr18:12341465 | A | G | 54 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(51): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1780-1064T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341465 | |||||||
| chr18:12341540 | T | C | 12 | a0001c0002t0003g0002 a0001c0002t0003g0003 a0001c0002t0003g0110 others(9): Show |
18 | HG01192.hp2 HG01358.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1780-1139A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341540 | |||||||
| chr18:12341632 | C | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1780-1231G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341632 | |||||||
| chr18:12341721 | C | T | 330 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(327): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1780-1320G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341721 | |||||||
| chr18:12341793 | G | A | 1 | a0001c0002t0003g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1780-1392C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341793 | |||||||
| chr18:12341908 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1780-1507G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341908 | |||||||
| chr18:12341976 | C | T | 1 | a0001c0002t0002g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1780-1575G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12341976 | |||||||
| chr18:12342110 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(164): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1780-1709G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12342110 | |||||||
| chr18:12342134 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0198 a0001c0001t0001g0211 others(3): Show |
8 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-1733C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12342134 | |||||||
| chr18:12342161 | C | T | 64 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1780-1760G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12342161 | |||||||
| chr18:12342568 | G | A | 13 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1779+1564C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12342568 | |||||||
| chr18:12342628 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1779+1504T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12342628 | |||||||
| chr18:12343006 | CA | C | 157 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(154): Show |
171 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1779+1125delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343006 | |||||||
| chr18:12343559 | G | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG01952.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1779+573C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343559 | |||||||
| chr18:12343560 | T | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG01952.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1779+572A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343560 | |||||||
| chr18:12343659 | T | G | 7 | a0001c0001t0004g0021 a0001c0003t0001g0317 a0001c0003t0004g0057 others(4): Show |
7 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1779+473A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343659 | |||||||
| chr18:12343682 | G | A | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1779+450C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343682 | |||||||
| chr18:12343872 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(179): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1779+260T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343872 | |||||||
| chr18:12343970 | A | C | 1 | a0001c0002t0003g0340 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1779+162T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12343970 | |||||||
| chr18:12344280 | T | C | 1 | a0001c0001t0004g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1664-33A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344280 | |||||||
| chr18:12344286 | C | T | 19 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0221 others(16): Show |
19 | HG01256.hp2 HG01891.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1664-39G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344286 | |||||||
| chr18:12344376 | C | T | 6 | a0001c0001t0004g0101 a0001c0002t0002g0096 a0001c0002t0002g0097 others(3): Show |
6 | HG01167.hp1 HG02717.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1664-129G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344376 | |||||||
| chr18:12344412 | T | C | 1 | a0001c0002t0002g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1664-165A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344412 | |||||||
| chr18:12344413 | G | A | 1 | a0001c0002t0002g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1664-166C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344413 | |||||||
| chr18:12344470 | T | A | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1664-223A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344470 | |||||||
| chr18:12344472 | C | T | 1 | a0001c0002t0002g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1664-225G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344472 | |||||||
| chr18:12344477 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1664-230G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344477 | |||||||
| chr18:12344478 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1664-231G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344478 | |||||||
| chr18:12344482 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1664-235G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344482 | |||||||
| chr18:12344487 | C | T | 1 | a0001c0002t0003g0283 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1664-240G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344487 | |||||||
| chr18:12344494 | G | A | 3 | a0001c0001t0007g0020 a0001c0002t0002g0102 a0001c0002t0002g0103 |
3 | HG02451.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1664-247C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344494 | |||||||
| chr18:12344547 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1664-300C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344547 | |||||||
| chr18:12344692 | ATTAAG | A | 11 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(8): Show |
11 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1664-450_1664-446d others(7): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344692 | |||||||
| chr18:12344697 | G | A | 2 | a0001c0003t0002g0084 a0001c0003t0002g0086 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1664-450C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344697 | |||||||
| chr18:12344844 | G | A | 12 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1664-597C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344844 | |||||||
| chr18:12344870 | A | G | 8 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0003g0305 others(5): Show |
8 | HG00438.hp2 HG00639.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1664-623T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344870 | |||||||
| chr18:12344911 | A | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG00280.hp1 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1664-664T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344911 | |||||||
| chr18:12344950 | T | C | 1 | a0001c0002t0003g0314 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1664-703A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344950 | |||||||
| chr18:12344982 | T | C | 1 | a0001c0003t0005g0018 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1664-735A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12344982 | |||||||
| chr18:12345240 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(197): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1664-993A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345240 | |||||||
| chr18:12345241 | G | A | 4 | a0001c0001t0004g0021 a0001c0003t0002g0077 a0001c0003t0002g0090 others(1): Show |
4 | HG01891.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1664-994C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345241 | |||||||
| chr18:12345262 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1664-1015C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345262 | |||||||
| chr18:12345277 | C | G | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1664-1030G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345277 | |||||||
| chr18:12345349 | C | G | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1664-1102G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345349 | |||||||
| chr18:12345390 | A | G | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1664-1143T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345390 | |||||||
| chr18:12345391 | A | AGT | 8 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(5): Show |
8 | HG02083.hp1 NA18942.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1664-1146_1664-114 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345391 | |||||||
| chr18:12345508 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(173): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1664-1261G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345508 | |||||||
| chr18:12345823 | C | A | 2 | a0001c0002t0003g0271 a0001c0002t0003g0330 |
2 | HG00733.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1664-1576G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345823 | |||||||
| chr18:12345874 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(272): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1664-1627T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345874 | |||||||
| chr18:12345878 | G | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(272): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1664-1631C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345878 | |||||||
| chr18:12345888 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1664-1641G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345888 | |||||||
| chr18:12346388 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+1885C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346388 | |||||||
| chr18:12346393 | A | G | 1 | a0001c0002t0003g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1663+1880T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346393 | |||||||
| chr18:12346504 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1663+1769G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346504 | |||||||
| chr18:12346653 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1663+1620C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346653 | |||||||
