Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10972 |
|---|---|
| ensemblid | ENSG00000170348.9 |
| hgncid | 16998 |
| symbol | TMED10 |
| name | transmembrane p24 trafficking protein 10 |
| refseq_nuc | NM_006827.6 |
| refseq_prot | NP_006818.3 |
| ensembl_nuc | ENST00000303575.9 |
| ensembl_prot | ENSP00000303145.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 75131469 |
| end | 75176612 |
| strand | - |
| ver | v1.2 |
| region | chr14:75131469-75176612 |
| region5000 | chr14:75126469-75181612 |
| regionname0 | TMED10_chr14_75131469_75176612 |
| regionname5000 | TMED10_chr14_75126469_75181612 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 219 | 261 | 86 | 48 | 85 | 8 | 32 | 63 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0002 | 0/0 | 219 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 660 | 242 | 72 | 46 | 85 | 8 | 29 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| c0002 | 0/0 | 660 | 19 | 14 | 2 | 0 | 0 | 3 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| c0003 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3451 | 84 | 13 | 15 | 43 | 2 | 10 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0002 | 0/0 | 3449 | 64 | 26 | 13 | 14 | 4 | 7 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0003 | 0/0 | 3452 | 25 | 5 | 4 | 11 | 0 | 5 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0004 | 0/0 | 3450 | 25 | 11 | 4 | 5 | 0 | 5 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0005 | 0/0 | 3450 | 11 | 3 | 1 | 5 | 1 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0006 | 0/0 | 3449 | 8 | 2 | 4 | 0 | 1 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0007 | 0/0 | 3451 | 7 | 5 | 1 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0008 | 0/0 | 3450 | 6 | 4 | 1 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0009 | 1/0 | 3450 | 5 | 2 | 2 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0010 | 0/0 | 3451 | 5 | 1 | 0 | 3 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0011 | 0/0 | 3450 | 4 | 1 | 2 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0012 | 0/0 | 3452 | 4 | 4 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0013 | 0/0 | 3450 | 3 | 0 | 0 | 3 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0014 | 0/0 | 3452 | 3 | 3 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0015 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0016 | 0/0 | 3449 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0017 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0018 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0019 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0020 | 0/0 | 3451 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0021 | 0/0 | 3449 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| t0022 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 660 | 242 | 72 | 46 | 85 | 8 | 29 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0002 | 0/0 | 660 | 19 | 14 | 2 | 0 | 0 | 3 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0002c0003 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4110 | 68 | 2 | 13 | 42 | 2 | 8 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0002 | 0/0 | 4108 | 64 | 26 | 13 | 14 | 4 | 7 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0003 | 0/0 | 4111 | 22 | 2 | 4 | 11 | 0 | 5 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0004 | 0/0 | 4109 | 25 | 11 | 4 | 5 | 0 | 5 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0005 | 0/0 | 4109 | 10 | 3 | 1 | 5 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0006 | 0/0 | 4108 | 8 | 2 | 4 | 0 | 1 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0007 | 0/0 | 4110 | 7 | 5 | 1 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0008 | 0/0 | 4109 | 6 | 4 | 1 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0009 | 1/0 | 4109 | 5 | 2 | 2 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0010 | 0/0 | 4110 | 5 | 1 | 0 | 3 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0011 | 0/0 | 4109 | 4 | 1 | 2 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0012 | 0/0 | 4111 | 4 | 4 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0013 | 0/0 | 4109 | 3 | 0 | 0 | 3 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0014 | 0/0 | 4111 | 3 | 3 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0015 | 0/0 | 4111 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0016 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0017 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0018 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0019 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0020 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0021 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0001t0022 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0002t0001 | 0/0 | 4110 | 15 | 11 | 2 | 0 | 0 | 2 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0002t0003 | 0/0 | 4111 | 3 | 3 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0001c0002t0005 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| a0002c0003t0001 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | copy fasta | chr14 | 75126469 | 75181612 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0013g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0013g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0014g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0017g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0018g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0019g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0020g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0021g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0022g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0002c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | GBR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0032 | EUR | FIN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0100 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00642 | hp2 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0178 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0055 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0251 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0239 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0168 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0118 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0006 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0044 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0256 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02074 | hp1 | a0001 | c0001 | t0013 | g0128 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0075 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0072 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0180 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0200 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0248 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0240 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0238 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0121 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0123 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0241 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0246 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0252 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0258 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03195 | hp2 | a0001 | c0001 | t0022 | g0244 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03490 | hp1 | a0001 | c0001 | t0021 | g0179 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0205 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0062 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0043 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0232 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04184 | hp1 | a0001 | c0001 | t0011 | g0111 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0074 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0257 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0242 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18980 | hp1 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19068 | hp2 | a0001 | c0001 | t0013 | g0230 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19084 | hp1 | a0001 | c0001 | t0013 | g0221 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ASW | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0056 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0076 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0188 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0250 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0236 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0227 | REF | REF | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75176429
|
C | T | 1 | a0002 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.151G>A | p.Asp51Asn | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/5 | 184/4109 | 151/660 | 51/219 | chr14 | 75176429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75134960
|
G | A | 1 | a0001c0002 | 19 | HG00741.hp2 HG01346.hp2 HG01884.hp1 others(16): Show |
synonymous_variant | LOW | c.585C>T | p.Phe195Phe | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 618/4109 | 585/660 | 195/219 | chr14 | 75134960 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75132336
|
T | C | 1 | a0001c0001t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2549 | chr14 | 75132336 | |||||
| chr14:75132384
|
T | TC | 6 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(3): Show | 97 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2500dupG | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | |||||
| chr14:75132384
|
T | TCC | 4 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(1): Show | 30 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2499_*2500dupGG | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | |||||
| chr14:75132384
|
T | TTC | 1 | a0001c0001t0014 | 3 | HG02717.hp1 HG02895.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2500_*2501insGA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | |||||
| chr14:75132396
|
CA | C | 4 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(1): Show | 74 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2488delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2488 | chr14 | 75132396 | |||||
| chr14:75132397
|
A | C | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0011others(4): Show | 45 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2488T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2488 | chr14 | 75132397 | |||||
| chr14:75132398
|
A | C | 2 | a0001c0001t0006a0001c0001t0011 | 12 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2487T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2487 | chr14 | 75132398 | |||||
| chr14:75132426
|
A | G | 2 | a0001c0001t0010a0001c0001t0022 | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2459T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2459 | chr14 | 75132426 | |||||
| chr14:75132452
|
G | A | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2433C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2433 | chr14 | 75132452 | |||||
| chr14:75132625
|
G | C | 2 | a0001c0001t0010a0001c0001t0022 | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2260C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2260 | chr14 | 75132625 | |||||
| chr14:75132944
|
