Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 | copy fasta | chr18 | 12323944 | 12382227 |
| a0002 | 0/0 | 797 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0003 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2394 | 186 | 36 | 44 | 70 | 11 | 24 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0002 | 1/0 | 2394 | 155 | 30 | 32 | 81 | 3 | 8 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0003 | 0/0 | 2394 | 30 | 24 | 2 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0004 | 0/0 | 2394 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0005 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0006 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| c0007 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 767 | 191 | 34 | 42 | 74 | 11 | 28 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0002 | 0/0 | 767 | 85 | 36 | 9 | 35 | 1 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0003 | 0/0 | 767 | 82 | 7 | 23 | 46 | 2 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0004 | 0/0 | 767 | 9 | 7 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0005 | 0/0 | 767 | 4 | 2 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0006 | 0/0 | 767 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0007 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0008 | 0/0 | 767 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| t0009 | 0/0 | 767 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2394 | 186 | 36 | 44 | 70 | 11 | 24 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0002 | 1/0 | 2394 | 155 | 30 | 32 | 81 | 3 | 8 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003 | 0/0 | 2394 | 30 | 24 | 2 | 4 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0005 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0007 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0002c0004 | 0/0 | 2394 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0003c0006 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | 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 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0001t0002 | 0/0 | 3160 | 4 | 4 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0001t0004 | 0/0 | 3160 | 4 | 2 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0001t0006 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0001t0007 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0001t0009 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0002t0001 | 1/0 | 3160 | 9 | 6 | 0 | 2 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0002t0002 | 0/0 | 3160 | 65 | 17 | 9 | 34 | 1 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0002t0003 | 0/0 | 3160 | 81 | 7 | 23 | 45 | 2 | 4 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0001 | 0/0 | 3160 | 4 | 1 | 0 | 3 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0002 | 0/0 | 3160 | 15 | 15 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0003 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0004 | 0/0 | 3160 | 5 | 5 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0005 | 0/0 | 3160 | 4 | 2 | 2 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0003t0008 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0005t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0001c0007t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0002c0004t0001 | 0/0 | 3160 | 2 | 0 | 0 | 0 | 0 | 2 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | chr18 | 12323944 | 12382227 |
| a0003c0006t0002 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | copy fasta | 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 |
| a0001c0001t0001g0004 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0001t0001g0347 | 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 |
| a0001c0001t0006g0238 | 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 |
| a0001c0002t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0003 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0003g0005 | 0/0 | 3 | 0 | 2 | 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 |
| a0001c0002t0003g0185 | 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 |
| 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 | 0 | 0 | 1 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0277 | 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 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0335 | 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 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0002t0003g0342 | 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 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0003t0002g0093 | 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 |
| a0001c0003t0003g0306 | 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 |
| a0001c0003t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| a0001c0005t0001g0170 | 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 | g0038 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0185 | 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 | g0159 | 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 | g0053 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0342 | 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 | g0172 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0295 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0303 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0033 | 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 | g0013 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0319 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | CHS | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0279 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | 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 | g0322 | 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 | g0312 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0242 | 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 | g0184 | 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 | g0246 | 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 | g0152 | 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 | g0153 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0314 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0096 | 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 | g0313 | 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 | g0286 | 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 | g0150 | 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 | g0192 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0301 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0288 | 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 | g0168 | 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 | g0297 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0277 | 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 | g0278 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0027 | 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 | g0346 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0289 | 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 | g0155 | 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 | g0088 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0080 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0079 | 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 | g0048 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0283 | 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 | g0186 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0156 | 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 | g0334 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | 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 | g0300 | AMR | PEL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0318 | 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 | g0298 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0165 | 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 | g0252 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0293 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0046 | 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 | g0284 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0338 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0311 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0083 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0330 | 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 | g0290 | 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 | g0308 | EAS | CDX | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0317 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0190 | 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 | g0268 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0274 | EAS | KHV | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0336 | 