| chr18:12346747 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(171): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1663+1526A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346747 | |||||||
| chr18:12346815 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1663+1458T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346815 | |||||||
| chr18:12346903 | CA | C | 126 | a0001c0001t0001g0109 a0001c0001t0001g0121 a0001c0001t0001g0129 others(123): Show |
138 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1663+1369delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346903 | |||||||
| chr18:12346903 | CAA | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(185): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1663+1368_1663+136 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12346903 | |||||||
| chr18:12347009 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1663+1264A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347009 | |||||||
| chr18:12347090 | G | A | 3 | a0001c0002t0003g0326 a0001c0002t0003g0328 a0001c0002t0003g0329 |
3 | HG02145.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1663+1183C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347090 | |||||||
| chr18:12347121 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1663+1152A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347121 | |||||||
| chr18:12347160 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1663+1113G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347160 | |||||||
| chr18:12347483 | C | T | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1663+790G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347483 | |||||||
| chr18:12347553 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(166): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1663+720A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347553 | |||||||
| chr18:12347553 | TA | T | 68 | a0001c0001t0004g0101 a0001c0002t0001g0338 a0001c0002t0001g0339 others(65): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1663+719delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347553 | |||||||
| chr18:12347554 | A | AT | 13 | a0001c0002t0003g0297 a0001c0003t0002g0078 a0001c0003t0002g0079 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1663+718dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347554 | |||||||
| chr18:12347554 | A | T | 2 | a0001c0002t0003g0196 a0001c0002t0003g0315 |
2 | NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1663+719T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347554 | |||||||
| chr18:12347554 | AT | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(174): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1663+718delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347554 | |||||||
| chr18:12347614 | G | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+659C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347614 | |||||||
| chr18:12347795 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(198): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1663+478A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347795 | |||||||
| chr18:12347844 | C | T | 5 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0060 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663+429G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347844 | |||||||
| chr18:12348000 | C | T | 72 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0002g0049 others(69): Show |
79 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1663+273G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12348000 | |||||||
| chr18:12348008 | G | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1663+265C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12348008 | |||||||
| chr18:12348080 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+193C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12348080 | |||||||
| chr18:12348092 | A | G | 12 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1663+181T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12348092 | |||||||
| chr18:12348444 | A | G | 1 | a0001c0002t0001g0322 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1553-61T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12348444 | |||||||
| chr18:12348716 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1553-333G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12348716 | |||||||
| chr18:12348995 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553-612C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12348995 | |||||||
| chr18:12349030 | C | T | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553-647G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349030 | |||||||
| chr18:12349059 | A | C | 10 | a0001c0002t0002g0007 a0001c0002t0002g0035 a0001c0002t0002g0041 others(7): Show |
11 | HG02040.hp1 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1553-676T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349059 | |||||||
| chr18:12349254 | G | A | 15 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1553-871C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349254 | |||||||
| chr18:12349254 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(166): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1553-871C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349254 | |||||||
| chr18:12349407 | T | C | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1553-1024A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349407 | |||||||
| chr18:12349446 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(166): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1553-1063G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349446 | |||||||
| chr18:12349634 | A | C | 1 | a0001c0002t0003g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1553-1251T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349634 | |||||||
| chr18:12349656 | CAT | C | 5 | a0001c0001t0001g0111 a0001c0002t0002g0050 a0001c0003t0004g0061 others(2): Show |
5 | HG02976.hp1 HG04184.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553-1275_1553-127 others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349656 | |||||||
| chr18:12349659 | GTTTTTA | G | 4 | a0001c0001t0001g0323 a0001c0001t0001g0327 a0001c0001t0006g0206 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553-1282_1553-127 others(10): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349659 | |||||||
| chr18:12349695 | C | T | 15 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1553-1312G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349695 | |||||||
| chr18:12349954 | AC | A | 15 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(12): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1552+1130delG | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12349954 | |||||||
| chr18:12350187 | T | G | 1 | a0001c0002t0002g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1552+898A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350187 | |||||||
| chr18:12350231 | G | A | 2 | a0001c0003t0001g0333 a0001c0003t0001g0335 |
2 | NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1552+854C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350231 | |||||||
| chr18:12350418 | G | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1552+667C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350418 | |||||||
| chr18:12350435 | CTTAGGAA | C | 24 | a0001c0003t0001g0317 a0001c0003t0002g0077 a0001c0003t0002g0078 others(21): Show |
26 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1552+643_1552+649d others(9): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350435 | |||||||
| chr18:12350478 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(197): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1552+607G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350478 | |||||||
| chr18:12350503 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1552+582A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350503 | |||||||
| chr18:12350506 | C | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(272): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1552+579G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350506 | |||||||
| chr18:12350833 | A | C | 1 | a0001c0002t0003g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1552+252T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 12/16 | chr18 | 12350833 | |||||||
| chr18:12351266 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1426+40G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 11/16 | chr18 | 12351266 | |||||||
| chr18:12351420 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.1319-7C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351420 | |||||||
| chr18:12351453 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1319-40C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351453 | |||||||
| chr18:12351464 | C | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1319-51G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351464 | |||||||
| chr18:12351549 | G | GT | 16 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0144 others(13): Show |
16 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1319-137dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351549 | |||||||
| chr18:12351553 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0009g0107 |
3 | HG00621.hp2 HG02165.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1319-140A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351553 | |||||||
| chr18:12351608 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1319-195C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351608 | |||||||
| chr18:12351677 | G | C | 74 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0002g0049 others(71): Show |
81 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1319-264C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351677 | |||||||
| chr18:12351692 | A | G | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1319-279T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351692 | |||||||
| chr18:12351755 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1319-342G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351755 | |||||||
| chr18:12351855 | GTTT | G | 7 | a0001c0003t0002g0083 a0001c0003t0002g0084 a0001c0003t0002g0085 others(4): Show |
7 | HG01884.hp1 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-445_1319-443d others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351855 | |||||||
| chr18:12351939 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1319-526G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351939 | |||||||
| chr18:12351941 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1319-528T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351941 | |||||||