A | G | 8 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | 123 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1941T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1941 | chr14 | 75132944 | |||||
| chr14:75133007
|
T | C | 1 | a0001c0001t0021 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1878A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1878 | chr14 | 75133007 | |||||
| chr14:75133832
|
C | T | 1 | a0001c0001t0018 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1053 | chr14 | 75133832 | |||||
| chr14:75133849
|
G | A | 2 | a0001c0001t0010a0001c0001t0022 | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1036C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1036 | chr14 | 75133849 | |||||
| chr14:75133994
|
C | T | 10 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 891 | chr14 | 75133994 | |||||
| chr14:75134258
|
C | T | 1 | a0001c0001t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*627G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 627 | chr14 | 75134258 | |||||
| chr14:75134541
|
G | T | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*344C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 344 | chr14 | 75134541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75135034
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(113): Show | 119 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.539-28T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135034 | ||||||
| chr14:75135068
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0011 | 3 | HG01243.hp2 HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.539-62A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135068 | ||||||
| chr14:75135079
|
G | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(80): Show | 84 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.539-73C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135079 | ||||||
| chr14:75135120
|
C | CTAACA | 13 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0080others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.539-119_539-115dup others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135120 | ||||||
| chr14:75135159
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.539-153T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135159 | ||||||
| chr14:75135260
|
C | T | 113 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(110): Show | 114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.539-254G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135260 | ||||||
| chr14:75135325
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.539-319T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135325 | ||||||
| chr14:75136131
|
A | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.412-245T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136131 | ||||||
| chr14:75136325
|
A | C | 13 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0080others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-439T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136325 | ||||||
| chr14:75136405
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.412-519G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136405 | ||||||
| chr14:75136536
|
A | G | 4 | a0001c0001t0014g0238a0001c0001t0014g0240a0001c0001t0014g0241others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-650T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136536 | ||||||
| chr14:75136703
|
T | C | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-817A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136703 | ||||||
| chr14:75136861
|
T | C | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.412-975A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136861 | ||||||
| chr14:75136962
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.412-1076A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136962 | ||||||
| chr14:75137015
|
C | CT | 7 | a0001c0001t0001g0148a0001c0001t0002g0247a0001c0001t0009g0257others(4): Show | 7 | HG02615.hp2 HG03017.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-1130dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137015 | ||||||
| chr14:75137246
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(113): Show | 119 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.412-1360C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137246 | ||||||
| chr14:75137514
|
T | A | 1 | a0001c0001t0002g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.412-1628A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137514 | ||||||
| chr14:75137606
|
C | T | 2 | a0001c0001t0010g0233a0001c0001t0010g0243 | 2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.412-1720G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137606 | ||||||
| chr14:75137622
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.412-1736A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137622 | ||||||
| chr14:75137691
|
A | AT | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(9): Show | 12 | HG01099.hp1 HG01109.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.412-1806dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137691 | ||||||
| chr14:75137691
|
A | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(236): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.412-1805T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137691 | ||||||
| chr14:75137694
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.412-1808G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137694 | ||||||
| chr14:75137696
|
G | GTTTC | 108 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 109 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.412-1814_412-1811d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137696 | ||||||
| chr14:75137708
|
CT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(114): Show | 120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.412-1823delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137708 | ||||||
| chr14:75137708
|
CTT | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0189others(2): Show | 5 | HG01099.hp1 HG01884.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1824_412-1823d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137708 | ||||||
| chr14:75137874
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.412-1988T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137874 | ||||||
| chr14:75138035
|
T | G | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2149A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138035 | ||||||
| chr14:75138073
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 6 | HG00558.hp1 NA18939.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-2187G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138073 | ||||||
| chr14:75138352
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0143a0001c0001t0001g0189others(44): Show | 49 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.412-2466C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138352 | ||||||
| chr14:75138399
|
A | C | 1 | a0001c0001t0005g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.412-2513T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138399 | ||||||
| chr14:75138501
|
A | T | 1 | a0001c0001t0021g0179 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.412-2615T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138501 | ||||||
| chr14:75138812
|
C | CT | 22 | a0001c0001t0002g0093a0001c0001t0002g0115a0001c0001t0002g0247others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.412-2927dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | ||||||
| chr14:75138812
|
C | CTT | 85 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.412-2928_412-2927d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | ||||||
| chr14:75138812
|
C | CTTT | 13 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(10): Show | 13 | HG00642.hp1 HG01255.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.412-2929_412-2927d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | ||||||
| chr14:75138824
|
T | TTA | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2939_412-2938i others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138824 | ||||||
| chr14:75138825
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0177 | 2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.412-2939A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138825 | ||||||
| chr14:75138825
|
T | TA | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(119): Show | 125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.412-2940_412-2939i others(3): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138825 | ||||||
| chr14:75138833
|
A | C | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.412-2947T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138833 | ||||||
| chr14:75138901
|
T | C | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-3015A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138901 | ||||||
| chr14:75138982
|
A | G | 3 | a0001c0001t0002g0247a0001c0001t0015g0246a0001c0001t0018g0248 | 3 | HG02615.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.412-3096T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138982 | ||||||
| chr14:75139089
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 123 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.412-3203T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139089 | ||||||
| chr14:75139360
|
TAATC | T | 88 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.412-3478_412-3475d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139360 | ||||||
| chr14:75139635
|
C | CA | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(113): Show | 119 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.412-3750dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139635 | ||||||
| chr14:75139635
|
C | CAA | 11 | a0001c0001t0003g0172a0001c0001t0003g0213a0001c0001t0004g0102others(8): Show | 11 | HG00673.hp1 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.412-3751_412-3750d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139635 | ||||||
| chr14:75140016
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.412-4130A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140016 | ||||||
| chr14:75140185
|
A | C | 2 | a0001c0001t0007g0059a0001c0001t0007g0060 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.412-4299T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140185 | ||||||
| chr14:75140186
|
C | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.412-4300G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140186 | ||||||
| chr14:75140321
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.412-4435C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140321 | ||||||
| chr14:75140342
|
G | A | 94 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(91): Show | 95 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.412-4456C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140342 | ||||||
| chr14:75140743
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412-4857A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140743 | ||||||
| chr14:75140861
|
C | G | 4 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243others(1): Show | 4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-4975G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140861 | ||||||
| chr14:75140863
|
C | G | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412-4977G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140863 | ||||||
| chr14:75141050
|