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 | g0142 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0235 | 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 | g0258 | 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 | g0082 | 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 | g0145 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0151 | 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 | g0071 | 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 | g0332 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0329 | 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 | g0333 | 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 | g0257 | 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 | g0072 | 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 | g0253 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0254 | 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 | g0099 | 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 | g0244 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0084 | 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 | g0247 | AFR | GWD | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0272 | 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 | g0090 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0266 | 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 | g0087 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0089 | 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 | g0267 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0191 | 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 | g0092 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0086 | 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 | g0307 | 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 | g0098 | 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 | g0238 | 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 | g0236 | SAS | PJL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0045 | 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 | g0176 | 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 | g0280 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0043 | 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 | g0170 | 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 | g0173 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0078 | 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 | g0180 | SAS | STU | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0291 | 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 | g0085 | 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 | g0337 | 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 | g0309 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0248 | 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 | g0316 | 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 | g0304 | 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 | g0118 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0105 | 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 | g0321 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0285 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0245 | 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 | g0260 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0034 | 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 | g0012 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | 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 | g0003 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0327 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0039 | 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 | g0012 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0344 | 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 | g0047 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0143 | 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 | g0175 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0292 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0306 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0325 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0005 | 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 | g0305 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0273 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0324 | 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 | g0136 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0310 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0177 | 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 | g0164 | 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 | g0179 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0183 | 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 | g0093 | 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 | g0036 | 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 | g0188 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0302 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0326 | 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 | g0178 | 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 | g0161 | 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 | g0299 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0134 | 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 | g0037 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0328 | 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 | g0296 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0081 | AFR | YRI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0341 | AFR | ASW | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0097 | 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 | g0276 | 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 | g0154 | EUR | TSI | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0335 | 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 | g0271 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0315 | AFR | ACB | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0250 | 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 | g0091 | AFR | MSL | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0243 | 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 | g0147 | EAS | JPT | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0323 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0265 | AFR | USA | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0157 | 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 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0237 | REF | REF | AFG3L2_chr18_12323944_12382227 | AFG3L2 | chr18 | 12323944 | 12382227 |
| 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 |
| 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 | a0001c0001a0001c0003a0001c0005others(2): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): 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 | a0001c0001a0001c0005a0001c0007others(1): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): 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 |
| 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 | a0001c0003t0005a0001c0003t0008 | 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 | a0001c0001t0006a0001c0001t0007 | 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 | a0001c0001t0002a0001c0002t0002a0001c0002t0003others(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 | a0001c0003t0005a0001c0003t0008 | 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 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(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 |
| 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 | 70 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0002t0002g0097others(67): 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | a0001c0002t0003g0323 | 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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(168): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(158): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2176-552dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12330334 | ||||||
| chr18:12330334
|
C | CAA | 6 | a0001c0001t0001g0175a0001c0001t0001g0221a0001c0001t0001g0229others(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 | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(164): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): 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 | a0001c0001t0001g0112a0001c0001t0001g0169a0001c0001t0001g0200others(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 | 159 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(156): 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 | 66 | a0001c0002t0002g0048a0001c0002t0003g0002a0001c0002t0003g0005others(63): 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 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0231others(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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(337): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): 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 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0239others(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 | a0001c0002t0002g0036 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0010a0001c0001t0001g0130 | 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 | 298 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(295): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0002t0002g0008a0001c0002t0002g0068a0001c0002t0002g0069others(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 | a0001c0002t0003g0294 | 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 | a0001c0003t0001g0326 | 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 | a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0001g0268a0001c0002t0001g0269 | 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 | a0001c0002t0002g0052 | 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 | a0001c0002t0002g0046a0001c0003t0002g0080a0001c0003t0002g0093others(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 | 150 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(147): 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 | a0001c0002t0003g0290 | 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 | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(167): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): 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 | a0001c0003t0001g0265 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0150a0001c0001t0001g0153 | 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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(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 | 128 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(125): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): 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 | a0001c0001t0001g0159a0001c0001t0001g0241a0001c0002t0002g0006others(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 | a0001c0002t0002g0097a0001c0002t0002g0098a0001c0002t0002g0099others(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 | a0001c0002t0002g0008a0001c0002t0002g0068a0001c0002t0002g0069others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(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 | a0001c0001t0001g0242a0001c0002t0003g0274a0001c0002t0003g0290others(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 | 34 | a0001c0001t0001g0119a0001c0001t0001g0139a0001c0001t0001g0149others(31): Show | 36 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.2176-2901delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332683 | ||||||
| chr18:12332684
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(299): 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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098 | 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 | a0001c0001t0001g0203a0001c0001t0001g0232 | 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 | 55 | a0001c0002t0002g0048a0001c0002t0003g0002a0001c0002t0003g0005others(52): 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 | a0001c0002t0003g0185a0001c0002t0003g0281a0001c0002t0003g0282others(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 | 198 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): 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 | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2176-3083C>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12332866 | ||||||
| chr18:12332867
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): 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 |
128 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): 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 | a0001c0001t0001g0235a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230others(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 | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(271): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): 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 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0161others(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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | 73 | a0001c0001t0001g0111a0001c0002t0002g0048a0001c0002t0002g0096others(70): 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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | 70 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0002t0002g0097others(67): 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 | 130 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(127): 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 | a0001c0001t0001g0146a0001c0001t0001g0188a0001c0001t0001g0251others(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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0001g0255 | 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 | 14 | a0001c0001t0001g0112a0001c0001t0001g0146a0001c0001t0001g0149others(11): Show | 14 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(11): 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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(249): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): 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 | a0001c0001t0004g0101a0001c0003t0001g0326a0001c0003t0001g0327others(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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0341others(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 | 72 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0002t0002g0097others(69): 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 | a0001c0001t0001g0166 | 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 | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.2176-3586A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12333369 | ||||||
| chr18:12333370
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(171): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): 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 | 72 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0002t0002g0097others(69): 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 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(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 | a0001c0002t0003g0309 | 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 | 70 | a0001c0002t0002g0048a0001c0002t0002g0096a0001c0002t0002g0097others(67): 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 | a0001c0002t0002g0003a0001c0002t0002g0026a0001c0002t0002g0027others(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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0001g0161 | 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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | 330 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(327): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(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 | a0001c0002t0003g0315a0001c0002t0003g0319a0001c0002t0003g0338others(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 | a0001c0002t0001g0269 | 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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0216a0001c0001t0001g0217 | 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): 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 | a0001c0003t0001g0328 | 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 | 158 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(155): 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 | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2175+1293T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 16/16 | chr18 | 12336048 | ||||||
| chr18:12336057
|
C | T | 330 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(327): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0003t0002g0086a0001c0003t0002g0087a0001c0003t0002g0088others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | a0001c0002t0003g0263a0001c0002t0003g0264a0001c0002t0003g0344others(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 | a0001c0001t0001g0258 | 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 | a0001c0002t0002g0048a0001c0002t0003g0019a0001c0002t0003g0195others(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 | a0001c0002t0003g0315a0001c0002t0003g0319a0001c0002t0003g0338others(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 | a0001c0001t0001g0187 | 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 | 12 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150others(9): Show | 12 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(9): 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 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0257 | 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 | a0001c0002t0003g0311 | 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 | a0001c0002t0003g0322 | 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 | a0001c0001t0001g0243 | 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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(337): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): 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 | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): 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 | a0001c0001t0004g0101a0001c0003t0001g0326a0001c0003t0001g0327others(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 | a0001c0001t0001g0010a0001c0001t0001g0130a0001c0001t0001g0131others(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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0002t0002g0003a0001c0002t0002g0026a0001c0002t0002g0027others(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 | a0001c0002t0002g0041a0001c0002t0002g0044 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0259a0001c0002t0001g0268a0001c0002t0002g0026others(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 | 28 | a0001c0002t0002g0033a0001c0002t0002g0098a0001c0002t0002g0103others(25): 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 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0130others(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 | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(117): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | a0001c0002t0003g0290 | 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 | a0001c0002t0003g0299 | 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 | 98 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0150others(95): Show | 106 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1980+648dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339552 | ||||||
| chr18:12339552
|
C | CAA | 8 | a0001c0001t0001g0259a0001c0002t0002g0062a0001c0002t0003g0197others(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 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(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 | a0001c0001t0001g0249a0001c0001t0001g0252a0001c0001t0001g0343others(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 | a0001c0002t0003g0322a0001c0002t0003g0323 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0003t0002g0086 | 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 | a0001c0002t0001g0270a0001c0002t0002g0032a0001c0002t0002g0068others(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 | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(222): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1980+352delT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 15/16 | chr18 | 12339848 | ||||||
| chr18:12339968
|
C | T | 66 | a0001c0002t0002g0048a0001c0002t0003g0002a0001c0002t0003g0005others(63): 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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(337): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1780-196delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340596 | ||||||
| chr18:12340627
|
G | A | 4 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0055others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0004g0101a0001c0002t0001g0337a0001c0002t0001g0340others(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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1780-519delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 14/16 | chr18 | 12340919 | ||||||
| chr18:12340937
|
A | G | 3 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0003g0273a0001c0002t0003g0325 | 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 | a0001c0002t0003g0289 | 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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(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 | 13 | a0001c0002t0003g0002a0001c0002t0003g0005a0001c0002t0003g0110others(10): 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 | 332 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(329): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): 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 | a0001c0002t0003g0312 | 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 | a0001c0001t0001g0242 | 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 | a0001c0002t0002g0071 | 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): 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 | a0001c0001t0001g0004a0001c0001t0001g0198a0001c0001t0001g0211others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0001t0001g0250 | 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 | 158 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(155): 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 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230 | 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 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0230 | 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 | a0001c0001t0004g0021a0001c0003t0001g0265a0001c0003t0004g0057others(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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(180): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): 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 | a0001c0002t0003g0341 | 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 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0221others(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 | a0001c0001t0004g0101a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0002t0002g0039 | 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 | a0001c0002t0002g0039 | 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 | a0001c0002t0002g0033 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0147 | 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 | a0001c0002t0003g0293 | 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 | a0001c0001t0007g0020a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0001t0001g0250 | 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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0003t0002g0087a0001c0003t0002g0089 | 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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0003g0315others(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 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0002t0003g0323 | 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 | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(198): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): 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 | a0001c0001t0004g0021a0001c0003t0002g0080a0001c0003t0002g0093others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(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 | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(174): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): 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 | a0001c0002t0003g0279a0001c0002t0003g0335 | 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 | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(274): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1664-1627T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12345874 | ||||||
| chr18:12345878
|
G | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(274): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0002t0003g0185 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0175 | 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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(172): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): 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 | a0001c0001t0001g0180 | 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 | 127 | a0001c0001t0001g0109a0001c0001t0001g0121a0001c0001t0001g0129others(124): 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 | 189 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(186): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): 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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0001c0002t0003g0330a0001c0002t0003g0332a0001c0002t0003g0333 | 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 | a0001c0001t0001g0148 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(167): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1663+720A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347553 | ||||||
| chr18:12347553
|
TA | T | 69 | a0001c0001t0004g0101a0001c0002t0001g0337a0001c0002t0001g0340others(66): 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 | a0001c0002t0003g0307a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0002t0003g0196a0001c0002t0003g0324 | 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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(175): Show | 192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1663+718delA | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 13/16 | chr18 | 12347554 | ||||||
| chr18:12347614
|
G | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(199): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0060others(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 | 73 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0002g0048others(70): 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083others(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 | a0001c0002t0001g0270 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | a0001c0002t0002g0007a0001c0002t0002g0034a0001c0002t0002g0040others(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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(167): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): 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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(167): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): 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 | a0001c0002t0003g0288 | 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 | a0001c0001t0001g0111a0001c0002t0002g0049a0001c0003t0004g0061others(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 | a0001c0001t0001g0271a0001c0001t0001g0331a0001c0001t0006g0206others(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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0002t0002g0033 | 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 | a0001c0003t0001g0326a0001c0003t0001g0328 | 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 | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(171): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): 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 | a0001c0003t0001g0265a0001c0003t0002g0080a0001c0003t0002g0081others(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 | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(198): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): 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 | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(274): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): 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 | a0001c0002t0003g0322 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0142 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0141others(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 | a0001c0001t0001g0121a0001c0001t0001g0140a0001c0001t0009g0107 | 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 | a0001c0001t0001g0163 | 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 | 75 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0002g0048others(72): 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 | a0001c0001t0001g0246 | 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 | a0001c0003t0002g0086a0001c0003t0002g0087a0001c0003t0002g0088others(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 | a0001c0001t0001g0153 | 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 | a0001c0002t0002g0070 | 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 | a0001c0002t0001g0269 | 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0002t0002g0006a0001c0002t0002g0043 | 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 | a0001c0001t0001g0218a0001c0001t0001g0245 | 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 | a0001c0001t0001g0198a0001c0001t0001g0243 | 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 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(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 | a0001c0001t0001g0287 | 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 | a0001c0002t0003g0292 | 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 | 60 | a0001c0002t0002g0048a0001c0002t0003g0002a0001c0002t0003g0005others(57): 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | 77 | a0001c0001t0001g0182a0001c0001t0001g0212a0001c0002t0002g0038others(74): 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 | a0001c0002t0002g0022a0001c0002t0002g0078a0001c0002t0003g0110others(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 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0003g0338others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(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 | a0001c0001t0001g0010a0001c0001t0001g0130a0001c0001t0001g0131others(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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(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 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(337): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): 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 | a0001c0001t0004g0101a0001c0002t0001g0266a0001c0002t0001g0267others(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 | 73 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0002g0048others(70): 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 | a0001c0003t0008g0079 | 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 | a0001c0003t0005g0017a0001c0003t0005g0018 | 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 | a0001c0001t0001g0013a0001c0001t0001g0209a0001c0001t0001g0210others(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 | a0001c0001t0001g0112a0001c0001t0001g0169 | 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 | 76 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0002g0048others(73): 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 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(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 | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(127): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(165): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): 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 | a0001c0001t0001g0112a0001c0001t0001g0169 | 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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(199): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): 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 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0001t0001g0130others(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 | a0001c0002t0001g0268 | 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 | a0001c0002t0002g0037 | 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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0003t0002g0080a0001c0003t0002g0093a0001c0003t0002g0094 | 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 | a0001c0003t0002g0080a0001c0003t0002g0093 | 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 | a0001c0003t0001g0327 | 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 | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(176): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): 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 | a0001c0002t0003g0330a0001c0002t0003g0332a0001c0002t0003g0333 | 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 | a0001c0003t0001g0326a0001c0003t0001g0328 | 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 | a0001c0001t0001g0190a0001c0001t0001g0192 | 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 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0003g0338others(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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(166): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1164+1333A>G | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355361 | ||||||
| chr18:12355371
|
G | A | 75 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0002g0048others(72): 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 | a0001c0002t0003g0279a0001c0002t0003g0335 | 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 | a0001c0002t0002g0038a0001c0002t0002g0078 | 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 | a0001c0001t0001g0202a0001c0001t0001g0226a0001c0001t0001g0236others(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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(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 | ||||||
| chr18:12355713
|
A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(343): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1164+981T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12355713 | ||||||
| chr18:12355732
|
G | A | 24 | a0001c0003t0001g0265a0001c0003t0002g0080a0001c0003t0002g0081others(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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(175): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1164+572dupT | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 9/16 | chr18 | 12356121 | ||||||
| chr18:12356149
|
C | CA | 3 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0138a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0245a0001c0001t0009g0107a0001c0002t0001g0267others(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 | a0001c0001t0001g0122a0001c0001t0001g0182a0001c0003t0002g0081others(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 | a0001c0003t0001g0326a0001c0003t0001g0328 | 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 | a0001c0002t0003g0334 | 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 | a0001c0001t0004g0101a0001c0002t0003g0019a0001c0002t0003g0286others(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 | a0001c0001t0001g0191 | 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0002t0003g0281a0001c0002t0003g0282 | 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 | a0001c0003t0001g0265a0001c0003t0004g0057a0001c0003t0004g0058others(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 | a0001c0002t0003g0195a0001c0002t0003g0196a0001c0002t0003g0197 | 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 | a0001c0001t0001g0255 | 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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(175): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): 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 | a0001c0001t0001g0137a0001c0001t0001g0171 | 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 | a0001c0003t0002g0081a0001c0003t0002g0082a0001c0003t0002g0083 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(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 | a0001c0002t0003g0320 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0111a0001c0001t0001g0133a0001c0001t0001g0134others(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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(199): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): 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 | a0001c0001t0001g0123a0001c0001t0001g0124 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0190a0001c0001t0001g0192 | 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 | a0001c0001t0001g0183 | 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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(175): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.753-55T>C | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 7/16 | chr18 | 12358998 | ||||||
| chr18:12359216
|
A | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(172): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): 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 | a0001c0003t0002g0081 | 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 | a0001c0002t0003g0263a0001c0002t0003g0264a0001c0002t0003g0284others(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 | a0001c0003t0002g0086a0001c0003t0002g0087a0001c0003t0002g0088others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0154a0001c0001t0001g0155 | 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 | a0001c0001t0001g0243 | 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 | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(171): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): 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 | a0001c0001t0001g0158 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0003t0005g0017a0001c0003t0005g0018a0001c0003t0008g0079 | 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 | a0001c0003t0002g0091a0001c0003t0002g0092 | 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 | a0001c0002t0003g0307 | 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 | a0001c0002t0001g0269a0001c0003t0001g0326a0001c0003t0001g0327others(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 | a0001c0002t0003g0332 | 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 | a0001c0002t0003g0290 | 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 | a0001c0002t0003g0319a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0001t0001g0198a0001c0003t0002g0084 | 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 | a0001c0003t0004g0061a0001c0003t0004g0064 | 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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(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 | a0001c0002t0003g0289 | 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 | a0001c0002t0003g0308 | 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 | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): 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 | a0001c0002t0002g0102a0001c0002t0002g0103a0001c0003t0001g0326others(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 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0205a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0108others(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 | a0001c0002t0003g0333 | 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 | a0001c0003t0002g0086a0001c0003t0002g0087a0001c0003t0002g0088others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0001g0179 | 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 | 136 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0004g0030others(133): 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0002t0001g0268 | 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 | a0001c0001t0001g0220a0001c0001t0001g0241 | 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 | a0001c0001t0001g0240 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0002g0054 | 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 | a0001c0002t0003g0322a0001c0002t0003g0323 | 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 | 139 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0004g0030others(136): 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 | a0001c0002t0001g0268a0001c0002t0001g0270 | 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 | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(196): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): 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 | a0001c0001t0004g0030a0001c0002t0002g0003a0001c0002t0002g0006others(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 | a0001c0001t0001g0127a0001c0001t0001g0181 | 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 | a0001c0001t0001g0109a0001c0001t0001g0166a0001c0001t0001g0179others(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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(193): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): 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 | a0001c0001t0001g0176 | 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(162): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): 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 | a0001c0002t0003g0341 | 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 | 154 | a0001c0001t0001g0011a0001c0001t0001g0131a0001c0001t0001g0132others(151): 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 | a0001c0001t0002g0067a0001c0001t0002g0095a0001c0001t0004g0101others(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 | a0001c0002t0002g0024a0001c0003t0002g0080a0001c0003t0002g0081others(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 | a0001c0002t0003g0279 | 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 | a0001c0002t0003g0274 | 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 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(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 | a0001c0002t0003g0344 | 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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0001t0001g0112a0001c0001t0001g0169 | 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 | a0001c0002t0002g0023a0001c0002t0002g0025 | 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 | 178 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0001g0331others(175): 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 | a0001c0002t0003g0311 | 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | a0001c0001t0001g0287 | 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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | 80 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0002t0001g0337others(77): 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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0055others(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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | a0001c0001t0001g0271a0001c0002t0001g0266a0001c0002t0001g0267others(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 | a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0002t0003g0286a0001c0002t0003g0313 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0002t0002g0008a0001c0002t0002g0068a0001c0002t0002g0069others(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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | a0001c0002t0003g0309a0001c0002t0003g0310a0001c0002t0003g0311others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0002t0002g0034 | 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 | a0001c0001t0001g0271a0001c0002t0001g0266a0001c0002t0001g0267others(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 | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(280): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0006g0206a0001c0001t0006g0238a0001c0001t0007g0020 | 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 | a0001c0001t0001g0343 | 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 | 180 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0001g0331others(177): 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 | a0001c0001t0001g0167a0001c0001t0001g0168 | 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 | a0001c0001t0001g0010a0001c0001t0001g0130 | 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0003g0334 | 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 | 167 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0002g0059others(164): 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 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0169others(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 | a0001c0001t0002g0059a0001c0001t0002g0067a0001c0002t0002g0073others(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 | a0001c0001t0002g0063a0001c0001t0002g0095a0001c0001t0004g0030others(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 | a0001c0002t0002g0026a0001c0002t0002g0027a0001c0002t0002g0031others(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 | a0001c0001t0004g0021a0001c0002t0001g0266a0001c0002t0001g0267others(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 | a0001c0003t0002g0080a0001c0003t0002g0081a0001c0003t0002g0082others(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 | 139 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0004g0030others(136): 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 | a0001c0002t0002g0033 | 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 | a0001c0002t0003g0276a0001c0002t0003g0277a0001c0002t0003g0278 | 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 | a0001c0001t0004g0030a0001c0002t0002g0003a0001c0002t0002g0006others(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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(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 | a0001c0001t0004g0030a0001c0002t0002g0027a0001c0002t0002g0028others(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 | a0001c0001t0001g0128a0001c0001t0001g0188a0001c0001t0001g0205others(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 | a0001c0002t0002g0056a0001c0002t0002g0099a0001c0003t0002g0080others(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 | a0001c0001t0004g0030a0001c0002t0002g0003a0001c0002t0002g0006others(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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0002t0001g0340others(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 | a0001c0002t0001g0337a0001c0002t0003g0110a0001c0002t0003g0283others(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 | a0001c0003t0005g0017a0001c0003t0005g0018 | 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 | a0001c0001t0001g0271a0001c0001t0004g0101a0001c0002t0001g0266others(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 | a0001c0002t0003g0320 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0001g0180 | 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 | a0001c0003t0005g0017a0001c0003t0005g0018 | 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 | a0001c0001t0001g0198a0001c0001t0001g0243 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0003g0281a0001c0002t0003g0282 | 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 | 167 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0002g0059others(164): 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 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0113others(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 | a0001c0001t0001g0108a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0246 | 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 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025 | 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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0002t0002g0026a0001c0002t0002g0073 | 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 | a0001c0001t0001g0184 | 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 | 180 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0001g0331others(177): 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 | a0001c0001t0002g0067a0001c0001t0002g0095 | 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 | a0001c0002t0001g0272 | 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0271a0001c0002t0001g0266a0001c0002t0001g0267others(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 | a0001c0001t0001g0331a0001c0002t0003g0330a0001c0002t0003g0332others(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 | a0001c0002t0003g0280a0001c0002t0003g0329 | 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 | a0001c0002t0003g0279 | 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 | a0001c0002t0003g0322a0001c0002t0003g0323 | 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 | a0001c0002t0003g0185 | 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 | a0001c0002t0003g0324 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0255 | 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 | a0001c0002t0003g0276a0001c0002t0003g0277a0001c0002t0003g0278 | 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 | a0001c0002t0002g0008a0001c0002t0002g0068a0001c0002t0002g0069others(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 | 167 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0002g0059others(164): 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 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 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 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | 167 | a0001c0001t0001g0287a0001c0001t0001g0331a0001c0001t0002g0059others(164): 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 | a0001c0002t0003g0273a0001c0002t0003g0274a0001c0002t0003g0275others(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 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(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 | a0001c0001t0001g0111a0001c0001t0004g0021a0001c0002t0002g0100others(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 | 161 | a0001c0001t0001g0201a0001c0001t0001g0287a0001c0001t0001g0331others(158): 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 | 167 | a0001c0001t0001g0013a0001c0001t0001g0190a0001c0001t0001g0191others(164): 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 | a0001c0001t0001g0109a0001c0002t0002g0023a0001c0002t0002g0024others(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 | 99 | a0001c0001t0001g0193a0001c0001t0001g0261a0001c0001t0001g0271others(96): 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 | a0001c0001t0001g0331a0001c0002t0003g0329a0001c0002t0003g0330others(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 | a0001c0002t0001g0337a0001c0002t0001g0340a0001c0002t0003g0338others(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 | 181 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0001g0331others(178): 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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0002t0003g0195a0001c0002t0003g0196a0001c0002t0003g0197 | 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 | a0001c0001t0002g0059a0001c0001t0002g0063a0001c0001t0002g0067others(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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0002t0002g0102a0001c0002t0002g0103 | 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 | a0001c0002t0002g0104a0001c0002t0002g0105 | 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 | 96 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(93): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): 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 | a0001c0002t0003g0344a0001c0002t0003g0345 | 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 | a0001c0001t0001g0346 | 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 | a0001c0001t0001g0347 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.114+35C>T | AFG3L2 | ENSG00000141385.12 | transcript | ENST00000269143.8 | protein_coding | 1/16 | chr18 | 12376934 |