| chr18:12351972 | T | C | 1 | a0001c0002t0002g0065 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1319-559A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12351972 | |||||||
| chr18:12352002 | T | C | 1 | a0001c0002t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1319-589A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352002 | |||||||
| chr18:12352258 | T | C | 1 | a0001c0002t0001g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1318+747A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352258 | |||||||
| chr18:12352284 | G | A | 9 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(6): Show |
11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1318+721C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352284 | |||||||
| chr18:12352335 | T | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+670A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352335 | |||||||
| chr18:12352336 | C | T | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+669G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352336 | |||||||
| chr18:12352337 | A | G | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+668T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352337 | |||||||
| chr18:12352338 | T | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+667A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352338 | |||||||
| chr18:12352342 | AG | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+662delC | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352342 | |||||||
| chr18:12352345 | C | T | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+660G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352345 | |||||||
| chr18:12352346 | A | G | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+659T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352346 | |||||||
| chr18:12352348 | T | C | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+657A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352348 | |||||||
| chr18:12352349 | T | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+656A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352349 | |||||||
| chr18:12352350 | C | T | 2 | a0001c0002t0002g0006 a0001c0002t0002g0044 |
3 | HG01070.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1318+655G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352350 | |||||||
| chr18:12352384 | A | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0246 |
2 | NA18949.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1318+621T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352384 | |||||||
| chr18:12352546 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0244 |
2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1318+459C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 10/16 | chr18 | 12352546 | |||||||
| chr18:12353179 | A | T | 59 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(56): Show |
64 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1165-21T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353179 | |||||||
| chr18:12353182 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1165-24G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353182 | |||||||
| chr18:12353202 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1165-44A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353202 | |||||||
| chr18:12353320 | G | T | 1 | a0001c0002t0003g0282 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1165-162C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353320 | |||||||
| chr18:12353383 | G | A | 59 | a0001c0002t0002g0049 a0001c0002t0003g0002 a0001c0002t0003g0003 others(56): Show |
66 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1165-225C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353383 | |||||||
| chr18:12353409 | G | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-251C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353409 | |||||||
| chr18:12353514 | C | CA | 76 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0002t0002g0039 others(73): Show |
83 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1165-357dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353514 | |||||||
| chr18:12353514 | C | CAA | 13 | a0001c0002t0002g0022 a0001c0002t0002g0093 a0001c0002t0003g0110 others(10): Show |
13 | HG02257.hp1 HG02572.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1165-358_1165-357d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353514 | |||||||
| chr18:12353514 | C | CAAA | 6 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0003g0336 others(3): Show |
6 | HG02129.hp2 NA18612.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-359_1165-357d others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353514 | |||||||
| chr18:12353514 | CA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(133): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1165-357delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353514 | |||||||
| chr18:12353514 | CAA | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0130 a0001c0001t0001g0131 others(12): Show |
16 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165-358_1165-357d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353514 | |||||||
| chr18:12353539 | T | A | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-381A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353539 | |||||||
| chr18:12353852 | T | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(44): Show |
51 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1165-694A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353852 | |||||||
| chr18:12353921 | A | G | 4 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-763T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353921 | |||||||
| chr18:12353965 | G | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-807C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353965 | |||||||
| chr18:12353966 | G | A | 5 | a0001c0002t0002g0096 a0001c0002t0002g0097 a0001c0002t0002g0098 others(2): Show |
5 | HG01167.hp1 HG02717.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-808C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353966 | |||||||
| chr18:12353977 | C | T | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165-819G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12353977 | |||||||
| chr18:12354100 | A | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(335): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1165-942T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354100 | |||||||
| chr18:12354132 | A | AC | 49 | a0001c0001t0004g0101 a0001c0002t0001g0318 a0001c0002t0001g0319 others(46): Show |
50 | HG00423.hp2 HG00597.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1165-975dupG | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354132 | |||||||
| chr18:12354133 | C | CCCG | 72 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0002g0049 others(69): Show |
79 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1165-976_1165-975i others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354133 | |||||||
| chr18:12354135 | C | A | 1 | a0001c0003t0008g0076 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1165-977G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354135 | |||||||
| chr18:12354136 | C | A | 2 | a0001c0003t0005g0017 a0001c0003t0005g0018 |
4 | HG01167.hp2 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-978G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354136 | |||||||
| chr18:12354136 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG00609.hp2 HG02083.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-978G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354136 | |||||||
| chr18:12354138 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0171 |
2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1165-980G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354138 | |||||||
| chr18:12354140 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1165-982G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354140 | |||||||
| chr18:12354141 | C | T | 75 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0002g0049 others(72): Show |
82 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1165-983G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354141 | |||||||
| chr18:12354143 | C | CG | 35 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(32): Show |
36 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1165-986_1165-985i others(3): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354143 | |||||||
| chr18:12354143 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(126): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1165-985G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354143 | |||||||
| chr18:12354144 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1165-986G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354144 | |||||||
| chr18:12354145 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(164): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165-987G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354145 | |||||||
| chr18:12354168 | G | A | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1165-1010C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354168 | |||||||
| chr18:12354203 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0171 |
2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1165-1045G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354203 | |||||||
| chr18:12354320 | T | C | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1165-1162A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354320 | |||||||
| chr18:12354468 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(198): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1165-1310A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354468 | |||||||
| chr18:12354478 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0130 others(14): Show |
18 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1165-1320T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354478 | |||||||
| chr18:12354613 | G | A | 1 | a0001c0002t0001g0320 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1165-1455C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354613 | |||||||
| chr18:12354635 | T | C | 1 | a0001c0002t0002g0038 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1165-1477A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354635 | |||||||
| chr18:12354816 | C | T | 19 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(16): Show |
21 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1165-1658G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354816 | |||||||
| chr18:12354873 | C | G | 3 | a0001c0003t0002g0077 a0001c0003t0002g0090 a0001c0003t0002g0094 |
3 | HG01891.hp1 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1165-1715G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354873 | |||||||
| chr18:12354937 | G | A | 2 | a0001c0003t0002g0077 a0001c0003t0002g0090 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1164+1757C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12354937 | |||||||
| chr18:12355089 | G | C | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1164+1605C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355089 | |||||||
| chr18:12355175 | G | A | 1 | a0001c0003t0001g0334 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1164+1519C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355175 | |||||||
| chr18:12355208 | TA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(175): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1164+1485delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355208 | |||||||
| chr18:12355210 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1164+1484T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355210 | |||||||
| chr18:12355227 | C | T | 3 | a0001c0002t0003g0326 a0001c0002t0003g0328 a0001c0002t0003g0329 |
3 | HG02145.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1164+1467G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355227 | |||||||
| chr18:12355292 | C | T | 2 | a0001c0003t0001g0333 a0001c0003t0001g0335 |
2 | NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1164+1402G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355292 | |||||||
| chr18:12355331 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0172 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1164+1363G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355331 | |||||||
| chr18:12355357 | C | T | 6 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0003g0336 others(3): Show |
6 | HG00438.hp2 HG02129.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+1337G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355357 | |||||||
| chr18:12355361 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(165): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1164+1333A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355361 | |||||||
| chr18:12355371 | G | A | 74 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0002g0049 others(71): Show |
81 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1164+1323C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355371 | |||||||
| chr18:12355385 | C | T | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1164+1309G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355385 | |||||||
| chr18:12355438 | G | A | 2 | a0001c0002t0003g0271 a0001c0002t0003g0330 |
2 | HG00733.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1164+1256C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355438 | |||||||
| chr18:12355652 | C | T | 2 | a0001c0002t0002g0039 a0001c0002t0002g0093 |
2 | HG00099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1164+1042G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355652 | |||||||
| chr18:12355673 | A | AT | 64 | a0001c0001t0001g0202 a0001c0001t0001g0226 a0001c0001t0001g0237 others(61): Show |
69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1164+1020dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355673 | |||||||
| chr18:12355693 | G | A | 4 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+1001C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355693 | |||||||
| chr18:12355732 | G | A | 24 | a0001c0003t0001g0317 a0001c0003t0002g0077 a0001c0003t0002g0078 others(21): Show |
26 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1164+962C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355732 | |||||||
| chr18:12356121 | C | CA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(174): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1164+572dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356121 | |||||||
| chr18:12356149 | C | CA | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1164+544dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356149 | |||||||
| chr18:12356153 | A | AT | 10 | a0001c0001t0001g0140 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
10 | HG02004.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1164+540dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356153 | |||||||
| chr18:12356153 | AT | A | 6 | a0001c0001t0001g0246 a0001c0001t0009g0107 a0001c0002t0001g0319 others(3): Show |
6 | HG00639.hp1 HG02165.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+540delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356153 | |||||||
| chr18:12356154 | T | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0003t0002g0078 others(4): Show |
7 | HG02145.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+540A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356154 | |||||||
| chr18:12356177 | C | T | 2 | a0001c0003t0001g0333 a0001c0003t0001g0335 |
2 | NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1164+517G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356177 | |||||||
| chr18:12356178 | G | A | 1 | a0001c0002t0003g0332 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1164+516C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356178 | |||||||
| chr18:12356241 | G | A | 6 | a0001c0001t0004g0101 a0001c0002t0003g0019 a0001c0002t0003g0276 others(3): Show |
7 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+453C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356241 | |||||||
| chr18:12356265 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1164+429G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356265 | |||||||
| chr18:12356300 | C | T | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+394G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356300 | |||||||
| chr18:12356372 | G | A | 2 | a0001c0002t0003g0273 a0001c0002t0003g0274 |
2 | NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1164+322C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356372 | |||||||
| chr18:12356442 | G | A | 6 | a0001c0003t0001g0317 a0001c0003t0004g0057 a0001c0003t0004g0058 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+252C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356442 | |||||||
| chr18:12356499 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1164+195C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356499 | |||||||
| chr18:12356559 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1164+135C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356559 | |||||||
| chr18:12356963 | T | G | 3 | a0001c0002t0003g0195 a0001c0002t0003g0196 a0001c0002t0003g0197 |
3 | NA18994.hp2 NA19009.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1027-132A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12356963 | |||||||
| chr18:12357056 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1027-225T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357056 | |||||||
| chr18:12357291 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(174): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1027-460T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357291 | |||||||
| chr18:12357498 | A | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0174 |
2 | NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1027-667T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357498 | |||||||
| chr18:12357548 | C | A | 3 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 |
3 | HG02145.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027-717G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357548 | |||||||
| chr18:12357622 | T | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-791A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357622 | |||||||
| chr18:12357772 | T | C | 1 | a0001c0002t0003g0311 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1026+898A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357772 | |||||||
| chr18:12357856 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1026+814G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357856 | |||||||
| chr18:12357890 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | NA18942.hp1 NA18998.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+780G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12357890 | |||||||
| chr18:12358020 | A | AAAT | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(198): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1026+647_1026+649d others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12358020 | |||||||
| chr18:12358029 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18959.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1026+641A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12358029 | |||||||
| chr18:12358318 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1026+352C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12358318 | |||||||
| chr18:12358481 | A | C | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1026+189T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12358481 | |||||||
| chr18:12358662 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0172 |
2 | HG01192.hp1 HG02280.hp1 |
splice_region_variant&intron_variant | LOW | c.1026+8G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 8/16 | chr18 | 12358662 | |||||||
| chr18:12358959 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.753-16C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12358959 | |||||||
| chr18:12358998 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(174): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.753-55T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12358998 | |||||||
| chr18:12359216 | A | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(171): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.753-273T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359216 | |||||||
| chr18:12359275 | A | G | 1 | a0001c0003t0002g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.753-332T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359275 | |||||||
| chr18:12359316 | G | A | 5 | a0001c0002t0003g0263 a0001c0002t0003g0264 a0001c0002t0003g0307 others(2): Show |
5 | HG02080.hp2 NA18977.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.753-373C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359316 | |||||||
| chr18:12359354 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.753-411T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359354 | |||||||
| chr18:12359574 | AC | A | 7 | a0001c0003t0002g0083 a0001c0003t0002g0084 a0001c0003t0002g0085 others(4): Show |
7 | HG01884.hp1 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.752+352delG | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359574 | |||||||
| chr18:12359697 | A | G | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.752+230T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359697 | |||||||
| chr18:12359757 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.752+170A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359757 | |||||||
| chr18:12359852 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.752+75A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359852 | |||||||
| chr18:12359921 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(170): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
splice_region_variant&intron_variant | LOW | c.752+6C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12359921 | |||||||
| chr18:12360187 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.628-136T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360187 | |||||||
| chr18:12360224 | T | C | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.628-173A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360224 | |||||||
| chr18:12360523 | T | C | 3 | a0001c0003t0005g0017 a0001c0003t0005g0018 a0001c0003t0008g0076 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-472A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360523 | |||||||
| chr18:12360600 | T | C | 2 | a0001c0003t0002g0088 a0001c0003t0002g0089 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.628-549A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360600 | |||||||
| chr18:12360603 | G | A | 1 | a0001c0002t0003g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.628-552C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360603 | |||||||
| chr18:12360707 | T | C | 4 | a0001c0002t0001g0321 a0001c0003t0001g0333 a0001c0003t0001g0334 others(1): Show |
4 | HG03486.hp1 NA18964.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-656A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360707 | |||||||
| chr18:12360977 | T | C | 1 | a0001c0002t0003g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.628-926A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360977 | |||||||
| chr18:12360989 | A | G | 1 | a0001c0002t0003g0280 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.628-938T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12360989 | |||||||
| chr18:12361015 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.628-964A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361015 | |||||||
| chr18:12361027 | T | C | 12 | a0001c0002t0003g0310 a0001c0003t0002g0078 a0001c0003t0002g0079 others(9): Show |
12 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.628-976A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361027 | |||||||
| chr18:12361117 | T | C | 2 | a0001c0001t0001g0198 a0001c0003t0002g0081 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.628-1066A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361117 | |||||||
| chr18:12361248 | T | C | 2 | a0001c0003t0004g0061 a0001c0003t0004g0064 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.628-1197A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361248 | |||||||
| chr18:12361376 | C | G | 5 | a0001c0002t0002g0096 a0001c0002t0002g0097 a0001c0002t0002g0098 others(2): Show |
5 | HG01167.hp1 HG02717.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1325G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361376 | |||||||
| chr18:12361382 | C | T | 1 | a0001c0002t0003g0279 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.628-1331G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361382 | |||||||
| chr18:12361387 | G | A | 1 | a0001c0002t0003g0298 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.628-1336C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361387 | |||||||
| chr18:12361449 | T | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(336): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.628-1398A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361449 | |||||||
| chr18:12361456 | G | C | 5 | a0001c0002t0002g0102 a0001c0002t0002g0103 a0001c0003t0001g0333 others(2): Show |
5 | HG02451.hp1 HG03579.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-1405C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361456 | |||||||
| chr18:12361509 | A | G | 14 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(11): Show |
16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.628-1458T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361509 | |||||||
| chr18:12361702 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.628-1651A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361702 | |||||||
| chr18:12361792 | T | C | 1 | a0001c0002t0002g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628-1741A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361792 | |||||||
| chr18:12361947 | C | T | 8 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG00140.hp2 HG00738.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+1835G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12361947 | |||||||
| chr18:12362113 | C | G | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.627+1669G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362113 | |||||||
| chr18:12362134 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.627+1648G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362134 | |||||||
| chr18:12362220 | C | T | 61 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0108 others(58): Show |
64 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.627+1562G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362220 | |||||||
| chr18:12362259 | C | A | 1 | a0001c0002t0003g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.627+1523G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362259 | |||||||
| chr18:12362303 | T | C | 7 | a0001c0003t0002g0083 a0001c0003t0002g0084 a0001c0003t0002g0085 others(4): Show |
7 | HG01884.hp1 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+1479A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362303 | |||||||
| chr18:12362724 | C | CTGACATG others(43): Show |
11 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(8): Show |
11 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+1008_627+1057d others(52): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362724 | |||||||
| chr18:12362745 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.627+1037A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362745 | |||||||
| chr18:12362953 | A | C | 135 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0004g0030 others(132): Show |
147 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.627+829T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362953 | |||||||
| chr18:12362965 | A | G | 11 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(8): Show |
11 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+817T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12362965 | |||||||
| chr18:12363114 | C | A | 1 | a0001c0002t0001g0320 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.627+668G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363114 | |||||||
| chr18:12363294 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.627+488C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363294 | |||||||
| chr18:12363382 | A | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0242 |
2 | HG01109.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.627+400T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363382 | |||||||
| chr18:12363595 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.627+187T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363595 | |||||||
| chr18:12363608 | A | G | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.627+174T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363608 | |||||||
| chr18:12363645 | T | C | 1 | a0001c0002t0002g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.627+137A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363645 | |||||||
| chr18:12363671 | G | A | 2 | a0001c0002t0003g0313 a0001c0002t0003g0314 |
2 | HG00735.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.627+111C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363671 | |||||||
| chr18:12363684 | C | T | 138 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0004g0030 others(135): Show |
150 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.627+98G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 6/16 | chr18 | 12363684 | |||||||
| chr18:12363890 | C | T | 2 | a0001c0002t0001g0320 a0001c0002t0001g0322 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.553-34G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12363890 | |||||||
| chr18:12363934 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.553-78T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12363934 | |||||||
| chr18:12363951 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.553-95G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12363951 | |||||||
| chr18:12364186 | C | A | 45 | a0001c0001t0004g0030 a0001c0002t0002g0004 a0001c0002t0002g0006 others(42): Show |
49 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.553-330G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364186 | |||||||
| chr18:12364234 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0184 |
2 | HG02155.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.553-378C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364234 | |||||||
| chr18:12364250 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0168 a0001c0001t0001g0182 others(1): Show |
4 | NA18939.hp1 NA18981.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-394C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364250 | |||||||
| chr18:12364321 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(192): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.553-465G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364321 | |||||||
| chr18:12364325 | T | C | 1 | a0001c0001t0004g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.553-469A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364325 | |||||||
| chr18:12364354 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.553-498G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364354 | |||||||
| chr18:12364791 | T | C | 1 | a0001c0002t0002g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.553-935A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364791 | |||||||
| chr18:12364858 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.553-1002A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12364858 | |||||||
| chr18:12365001 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.553-1145T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365001 | |||||||
| chr18:12365161 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.553-1305G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365161 | |||||||
| chr18:12365358 | G | A | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.553-1502C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365358 | |||||||
| chr18:12365367 | C | A | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.553-1511G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365367 | |||||||
| chr18:12365516 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(161): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.552+1449G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365516 | |||||||
| chr18:12365553 | T | G | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.552+1412A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365553 | |||||||
| chr18:12365571 | G | A | 1 | a0001c0002t0003g0340 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.552+1394C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365571 | |||||||
| chr18:12365871 | C | CT | 153 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0132 others(150): Show |
166 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.552+1093dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365871 | |||||||
| chr18:12365871 | C | CTT | 19 | a0001c0001t0002g0067 a0001c0001t0002g0095 a0001c0001t0004g0101 others(16): Show |
19 | HG01243.hp2 HG01884.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.552+1092_552+1093d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365871 | |||||||
| chr18:12365871 | C | CTTT | 7 | a0001c0002t0002g0024 a0001c0003t0002g0077 a0001c0003t0002g0078 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+1091_552+1093d others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365871 | |||||||
| chr18:12365944 | G | A | 1 | a0001c0003t0004g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.552+1021C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365944 | |||||||
| chr18:12365963 | C | T | 1 | a0001c0002t0003g0271 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.552+1002G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365963 | |||||||
| chr18:12365971 | T | A | 1 | a0001c0002t0003g0266 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.552+994A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365971 | |||||||
| chr18:12365975 | C | T | 4 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(1): Show |
4 | NA18942.hp2 NA18970.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+990G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12365975 | |||||||
| chr18:12366155 | C | T | 1 | a0001c0002t0003g0343 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.552+810G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366155 | |||||||
| chr18:12366172 | G | A | 16 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.552+793C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366172 | |||||||
| chr18:12366267 | G | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0171 |
2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.552+698C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366267 | |||||||
| chr18:12366427 | C | T | 2 | a0001c0002t0002g0023 a0001c0002t0002g0025 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.552+538G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366427 | |||||||
| chr18:12366611 | T | C | 177 | a0001c0001t0001g0277 a0001c0001t0001g0323 a0001c0001t0001g0327 others(174): Show |
189 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.552+354A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366611 | |||||||
| chr18:12366631 | G | C | 1 | a0001c0002t0003g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.552+334C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366631 | |||||||
| chr18:12366672 | C | T | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.552+293G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366672 | |||||||
| chr18:12366710 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.552+255A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366710 | |||||||
| chr18:12366886 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.552+79G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366886 | |||||||
| chr18:12366912 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.552+53A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366912 | |||||||
| chr18:12366938 | C | T | 16 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.552+27G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 5/16 | chr18 | 12366938 | |||||||
| chr18:12367443 | T | C | 79 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0002t0001g0338 others(76): Show |
86 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.293-61A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12367443 | |||||||
| chr18:12367607 | C | T | 16 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-225G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12367607 | |||||||
| chr18:12367659 | G | A | 4 | a0001c0002t0002g0027 a0001c0002t0002g0050 a0001c0002t0002g0051 others(1): Show |
4 | NA18990.hp1 NA19003.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-277C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12367659 | |||||||
| chr18:12367730 | C | A | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.293-348G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12367730 | |||||||
| chr18:12367896 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.293-514G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12367896 | |||||||
| chr18:12368076 | A | G | 11 | a0001c0001t0001g0323 a0001c0002t0001g0318 a0001c0002t0001g0319 others(8): Show |
11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-694T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368076 | |||||||
| chr18:12368099 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01978.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.293-717C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368099 | |||||||
| chr18:12368141 | T | C | 10 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-759A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368141 | |||||||
| chr18:12368145 | C | A | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.293-763G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368145 | |||||||
| chr18:12368214 | C | T | 2 | a0001c0002t0003g0276 a0001c0002t0003g0303 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.293-832G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368214 | |||||||
| chr18:12368323 | C | G | 10 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-941G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368323 | |||||||
| chr18:12368509 | T | C | 6 | a0001c0002t0002g0008 a0001c0002t0002g0068 a0001c0002t0002g0069 others(3): Show |
7 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-1127A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368509 | |||||||
| chr18:12368532 | T | C | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.293-1150A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368532 | |||||||
| chr18:12368762 | G | A | 4 | a0001c0002t0003g0299 a0001c0002t0003g0300 a0001c0002t0003g0301 others(1): Show |
4 | HG02132.hp2 NA18747.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-1380C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368762 | |||||||
| chr18:12368793 | G | A | 27 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(24): Show |
27 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-1411C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368793 | |||||||
| chr18:12368862 | A | C | 1 | a0001c0002t0002g0035 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.293-1480T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12368862 | |||||||
| chr18:12369027 | C | T | 8 | a0001c0001t0001g0323 a0001c0002t0001g0318 a0001c0002t0001g0319 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-1645G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369027 | |||||||
| chr18:12369129 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(278): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.292+1720T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369129 | |||||||
| chr18:12369177 | C | T | 3 | a0001c0001t0006g0206 a0001c0001t0006g0239 a0001c0001t0007g0020 |
3 | HG02055.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.292+1672G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369177 | |||||||
| chr18:12369234 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292+1615G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369234 | |||||||
| chr18:12369342 | T | C | 179 | a0001c0001t0001g0277 a0001c0001t0001g0323 a0001c0001t0001g0327 others(176): Show |
193 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.292+1507A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369342 | |||||||
| chr18:12369343 | G | A | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.292+1506C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369343 | |||||||
| chr18:12369365 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.292+1484A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369365 | |||||||
| chr18:12369368 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.292+1481G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369368 | |||||||
| chr18:12369396 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0130 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.292+1453T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369396 | |||||||
| chr18:12369409 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.292+1440G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369409 | |||||||
| chr18:12369692 | G | A | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.292+1157C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369692 | |||||||
| chr18:12369711 | C | CA | 11 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(8): Show |
11 | HG00741.hp1 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+1137dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369711 | |||||||
| chr18:12369727 | G | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.292+1122C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369727 | |||||||
| chr18:12369751 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.292+1098G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369751 | |||||||
| chr18:12369835 | T | C | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.292+1014A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369835 | |||||||
| chr18:12369892 | T | C | 1 | a0001c0002t0003g0332 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.292+957A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369892 | |||||||
| chr18:12369900 | CA | C | 166 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0002g0059 others(163): Show |
178 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.292+948delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12369900 | |||||||
| chr18:12370054 | C | CA | 49 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0171 others(46): Show |
49 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+794dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370054 | C | CAAA | 7 | a0001c0001t0002g0059 a0001c0001t0002g0067 a0001c0002t0002g0073 others(4): Show |
7 | HG02572.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+792_292+794dup others(3): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370054 | C | CAAAA | 37 | a0001c0001t0002g0063 a0001c0001t0002g0095 a0001c0001t0004g0030 others(34): Show |
42 | HG00099.hp1 HG00597.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+791_292+794dup others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370054 | C | CAAAAA | 21 | a0001c0002t0002g0026 a0001c0002t0002g0031 a0001c0002t0002g0032 others(18): Show |
21 | HG00423.hp2 HG00438.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+790_292+794dup others(5): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370054 | CA | C | 10 | a0001c0001t0004g0021 a0001c0002t0001g0318 a0001c0002t0001g0319 others(7): Show |
10 | HG02451.hp2 HG02572.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+794delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370054 | CAAAAAAA others(2): Show |
C | 16 | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0079 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+786_292+794del others(9): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370054 | |||||||
| chr18:12370133 | G | A | 138 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0004g0030 others(135): Show |
150 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.292+716C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370133 | |||||||
| chr18:12370153 | C | T | 1 | a0001c0002t0002g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.292+696G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370153 | |||||||
| chr18:12370170 | G | A | 3 | a0001c0002t0003g0268 a0001c0002t0003g0269 a0001c0002t0003g0270 |
3 | HG01261.hp2 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.292+679C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370170 | |||||||
| chr18:12370205 | C | T | 45 | a0001c0001t0004g0030 a0001c0002t0002g0004 a0001c0002t0002g0006 others(42): Show |
49 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.292+644G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370205 | |||||||
| chr18:12370221 | T | G | 4 | a0001c0002t0002g0097 a0001c0002t0002g0098 a0001c0002t0002g0099 others(1): Show |
4 | HG01167.hp1 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+628A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370221 | |||||||
| chr18:12370455 | A | G | 6 | a0001c0001t0004g0030 a0001c0002t0002g0028 a0001c0002t0002g0029 others(3): Show |
6 | HG01099.hp2 HG01346.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+394T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370455 | |||||||
| chr18:12370463 | C | CT | 7 | a0001c0001t0001g0128 a0001c0001t0001g0191 a0001c0001t0001g0205 others(4): Show |
7 | HG00140.hp2 HG02080.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+385dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370463 | |||||||
| chr18:12370472 | TTTTTTTT others(1): Show |
T | 18 | a0001c0002t0002g0027 a0001c0002t0002g0096 a0001c0003t0002g0077 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.292+369_292+376del others(8): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370472 | |||||||
| chr18:12370473 | TTTTTTTC | T | 54 | a0001c0001t0004g0030 a0001c0002t0002g0004 a0001c0002t0002g0006 others(51): Show |
59 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.292+369_292+375del others(7): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370473 | |||||||
| chr18:12370474 | TTTTTTC | T | 14 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(11): Show |
14 | HG01358.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.292+369_292+374del others(6): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370474 | |||||||
| chr18:12370477 | TTTC | T | 72 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0002t0001g0339 others(69): Show |
78 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.292+369_292+371del others(3): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370477 | |||||||
| chr18:12370478 | TTC | T | 6 | a0001c0002t0001g0338 a0001c0002t0003g0003 a0001c0002t0003g0110 others(3): Show |
6 | HG01952.hp1 HG01981.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+369_292+370del others(2): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370478 | |||||||
| chr18:12370479 | T | C | 2 | a0001c0003t0005g0017 a0001c0003t0005g0018 |
4 | HG01167.hp2 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+370A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370479 | |||||||
| chr18:12370480 | C | T | 14 | a0001c0001t0001g0323 a0001c0001t0004g0101 a0001c0002t0001g0318 others(11): Show |
16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+369G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370480 | |||||||
| chr18:12370490 | T | A | 1 | a0001c0002t0003g0311 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.292+359A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370490 | |||||||
| chr18:12370755 | G | A | 10 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+94C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 3/16 | chr18 | 12370755 | |||||||
| chr18:12370931 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp2 | splice_region_variant&intron_variant | LOW | c.215-5A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12370931 | |||||||
| chr18:12371008 | T | C | 2 | a0001c0003t0005g0017 a0001c0003t0005g0018 |
4 | HG01167.hp2 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-82A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371008 | |||||||
| chr18:12371039 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0244 |
2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.215-113C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371039 | |||||||
| chr18:12371141 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.215-215G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371141 | |||||||
| chr18:12371221 | G | A | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.215-295C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371221 | |||||||
| chr18:12371245 | C | T | 2 | a0001c0002t0003g0273 a0001c0002t0003g0274 |
2 | NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.215-319G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371245 | |||||||
| chr18:12371259 | C | A | 166 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0002g0059 others(163): Show |
178 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.214+333G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371259 | |||||||
| chr18:12371292 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(20): Show |
30 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+300G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371292 | |||||||
| chr18:12371315 | C | CA | 16 | a0001c0001t0001g0108 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00544.hp1 HG01167.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+276dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371315 | |||||||
| chr18:12371340 | T | A | 1 | a0001c0003t0002g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214+252A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371340 | |||||||
| chr18:12371559 | T | C | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.214+33A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 2/16 | chr18 | 12371559 | |||||||
| chr18:12371741 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.115-50A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12371741 | |||||||
| chr18:12371753 | C | A | 3 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0025 |
3 | HG02572.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.115-62G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12371753 | |||||||
| chr18:12371883 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-192C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12371883 | |||||||
| chr18:12371955 | A | T | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.115-264T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12371955 | |||||||
| chr18:12372001 | G | C | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.115-310C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372001 | |||||||
| chr18:12372068 | G | A | 1 | a0001c0002t0002g0066 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.115-377C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372068 | |||||||
| chr18:12372194 | C | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0073 |
2 | NA18941.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.115-503G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372194 | |||||||
| chr18:12372211 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.115-520C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372211 | |||||||
| chr18:12372215 | T | C | 179 | a0001c0001t0001g0277 a0001c0001t0001g0323 a0001c0001t0001g0327 others(176): Show |
193 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.115-524A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372215 | |||||||
| chr18:12372404 | T | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0095 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.115-713A>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372404 | |||||||
| chr18:12372413 | C | A | 1 | a0001c0002t0001g0324 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115-722G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372413 | |||||||
| chr18:12372739 | T | C | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.115-1048A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372739 | |||||||
| chr18:12372777 | A | G | 8 | a0001c0001t0001g0323 a0001c0002t0001g0318 a0001c0002t0001g0319 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-1086T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372777 | |||||||
| chr18:12372908 | A | C | 4 | a0001c0001t0001g0327 a0001c0002t0003g0326 a0001c0002t0003g0328 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-1217T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372908 | |||||||
| chr18:12372915 | G | T | 2 | a0001c0002t0003g0272 a0001c0002t0003g0325 |
2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.115-1224C>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12372915 | |||||||
| chr18:12373065 | A | C | 1 | a0002c0004t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.115-1374T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373065 | |||||||
| chr18:12373224 | C | G | 1 | a0001c0002t0003g0271 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.115-1533G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373224 | |||||||
| chr18:12373315 | G | C | 2 | a0001c0002t0003g0313 a0001c0002t0003g0314 |
2 | HG00735.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.115-1624C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373315 | |||||||
| chr18:12373470 | G | A | 1 | a0001c0002t0003g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.115-1779C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373470 | |||||||
| chr18:12373530 | G | A | 1 | a0001c0002t0003g0315 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.115-1839C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373530 | |||||||
| chr18:12373533 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.115-1842A>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373533 | |||||||
| chr18:12373657 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115-1966G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373657 | |||||||
| chr18:12373888 | C | G | 3 | a0001c0002t0003g0268 a0001c0002t0003g0269 a0001c0002t0003g0270 |
3 | HG01261.hp2 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.115-2197G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373888 | |||||||
| chr18:12373926 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115-2235T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373926 | |||||||
| chr18:12373936 | G | A | 6 | a0001c0002t0002g0008 a0001c0002t0002g0068 a0001c0002t0002g0069 others(3): Show |
7 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-2245C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12373936 | |||||||
| chr18:12374248 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-2557T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374248 | |||||||
| chr18:12374363 | A | T | 166 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0002g0059 others(163): Show |
178 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.114+2606T>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374363 | |||||||
| chr18:12374431 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114+2538G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374431 | |||||||
| chr18:12374548 | T | C | 3 | a0001c0003t0001g0333 a0001c0003t0001g0334 a0001c0003t0001g0335 |
3 | NA18964.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.114+2421A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374548 | |||||||
| chr18:12374647 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114+2322G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374647 | |||||||
| chr18:12374684 | C | A | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+2285G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374684 | |||||||
| chr18:12374716 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.114+2253C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374716 | |||||||
| chr18:12374733 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114+2236C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374733 | |||||||
| chr18:12374824 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+2145C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374824 | |||||||
| chr18:12374826 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+2143G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374826 | |||||||
| chr18:12374924 | C | T | 166 | a0001c0001t0001g0277 a0001c0001t0001g0327 a0001c0001t0002g0059 others(163): Show |
178 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.114+2045G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12374924 | |||||||
| chr18:12375042 | C | T | 4 | a0001c0002t0003g0265 a0001c0002t0003g0266 a0001c0002t0003g0267 others(1): Show |
4 | HG02523.hp1 NA18975.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1927G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375042 | |||||||
| chr18:12375055 | C | CA | 13 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(10): Show |
13 | HG00621.hp1 HG01884.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.114+1913dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375055 | |||||||
| chr18:12375055 | CA | C | 5 | a0001c0001t0001g0111 a0001c0001t0004g0021 a0001c0002t0002g0100 others(2): Show |
7 | HG01167.hp2 HG01169.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+1913delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375055 | |||||||
| chr18:12375055 | CAA | C | 160 | a0001c0001t0001g0201 a0001c0001t0001g0277 a0001c0001t0001g0327 others(157): Show |
172 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.114+1912_114+1913d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375055 | |||||||
| chr18:12375128 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.114+1841G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375128 | |||||||
| chr18:12375258 | T | C | 166 | a0001c0001t0001g0012 a0001c0001t0001g0133 a0001c0001t0001g0139 others(163): Show |
179 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.114+1711A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375258 | |||||||
| chr18:12375259 | C | CT | 9 | a0001c0001t0001g0109 a0001c0002t0002g0023 a0001c0002t0002g0024 others(6): Show |
9 | HG02572.hp2 HG02683.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+1709dupA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375259 | |||||||
| chr18:12375260 | T | C | 1 | a0001c0002t0002g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.114+1709A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375260 | |||||||
| chr18:12375411 | G | GA | 98 | a0001c0001t0001g0193 a0001c0001t0001g0261 a0001c0001t0001g0277 others(95): Show |
105 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+1557dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375411 | |||||||
| chr18:12375411 | G | GAA | 11 | a0001c0001t0001g0327 a0001c0002t0003g0325 a0001c0002t0003g0326 others(8): Show |
11 | HG01123.hp1 HG01243.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1556_114+1557d others(4): Show |
AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375411 | |||||||
| chr18:12375428 | C | A | 6 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0001c0002t0003g0336 others(3): Show |
6 | HG00438.hp2 HG02129.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1541G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375428 | |||||||
| chr18:12375430 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+1539T>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375430 | |||||||
| chr18:12375449 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114+1520A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375449 | |||||||
| chr18:12375614 | T | C | 180 | a0001c0001t0001g0277 a0001c0001t0001g0323 a0001c0001t0001g0327 others(177): Show |
194 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.114+1355A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375614 | |||||||
| chr18:12375743 | C | T | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.114+1226G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375743 | |||||||
| chr18:12375800 | G | C | 5 | a0001c0002t0002g0096 a0001c0002t0002g0097 a0001c0002t0002g0098 others(2): Show |
5 | HG01167.hp1 HG02717.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+1169C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375800 | |||||||
| chr18:12375821 | G | A | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.114+1148C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375821 | |||||||
| chr18:12375824 | C | T | 3 | a0001c0002t0003g0195 a0001c0002t0003g0196 a0001c0002t0003g0197 |
3 | NA18994.hp2 NA19009.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.114+1145G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375824 | |||||||
| chr18:12375872 | C | G | 90 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0067 others(87): Show |
95 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.114+1097G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375872 | |||||||
| chr18:12375950 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+1019G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375950 | |||||||
| chr18:12375951 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+1018C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12375951 | |||||||
| chr18:12376055 | T | C | 1 | a0001c0001t0004g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114+914A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376055 | |||||||
| chr18:12376202 | T | C | 2 | a0001c0002t0002g0102 a0001c0002t0002g0103 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.114+767A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376202 | |||||||
| chr18:12376223 | C | T | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+746G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376223 | |||||||
| chr18:12376336 | C | T | 1 | a0001c0002t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.114+633G>A | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376336 | |||||||
| chr18:12376432 | C | A | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | NA18944.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.114+537G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376432 | |||||||
| chr18:12376433 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.114+536G>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376433 | |||||||
| chr18:12376440 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.114+529C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376440 | |||||||
| chr18:12376483 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.114+486T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376483 | |||||||
| chr18:12376662 | G | A | 1 | a0003c0006t0002g0106 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.114+307C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376662 | |||||||
| chr18:12376671 | G | A | 2 | a0001c0002t0003g0343 a0001c0002t0003g0344 |
2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.114+298C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376671 | |||||||
| chr18:12376695 | A | G | 1 | a0001c0001t0004g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+274T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376695 | |||||||
| chr18:12376757 | C | A | 1 | a0001c0001t0001g0345 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+212G>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376757 | |||||||
| chr18:12376934 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.114+35C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376934 |