A | G | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-5164T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141050 | ||||||
| chr14:75141064
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.412-5178G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141064 | ||||||
| chr14:75141083
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(249): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.412-5197A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141083 | ||||||
| chr14:75141141
|
A | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0156others(2): Show | 6 | HG01361.hp2 HG02293.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-5255T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141141 | ||||||
| chr14:75141214
|
G | A | 1 | a0001c0001t0004g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-5328C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141214 | ||||||
| chr14:75141565
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-5679T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141565 | ||||||
| chr14:75141673
|
A | G | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412-5787T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141673 | ||||||
| chr14:75141721
|
T | C | 2 | a0001c0001t0002g0092a0001c0001t0002g0094 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.412-5835A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141721 | ||||||
| chr14:75141919
|
G | A | 1 | a0001c0002t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.411+5745C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141919 | ||||||
| chr14:75141980
|
C | G | 110 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(107): Show | 111 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.411+5684G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141980 | ||||||
| chr14:75142025
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(113): Show | 119 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.411+5639C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142025 | ||||||
| chr14:75142079
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.411+5585T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142079 | ||||||
| chr14:75142333
|
G | T | 1 | a0001c0001t0004g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.411+5331C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142333 | ||||||
| chr14:75142387
|
C | T | 4 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243others(1): Show | 4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+5277G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142387 | ||||||
| chr14:75142565
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.411+5099T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142565 | ||||||
| chr14:75142607
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+5057A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142607 | ||||||
| chr14:75142864
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.411+4800A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142864 | ||||||
| chr14:75142890
|
G | C | 8 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4774C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142890 | ||||||
| chr14:75143181
|
G | A | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+4483C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143181 | ||||||
| chr14:75143297
|
C | T | 1 | a0001c0001t0005g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.411+4367G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143297 | ||||||
| chr14:75143467
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.411+4197C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143467 | ||||||
| chr14:75143933
|
C | CA | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(201): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.411+3730dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143933 | ||||||
| chr14:75143933
|
C | CAA | 5 | a0001c0001t0001g0141a0001c0001t0001g0228a0001c0001t0003g0129others(2): Show | 5 | HG03516.hp2 HG03831.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+3729_411+3730d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143933 | ||||||
| chr14:75143987
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.411+3677G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143987 | ||||||
| chr14:75143994
|
A | C | 1 | a0001c0001t0002g0071 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.411+3670T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143994 | ||||||
| chr14:75144022
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.411+3642T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144022 | ||||||
| chr14:75144069
|
A | G | 1 | a0001c0002t0003g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.411+3595T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144069 | ||||||
| chr14:75144278
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.411+3386G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144278 | ||||||
| chr14:75144458
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0003g0212 | 3 | HG01099.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.411+3206C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144458 | ||||||
| chr14:75144478
|
A | G | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+3186T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144478 | ||||||
| chr14:75144489
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0003g0212 | 3 | HG01099.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.411+3175G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144489 | ||||||
| chr14:75144581
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0220a0001c0001t0005g0219 | 3 | HG02080.hp2 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.411+3083G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144581 | ||||||
| chr14:75144609
|
AGTCCACA others(18): Show |
A | 1 | a0001c0001t0006g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+3030_411+3054d others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144609 | ||||||
| chr14:75144617
|
G | A | 5 | a0001c0002t0001g0198a0001c0002t0001g0201a0001c0002t0001g0202others(2): Show | 5 | HG00741.hp2 HG01346.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+3047C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144617 | ||||||
| chr14:75144752
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.411+2912G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144752 | ||||||
| chr14:75144782
|
C | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+2882G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144782 | ||||||
| chr14:75144819
|
G | A | 1 | a0001c0001t0010g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.411+2845C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144819 | ||||||
| chr14:75144856
|
G | T | 1 | a0001c0001t0004g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.411+2808C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144856 | ||||||
| chr14:75145322
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.411+2342G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145322 | ||||||
| chr14:75145324
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2340T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145324 | ||||||
| chr14:75145380
|
C | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.411+2284G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145380 | ||||||
| chr14:75145519
|
C | G | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+2145G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145519 | ||||||
| chr14:75145769
|
C | T | 14 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(11): Show | 14 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+1895G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145769 | ||||||
| chr14:75145770
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(249): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.411+1894T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145770 | ||||||
| chr14:75146146
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.411+1518G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146146 | ||||||
| chr14:75146388
|
C | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0164others(3): Show | 6 | HG00738.hp2 HG01256.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+1276G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146388 | ||||||
| chr14:75146406
|
A | G | 1 | a0001c0001t0005g0131 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.411+1258T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146406 | ||||||
| chr14:75146475
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0045a0001c0001t0006g0046others(5): Show | 8 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+1189G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146475 | ||||||
| chr14:75146908
|
C | CAGAT | 104 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.411+752_411+755dup others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | ||||||
| chr14:75146908
|
C | CAGATAGA others(1): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0135a0001c0001t0001g0139others(56): Show | 60 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.411+748_411+755dup others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | ||||||
| chr14:75146908
|
C | CAGATAGA others(5): Show |
18 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0146others(15): Show | 18 | HG00741.hp2 HG01256.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.411+744_411+755dup others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | ||||||
| chr14:75146908
|
C | CAGATAGA others(9): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0203 | 2 | HG03654.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.411+740_411+755dup others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | ||||||
| chr14:75146908
|
CAGAT | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0145others(11): Show | 14 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+752_411+755del others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | ||||||
| chr14:75146928
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+736A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146928 | ||||||
| chr14:75147184
|
T | C | 1 | a0001c0001t0004g0102 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.411+480A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147184 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0005g0009a0001c0001t0006g0046 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.411+469_411+478dup others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(7): Show |
5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0038others(2): Show | 5 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+478_411+479ins others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0002g0037a0001c0001t0004g0041a0001c0001t0004g0042 | 3 | HG03130.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+478_411+479ins others(15): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0005g0008a0001c0001t0006g0043a0001c0001t0006g0045others(1): Show | 4 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+468_411+478dup others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0005g0011a0001c0001t0011g0044a0001c0001t0011g0111 | 3 | HG01261.hp2 HG02630.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.411+467_411+478dup others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0006g0178a0001c0001t0011g0034 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.411+466_411+478dup others(13): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(7): Show |
7 | a0001c0001t0004g0077a0001c0001t0004g0081a0001c0001t0004g0126others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+465_411+478dup others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0004g0079a0001c0001t0012g0072a0001c0001t0012g0075 | 3 | HG02145.hp2 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.411+464_411+478dup others(15): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(9): Show |
2 | a0001c0001t0004g0122a0001c0001t0012g0076 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.411+463_411+478dup others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.411+461_411+478dup others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
GT | G | 6 | a0001c0001t0002g0023a0001c0001t0002g0052a0001c0001t0002g0069others(3): Show | 6 | HG00741.hp1 HG01981.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+478delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
GTT | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.411+477_411+478del others(2): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147185
|
GTTTTTTT | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(109): Show | 115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.411+472_411+478del others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | ||||||
| chr14:75147188
|
T | G | 1 | a0001c0001t0004g0102 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.411+476A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147188 | ||||||
| chr14:75147191
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0004g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.411+472_411+473ins others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147191 | ||||||
| chr14:75147287
|
C | T | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+377G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147287 | ||||||
| chr14:75147431
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+233G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147431 | ||||||
| chr14:75147801
|
A | ACCCG | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(110): Show | 116 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.338-68_338-65dupCG others(2): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147801 | ||||||
| chr14:75147805
|
G | C | 1 | a0001c0001t0003g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.338-68C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147805 | ||||||
| chr14:75147852
|
A | G | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-115T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147852 | ||||||
| chr14:75148139
|
T | C | 2 | a0001c0001t0002g0247a0001c0001t0018g0248 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.338-402A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148139 | ||||||
| chr14:75148185
|
A | G | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-448T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148185 | ||||||
| chr14:75148222
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.338-485C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148222 | ||||||
| chr14:75148514
|
AATC | A | 3 | a0001c0001t0001g0135a0001c0001t0005g0153a0001c0001t0005g0175 | 3 | NA18954.hp1 NA18981.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.338-780_338-778del others(3): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148514 | ||||||
| chr14:75148524
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.338-787A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148524 | ||||||
| chr14:75148543
|
C | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(93): Show | 97 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.338-806G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148543 | ||||||
| chr14:75148565
|
C | T | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.338-828G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148565 | ||||||
| chr14:75148890
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.338-1153T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148890 | ||||||
| chr14:75148923
|
A | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(148): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.338-1186T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148923 | ||||||
| chr14:75148976
|
G | A | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-1239C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148976 | ||||||
| chr14:75148992
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0005g0009 | 2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.338-1255G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148992 | ||||||
| chr14:75149279
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.338-1542A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149279 | ||||||
| chr14:75149472
|
A | ATAAAT | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.338-1736_338-1735i others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149472 | ||||||
| chr14:75149746
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(254): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.338-2009G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149746 | ||||||
| chr14:75149781
|
C | T | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-2044G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149781 | ||||||
| chr14:75149837
|
GCT | G | 109 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2102_338-2101d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149837 | ||||||
| chr14:75149840
|
C | G | 109 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2103G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149840 | ||||||
| chr14:75149842
|
T | G | 109 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2105A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149842 | ||||||
| chr14:75149845
|
CTGT | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2111_338-2109d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149845 | ||||||
| chr14:75149849
|
A | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2112T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149849 | ||||||
| chr14:75149964
|
G | A | 8 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+2068C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149964 | ||||||
| chr14:75150110
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0176others(1): Show | 5 | NA18982.hp1 NA18984.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+1922T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150110 | ||||||
| chr14:75150149
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0003g0222 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.337+1883G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150149 | ||||||
| chr14:75150226
|
G | T | 1 | a0001c0001t0003g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.337+1806C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150226 | ||||||
| chr14:75150319
|
C | T | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.337+1713G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150319 | ||||||
| chr14:75150737
|
G | A | 6 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0092others(3): Show | 6 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1295C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150737 | ||||||
| chr14:75150770
|
G | A | 1 | a0001c0001t0009g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.337+1262C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150770 | ||||||
| chr14:75151022
|
C | T | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1010G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151022 | ||||||
| chr14:75151116
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.337+916C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151116 | ||||||
| chr14:75151215
|
G | T | 2 | a0001c0001t0002g0089a0001c0001t0009g0250 | 2 | HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.337+817C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151215 | ||||||
| chr14:75151425
|
G | C | 1 | a0001c0001t0004g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.337+607C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151425 | ||||||
| chr14:75151426
|
C | G | 1 | a0001c0001t0004g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.337+606G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151426 | ||||||
| chr14:75151431
|
C | T | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+601G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151431 | ||||||
| chr14:75151457
|
G | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.337+575C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151457 | ||||||
| chr14:75151849
|
T | C | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+183A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151849 | ||||||
| chr14:75151872
|
C | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.337+160G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151872 | ||||||
| chr14:75152218
|
G | A | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-75C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152218 | ||||||
| chr14:75152332
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(249): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.226-189G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152332 | ||||||
| chr14:75152391
|
A | C | 1 | a0001c0001t0004g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.226-248T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152391 | ||||||
| chr14:75152397
|
C | T | 6 | a0001c0001t0007g0073a0001c0001t0007g0082a0001c0001t0012g0072others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-254G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152397 | ||||||
| chr14:75152415
|
T | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.226-272A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152415 | ||||||
| chr14:75152421
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.226-278A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152421 | ||||||
| chr14:75152431
|
A | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-288T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152431 | ||||||
| chr14:75152490
|
C | T | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-347G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152490 | ||||||
| chr14:75152586
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226-443C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152586 | ||||||
| chr14:75152604
|
A | C | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.226-461T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152604 | ||||||
| chr14:75152765
|
G | C | 12 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0001g0149others(9): Show | 12 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.226-622C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152765 | ||||||
| chr14:75152847
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0008g0062 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.226-704G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152847 | ||||||
| chr14:75152894
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226-751A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152894 | ||||||
| chr14:75153075
|
T | C | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-932A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153075 | ||||||
| chr14:75153275
|
AAAAAAC | A | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-1138_226-1133d others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153275 | ||||||
| chr14:75153315
|
T | TA | 9 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(6): Show | 9 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.226-1173dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153315 | ||||||
| chr14:75153416
|
T | C | 1 | a0001c0001t0004g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226-1273A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153416 | ||||||
| chr14:75153550
|
G | C | 1 | a0001c0002t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-1407C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153550 | ||||||
| chr14:75153777
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0033a0001c0001t0001g0132a0001c0001t0001g0139others(2): Show | 5 | HG01081.hp2 HG01257.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-1642_226-1635d others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | ||||||
| chr14:75153777
|
C | CTTTTTTT others(2): Show |
119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(116): Show | 122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-1643_226-1635d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | ||||||
| chr14:75153777
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0229a0001c0001t0014g0238a0001c0001t0014g0240others(1): Show | 4 | HG01109.hp2 HG01981.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1644_226-1635d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | ||||||
| chr14:75153855
|
C | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-1712G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153855 | ||||||
| chr14:75153862
|
C | T | 1 | a0001c0001t0011g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.226-1719G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153862 | ||||||
| chr14:75154168
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226-2025C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154168 | ||||||
| chr14:75154237
|
CA | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(242): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.226-2095delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154237 | ||||||
| chr14:75154317
|
G | A | 43 | a0001c0001t0002g0001a0001c0001t0002g0052a0001c0001t0002g0054others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.226-2174C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154317 | ||||||
| chr14:75154373
|
G | T | 8 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-2230C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154373 | ||||||
| chr14:75154385
|
C | G | 1 | a0001c0001t0002g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.226-2242G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154385 | ||||||
| chr14:75154401
|
C | CA | 83 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(80): Show | 84 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.226-2259dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAA | 30 | a0001c0001t0002g0058a0001c0001t0002g0071a0001c0001t0002g0083others(27): Show | 30 | HG00621.hp1 HG01192.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.226-2260_226-2259d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAA | 8 | a0001c0001t0002g0052a0001c0001t0002g0068a0001c0001t0004g0061others(5): Show | 8 | HG01243.hp1 HG01981.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-2261_226-2259d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(1): Show |
22 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0130others(19): Show | 22 | HG00423.hp1 HG01496.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.226-2266_226-2259d others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(2): Show |
49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(46): Show | 52 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-2267_226-2259d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(3): Show |
27 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0001g0138others(24): Show | 27 | HG00544.hp2 HG00741.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.226-2268_226-2259d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0208a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2269_226-2259d others(13): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0209a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG01099.hp1 HG01257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.226-2270_226-2259d others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.226-2272_226-2259d others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(8): Show |
2 | a0001c0002t0001g0187a0001c0002t0003g0188 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.226-2273_226-2259d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0001g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.226-2274_226-2259d others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
CA | C | 6 | a0001c0001t0009g0250a0001c0001t0010g0232a0001c0001t0010g0233others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-2259delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0008g0006 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226-2268_226-2259d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154401
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0194a0001c0001t0003g0222 | 2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-2272_226-2259d others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | ||||||
| chr14:75154542
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.226-2399C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154542 | ||||||
| chr14:75154824
|
C | T | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-2681G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154824 | ||||||
| chr14:75154963
|
CT | C | 15 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2821delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154963 | ||||||
| chr14:75154964
|
T | C | 2 | a0001c0001t0005g0153a0001c0001t0005g0175 | 2 | NA18954.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.226-2821A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154964 | ||||||
| chr14:75154965
|
T | C | 1 | a0001c0001t0005g0175 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.226-2822A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154965 | ||||||
| chr14:75155020
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0173a0001c0001t0003g0154 | 3 | HG03704.hp2 HG03942.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.226-2877C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155020 | ||||||
| chr14:75155208
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0081others(2): Show | 5 | HG02647.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-3065G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155208 | ||||||
| chr14:75155219
|
C | T | 1 | a0001c0001t0007g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.226-3076G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155219 | ||||||
| chr14:75155589
|
C | T | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-3446G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155589 | ||||||
| chr14:75155711
|
T | C | 6 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0092others(3): Show | 6 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-3568A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155711 | ||||||
| chr14:75155783
|
C | A | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-3640G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155783 | ||||||
| chr14:75156145
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0177 | 2 | HG01256.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.226-4002G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156145 | ||||||
| chr14:75156341
|
T | C | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-4198A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156341 | ||||||
| chr14:75156550
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0013g0128 | 2 | HG02074.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.226-4407G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156550 | ||||||
| chr14:75156784
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-4641A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156784 | ||||||
| chr14:75156916
|
A | AAAAAG | 107 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0027others(104): Show | 109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.226-4778_226-4774d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(3): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0139others(56): Show | 60 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.226-4783_226-4774d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(8): Show |
31 | a0001c0001t0001g0226a0001c0001t0002g0012a0001c0001t0002g0014others(28): Show | 31 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.226-4788_226-4774d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(13): Show |
12 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0023others(9): Show | 12 | HG01243.hp1 HG01358.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-4793_226-4774d others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(18): Show |
1 | a0001c0001t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4798_226-4774d others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(23): Show |
1 | a0001c0001t0006g0043 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.226-4803_226-4774d others(32): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | AAAAAGAA others(28): Show |
6 | a0001c0001t0006g0045a0001c0001t0006g0046a0001c0001t0006g0178others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-4808_226-4774d others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
A | G | 1 | a0001c0001t0003g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.226-4773T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
AAAAAG | A | 9 | a0001c0001t0001g0155a0001c0001t0009g0257a0001c0001t0010g0232others(6): Show | 9 | HG03130.hp1 HG03195.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-4778_226-4774d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.226-4783_226-4774d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75156916
|
AAAAAGAA others(8): Show |
A | 1 | a0001c0001t0012g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-4788_226-4774d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | ||||||
| chr14:75157063
|
T | C | 1 | a0001c0001t0004g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-4920A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157063 | ||||||
| chr14:75157075
|
T | G | 4 | a0001c0001t0014g0238a0001c0001t0014g0240a0001c0001t0014g0241others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-4932A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157075 | ||||||
| chr14:75157285
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 123 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.226-5142A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157285 | ||||||
| chr14:75157292
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.226-5149A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157292 | ||||||
| chr14:75157431
|
C | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-5288G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157431 | ||||||
| chr14:75157603
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-5460A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157603 | ||||||
| chr14:75157642
|
CAT | C | 88 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-5501_226-5500d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157642 | ||||||
| chr14:75157647
|
C | T | 113 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(110): Show | 114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.226-5504G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157647 | ||||||
| chr14:75157760
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-5617G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157760 | ||||||
| chr14:75158444
|
C | G | 2 | a0001c0001t0002g0069a0001c0001t0004g0104 | 2 | NA18979.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.226-6301G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158444 | ||||||
| chr14:75158648
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226-6505C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158648 | ||||||
| chr14:75158849
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.226-6706C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158849 | ||||||
| chr14:75158855
|
T | C | 1 | a0001c0001t0008g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.226-6712A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158855 | ||||||
| chr14:75158883
|
C | CA | 6 | a0001c0001t0002g0001a0001c0001t0002g0054a0001c0001t0002g0113others(3): Show | 7 | NA18747.hp2 NA18955.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-6741dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158883 | ||||||
| chr14:75158919
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.226-6776G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158919 | ||||||
| chr14:75158925
|
A | AAAAT | 3 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243 | 3 | NA18953.hp1 NA18954.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.226-6786_226-6783d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158925 | ||||||
| chr14:75158953
|
T | A | 13 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0080others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-6810A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158953 | ||||||
| chr14:75158973
|
A | G | 1 | a0001c0001t0011g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.226-6830T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158973 | ||||||
| chr14:75158979
|
G | A | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-6836C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158979 | ||||||
| chr14:75159339
|
A | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-7196T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159339 | ||||||
| chr14:75159428
|
T | C | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-7285A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159428 | ||||||
| chr14:75159457
|
A | C | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-7314T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159457 | ||||||
| chr14:75159554
|
T | C | 88 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-7411A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159554 | ||||||
| chr14:75160012
|
G | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(249): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.226-7869C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160012 | ||||||
| chr14:75160233
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.226-8090C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160233 | ||||||
| chr14:75160303
|
T | C | 1 | a0001c0001t0016g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.226-8160A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160303 | ||||||
| chr14:75160394
|
AT | A | 6 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-8252delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160394 | ||||||
| chr14:75160616
|
T | A | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-8473A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160616 | ||||||
| chr14:75160918
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-8775G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160918 | ||||||
| chr14:75160998
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-8855A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160998 | ||||||
| chr14:75161470
|
C | G | 1 | a0001c0002t0003g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.226-9327G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161470 | ||||||
| chr14:75161496
|
AG | A | 43 | a0001c0001t0002g0001a0001c0001t0002g0052a0001c0001t0002g0054others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.226-9354delC | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161496 | ||||||
| chr14:75161696
|
T | C | 1 | a0001c0001t0008g0006 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226-9553A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161696 | ||||||
| chr14:75161790
|
C | A | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226-9647G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161790 | ||||||
| chr14:75161809
|
A | G | 5 | a0001c0001t0009g0251a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-9666T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161809 | ||||||
| chr14:75161968
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.226-9825T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161968 | ||||||
| chr14:75161998
|
G | C | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-9855C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161998 | ||||||
| chr14:75162021
|
C | CCGGGG | 12 | a0001c0001t0006g0043a0001c0001t0006g0045a0001c0001t0006g0046others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-9883_226-9879d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162021 | ||||||
| chr14:75162022
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.226-9879G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162022 | ||||||
| chr14:75162153
|
T | C | 2 | a0001c0001t0004g0101a0001c0001t0004g0125 | 2 | HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.226-10010A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162153 | ||||||
| chr14:75162182
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.226-10039A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162182 | ||||||
| chr14:75162252
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-10109T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162252 | ||||||
| chr14:75162352
|
A | G | 15 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(12): Show | 15 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-10209T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162352 | ||||||
| chr14:75162697
|
CCTGACAA others(26): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.226-10587_226-1055 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162697 | ||||||
| chr14:75162702
|
C | T | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-10559G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162702 | ||||||
| chr14:75162741
|
C | T | 1 | a0001c0001t0002g0114 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.226-10598G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162741 | ||||||
| chr14:75162884
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0005g0219 | 2 | HG02080.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.226-10741A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162884 | ||||||
| chr14:75163039
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0156others(2): Show | 6 | HG01361.hp2 HG02293.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-10896T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163039 | ||||||
| chr14:75163042
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.226-10899G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163042 | ||||||
| chr14:75163079
|
T | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-10936A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163079 | ||||||
| chr14:75163081
|
A | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.226-10938T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163081 | ||||||
| chr14:75163145
|
GGGA | G | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-11005_226-1100 others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163145 | ||||||
| chr14:75163214
|
C | G | 5 | a0001c0001t0009g0251a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-11071G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163214 | ||||||
| chr14:75163250
|
C | T | 2 | a0001c0001t0009g0257a0001c0001t0019g0258 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.226-11107G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163250 | ||||||
| chr14:75163254
|
C | T | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226-11111G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163254 | ||||||
| chr14:75163269
|
C | T | 88 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-11126G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163269 | ||||||
| chr14:75163294
|
T | C | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-11151A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163294 | ||||||
| chr14:75163294
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.226-11151A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163294 | ||||||
| chr14:75163310
|
T | C | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-11167A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163310 | ||||||
| chr14:75163358
|
T | C | 4 | a0001c0001t0014g0238a0001c0001t0014g0240a0001c0001t0014g0241others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-11215A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163358 | ||||||
| chr14:75163507
|
C | T | 1 | a0001c0001t0009g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.226-11364G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163507 | ||||||
| chr14:75163552
|
C | CA | 25 | a0001c0001t0001g0030a0001c0001t0001g0138a0001c0001t0001g0157others(22): Show | 25 | HG00621.hp2 HG00741.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.226-11410dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | ||||||
| chr14:75163552
|
CA | C | 110 | a0001c0001t0001g0010a0001c0001t0001g0164a0001c0001t0002g0012others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.226-11410delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | ||||||
| chr14:75163552
|
CAAAAAA | C | 5 | a0001c0001t0009g0251a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-11415_226-1141 others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | ||||||
| chr14:75163587
|
C | T | 2 | a0001c0001t0006g0055a0001c0001t0006g0056 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.226-11444G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163587 | ||||||
| chr14:75163675
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-11532C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163675 | ||||||
| chr14:75164072
|
C | T | 13 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0080others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-11929G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164072 | ||||||
| chr14:75164211
|
G | A | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-12068C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164211 | ||||||
| chr14:75164229
|
C | CT | 54 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0135others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.226-12087dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164229 | ||||||
| chr14:75164238
|
T | TC | 4 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243others(1): Show | 4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-12096_226-1209 others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164238 | ||||||
| chr14:75164309
|
G | GCACAAAA others(26): Show |
1 | a0001c0001t0001g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225+12045_225+1204 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164309 | ||||||
| chr14:75164312
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225+12043T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164312 | ||||||
| chr14:75164324
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.225+12031C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164324 | ||||||
| chr14:75164380
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.225+11975G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164380 | ||||||
| chr14:75164426
|
T | A | 1 | a0001c0001t0003g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.225+11929A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164426 | ||||||
| chr14:75164492
|
A | G | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+11863T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164492 | ||||||
| chr14:75164532
|
AAT | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0165a0001c0001t0001g0190others(2): Show | 6 | NA18939.hp1 NA18953.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+11821_225+1182 others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164532
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0004g0079a0001c0001t0007g0078 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.225+11811_225+1182 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164532
|
AATATATA others(7): Show |
A | 1 | a0001c0001t0004g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.225+11809_225+1182 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164532
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0005g0254 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.225+11807_225+1182 others(20): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164532
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0002g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.225+11801_225+1182 others(26): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164532
|
AATATATA others(19): Show |
A | 57 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.225+11797_225+1182 others(30): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | ||||||
| chr14:75164545
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.225+11777_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164545 | ||||||
| chr14:75164546
|
TATATATA others(18): Show |
T | 3 | a0001c0001t0003g0129a0001c0001t0003g0134a0001c0001t0005g0175 | 3 | HG03831.hp1 NA19012.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.225+11784_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164546 | ||||||
| chr14:75164546
|
TATATATA others(20): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.225+11782_225+1180 others(31): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164546 | ||||||
| chr14:75164547
|
ATATATAT others(26): Show |
A | 3 | a0001c0001t0010g0233a0001c0001t0010g0243a0001c0001t0022g0244 | 3 | HG03195.hp2 NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.225+11775_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164547 | ||||||
| chr14:75164547
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0010g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225+11774_225+1180 others(38): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164547 | ||||||
| chr14:75164548
|
TATATATA others(18): Show |
T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18990.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.225+11782_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164548 | ||||||
| chr14:75164549
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0010g0242 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.225+11773_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164549 | ||||||
| chr14:75164551
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+11773_225+1180 others(35): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164551 | ||||||
| chr14:75164553
|
ATATATAT others(18): Show |
A | 5 | a0001c0001t0001g0169a0001c0001t0006g0043a0001c0001t0009g0250others(2): Show | 5 | HG01361.hp1 HG01496.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11777_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164553 | ||||||
| chr14:75164553
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0002g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225+11775_225+1180 others(31): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164553 | ||||||
| chr14:75164555
|
ATATATAT others(16): Show |
A | 9 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(6): Show | 9 | HG01243.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+11777_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | ||||||
| chr14:75164555
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.225+11776_225+1179 others(28): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | ||||||
| chr14:75164555
|
ATATATAT others(18): Show |
A | 9 | a0001c0001t0006g0045a0001c0001t0006g0178a0001c0001t0009g0251others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | ||||||
| chr14:75164556
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0002g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.225+11780_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164556 | ||||||
| chr14:75164557
|
ATATATAT others(14): Show |
A | 12 | a0001c0001t0002g0066a0001c0001t0002g0084a0001c0001t0002g0085others(9): Show | 12 | HG00280.hp2 HG00741.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+11777_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | ||||||
| chr14:75164557
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.225+11776_225+1179 others(26): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | ||||||
| chr14:75164557
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0006g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.225+11774_225+1179 others(28): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | ||||||
| chr14:75164557
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0011g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+11773_225+1179 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | ||||||
| chr14:75164558
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0002g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225+11778_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164558 | ||||||
| chr14:75164559
|
ATATATAT others(12): Show |
A | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0021g0179 | 3 | HG01891.hp2 HG02809.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.225+11777_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | ||||||
| chr14:75164559
|
ATATATAT others(13): Show |
A | 4 | a0001c0001t0002g0054a0001c0001t0004g0051a0001c0001t0004g0116others(1): Show | 4 | HG02818.hp1 HG04228.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+11776_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | ||||||
| chr14:75164559
|
ATATATAT others(14): Show |
A | 23 | a0001c0001t0002g0001a0001c0001t0002g0052a0001c0001t0002g0068others(20): Show | 24 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | ||||||
| chr14:75164559
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0004g0041a0001c0001t0004g0042 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+11773_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | ||||||
| chr14:75164561
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0004g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+11777_225+1179 others(21): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164561
|
ATATATAT others(11): Show |
A | 5 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11776_225+1179 others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164561
|
ATATATAT others(12): Show |
A | 17 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0023others(14): Show | 17 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164561
|
ATATATAT others(13): Show |
A | 4 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0112others(1): Show | 4 | HG00639.hp2 HG03831.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11774_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164561
|
ATATATAT others(14): Show |
A | 3 | a0001c0001t0002g0247a0001c0001t0002g0255a0001c0001t0006g0057 | 3 | HG02895.hp2 HG03471.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.225+11773_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164561
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0018g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+11771_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | ||||||
| chr14:75164563
|
ATATATAT others(10): Show |
A | 4 | a0001c0001t0002g0022a0001c0001t0002g0093a0001c0001t0002g0094others(1): Show | 4 | HG00140.hp1 HG02976.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(21): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | ||||||
| chr14:75164563
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0004g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+11773_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | ||||||
| chr14:75164563
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225+11772_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | ||||||
| chr14:75164565
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0004g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225+11776_225+1178 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164565 | ||||||
| chr14:75164565
|
ATATATAT others(8): Show |
A | 4 | a0001c0001t0002g0092a0001c0001t0004g0021a0001c0001t0004g0061others(1): Show | 4 | HG00738.hp1 HG02647.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+11775_225+1178 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164565 | ||||||
| chr14:75164567
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0004g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225+11776_225+1178 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164567 | ||||||
| chr14:75164569
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0004g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.225+11771_225+1178 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164569 | ||||||
| chr14:75164570
|
TATATATA | T | 4 | a0001c0001t0007g0073a0001c0001t0012g0072a0001c0001t0012g0074others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11778_225+1178 others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164570 | ||||||
| chr14:75164571
|
A | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01884.hp2 NA18939.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11784T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164571 | ||||||
| chr14:75164573
|
A | ATT | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG01257.hp2 NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.225+11781_225+1178 others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164573 | ||||||
| chr14:75164573
|
A | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0130others(49): Show | 54 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.225+11782T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164573 | ||||||
| chr14:75164575
|
A | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(75): Show | 80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.225+11780T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164575 | ||||||
| chr14:75164577
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0001g0215 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0201 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(20): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0253 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(7): Show |
6 | a0001c0001t0001g0203a0001c0002t0001g0204a0001c0002t0001g0206others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+11777_225+1177 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0202 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0003g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | ATATTTTT others(5): Show |
1 | a0001c0002t0003g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164577
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(82): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.225+11778T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | ||||||
| chr14:75164580
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.225+11775A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164580 | ||||||
| chr14:75164581
|
T | A | 2 | a0001c0001t0014g0240a0001c0001t0014g0241 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.225+11774A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164581 | ||||||
| chr14:75164842
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.225+11513T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164842 | ||||||
| chr14:75164974
|
G | A | 1 | a0001c0001t0003g0171 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.225+11381C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164974 | ||||||
| chr14:75165389
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.225+10966C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165389 | ||||||
| chr14:75165435
|
C | A | 1 | a0001c0001t0018g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+10920G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165435 | ||||||
| chr14:75165597
|
A | G | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+10758T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165597 | ||||||
| chr14:75165658
|
T | A | 2 | a0001c0001t0006g0178a0001c0001t0011g0034 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.225+10697A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165658 | ||||||
| chr14:75165813
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.225+10542C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165813 | ||||||
| chr14:75165896
|
A | G | 13 | a0001c0001t0004g0077a0001c0001t0004g0079a0001c0001t0004g0080others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+10459T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165896 | ||||||
| chr14:75165974
|
C | CT | 8 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+10380dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165974 | ||||||
| chr14:75166127
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.225+10228G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166127 | ||||||
| chr14:75166144
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225+10211C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166144 | ||||||
| chr14:75166305
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.225+10050T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166305 | ||||||
| chr14:75166385
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.225+9970C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166385 | ||||||
| chr14:75166547
|
G | A | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+9808C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166547 | ||||||
| chr14:75166563
|
G | T | 1 | a0001c0001t0002g0071 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.225+9792C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166563 | ||||||
| chr14:75166772
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(253): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.225+9583T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166772 | ||||||
| chr14:75166797
|
T | G | 2 | a0001c0001t0010g0233a0001c0001t0010g0243 | 2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.225+9558A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166797 | ||||||
| chr14:75166939
|
CT | C | 115 | a0001c0001t0001g0033a0001c0001t0002g0001a0001c0001t0002g0012others(112): Show | 116 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.225+9415delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166939 | ||||||
| chr14:75167038
|
T | G | 6 | a0001c0001t0002g0001a0001c0001t0002g0054a0001c0001t0002g0113others(3): Show | 7 | NA18747.hp2 NA18955.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+9317A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167038 | ||||||
| chr14:75167095
|
C | A | 28 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(25): Show | 28 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.225+9260G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167095 | ||||||
| chr14:75167099
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0004g0116 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225+9256C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167099 | ||||||
| chr14:75167117
|
T | C | 1 | a0001c0001t0011g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+9238A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167117 | ||||||
| chr14:75167250
|
ATTCT | A | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9101_225+9104d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167250 | ||||||
| chr14:75167446
|
G | A | 4 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243others(1): Show | 4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+8909C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167446 | ||||||
| chr14:75168031
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.225+8324A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168031 | ||||||
| chr14:75168198
|
C | T | 1 | a0001c0001t0011g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+8157G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168198 | ||||||
| chr14:75168354
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225+8001A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168354 | ||||||
| chr14:75168495
|
GA | G | 4 | a0001c0001t0010g0233a0001c0001t0010g0242a0001c0001t0010g0243others(1): Show | 4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+7859delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168495 | ||||||
| chr14:75168670
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225+7685C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168670 | ||||||
| chr14:75168841
|
T | G | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+7514A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168841 | ||||||
| chr14:75168902
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225+7453G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168902 | ||||||
| chr14:75168950
|
T | C | 1 | a0001c0001t0016g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+7405A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168950 | ||||||
| chr14:75169008
|
C | T | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+7347G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169008 | ||||||
| chr14:75169013
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.225+7342T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169013 | ||||||
| chr14:75169058
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.225+7297C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169058 | ||||||
| chr14:75169273
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+7082A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169273 | ||||||
| chr14:75169486
|
C | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0057 | 3 | HG00741.hp1 HG02895.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.225+6869G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169486 | ||||||
| chr14:75169646
|
G | A | 4 | a0001c0001t0006g0118a0001c0001t0008g0119a0001c0001t0008g0120others(1): Show | 4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+6709C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169646 | ||||||
| chr14:75170047
|
GAAATACA others(2): Show |
G | 6 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0009g0256others(3): Show | 6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+6299_225+6307d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170047 | ||||||
| chr14:75170084
|
G | A | 1 | a0001c0001t0004g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+6271C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170084 | ||||||
| chr14:75170087
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225+6268G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170087 | ||||||
| chr14:75170104
|
G | C | 1 | a0001c0001t0006g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.225+6251C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170104 | ||||||
| chr14:75170152
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG00544.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.225+6203G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170152 | ||||||
| chr14:75170258
|
G | A | 4 | a0001c0001t0014g0238a0001c0001t0014g0240a0001c0001t0014g0241others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+6097C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170258 | ||||||
| chr14:75170264
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.225+6091G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170264 | ||||||
| chr14:75170284
|
G | A | 1 | a0001c0001t0022g0244 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.225+6071C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170284 | ||||||
| chr14:75170648
|
A | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.225+5707T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170648 | ||||||
| chr14:75170656
|
A | C | 141 | a0001c0001t0001g0010a0001c0001t0002g0001a0001c0001t0002g0012others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+5699T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170656 | ||||||
| chr14:75170761
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.225+5594T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170761 | ||||||
| chr14:75171196
|
GGAA | G | 6 | a0001c0001t0006g0043a0001c0001t0006g0045a0001c0001t0006g0046others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+5156_225+5158d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171196 | ||||||
| chr14:75171234
|
A | G | 3 | a0001c0001t0009g0256a0001c0001t0009g0257a0001c0001t0019g0258 | 3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.225+5121T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171234 | ||||||
| chr14:75171237
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225+5118C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171237 | ||||||
| chr14:75171264
|
C | G | 1 | a0001c0001t0010g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+5091G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171264 | ||||||
| chr14:75171281
|
A | AT | 15 | a0001c0001t0002g0013a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 15 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.225+5073dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171281 | ||||||
| chr14:75171281
|
AT | A | 5 | a0001c0001t0004g0122a0001c0001t0004g0124a0001c0001t0010g0233others(2): