Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 89894 |
|---|---|
| ensemblid | ENSG00000198270.13 |
| hgncid | 25084 |
| symbol | TMEM116 |
| name | transmembrane protein 116 |
| refseq_nuc | NM_001193531.2 |
| refseq_prot | NP_001180460.1 |
| ensembl_nuc | ENST00000552374.7 |
| ensembl_prot | ENSP00000447731.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 111931298 |
| end | 112013165 |
| strand | - |
| ver | v1.2 |
| region | chr12:111931298-112013165 |
| region5000 | chr12:111926298-112018165 |
| regionname0 | TMEM116_chr12_111931298_112013165 |
| regionname5000 | TMEM116_chr12_111926298_112018165 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 337 | 231 | 51 | 43 | 105 | 4 | 26 | 89 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002 | 0/0 | 337 | 104 | 40 | 8 | 48 | 2 | 6 | 38 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0003 | 0/0 | 337 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0004 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0005 | 0/0 | 337 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0006 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0007 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0008 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0009 | 0/0 | 337 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1014 | 231 | 51 | 43 | 105 | 4 | 26 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0002 | 0/0 | 1014 | 99 | 39 | 8 | 44 | 2 | 6 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0003 | 0/0 | 1014 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0004 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0005 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0006 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0007 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0008 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0009 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| c0011 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 521 | 336 | 89 | 51 | 154 | 6 | 34 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| t0002 | 0/0 | 521 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| t0003 | 0/0 | 521 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| t0004 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1014 | 231 | 51 | 43 | 105 | 4 | 26 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0002 | 0/0 | 1014 | 99 | 39 | 8 | 44 | 2 | 6 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0003 | 0/0 | 1014 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0010 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0003c0009 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0004c0008 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0005c0007 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0006c0006 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0007c0005 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0008c0004 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0009c0011 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1534 | 228 | 49 | 42 | 105 | 4 | 26 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0001c0001t0003 | 0/0 | 1534 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0001c0001t0004 | 0/0 | 1534 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0002t0001 | 0/0 | 1534 | 96 | 36 | 8 | 44 | 2 | 6 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0002t0002 | 0/0 | 1534 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0003t0001 | 0/0 | 1534 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0002c0010t0001 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0003c0009t0001 | 0/0 | 1534 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0004c0008t0001 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0005c0007t0001 | 0/0 | 1534 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0006c0006t0001 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0007c0005t0001 | 0/0 | 1534 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0008c0004t0001 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| a0009c0011t0001 | 0/0 | 1534 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | copy fasta | chr12 | 111926298 | 112018165 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0002c0010t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0003c0009t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0004c0008t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0005c0007t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0007c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0008c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| a0009c0011t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0128 | EUR | GBR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0243 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | CHS | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01175 | hp2 | a0003 | c0009 | t0001 | g0125 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0329 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | KHV | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0261 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0321 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0284 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0302 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0260 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02897 | hp1 | a0006 | c0006 | t0001 | g0263 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02922 | hp2 | a0002 | c0010 | t0001 | g0305 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03017 | hp1 | a0005 | c0007 | t0001 | g0040 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0307 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | ESN | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03540 | hp2 | a0004 | c0008 | t0001 | g0233 | AFR | GWD | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0296 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0333 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0241 | SAS | BEB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04204 | hp2 | a0009 | c0011 | t0001 | g0209 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0288 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0278 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19012 | hp1 | a0007 | c0005 | t0001 | g0266 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | ASW | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0292 | EUR | TSI | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0306 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | MSL | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| HG06807 | hp2 | a0008 | c0004 | t0001 | g0118 | AFR | USA | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | USA | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | TMEM116_chr12_111926298_112018165 | TMEM116 | chr12 | 111926298 | 112018165 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111931640
|
C | T | 1 | a0005 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.995G>A | p.Ser332Asn | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 11/11 | 1192/1534 | 995/1014 | 332/337 | chr12 | 111931640 | ||
| chr12:111931658
|
G | A | 1 | a0006 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.977C>T | p.Thr326Ile | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 11/11 | 1174/1534 | 977/1014 | 326/337 | chr12 | 111931658 | ||
| chr12:111932615
|
T | C | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.778A>G | p.Lys260Glu | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/11 | 975/1534 | 778/1014 | 260/337 | chr12 | 111932615 | ||
| chr12:111932657
|
C | A | 1 | a0003 | 1 | HG01175.hp2 | missense_variant&splice_region_variant | MODERATE | c.736G>T | p.Val246Phe | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/11 | 933/1534 | 736/1014 | 246/337 | chr12 | 111932657 | ||
| chr12:111937162
|
G | T | 1 | a0007 | 1 | NA19012.hp1 | missense_variant&splice_region_variant | MODERATE | c.447C>A | p.His149Gln | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/11 | 644/1534 | 447/1014 | 149/337 | chr12 | 111937162 | ||
| chr12:111938186
|
A | C | 3 | a0002a0006a0007 | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
missense_variant | MODERATE | c.340T>G | p.Cys114Gly | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/11 | 537/1534 | 340/1014 | 114/337 | chr12 | 111938186 | ||
| chr12:111938206
|
A | G | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.320T>C | p.Ile107Thr | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/11 | 517/1534 | 320/1014 | 107/337 | chr12 | 111938206 | ||
| chr12:111943335
|
T | G | 1 | a0009 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.245A>C | p.Asn82Thr | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/11 | 442/1534 | 245/1014 | 82/337 | chr12 | 111943335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111931744
|
C | T | 1 | a0002c0003 | 4 | HG00558.hp2 NA18971.hp2 NA18980.hp1 others(1): Show |
synonymous_variant | LOW | c.891G>A | p.Glu297Glu | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 11/11 | 1088/1534 | 891/1014 | 297/337 | chr12 | 111931744 | ||
| chr12:111943267
|
G | A | 1 | a0002c0010 | 1 | HG02922.hp2 | splice_region_variant&synonymous_variant | LOW | c.313C>T | p.Leu105Leu | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/11 | 510/1534 | 313/1014 | 105/337 | chr12 | 111943267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111931480
|
A | G | 1 | a0002c0002t0002 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 11/11 | 141 | chr12 | 111931480 | |||||
| chr12:111931530
|
T | C | 1 | a0001c0001t0003 | 2 | HG02572.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 11/11 | 91 | chr12 | 111931530 | |||||
| chr12:112013073
|
C | T | 1 | a0001c0001t0004 | 1 | HG01952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/11 | 7803 | chr12 | 112013073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111931943
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.808-116T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111931943 | ||||||
| chr12:111932030
|
C | T | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.808-203G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111932030 | ||||||
| chr12:111932074
|
G | GC | 81 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.808-248dupG | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111932074 | ||||||
| chr12:111932156
|
T | C | 6 | a0002c0002t0001g0279a0002c0002t0001g0280a0002c0002t0001g0294others(3): Show | 6 | NA18942.hp2 NA18960.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-329A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111932156 | ||||||
| chr12:111932371
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0143a0001c0001t0001g0152others(1): Show | 4 | HG02080.hp2 NA18961.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+215G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111932371 | ||||||
| chr12:111932491
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.807+95G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 10/10 | chr12 | 111932491 | ||||||
| chr12:111932792
|
T | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-133A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 9/10 | chr12 | 111932792 | ||||||
| chr12:111933240
|
C | CA | 183 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(180): Show | 190 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.734-582dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 9/10 | chr12 | 111933240 | ||||||
| chr12:111933489
|
C | CT | 21 | a0001c0001t0001g0026a0001c0001t0001g0064a0001c0001t0001g0084others(18): Show | 21 | HG00735.hp2 HG02056.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.733+396dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 9/10 | chr12 | 111933489 | ||||||
| chr12:111933655
|
A | AT | 6 | a0001c0001t0001g0023a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01433.hp1 NA18981.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+230dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 9/10 | chr12 | 111933655 | ||||||
| chr12:111933655
|
AT | A | 99 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(96): Show | 103 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.733+230delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 9/10 | chr12 | 111933655 | ||||||
| chr12:111934080
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-50G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934080 | ||||||
| chr12:111934105
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.589-75A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934105 | ||||||
| chr12:111934155
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.589-125A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934155 | ||||||
| chr12:111934232
|
T | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0131a0002c0002t0001g0132 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.589-202A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934232 | ||||||
| chr12:111934484
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.589-454G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934484 | ||||||
| chr12:111934501
|
C | T | 3 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129 | 3 | HG00099.hp2 HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.589-471G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934501 | ||||||
| chr12:111934626
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.589-596G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934626 | ||||||
| chr12:111934667
|
A | G | 1 | a0002c0003t0001g0243 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.589-637T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934667 | ||||||
| chr12:111934714
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-684C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934714 | ||||||
| chr12:111934886
|
A | G | 9 | a0002c0002t0001g0002a0002c0002t0001g0254a0002c0002t0001g0255others(6): Show | 11 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-856T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111934886 | ||||||
| chr12:111935048
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.589-1018C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935048 | ||||||
| chr12:111935285
|
T | C | 111 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(108): Show | 115 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-1255A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935285 | ||||||
| chr12:111935375
|
G | T | 3 | a0002c0002t0001g0262a0002c0002t0001g0264a0006c0006t0001g0263 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588+1317C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935375 | ||||||
| chr12:111935613
|
C | CGGTGTGT others(4): Show |
1 | a0001c0001t0001g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.588+1078_588+1079i others(13): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGT | 38 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(35): Show | 38 | HG01081.hp1 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.588+1077_588+1078d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGT | 56 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 56 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.588+1075_588+1078d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGT | 56 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0020others(53): Show | 56 | HG01106.hp1 HG01106.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.588+1073_588+1078d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(1): Show |
32 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0050others(29): Show | 32 | HG00597.hp1 HG01071.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.588+1071_588+1078d others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(3): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0145a0001c0001t0001g0158others(3): Show | 6 | HG00544.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1069_588+1078d others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(5): Show |
12 | a0001c0001t0001g0090a0001c0001t0001g0117a0001c0001t0001g0144others(9): Show | 12 | HG03195.hp1 HG03486.hp1 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.588+1067_588+1078d others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(7): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0173a0001c0001t0001g0177others(1): Show | 4 | NA18939.hp1 NA19011.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1065_588+1078d others(16): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0168a0002c0002t0001g0313 | 6 | HG02027.hp2 HG02132.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1063_588+1078d others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(11): Show |
11 | a0001c0001t0001g0008a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG03927.hp1 NA18946.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+1061_588+1078d others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(13): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0214 | 2 | NA18951.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.588+1059_588+1078d others(22): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0001g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.588+1057_588+1078d others(24): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
C | CGTGTGTG others(17): Show |
1 | a0001c0001t0001g0159 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.588+1055_588+1078d others(26): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
CGT | C | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(16): Show | 19 | HG00544.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.588+1077_588+1078d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
CGTGTGT | C | 3 | a0002c0002t0001g0250a0002c0002t0001g0253a0002c0002t0001g0330 | 3 | HG02258.hp2 NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.588+1073_588+1078d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935613
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0005a0001c0001t0004g0006 | 3 | HG01496.hp2 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.588+1065_588+1078d others(16): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935613 | ||||||
| chr12:111935637
|
T | TGTGTGTG others(3): Show |
1 | a0002c0002t0001g0270 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.588+1054_588+1055i others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935637 | ||||||
| chr12:111935661
|
T | TGTGTGTG | 4 | a0001c0001t0001g0120a0001c0001t0001g0134a0001c0001t0001g0201others(1): Show | 4 | HG01433.hp1 HG01993.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+1030_588+1031i others(9): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935661 | ||||||
| chr12:111935661
|
T | TGTGTGTG others(4): Show |
2 | a0001c0001t0001g0170a0002c0002t0001g0300 | 2 | HG01099.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.588+1030_588+1031i others(13): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935661 | ||||||
| chr12:111935662
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.588+1030A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935662 | ||||||
| chr12:111935783
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588+909A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111935783 | ||||||
| chr12:111936150
|
G | A | 1 | a0004c0008t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+542C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111936150 | ||||||
| chr12:111936282
|
C | A | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.588+410G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111936282 | ||||||
| chr12:111936613
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.588+79A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 8/10 | chr12 | 111936613 | ||||||
| chr12:111937027
|
C | A | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+133G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937027 | ||||||
| chr12:111937028
|
A | T | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+132T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937028 | ||||||
| chr12:111937033
|
G | T | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+127C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937033 | ||||||
| chr12:111937039
|
T | A | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+121A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937039 | ||||||
| chr12:111937046
|
T | A | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+114A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937046 | ||||||
| chr12:111937073
|
T | G | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+87A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937073 | ||||||
| chr12:111937138
|
T | G | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+22A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937138 | ||||||
| chr12:111937147
|
A | T | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+13T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937147 | ||||||
| chr12:111937150
|
T | G | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.449+10A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937150 | ||||||
| chr12:111937153
|
T | G | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | splice_region_variant&intron_variant | LOW | c.449+7A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937153 | ||||||
| chr12:111937157
|
T | A | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | splice_region_variant&intron_variant | LOW | c.449+3A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937157 | ||||||
| chr12:111937159
|
C | G | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | splice_donor_variant&intron_variant | HIGH | c.449+1G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 7/10 | chr12 | 111937159 | ||||||
| chr12:111937504
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(198): Show | 208 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.366-261A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937504 | ||||||
| chr12:111937580
|
G | T | 1 | a0002c0002t0001g0331 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.366-337C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937580 | ||||||
| chr12:111937676
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.366-433G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937676 | ||||||
| chr12:111937712
|
G | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0004c0008t0001g0233 | 3 | HG03098.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+449C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937712 | ||||||
| chr12:111937972
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.365+189G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937972 | ||||||
| chr12:111937974
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+187A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937974 | ||||||
| chr12:111937998
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+163C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 6/10 | chr12 | 111937998 | ||||||
| chr12:111938353
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.316-143T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938353 | ||||||
| chr12:111938493
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.316-283G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938493 | ||||||
| chr12:111938539
|
T | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.316-329A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938539 | ||||||
| chr12:111938709
|
G | T | 1 | a0001c0001t0001g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.316-499C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938709 | ||||||
| chr12:111938793
|
G | A | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.316-583C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938793 | ||||||
| chr12:111938871
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.316-661C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938871 | ||||||
| chr12:111938898
|
A | ATAT | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.316-691_316-689dup others(3): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111938898 | ||||||
| chr12:111939145
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.316-935T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939145 | ||||||
| chr12:111939237
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.316-1027C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939237 | ||||||
| chr12:111939451
|
CA | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(240): Show | 251 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(248): Show |
intron_variant | MODIFIER | c.316-1242delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939451 | ||||||
| chr12:111939451
|
CAA | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0020others(13): Show | 16 | HG01169.hp2 HG01943.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.316-1243_316-1242d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939451 | ||||||
| chr12:111939530
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.316-1320C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939530 | ||||||
| chr12:111939585
|
C | G | 1 | a0002c0002t0001g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.316-1375G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939585 | ||||||
| chr12:111939733
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.316-1523G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939733 | ||||||
| chr12:111939880
|
C | CTG | 22 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0019others(19): Show | 23 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.316-1672_316-1671d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
C | CTGTG | 19 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(16): Show | 19 | HG01071.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.316-1674_316-1671d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
C | CTGTGTG | 6 | a0001c0001t0001g0053a0001c0001t0001g0073a0001c0001t0001g0074others(3): Show | 6 | HG02080.hp1 HG02683.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-1676_316-1671d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0205 | 3 | HG02148.hp1 HG02523.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.316-1678_316-1671d others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0082 | 3 | HG01934.hp2 HG01978.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.316-1680_316-1671d others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTG | C | 20 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00140.hp2 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.316-1672_316-1671d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTG | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(29): Show | 35 | HG01081.hp1 HG01168.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.316-1674_316-1671d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTG | C | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 52 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.316-1676_316-1671d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(1): Show |
C | 40 | a0001c0001t0001g0212a0002c0002t0001g0127a0002c0002t0001g0130others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.316-1678_316-1671d others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(3): Show |
C | 15 | a0001c0001t0001g0020a0001c0001t0001g0070a0002c0002t0001g0126others(12): Show | 15 | HG00099.hp2 HG01175.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.316-1680_316-1671d others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(5): Show |
C | 9 | a0002c0002t0001g0131a0002c0002t0001g0132a0002c0002t0001g0245others(6): Show | 9 | HG01361.hp2 HG02132.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-1682_316-1671d others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(9): Show |
C | 5 | a0001c0001t0001g0096a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02897.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-1686_316-1671d others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(11): Show |
C | 1 | a0002c0002t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.316-1688_316-1671d others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.316-1692_316-1671d others(24): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(17): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-1694_316-1671d others(26): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939880
|
CTGTGTGT others(27): Show |
C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.316-1704_316-1671d others(36): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939880 | ||||||
| chr12:111939908
|
G | A | 1 | a0007c0005t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.316-1698C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939908 | ||||||
| chr12:111939981
|
C | T | 6 | a0002c0002t0001g0268a0002c0002t0001g0269a0002c0002t0001g0270others(3): Show | 6 | NA18939.hp2 NA18959.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-1771G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111939981 | ||||||
| chr12:111940043
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.316-1833A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940043 | ||||||
| chr12:111940204
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-1994G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940204 | ||||||
| chr12:111940279
|
T | A | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(10): Show | 13 | HG00140.hp1 HG01106.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-2069A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940279 | ||||||
| chr12:111940334
|
A | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.316-2124T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940334 | ||||||
| chr12:111940472
|
T | TACACACA others(5): Show |
1 | a0002c0002t0002g0261 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.316-2263_316-2262i others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940472 | ||||||
| chr12:111940472
|
T | TACACACA others(7): Show |
2 | a0002c0002t0002g0247a0002c0002t0002g0260 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.316-2263_316-2262i others(16): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940472 | ||||||
| chr12:111940474
|
T | C | 3 | a0002c0002t0002g0247a0002c0002t0002g0260a0002c0002t0002g0261 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.316-2264A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940474
|
T | TACACACA others(3): Show |
1 | a0002c0002t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.316-2265_316-2264i others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940474
|
T | TACACACA others(7): Show |
11 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0128others(8): Show | 13 | HG00099.hp2 HG00733.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.316-2265_316-2264i others(16): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940474
|
T | TACACACA others(9): Show |
3 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0259 | 3 | HG01099.hp1 HG01175.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.316-2265_316-2264i others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940474
|
T | TACACACA others(11): Show |
1 | a0002c0002t0001g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.316-2265_316-2264i others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940474
|
T | TACACACA others(13): Show |
1 | a0002c0002t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-2265_316-2264i others(22): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940474 | ||||||
| chr12:111940476
|
T | C | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.316-2266A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940476 | ||||||
| chr12:111940476
|
T | TACACACA others(3): Show |
1 | a0002c0002t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.316-2267_316-2266i others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940476 | ||||||
| chr12:111940480
|
T | C | 22 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(19): Show | 24 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.316-2270A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940480
|
T | TAC | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(118): Show | 123 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.316-2272_316-2271d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940480
|
T | TACAC | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.316-2274_316-2271d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940480
|
T | TACACACA others(1): Show |
7 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0285others(4): Show | 7 | HG00558.hp1 HG00558.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-2278_316-2271d others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940480
|
T | TACACACA others(3): Show |
63 | a0002c0002t0001g0003a0002c0002t0001g0246a0002c0002t0001g0248others(60): Show | 65 | HG00597.hp2 HG01081.hp1 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.316-2280_316-2271d others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940480
|
T | TACACACA others(5): Show |
10 | a0002c0002t0001g0241a0002c0002t0001g0262a0002c0002t0001g0264others(7): Show | 10 | HG02622.hp2 HG02897.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-2282_316-2271d others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940480 | ||||||
| chr12:111940498
|
C | CACACACA others(9): Show |
1 | a0002c0002t0001g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.316-2289_316-2288i others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940498 | ||||||
| chr12:111940498
|
C | CACATATA others(33): Show |
1 | a0001c0001t0001g0019 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.316-2289_316-2288i others(42): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940498 | ||||||
| chr12:111940500
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 5 | HG03098.hp1 HG03516.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-2290A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940500 | ||||||
| chr12:111940508
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.316-2298G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940508 | ||||||
| chr12:111940514
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0174others(5): Show | 8 | HG01256.hp1 HG01258.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-2304A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940514 | ||||||
| chr12:111940521
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.316-2311C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940521 | ||||||
| chr12:111940523
|
G | GTA | 3 | a0001c0001t0003g0077a0001c0001t0003g0078a0003c0009t0001g0125 | 3 | HG01175.hp2 HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.316-2315_316-2314d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0182 | 2 | HG02148.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.316-2325_316-2314d others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(7): Show |
20 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(17): Show | 20 | HG01071.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.316-2327_316-2314d others(16): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(9): Show |
14 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0133others(11): Show | 14 | HG01123.hp1 HG02071.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.316-2329_316-2314d others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(11): Show |
14 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0033others(11): Show | 14 | HG00597.hp1 HG00735.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.316-2331_316-2314d others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(13): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0136a0001c0001t0001g0148others(16): Show | 22 | HG00544.hp2 HG02027.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.316-2333_316-2314d others(22): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0001g0181others(1): Show | 4 | HG02135.hp2 HG02165.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-2335_316-2314d others(24): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0001g0153 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.316-2314_316-2313i others(28): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
G | GTGTATAT others(13): Show |
1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.316-2314_316-2313i others(22): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940523
|
GTA | G | 33 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0045others(30): Show | 33 | HG00140.hp1 HG01106.hp1 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.316-2315_316-2314d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940523 | ||||||
| chr12:111940525
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG00597.hp2 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-2315T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940525 | ||||||
| chr12:111940527
|
ATATATAT others(33): Show |
A | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.316-2357_316-2318d others(42): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940527 | ||||||
| chr12:111940529
|
A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.316-2320_316-2319i others(32): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940529 | ||||||
| chr12:111940529
|
A | ATATATAT others(21): Show |
48 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(45): Show | 50 | HG00558.hp1 HG00558.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.316-2320_316-2319i others(30): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940529 | ||||||
| chr12:111940529
|
A | ATATATAT others(21): Show |
16 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(13): Show | 16 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.316-2320_316-2319i others(30): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940529 | ||||||
| chr12:111940529
|
ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.316-2357_316-2320d others(40): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940529 | ||||||
| chr12:111940531
|
A | ATATATAT others(21): Show |
8 | a0002c0002t0001g0248a0002c0002t0001g0277a0002c0002t0001g0281others(5): Show | 8 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-2322_316-2321i others(30): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940531 | ||||||
| chr12:111940531
|
A | ATATATAT others(21): Show |
3 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.316-2322_316-2321i others(30): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940531 | ||||||
| chr12:111940533
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0001g0137 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.316-2357_316-2324d others(36): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940533 | ||||||
| chr12:111940538
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.316-2328A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940538 | ||||||
| chr12:111940538
|
TATATATA others(1): Show |
T | 16 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.316-2336_316-2329d others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940538 | ||||||
| chr12:111940538
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.316-2338_316-2329d others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940538 | ||||||
| chr12:111940540
|
TATATAC | T | 4 | a0001c0001t0001g0224a0002c0002t0001g0251a0002c0002t0001g0264others(1): Show | 4 | HG02559.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-2336_316-2331d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940540 | ||||||
| chr12:111940541
|
ATATACAC others(19): Show |
A | 1 | a0001c0001t0001g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.316-2357_316-2332d others(28): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940541 | ||||||
| chr12:111940542
|
TATAC | T | 13 | a0002c0002t0001g0061a0002c0002t0001g0126a0002c0002t0001g0127others(10): Show | 13 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-2336_316-2333d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940542 | ||||||
| chr12:111940542
|
TATACACA others(5): Show |
T | 1 | a0001c0001t0001g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.316-2344_316-2333d others(14): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940542 | ||||||
| chr12:111940543
|
ATACACAC others(17): Show |
A | 2 | a0001c0001t0001g0164a0001c0001t0001g0215 | 2 | NA18950.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.316-2357_316-2334d others(26): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940543 | ||||||
| chr12:111940544
|
T | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01943.hp1 HG02109.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-2334A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940544 | ||||||
| chr12:111940544
|
TAC | T | 12 | a0001c0001t0001g0226a0001c0001t0001g0236a0002c0002t0001g0002others(9): Show | 14 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.316-2336_316-2335d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940544 | ||||||
| chr12:111940545
|
ACACACAC others(15): Show |
A | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02257.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-2357_316-2336d others(24): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940545 | ||||||
| chr12:111940546
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0032others(143): Show | 151 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.316-2336G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940546 | ||||||
| chr12:111940548
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.316-2339_316-2338i others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940548 | ||||||
| chr12:111940548
|
C | CATATATG others(3): Show |
1 | a0001c0001t0001g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.316-2339_316-2338i others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940548 | ||||||
| chr12:111940549
|
A | ATATATGT others(1): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01943.hp1 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-2340_316-2339i others(10): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940549 | ||||||
| chr12:111940550
|
C | CATATATG others(23): Show |
1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-2341_316-2340i others(32): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940550 | ||||||
| chr12:111940550
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(7): Show | 10 | HG01943.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-2340G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940550 | ||||||
| chr12:111940551
|
A | ATATGTG | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0237 | 3 | HG02257.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.316-2342_316-2341i others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940551 | ||||||
| chr12:111940552
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(7): Show | 10 | HG01943.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-2342G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940552 | ||||||
| chr12:111940554
|
C | T | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01243.hp1 HG01943.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.316-2344G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940554 | ||||||
| chr12:111940556
|
T | C | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-2346A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940556 | ||||||
| chr12:111940559
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.316-2349T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940559 | ||||||
| chr12:111940561
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 210 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.316-2351T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940561 | ||||||
| chr12:111940563
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG01943.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.316-2353C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940563 | ||||||
| chr12:111940563
|
G | GTA | 9 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0277others(6): Show | 9 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-2354_316-2353i others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940563 | ||||||
| chr12:111940565
|
G | A | 110 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 114 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.316-2355C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940565 | ||||||
| chr12:111940567
|
G | A | 116 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(113): Show | 120 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.316-2357C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940567 | ||||||
| chr12:111940567
|
G | GTATA | 75 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(72): Show | 78 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.316-2361_316-2358d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940567 | ||||||
| chr12:111940569
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.316-2359T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940569 | ||||||
| chr12:111940964
|
A | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.315+2301T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111940964 | ||||||
| chr12:111941105
|
C | T | 57 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(54): Show | 59 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+2160G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941105 | ||||||
| chr12:111941106
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+2159C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941106 | ||||||
| chr12:111941140
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+2125C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941140 | ||||||
| chr12:111941209
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+2056G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941209 | ||||||
| chr12:111941291
|
G | A | 8 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.315+1974C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941291 | ||||||
| chr12:111941324
|
C | T | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+1941G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941324 | ||||||
| chr12:111941374
|
CA | C | 11 | a0001c0001t0001g0046a0001c0001t0001g0145a0001c0001t0001g0166others(8): Show | 11 | HG02735.hp2 HG03098.hp1 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.315+1890delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941374 | ||||||
| chr12:111941396
|
A | G | 3 | a0002c0002t0001g0262a0002c0002t0001g0264a0006c0006t0001g0263 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.315+1869T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941396 | ||||||
| chr12:111941467
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.315+1798A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941467 | ||||||
| chr12:111941491
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.315+1774T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941491 | ||||||
| chr12:111941581
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+1684T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941581 | ||||||
| chr12:111941694
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.315+1571C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941694 | ||||||
| chr12:111941783
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.315+1482T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941783 | ||||||
| chr12:111941802
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 26 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.315+1463G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941802 | ||||||
| chr12:111941831
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.315+1434T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941831 | ||||||
| chr12:111941975
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315+1290C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111941975 | ||||||
| chr12:111942029
|
C | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.315+1236G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942029 | ||||||
| chr12:111942120
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.315+1145A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942120 | ||||||
| chr12:111942124
|
G | C | 1 | a0002c0002t0001g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.315+1141C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942124 | ||||||
| chr12:111942148
|
G | T | 3 | a0002c0002t0001g0272a0002c0002t0001g0274a0002c0002t0001g0275 | 3 | HG02818.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.315+1117C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942148 | ||||||
| chr12:111942211
|
T | C | 1 | a0002c0002t0001g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1054A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942211 | ||||||
| chr12:111942223
|
C | A | 75 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(72): Show | 77 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.315+1042G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942223 | ||||||
| chr12:111942365
|
C | T | 1 | a0002c0002t0001g0296 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.315+900G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942365 | ||||||
| chr12:111942465
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.315+800T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942465 | ||||||
| chr12:111942568
|
G | A | 101 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(98): Show | 105 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.315+697C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942568 | ||||||
| chr12:111942638
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.315+627G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942638 | ||||||
| chr12:111942666
|
G | C | 101 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(98): Show | 105 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.315+599C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942666 | ||||||
| chr12:111942771
|
TGTGTGTG others(5): Show |
T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.315+482_315+493del others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942771 | ||||||
| chr12:111942777
|
T | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.315+488A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942777 | ||||||
| chr12:111942834
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315+431C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111942834 | ||||||
| chr12:111943227
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+38G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 5/10 | chr12 | 111943227 | ||||||
| chr12:111943681
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.211-312G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111943681 | ||||||
| chr12:111943706
|
A | G | 1 | a0002c0002t0001g0295 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.211-337T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111943706 | ||||||
| chr12:111944426
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0232 | 3 | HG02970.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.211-1057C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111944426 | ||||||
| chr12:111944447
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-1078A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111944447 | ||||||
| chr12:111944518
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-1149T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111944518 | ||||||
| chr12:111944898
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.211-1529C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111944898 | ||||||
| chr12:111945073
|
T | TA | 44 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0063others(41): Show | 44 | HG00544.hp2 HG00597.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.211-1705dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945073 | ||||||
| chr12:111945073
|
T | TAA | 10 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 10 | HG01074.hp1 HG01928.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1706_211-1705d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945073 | ||||||
| chr12:111945073
|
TA | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0104a0001c0001t0001g0120others(21): Show | 26 | HG00099.hp2 HG00733.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.211-1705delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945073 | ||||||
| chr12:111945092
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.211-1723T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945092 | ||||||
| chr12:111945145
|
C | A | 1 | a0001c0001t0001g0225 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.211-1776G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945145 | ||||||
| chr12:111945343
|
C | CA | 17 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0097others(14): Show | 17 | HG00735.hp1 HG02055.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.211-1975dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945343 | ||||||
| chr12:111945343
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(117): Show | 123 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.211-1975delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945343 | ||||||
| chr12:111945343
|
CAA | C | 48 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 49 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.211-1976_211-1975d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945343 | ||||||
| chr12:111945343
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.211-1989_211-1975d others(17): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945343 | ||||||
| chr12:111945448
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-2079G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945448 | ||||||
| chr12:111945456
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-2087C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945456 | ||||||
| chr12:111945520
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.211-2151G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111945520 | ||||||
| chr12:111946224
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.211-2855C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946224 | ||||||
| chr12:111946349
|
C | T | 1 | a0002c0002t0001g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.211-2980G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946349 | ||||||
| chr12:111946378
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-3009C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946378 | ||||||
| chr12:111946587
|
C | T | 3 | a0002c0002t0001g0002a0002c0002t0001g0255a0002c0002t0001g0259 | 5 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-3218G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946587 | ||||||
| chr12:111946615
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.211-3246C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946615 | ||||||
| chr12:111946672
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.211-3303C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946672 | ||||||
| chr12:111946951
|
A | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226 | 3 | HG01884.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.211-3582T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111946951 | ||||||
| chr12:111947172
|
CT | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0237a0002c0002t0001g0248others(5): Show | 8 | HG01167.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-3804delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111947172 | ||||||
| chr12:111947178
|
T | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG01993.hp2 HG02135.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-3809A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111947178 | ||||||
| chr12:111947356
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.211-3987C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111947356 | ||||||
| chr12:111947725
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-4356T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111947725 | ||||||
| chr12:111947861
|
A | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(196): Show | 206 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.211-4492T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111947861 | ||||||
| chr12:111948381
|
G | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-5012C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111948381 | ||||||
| chr12:111948806
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.211-5437A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111948806 | ||||||
| chr12:111948836
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 23 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-5467A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111948836 | ||||||
| chr12:111949013
|
G | A | 1 | a0002c0002t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.211-5644C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111949013 | ||||||
| chr12:111949365
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.211-5996T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111949365 | ||||||
| chr12:111949881
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.211-6512C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111949881 | ||||||
| chr12:111949901
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.211-6532C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111949901 | ||||||
| chr12:111949921
|
C | G | 13 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0090others(10): Show | 13 | HG01175.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.211-6552G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111949921 | ||||||
| chr12:111950116
|
A | AAAAAC | 54 | a0001c0001t0001g0064a0002c0002t0001g0003a0002c0002t0001g0241others(51): Show | 56 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.211-6752_211-6748d others(7): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950116 | ||||||
| chr12:111950163
|
C | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-6794G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950163 | ||||||
| chr12:111950201
|
C | T | 9 | a0002c0002t0001g0002a0002c0002t0001g0254a0002c0002t0001g0255others(6): Show | 11 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-6832G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950201 | ||||||
| chr12:111950324
|
A | T | 110 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 114 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.211-6955T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950324 | ||||||
| chr12:111950469
|
T | TA | 16 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0042others(13): Show | 16 | HG01175.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-7101dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950469 | ||||||
| chr12:111950469
|
TA | T | 88 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0095others(85): Show | 90 | HG00099.hp2 HG00597.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.211-7101delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950469 | ||||||
| chr12:111950627
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-7258T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111950627 | ||||||
| chr12:111951684
|
G | A | 1 | a0002c0002t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211-8315C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111951684 | ||||||
| chr12:111951855
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.211-8486G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111951855 | ||||||
| chr12:111951938
|
ACGGTGGC others(11): Show |
A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0185 | 3 | HG01123.hp1 HG02273.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.211-8587_211-8570d others(20): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111951938 | ||||||
| chr12:111951940
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-8571C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111951940 | ||||||
| chr12:111952397
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-9028A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111952397 | ||||||
| chr12:111952456
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-9087T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111952456 | ||||||
| chr12:111952534
|
G | A | 1 | a0002c0002t0001g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-9165C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111952534 | ||||||
| chr12:111952817
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-9448A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111952817 | ||||||
| chr12:111953053
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226 | 3 | HG01884.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.211-9684A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953053 | ||||||
| chr12:111953228
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0166 | 2 | NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.211-9859A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953228 | ||||||
| chr12:111953262
|
A | G | 3 | a0002c0002t0001g0304a0002c0002t0001g0313a0002c0002t0001g0332 | 3 | HG02027.hp2 NA18949.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.211-9893T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953262 | ||||||
| chr12:111953489
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.211-10120G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953489 | ||||||
| chr12:111953557
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-10188A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953557 | ||||||
| chr12:111953564
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.211-10195A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953564 | ||||||
| chr12:111953571
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.211-10202G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953571 | ||||||
| chr12:111953628
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.211-10259C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953628 | ||||||
| chr12:111953799
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0078 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.211-10430C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111953799 | ||||||
| chr12:111954072
|
G | GA | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.211-10704dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111954072 | ||||||
| chr12:111954232
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(223): Show | 234 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.211-10863G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111954232 | ||||||
| chr12:111954382
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.211-11013A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111954382 | ||||||
| chr12:111954723
|
A | G | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(10): Show | 13 | HG00140.hp1 HG01106.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.211-11354T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111954723 | ||||||
| chr12:111955020
|
T | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.211-11651A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955020 | ||||||
| chr12:111955255
|
A | G | 3 | a0002c0002t0002g0247a0002c0002t0002g0260a0002c0002t0002g0261 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.211-11886T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955255 | ||||||
| chr12:111955261
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-11892C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955261 | ||||||
| chr12:111955318
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.211-11949C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955318 | ||||||
| chr12:111955435
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-12066T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955435 | ||||||
| chr12:111955738
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.211-12369G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111955738 | ||||||
| chr12:111956011
|
T | G | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-12642A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956011 | ||||||
| chr12:111956022
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-12653G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956022 | ||||||
| chr12:111956130
|
A | T | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.211-12761T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956130 | ||||||
| chr12:111956218
|
G | T | 103 | a0001c0001t0001g0074a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 107 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.211-12849C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956218 | ||||||
| chr12:111956263
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | NA18942.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.211-12894A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956263 | ||||||
| chr12:111956333
|
A | G | 4 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-12964T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956333 | ||||||
| chr12:111956456
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.211-13087G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956456 | ||||||
| chr12:111956514
|
C | T | 1 | a0005c0007t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.211-13145G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956514 | ||||||
| chr12:111956651
|
C | T | 1 | a0002c0002t0001g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.211-13282G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956651 | ||||||
| chr12:111956686
|
G | A | 3 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.211-13317C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956686 | ||||||
| chr12:111956794
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211-13425G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956794 | ||||||
| chr12:111956954
|
C | T | 1 | a0002c0002t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211-13585G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111956954 | ||||||
| chr12:111957049
|
C | A | 1 | a0002c0010t0001g0305 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.211-13680G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957049 | ||||||
| chr12:111957239
|
C | T | 1 | a0002c0002t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211-13870G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957239 | ||||||
| chr12:111957317
|
G | A | 101 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(98): Show | 105 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.211-13948C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957317 | ||||||
| chr12:111957320
|
A | AC | 20 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0030others(17): Show | 20 | HG00544.hp2 HG00597.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.211-13952dupG | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957320 | ||||||
| chr12:111957435
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-14066G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957435 | ||||||
| chr12:111957460
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.211-14091C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957460 | ||||||
| chr12:111957464
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0152 | 2 | HG02080.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.211-14095T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957464 | ||||||
| chr12:111957477
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.211-14108C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957477 | ||||||
| chr12:111957505
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.211-14136G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957505 | ||||||
| chr12:111957506
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.211-14137G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957506 | ||||||
| chr12:111957528
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.211-14159C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957528 | ||||||
| chr12:111957553
|
A | G | 1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.211-14184T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957553 | ||||||
| chr12:111957722
|
C | T | 1 | a0002c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.211-14353G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957722 | ||||||
| chr12:111957796
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG01993.hp2 HG02135.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-14427G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957796 | ||||||
| chr12:111957824
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.211-14455A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957824 | ||||||
| chr12:111957934
|
A | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0059 | 2 | HG01074.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.211-14565T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111957934 | ||||||
| chr12:111958191
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.211-14822A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958191 | ||||||
| chr12:111958201
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.211-14832G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958201 | ||||||
| chr12:111958247
|
G | A | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-14878C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958247 | ||||||
| chr12:111958277
|
T | TA | 15 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0059others(12): Show | 15 | HG01123.hp2 HG01175.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.211-14909dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958277 | ||||||
| chr12:111958277
|
TA | T | 93 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(90): Show | 95 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.211-14909delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958277 | ||||||
| chr12:111958277
|
TAA | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(62): Show | 68 | HG00099.hp2 HG00140.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.211-14910_211-1490 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958277 | ||||||
| chr12:111958277
|
TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0001g0179a0001c0001t0001g0207 | 2 | HG03239.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.211-14921_211-1490 others(17): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958277 | ||||||
| chr12:111958277
|
TAAAAAAA others(7): Show |
T | 87 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(84): Show | 90 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.211-14922_211-1490 others(18): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958277 | ||||||
| chr12:111958334
|
C | A | 1 | a0002c0002t0001g0271 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.211-14965G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958334 | ||||||
| chr12:111958423
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-15054G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958423 | ||||||
| chr12:111958563
|
A | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-15194T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958563 | ||||||
| chr12:111958692
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(1): Show | 4 | HG01928.hp1 HG01934.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-15323C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111958692 | ||||||
| chr12:111959260
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-15891A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959260 | ||||||
| chr12:111959290
|
G | A | 5 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(2): Show | 5 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-15921C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959290 | ||||||
| chr12:111959548
|
C | T | 3 | a0002c0002t0001g0306a0002c0002t0001g0328a0002c0010t0001g0305 | 3 | HG02055.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.211-16179G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959548 | ||||||
| chr12:111959821
|
T | C | 1 | a0002c0002t0001g0300 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.211-16452A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959821 | ||||||
| chr12:111959923
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0078 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.211-16554G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959923 | ||||||
| chr12:111959941
|
C | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-16572G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111959941 | ||||||
| chr12:111960083
|
T | C | 81 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.211-16714A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960083 | ||||||
| chr12:111960261
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-16892C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960261 | ||||||
| chr12:111960383
|
T | A | 1 | a0002c0002t0001g0244 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.211-17014A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960383 | ||||||
| chr12:111960384
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-17015A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960384 | ||||||
| chr12:111960430
|
T | G | 1 | a0002c0002t0001g0280 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.211-17061A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960430 | ||||||
| chr12:111960491
|
C | CA | 21 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0054others(18): Show | 21 | HG01071.hp1 HG01433.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.211-17123dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960491 | ||||||
| chr12:111960491
|
CA | C | 46 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 48 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.211-17123delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960491 | ||||||
| chr12:111960491
|
CAA | C | 68 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0244others(65): Show | 70 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.211-17124_211-1712 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960491 | ||||||
| chr12:111960647
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-17278T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960647 | ||||||
| chr12:111960719
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-17350C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960719 | ||||||
| chr12:111960890
|
C | G | 3 | a0002c0002t0001g0126a0002c0002t0001g0131a0002c0002t0001g0132 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.211-17521G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111960890 | ||||||
| chr12:111961065
|
A | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 5 | HG01243.hp1 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-17696T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961065 | ||||||
| chr12:111961106
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.211-17737A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961106 | ||||||
| chr12:111961441
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.211-18072G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961441 | ||||||
| chr12:111961469
|
A | T | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-18100T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961469 | ||||||
| chr12:111961538
|
G | A | 1 | a0002c0002t0001g0312 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211-18169C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961538 | ||||||
| chr12:111961650
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.211-18281A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961650 | ||||||
| chr12:111961850
|
T | A | 1 | a0002c0002t0001g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211-18481A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961850 | ||||||
| chr12:111961850
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-18481A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111961850 | ||||||
| chr12:111962205
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.211-18836A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962205 | ||||||
| chr12:111962208
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-18839C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962208 | ||||||
| chr12:111962264
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-18895G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962264 | ||||||
| chr12:111962273
|
TCAAGCTA others(1): Show |
T | 7 | a0002c0002t0001g0287a0002c0002t0001g0288a0002c0002t0001g0289others(4): Show | 7 | HG01081.hp1 HG01099.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-18912_211-1890 others(12): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962273 | ||||||
| chr12:111962362
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-18993A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962362 | ||||||
| chr12:111962709
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.211-19340T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111962709 | ||||||
| chr12:111963049
|
CAT | C | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG03098.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-19682_211-1968 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111963049 | ||||||
| chr12:111963764
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-20395T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111963764 | ||||||
| chr12:111964310
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-20941G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964310 | ||||||
| chr12:111964440
|
C | CA | 6 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0104others(3): Show | 6 | HG01243.hp1 HG06807.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-21072dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964440 | ||||||
| chr12:111964646
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-21277G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964646 | ||||||
| chr12:111964654
|
A | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-21285T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964654 | ||||||
| chr12:111964773
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.211-21404C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964773 | ||||||
| chr12:111964785
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.211-21416C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964785 | ||||||
| chr12:111964864
|
A | AT | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-21496_211-2149 others(5): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964864 | ||||||
| chr12:111964865
|
A | T | 103 | a0001c0001t0001g0234a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 107 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.211-21496T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964865 | ||||||
| chr12:111964885
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.211-21516G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964885 | ||||||
| chr12:111964913
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(197): Show | 207 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.211-21544T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111964913 | ||||||
| chr12:111965146
|
G | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-21777C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965146 | ||||||
| chr12:111965331
|
A | G | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.211-21962T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965331 | ||||||
| chr12:111965357
|
A | T | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.211-21988T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965357 | ||||||
| chr12:111965672
|
C | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-22303G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965672 | ||||||
| chr12:111965692
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.211-22323T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965692 | ||||||
| chr12:111965761
|
TA | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-22393delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965761 | ||||||
| chr12:111965868
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-22499C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965868 | ||||||
| chr12:111965983
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-22614A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111965983 | ||||||
| chr12:111966009
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-22640A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966009 | ||||||
| chr12:111966127
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(223): Show | 234 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.211-22758T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966127 | ||||||
| chr12:111966193
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-22824G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966193 | ||||||
| chr12:111966216
|
G | A | 2 | a0002c0002t0001g0291a0002c0002t0001g0312 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.211-22847C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966216 | ||||||
| chr12:111966333
|
G | C | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0100others(4): Show | 7 | HG03492.hp1 HG03710.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-22964C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966333 | ||||||
| chr12:111966347
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.211-22978T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966347 | ||||||
| chr12:111966879
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211-23510A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966879 | ||||||
| chr12:111966890
|
C | G | 2 | a0002c0002t0001g0306a0002c0002t0001g0328 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.211-23521G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111966890 | ||||||
| chr12:111967034
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(223): Show | 234 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.211-23665C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111967034 | ||||||
| chr12:111967091
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.211-23722G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111967091 | ||||||
| chr12:111967218
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.211-23849G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111967218 | ||||||
| chr12:111967362
|
C | T | 1 | a0003c0009t0001g0125 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211-23993G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111967362 | ||||||
| chr12:111968065
|
A | AAAAC | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+23689_210+2369 others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968065 | ||||||
| chr12:111968142
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.210+23616C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968142 | ||||||
| chr12:111968294
|
G | A | 7 | a0002c0002t0001g0287a0002c0002t0001g0288a0002c0002t0001g0289others(4): Show | 7 | HG01081.hp1 HG01099.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+23464C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968294 | ||||||
| chr12:111968444
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+23314T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968444 | ||||||
| chr12:111968602
|
A | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+23156T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968602 | ||||||
| chr12:111968696
|
T | A | 1 | a0001c0001t0003g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.210+23062A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968696 | ||||||
| chr12:111968849
|
C | T | 1 | a0002c0002t0001g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.210+22909G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968849 | ||||||
| chr12:111968862
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+22896C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968862 | ||||||
| chr12:111968945
|
G | A | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.210+22813C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968945 | ||||||
| chr12:111968967
|
T | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+22791A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968967 | ||||||
| chr12:111968992
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(112): Show | 118 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(115): Show |
intron_variant | MODIFIER | c.210+22765dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968992 | ||||||
| chr12:111968992
|
C | CAA | 6 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0047others(3): Show | 6 | HG01928.hp2 HG02135.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+22764_210+2276 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111968992 | ||||||
| chr12:111969007
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0114others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+22751T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969007 | ||||||
| chr12:111969009
|
A | G | 1 | a0002c0010t0001g0305 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.210+22749T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969009 | ||||||
| chr12:111969092
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210+22666C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969092 | ||||||
| chr12:111969111
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210+22647C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969111 | ||||||
| chr12:111969207
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+22551G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969207 | ||||||
| chr12:111969320
|
C | CA | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(174): Show | 184 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.210+22437dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969320 | ||||||
| chr12:111969320
|
C | CAA | 15 | a0001c0001t0001g0041a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG01256.hp1 HG01258.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+22436_210+2243 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969320 | ||||||
| chr12:111969390
|
GT | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+22367delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969390 | ||||||
| chr12:111969410
|
T | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(12): Show | 15 | HG01943.hp1 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+22348A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969410 | ||||||
| chr12:111969634
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+22124T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969634 | ||||||
| chr12:111969641
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.210+22117A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969641 | ||||||
| chr12:111969724
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210+22034G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969724 | ||||||
| chr12:111969739
|
G | A | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+22019C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969739 | ||||||
| chr12:111969761
|
G | T | 10 | a0002c0002t0001g0002a0002c0002t0001g0240a0002c0002t0001g0254others(7): Show | 12 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+21997C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969761 | ||||||
| chr12:111969784
|
TG | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+21973delC | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111969784 | ||||||
| chr12:111970572
|
T | C | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+21186A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111970572 | ||||||
| chr12:111970586
|
G | GT | 17 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0080others(14): Show | 17 | HG01243.hp1 HG01943.hp2 HG02738.hp1 others(14): Show |
intron_variant | MODIFIER | c.210+21171dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111970586 | ||||||
| chr12:111970586
|
GT | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(171): Show | 181 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.210+21171delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111970586 | ||||||
| chr12:111970586
|
GTT | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+21170_210+2117 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111970586 | ||||||
| chr12:111970617
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0031 | 2 | NA18942.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.210+21141G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111970617 | ||||||
| chr12:111971001
|
C | T | 6 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+20757G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971001 | ||||||
| chr12:111971057
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+20701C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971057 | ||||||
| chr12:111971094
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.210+20664C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971094 | ||||||
| chr12:111971141
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+20617T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971141 | ||||||
| chr12:111971489
|
C | T | 2 | a0001c0001t0001g0069a0005c0007t0001g0040 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.210+20269G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971489 | ||||||
| chr12:111971498
|
TA | T | 107 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0219others(104): Show | 111 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.210+20259delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971498 | ||||||
| chr12:111971617
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.210+20141G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971617 | ||||||
| chr12:111971979
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.210+19779C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111971979 | ||||||
| chr12:111972076
|
G | GA | 18 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0055others(15): Show | 18 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+19681dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972076 | ||||||
| chr12:111972076
|
G | GAAA | 81 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0128others(78): Show | 85 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.210+19679_210+1968 others(7): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972076 | ||||||
| chr12:111972076
|
G | GAAAA | 19 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0237others(16): Show | 19 | HG01099.hp1 HG01175.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.210+19678_210+1968 others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972076 | ||||||
| chr12:111972076
|
GA | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0149a0001c0001t0001g0211others(3): Show | 6 | HG02630.hp1 HG03225.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+19681delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972076 | ||||||
| chr12:111972097
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.210+19661G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972097 | ||||||
| chr12:111972273
|
C | A | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+19485G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972273 | ||||||
| chr12:111972382
|
T | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+19376A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972382 | ||||||
| chr12:111972531
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+19227A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972531 | ||||||
| chr12:111972850
|
T | TGGGTGAC others(135): Show |
1 | a0001c0001t0001g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.210+18766_210+1890 others(146): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972850 | ||||||
| chr12:111972885
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+18873T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111972885 | ||||||
| chr12:111973068
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.210+18690C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973068 | ||||||
| chr12:111973116
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+18642G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973116 | ||||||
| chr12:111973316
|
A | C | 2 | a0002c0002t0001g0306a0002c0002t0001g0328 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.210+18442T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973316 | ||||||
| chr12:111973386
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+18372A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973386 | ||||||
| chr12:111973391
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.210+18367A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973391 | ||||||
| chr12:111973697
|
A | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 22 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.210+18061T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973697 | ||||||
| chr12:111973725
|
G | A | 3 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.210+18033C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973725 | ||||||
| chr12:111973922
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | NA19006.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.210+17836G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111973922 | ||||||
| chr12:111974216
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+17542C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974216 | ||||||
| chr12:111974274
|
G | C | 1 | a0002c0002t0001g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.210+17484C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974274 | ||||||
| chr12:111974313
|
T | C | 1 | a0002c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.210+17445A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974313 | ||||||
| chr12:111974408
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.210+17350G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974408 | ||||||
| chr12:111974531
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.210+17227C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974531 | ||||||
| chr12:111974714
|
T | C | 4 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0314others(1): Show | 4 | HG00558.hp2 HG02132.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+17044A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111974714 | ||||||
| chr12:111975161
|
T | C | 3 | a0002c0002t0001g0306a0002c0002t0001g0328a0002c0010t0001g0305 | 3 | HG02055.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.210+16597A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975161 | ||||||
| chr12:111975168
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | NA18948.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.210+16590T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975168 | ||||||
| chr12:111975221
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.210+16537A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975221 | ||||||
| chr12:111975327
|
A | AT | 199 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(196): Show | 206 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.210+16430dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975327 | ||||||
| chr12:111975419
|
G | T | 1 | a0002c0002t0001g0267 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.210+16339C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975419 | ||||||
| chr12:111975436
|
AT | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+16321delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975436 | ||||||
| chr12:111975728
|
T | C | 1 | a0002c0002t0001g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.210+16030A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975728 | ||||||
| chr12:111975793
|
T | TA | 111 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(108): Show | 115 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.210+15964dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975793 | ||||||
| chr12:111975793
|
T | TAA | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+15963_210+1596 others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111975793 | ||||||
| chr12:111976154
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.210+15604C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111976154 | ||||||
| chr12:111976206
|
C | T | 3 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.210+15552G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111976206 | ||||||
| chr12:111976559
|
C | T | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+15199G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111976559 | ||||||
| chr12:111976747
|
G | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+15011C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111976747 | ||||||
| chr12:111976763
|
A | T | 1 | a0002c0002t0001g0324 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.210+14995T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111976763 | ||||||
| chr12:111977180
|
T | C | 6 | a0002c0002t0001g0003a0002c0002t0001g0265a0002c0002t0001g0267others(3): Show | 8 | NA18946.hp2 NA18950.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+14578A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111977180 | ||||||
| chr12:111977202
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210+14556C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111977202 | ||||||
| chr12:111977375
|
A | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+14383T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111977375 | ||||||
| chr12:111977550
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.210+14208T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111977550 | ||||||
| chr12:111977930
|
G | C | 3 | a0002c0002t0001g0304a0002c0002t0001g0313a0002c0002t0001g0332 | 3 | HG02027.hp2 NA18949.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.210+13828C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111977930 | ||||||
| chr12:111978129
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.210+13629G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978129 | ||||||
| chr12:111978185
|
A | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+13573T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978185 | ||||||
| chr12:111978405
|
G | GA | 103 | a0001c0001t0001g0036a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 107 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.210+13352dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978405 | ||||||
| chr12:111978710
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+13048G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978710 | ||||||
| chr12:111978782
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+12976G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978782 | ||||||
| chr12:111978990
|
T | C | 11 | a0002c0002t0001g0061a0002c0002t0001g0126a0002c0002t0001g0127others(8): Show | 11 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+12768A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111978990 | ||||||
| chr12:111979043
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+12715T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111979043 | ||||||
| chr12:111979145
|
C | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+12613G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111979145 | ||||||
| chr12:111979740
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0276 | 2 | NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.210+12018T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111979740 | ||||||
| chr12:111979832
|
A | C | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.210+11926T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111979832 | ||||||
| chr12:111980287
|
C | T | 1 | a0002c0002t0001g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.210+11471G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980287 | ||||||
| chr12:111980342
|
C | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(262): Show | 273 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(270): Show |
intron_variant | MODIFIER | c.210+11416G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980342 | ||||||
| chr12:111980440
|
T | TA | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+11317dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980440 | ||||||
| chr12:111980447
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.210+11311A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980447 | ||||||
| chr12:111980652
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.210+11106A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980652 | ||||||
| chr12:111980671
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.210+11087A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980671 | ||||||
| chr12:111980692
|
G | A | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+11066C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980692 | ||||||
| chr12:111980762
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0108 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.210+10996G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980762 | ||||||
| chr12:111980763
|
G | A | 2 | a0001c0001t0001g0075a0004c0008t0001g0233 | 2 | HG00140.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.210+10995C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980763 | ||||||
| chr12:111980835
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.210+10923T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980835 | ||||||
| chr12:111980852
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+10906A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111980852 | ||||||
| chr12:111981026
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.210+10732C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981026 | ||||||
| chr12:111981052
|
G | A | 2 | a0002c0002t0001g0291a0002c0002t0001g0312 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.210+10706C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981052 | ||||||
| chr12:111981064
|
CA | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 203 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.210+10693delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981064 | ||||||
| chr12:111981114
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(196): Show | 206 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.210+10644G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981114 | ||||||
| chr12:111981260
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226 | 3 | HG01884.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.210+10498C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981260 | ||||||
| chr12:111981584
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+10174C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981584 | ||||||
| chr12:111981712
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.210+10046A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111981712 | ||||||
| chr12:111982304
|
CT | C | 105 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(102): Show | 109 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.210+9453delA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111982304 | ||||||
| chr12:111982324
|
C | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+9434G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111982324 | ||||||
| chr12:111982559
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.210+9199G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111982559 | ||||||
| chr12:111983084
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.210+8674T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983084 | ||||||
| chr12:111983091
|
T | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+8667A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983091 | ||||||
| chr12:111983305
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.210+8453C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983305 | ||||||
| chr12:111983548
|
G | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+8210C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983548 | ||||||
| chr12:111983561
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.210+8197G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983561 | ||||||
| chr12:111983832
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.210+7926C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983832 | ||||||
| chr12:111983906
|
C | G | 1 | a0002c0002t0001g0329 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.210+7852G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983906 | ||||||
| chr12:111983952
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+7806C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983952 | ||||||
| chr12:111983968
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.210+7790T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111983968 | ||||||
| chr12:111984197
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.210+7561T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111984197 | ||||||
| chr12:111984591
|
CTAAAACA others(78): Show |
C | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.210+7082_210+7166d others(87): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111984591 | ||||||
| chr12:111984718
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+7040G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111984718 | ||||||
| chr12:111984813
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.210+6945A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111984813 | ||||||
| chr12:111984847
|
T | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226 | 3 | HG01884.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.210+6911A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111984847 | ||||||
| chr12:111985008
|
C | CTCATACT others(21): Show |
1 | a0001c0001t0001g0147 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.210+6722_210+6749d others(30): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985008 | ||||||
| chr12:111985121
|
T | C | 1 | a0002c0002t0001g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.210+6637A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985121 | ||||||
| chr12:111985258
|
T | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0061a0002c0002t0001g0126others(18): Show | 23 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+6500A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985258 | ||||||
| chr12:111985268
|
T | G | 3 | a0002c0002t0002g0247a0002c0002t0002g0260a0002c0002t0002g0261 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.210+6490A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985268 | ||||||
| chr12:111985277
|
T | TAC | 118 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(115): Show | 121 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.210+6479_210+6480d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985277 | ||||||
| chr12:111985277
|
TAC | T | 104 | a0001c0001t0003g0077a0001c0001t0003g0078a0002c0002t0001g0002others(101): Show | 108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.210+6479_210+6480d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985277 | ||||||
| chr12:111985310
|
TCAAA | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG01993.hp2 HG02135.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.210+6444_210+6447d others(6): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985310 | ||||||
| chr12:111985482
|
C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+6276G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985482 | ||||||
| chr12:111985776
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.210+5982A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985776 | ||||||
| chr12:111985862
|
G | A | 1 | a0002c0002t0001g0294 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+5896C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111985862 | ||||||
| chr12:111986025
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.210+5733A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986025 | ||||||
| chr12:111986169
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.210+5589T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986169 | ||||||
| chr12:111986183
|
C | T | 2 | a0002c0002t0001g0250a0002c0002t0001g0253 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.210+5575G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986183 | ||||||
| chr12:111986312
|
T | A | 3 | a0002c0002t0002g0247a0002c0002t0002g0260a0002c0002t0002g0261 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.210+5446A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986312 | ||||||
| chr12:111986415
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+5343G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986415 | ||||||
| chr12:111986540
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+5218A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986540 | ||||||
| chr12:111986549
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+5209G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986549 | ||||||
| chr12:111986607
|
C | G | 1 | a0002c0002t0001g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+5151G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986607 | ||||||
| chr12:111986627
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02135.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.210+5131A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986627 | ||||||
| chr12:111986667
|
G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+5091C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986667 | ||||||
| chr12:111986766
|
A | G | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(99): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.210+4992T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986766 | ||||||
| chr12:111986809
|
A | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.210+4949T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986809 | ||||||
| chr12:111986849
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+4909G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986849 | ||||||
| chr12:111986889
|
T | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0101others(4): Show | 7 | NA18941.hp1 NA18948.hp1 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+4869A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986889 | ||||||
| chr12:111986905
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0009c0011t0001g0209 | 3 | HG03017.hp2 HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.210+4853A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986905 | ||||||
| chr12:111986934
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0232 | 3 | HG02970.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.210+4824T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111986934 | ||||||
| chr12:111987236
|
G | A | 2 | a0001c0001t0001g0069a0005c0007t0001g0040 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.210+4522C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987236 | ||||||
| chr12:111987407
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.210+4351T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987407 | ||||||
| chr12:111987436
|
T | C | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG02257.hp2 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+4322A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987436 | ||||||
| chr12:111987509
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(81): Show | 87 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.210+4248dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987509 | ||||||
| chr12:111987509
|
C | CAA | 7 | a0001c0001t0001g0146a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01123.hp1 HG02109.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+4247_210+4248d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987509 | ||||||
| chr12:111987523
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.210+4235T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987523 | ||||||
| chr12:111987524
|
A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 23 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+4234T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987524 | ||||||
| chr12:111987581
|
A | T | 1 | a0002c0002t0001g0312 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+4177T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987581 | ||||||
| chr12:111987589
|
A | C | 1 | a0001c0001t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.210+4169T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987589 | ||||||
| chr12:111987646
|
C | T | 4 | a0002c0002t0001g0279a0002c0002t0001g0280a0002c0002t0001g0294others(1): Show | 4 | NA18942.hp2 NA18960.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+4112G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987646 | ||||||
| chr12:111987863
|
T | C | 6 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+3895A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987863 | ||||||
| chr12:111987942
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(223): Show | 234 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.210+3816A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111987942 | ||||||
| chr12:111988066
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.210+3692G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988066 | ||||||
| chr12:111988067
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0206 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.210+3691C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988067 | ||||||
| chr12:111988421
|
C | T | 1 | a0002c0003t0001g0278 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.210+3337G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988421 | ||||||
| chr12:111988618
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+3140C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988618 | ||||||
| chr12:111988704
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.210+3054G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988704 | ||||||
| chr12:111988838
|
A | T | 1 | a0002c0002t0001g0132 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.210+2920T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988838 | ||||||
| chr12:111988990
|
TCAAAAAC others(10): Show |
T | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0232 | 3 | HG02970.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.210+2751_210+2767d others(19): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111988990 | ||||||
| chr12:111989003
|
C | CAAAACA | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+2749_210+2754d others(8): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989003 | ||||||
| chr12:111989258
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.210+2500A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989258 | ||||||
| chr12:111989585
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.210+2173A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989585 | ||||||
| chr12:111989934
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+1824A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989934 | ||||||
| chr12:111989987
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.210+1771C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989987 | ||||||
| chr12:111989992
|
A | C | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.210+1766T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989992 | ||||||
| chr12:111989993
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.210+1765G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111989993 | ||||||
| chr12:111990177
|
C | T | 8 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(5): Show | 8 | HG01167.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+1581G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990177 | ||||||
| chr12:111990241
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210+1517G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990241 | ||||||
| chr12:111990269
|
AG | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(196): Show | 206 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.210+1488delC | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990269 | ||||||
| chr12:111990367
|
C | T | 76 | a0002c0002t0001g0003a0002c0002t0001g0241a0002c0002t0001g0242others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.210+1391G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990367 | ||||||
| chr12:111990578
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+1180A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990578 | ||||||
| chr12:111990943
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+815C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111990943 | ||||||
| chr12:111991217
|
C | CA | 47 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 48 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.210+540dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991217 | ||||||
| chr12:111991217
|
C | CAAAA | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | NA18952.hp1 NA18973.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+537_210+540dup others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991217 | ||||||
| chr12:111991217
|
CA | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(64): Show | 70 | HG00597.hp1 HG01071.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.210+540delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991217 | ||||||
| chr12:111991217
|
CAAA | C | 38 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0240others(35): Show | 38 | HG00597.hp2 HG00733.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.210+538_210+540del others(3): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991217 | ||||||
| chr12:111991217
|
CAAAA | C | 64 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0061others(61): Show | 68 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.210+537_210+540del others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991217 | ||||||
| chr12:111991221
|
A | C | 29 | a0002c0002t0001g0241a0002c0002t0001g0242a0002c0002t0001g0244others(26): Show | 29 | HG00597.hp2 HG01099.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.210+537T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991221 | ||||||
| chr12:111991222
|
A | C | 52 | a0002c0002t0001g0003a0002c0002t0001g0245a0002c0002t0001g0246others(49): Show | 54 | HG00558.hp1 HG00558.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.210+536T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991222 | ||||||
| chr12:111991251
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.210+507C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991251 | ||||||
| chr12:111991340
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226 | 3 | HG01884.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.210+418C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991340 | ||||||
| chr12:111991479
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | NA18985.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.210+279C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991479 | ||||||
| chr12:111991524
|
G | GA | 104 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(101): Show | 107 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.210+233dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991524 | ||||||
| chr12:111991525
|
A | AG | 101 | a0001c0001t0001g0256a0002c0002t0001g0002a0002c0002t0001g0003others(98): Show | 105 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.210+232_210+233ins others(1): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991525 | ||||||
| chr12:111991556
|
T | C | 5 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(2): Show | 5 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+202A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991556 | ||||||
| chr12:111991665
|
C | G | 103 | a0001c0001t0001g0256a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 107 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.210+93G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991665 | ||||||
| chr12:111991665
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+93G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991665 | ||||||
| chr12:111991751
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02630.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.210+7G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 4/10 | chr12 | 111991751 | ||||||
| chr12:111992030
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG01943.hp1 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-141T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992030 | ||||||
| chr12:111992269
|
C | CT | 9 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0143others(6): Show | 9 | HG01361.hp1 HG01934.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-381dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992269 | ||||||
| chr12:111992323
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01071.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.79-434C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992323 | ||||||
| chr12:111992358
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.79-469G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992358 | ||||||
| chr12:111992365
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.79-476C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992365 | ||||||
| chr12:111992485
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0232 | 3 | HG02970.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79-596C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992485 | ||||||
| chr12:111992542
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(262): Show | 273 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(270): Show |
intron_variant | MODIFIER | c.79-653G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992542 | ||||||
| chr12:111992744
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.79-855G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111992744 | ||||||
| chr12:111993084
|
G | A | 3 | a0002c0002t0001g0306a0002c0002t0001g0328a0002c0010t0001g0305 | 3 | HG02055.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.79-1195C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993084 | ||||||
| chr12:111993261
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 15 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.79-1372A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993261 | ||||||
| chr12:111993285
|
T | C | 1 | a0004c0008t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.79-1396A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993285 | ||||||
| chr12:111993408
|
T | C | 103 | a0001c0001t0001g0256a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 107 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.79-1519A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993408 | ||||||
| chr12:111993497
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79-1608C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993497 | ||||||
| chr12:111993672
|
G | A | 3 | a0002c0002t0001g0306a0002c0002t0001g0328a0002c0010t0001g0305 | 3 | HG02055.hp1 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.79-1783C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993672 | ||||||
| chr12:111993728
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.79-1839C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111993728 | ||||||
| chr12:111994089
|
T | G | 1 | a0002c0002t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.79-2200A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994089 | ||||||
| chr12:111994172
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.79-2283A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994172 | ||||||
| chr12:111994235
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2346A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994235 | ||||||
| chr12:111994351
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.79-2462C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994351 | ||||||
| chr12:111994869
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.79-2980T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994869 | ||||||
| chr12:111994905
|
A | G | 97 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(94): Show | 101 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.79-3016T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994905 | ||||||
| chr12:111994907
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79-3018G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111994907 | ||||||
| chr12:111995043
|
T | C | 3 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309 | 3 | HG03453.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.79-3154A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995043 | ||||||
| chr12:111995357
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.79-3468G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995357 | ||||||
| chr12:111995457
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.79-3568A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995457 | ||||||
| chr12:111995607
|
G | A | 97 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(94): Show | 101 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.79-3718C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995607 | ||||||
| chr12:111995664
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.79-3775C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995664 | ||||||
| chr12:111995670
|
G | A | 1 | a0002c0002t0001g0310 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.79-3781C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995670 | ||||||
| chr12:111995716
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79-3827G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995716 | ||||||
| chr12:111995752
|
A | G | 76 | a0001c0001t0001g0276a0002c0002t0001g0003a0002c0002t0001g0241others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.79-3863T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995752 | ||||||
| chr12:111995933
|
G | C | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.79-4044C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111995933 | ||||||
| chr12:111996039
|
C | CA | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(19): Show | 22 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.79-4151dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996039 | ||||||
| chr12:111996039
|
CA | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(22): Show | 26 | HG00544.hp2 HG01943.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.79-4151delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996039 | ||||||
| chr12:111996039
|
CAA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(74): Show | 80 | HG00597.hp1 HG00735.hp2 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.79-4152_79-4151del others(2): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996039 | ||||||
| chr12:111996348
|
C | T | 97 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(94): Show | 101 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.79-4459G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996348 | ||||||
| chr12:111996618
|
G | T | 1 | a0003c0009t0001g0125 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.79-4729C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996618 | ||||||
| chr12:111996665
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.79-4776A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996665 | ||||||
| chr12:111996700
|
A | G | 97 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(94): Show | 101 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.79-4811T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996700 | ||||||
| chr12:111996877
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.79-4988C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111996877 | ||||||
| chr12:111997275
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79-5386G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997275 | ||||||
| chr12:111997325
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.79-5436C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997325 | ||||||
| chr12:111997383
|
T | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0131a0002c0002t0001g0132 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.79-5494A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997383 | ||||||
| chr12:111997556
|
T | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5667A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997556 | ||||||
| chr12:111997660
|
C | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5771G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997660 | ||||||
| chr12:111997717
|
GAA | G | 2 | a0001c0001t0001g0005a0001c0001t0004g0006 | 3 | HG01496.hp2 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.79-5830_79-5829del others(2): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997717 | ||||||
| chr12:111997742
|
T | C | 1 | a0002c0002t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-5853A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997742 | ||||||
| chr12:111997959
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.78+5841T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997959 | ||||||
| chr12:111997969
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.78+5831T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111997969 | ||||||
| chr12:111998153
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+5647A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998153 | ||||||
| chr12:111998212
|
T | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+5588A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998212 | ||||||
| chr12:111998225
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.78+5575C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998225 | ||||||
| chr12:111998249
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0204 | 2 | HG02080.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.78+5551T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998249 | ||||||
| chr12:111998303
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+5497A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998303 | ||||||
| chr12:111998308
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.78+5492G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998308 | ||||||
| chr12:111998312
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0106 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.78+5488A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998312 | ||||||
| chr12:111998391
|
C | T | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+5409G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998391 | ||||||
| chr12:111998589
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.78+5211G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998589 | ||||||
| chr12:111998590
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+5210C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998590 | ||||||
| chr12:111998729
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(224): Show | 235 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.78+5071T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998729 | ||||||
| chr12:111998764
|
T | A | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(10): Show | 13 | HG00140.hp1 HG01106.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+5036A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998764 | ||||||
| chr12:111998873
|
G | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+4927C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111998873 | ||||||
| chr12:111999077
|
T | C | 2 | a0002c0002t0001g0250a0002c0002t0001g0253 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.78+4723A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999077 | ||||||
| chr12:111999156
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.78+4644C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999156 | ||||||
| chr12:111999206
|
T | C | 1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.78+4594A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999206 | ||||||
| chr12:111999226
|
C | CT | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+4573dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999226 | ||||||
| chr12:111999307
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.78+4493A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999307 | ||||||
| chr12:111999320
|
G | A | 4 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0314others(1): Show | 4 | HG00558.hp2 HG02132.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+4480C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999320 | ||||||
| chr12:111999323
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.78+4477G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999323 | ||||||
| chr12:111999345
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(80): Show | 86 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.78+4455G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999345 | ||||||
| chr12:111999593
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.78+4207G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999593 | ||||||
| chr12:111999656
|
A | C | 1 | a0002c0002t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.78+4144T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999656 | ||||||
| chr12:111999710
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(189): Show | 199 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(196): Show |
intron_variant | MODIFIER | c.78+4090G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 111999710 | ||||||
| chr12:112000242
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(189): Show | 199 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(196): Show |
intron_variant | MODIFIER | c.78+3558G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112000242 | ||||||
| chr12:112000458
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.78+3342C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112000458 | ||||||
| chr12:112000947
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+2853G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112000947 | ||||||
| chr12:112000966
|
C | G | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+2834G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112000966 | ||||||
| chr12:112001001
|
C | T | 5 | a0002c0002t0001g0272a0002c0002t0001g0273a0002c0002t0001g0274others(2): Show | 5 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+2799G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001001 | ||||||
| chr12:112001002
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+2798C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001002 | ||||||
| chr12:112001055
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+2745C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001055 | ||||||
| chr12:112001483
|
G | A | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+2317C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001483 | ||||||
| chr12:112001540
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+2260C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001540 | ||||||
| chr12:112001670
|
G | A | 1 | a0002c0002t0001g0324 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.78+2130C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001670 | ||||||
| chr12:112001860
|
C | T | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.78+1940G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001860 | ||||||
| chr12:112001897
|
G | T | 6 | a0002c0002t0001g0268a0002c0002t0001g0269a0002c0002t0001g0270others(3): Show | 6 | NA18939.hp2 NA18959.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+1903C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001897 | ||||||
| chr12:112001986
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.78+1814G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112001986 | ||||||
| chr12:112002029
|
C | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0206 | 2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.78+1771G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002029 | ||||||
| chr12:112002282
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.78+1518C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002282 | ||||||
| chr12:112002393
|
C | CA | 14 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0108others(11): Show | 14 | HG00597.hp2 HG01934.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+1406dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002393 | ||||||
| chr12:112002393
|
CA | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(10): Show | 13 | HG01169.hp1 HG01943.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+1406delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002393 | ||||||
| chr12:112002564
|
CA | C | 98 | a0001c0001t0001g0022a0001c0001t0001g0070a0001c0001t0001g0134others(95): Show | 102 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.78+1235delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002564 | ||||||
| chr12:112002706
|
T | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.78+1094A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002706 | ||||||
| chr12:112002927
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(263): Show | 274 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(271): Show |
intron_variant | MODIFIER | c.78+873C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112002927 | ||||||
| chr12:112003043
|
A | G | 14 | a0001c0001t0001g0256a0002c0002t0001g0002a0002c0002t0001g0240others(11): Show | 16 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.78+757T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003043 | ||||||
| chr12:112003084
|
T | C | 3 | a0002c0002t0002g0247a0002c0002t0002g0260a0002c0002t0002g0261 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.78+716A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003084 | ||||||
| chr12:112003194
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 31 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.78+606A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003194 | ||||||
| chr12:112003285
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(224): Show | 235 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.78+515T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003285 | ||||||
| chr12:112003295
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.78+505C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003295 | ||||||
| chr12:112003343
|
C | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+457G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003343 | ||||||
| chr12:112003364
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+436G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003364 | ||||||
| chr12:112003567
|
C | CA | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0222others(3): Show | 6 | HG02071.hp2 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+232dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003567 | ||||||
| chr12:112003567
|
CA | C | 10 | a0001c0001t0001g0004a0002c0002t0001g0003a0002c0002t0001g0250others(7): Show | 13 | HG02559.hp1 HG02622.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+232delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003567 | ||||||
| chr12:112003750
|
A | T | 1 | a0002c0002t0001g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.78+50T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 3/10 | chr12 | 112003750 | ||||||
| chr12:112003884
|
T | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.15-21A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112003884 | ||||||
| chr12:112003917
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.15-54C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112003917 | ||||||
| chr12:112003937
|
G | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.15-74C>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112003937 | ||||||
| chr12:112004484
|
G | A | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.15-621C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004484 | ||||||
| chr12:112004612
|
C | A | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.14+645G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004612 | ||||||
| chr12:112004628
|
A | G | 103 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(100): Show | 107 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.14+629T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004628 | ||||||
| chr12:112004645
|
G | C | 1 | a0002c0002t0001g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.14+612C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004645 | ||||||
| chr12:112004656
|
C | CT | 94 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(91): Show | 98 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.14+600dupA | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004656 | ||||||
| chr12:112004782
|
T | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.14+475A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004782 | ||||||
| chr12:112004839
|
A | T | 1 | a0002c0002t0001g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.14+418T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004839 | ||||||
| chr12:112004848
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.14+409G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112004848 | ||||||
| chr12:112005129
|
T | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+128A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112005129 | ||||||
| chr12:112005209
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+48G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112005209 | ||||||
| chr12:112005213
|
C | T | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.14+44G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 2/10 | chr12 | 112005213 | ||||||
| chr12:112005609
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-33-306G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112005609 | ||||||
| chr12:112005907
|
A | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0226others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-604T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112005907 | ||||||
| chr12:112006099
|
T | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-796A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006099 | ||||||
| chr12:112006100
|
C | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-797G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006100 | ||||||
| chr12:112006106
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG01074.hp2 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-33-803T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006106 | ||||||
| chr12:112006156
|
G | A | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-33-853C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006156 | ||||||
| chr12:112006305
|
A | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-33-1002T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006305 | ||||||
| chr12:112006350
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-33-1047C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006350 | ||||||
| chr12:112006454
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33-1151A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006454 | ||||||
| chr12:112006646
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-33-1343T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006646 | ||||||
| chr12:112006666
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33-1363A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006666 | ||||||
| chr12:112006688
|
C | T | 2 | a0002c0002t0001g0251a0002c0002t0001g0252 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-33-1385G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006688 | ||||||
| chr12:112006713
|
G | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-33-1410C>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006713 | ||||||
| chr12:112006733
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01071.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-33-1430A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006733 | ||||||
| chr12:112006737
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(86): Show | 92 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.-33-1434T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006737 | ||||||
| chr12:112006875
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG01993.hp2 HG02135.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-33-1572G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006875 | ||||||
| chr12:112006914
|
T | C | 1 | a0002c0002t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-33-1611A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006914 | ||||||
| chr12:112006946
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33-1643T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112006946 | ||||||
| chr12:112007028
|
C | T | 1 | a0002c0002t0001g0250 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-33-1725G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007028 | ||||||
| chr12:112007087
|
T | A | 102 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(99): Show | 106 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.-33-1784A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007087 | ||||||
| chr12:112007135
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-33-1832C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007135 | ||||||
| chr12:112007263
|
T | C | 3 | a0002c0002t0001g0262a0002c0002t0001g0264a0006c0006t0001g0263 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-33-1960A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007263 | ||||||
| chr12:112007374
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-33-2071T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007374 | ||||||
| chr12:112007486
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2183C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112007486 | ||||||
| chr12:112008036
|
T | C | 1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-33-2733A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008036 | ||||||
| chr12:112008165
|
C | A | 77 | a0001c0001t0001g0276a0002c0002t0001g0003a0002c0002t0001g0241others(74): Show | 79 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-33-2862G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008165 | ||||||
| chr12:112008242
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33-2939C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008242 | ||||||
| chr12:112008323
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-33-3020T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008323 | ||||||
| chr12:112008442
|
T | C | 102 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(99): Show | 106 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.-33-3139A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008442 | ||||||
| chr12:112008479
|
C | CA | 8 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0203others(5): Show | 8 | HG01175.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-3177dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008479 | ||||||
| chr12:112008551
|
T | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-33-3248A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008551 | ||||||
| chr12:112008601
|
T | C | 8 | a0001c0001t0001g0224a0002c0002t0001g0126a0002c0002t0001g0127others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-3298A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008601 | ||||||
| chr12:112008680
|
A | C | 1 | a0001c0001t0001g0239 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-33-3377T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008680 | ||||||
| chr12:112008689
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(189): Show | 199 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(196): Show |
intron_variant | MODIFIER | c.-33-3386T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008689 | ||||||
| chr12:112008906
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(189): Show | 199 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(196): Show |
intron_variant | MODIFIER | c.-33-3603A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008906 | ||||||
| chr12:112008962
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33-3659G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008962 | ||||||
| chr12:112008975
|
C | CA | 7 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(4): Show | 7 | HG02258.hp2 HG03017.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-3673dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008975 | ||||||
| chr12:112008975
|
CA | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0039a0001c0001t0001g0041others(4): Show | 7 | HG01168.hp1 HG03017.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-3673delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112008975 | ||||||
| chr12:112009238
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-34+3764G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009238 | ||||||
| chr12:112009484
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+3518C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009484 | ||||||
| chr12:112009534
|
T | TCA | 5 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+3467_-34+3468i others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009534 | ||||||
| chr12:112009535
|
T | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+3467A>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009535 | ||||||
| chr12:112009535
|
T | TA | 97 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(94): Show | 101 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(98): Show |
intron_variant | MODIFIER | c.-34+3466dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009535 | ||||||
| chr12:112009535
|
T | TAA | 8 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 8 | HG02074.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+3465_-34+3466d others(4): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009535 | ||||||
| chr12:112009535
|
TA | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(11): Show | 14 | HG01928.hp1 HG01928.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+3466delT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009535 | ||||||
| chr12:112009551
|
A | AG | 3 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0003t0001g0243 | 3 | HG00558.hp2 HG02132.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-34+3450_-34+3451i others(3): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009551 | ||||||
| chr12:112009556
|
T | G | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+3446A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009556 | ||||||
| chr12:112009607
|
G | A | 1 | a0001c0001t0004g0006 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-34+3395C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009607 | ||||||
| chr12:112009683
|
C | CA | 5 | a0001c0001t0001g0004a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 6 | HG02257.hp2 HG02559.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+3318dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009683 | ||||||
| chr12:112009843
|
C | CA | 7 | a0001c0001t0001g0005a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01496.hp2 HG01952.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+3158dupT | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009843 | ||||||
| chr12:112009848
|
A | C | 1 | a0002c0002t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-34+3154T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009848 | ||||||
| chr12:112009853
|
A | C | 1 | a0002c0002t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-34+3149T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009853 | ||||||
| chr12:112009863
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34+3139G>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009863 | ||||||
| chr12:112009871
|
A | G | 1 | a0002c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34+3131T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009871 | ||||||
| chr12:112009958
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-34+3044A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112009958 | ||||||
| chr12:112010057
|
CCCT | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+2942_-34+2944d others(5): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010057 | ||||||
| chr12:112010358
|
A | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+2644T>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010358 | ||||||
| chr12:112010449
|
T | C | 1 | a0002c0002t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-34+2553A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010449 | ||||||
| chr12:112010534
|
A | T | 1 | a0001c0001t0001g0020 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-34+2468T>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010534 | ||||||
| chr12:112010562
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG01943.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+2440G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010562 | ||||||
| chr12:112010681
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(327): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-34+2321A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010681 | ||||||
| chr12:112010827
|
C | T | 1 | a0002c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-34+2175G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010827 | ||||||
| chr12:112010847
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-34+2155G>A | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010847 | ||||||
| chr12:112010858
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-34+2144A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112010858 | ||||||
| chr12:112011005
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-34+1997A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011005 | ||||||
| chr12:112011072
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-34+1930C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011072 | ||||||
| chr12:112011079
|
A | G | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+1923T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011079 | ||||||
| chr12:112011292
|
T | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34+1710A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011292 | ||||||
| chr12:112011819
|
C | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+1183G>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011819 | ||||||
| chr12:112011973
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-34+1029C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112011973 | ||||||
| chr12:112012286
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-34+716C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012286 | ||||||
| chr12:112012420
|
G | A | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG02257.hp2 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+582C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012420 | ||||||
| chr12:112012549
|
GATTACAG others(41): Show |
G | 1 | a0001c0001t0001g0008 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-34+405_-34+452del others(48): Show |
TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012549 | ||||||
| chr12:112012629
|
A | G | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+373T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012629 | ||||||
| chr12:112012706
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-34+296C>T | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012706 | ||||||
| chr12:112012715
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-34+287T>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012715 | ||||||
| chr12:112012766
|
T | G | 1 | a0001c0001t0001g0239 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+236A>C | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012766 | ||||||
| chr12:112012950
|
T | C | 96 | a0001c0001t0001g0256a0001c0001t0001g0276a0002c0002t0001g0002others(93): Show | 100 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+52A>G | TMEM116 | ENSG00000198270.13 | transcript | ENST00000552374.7 | protein_coding | 1/10 | chr12 | 112012950 |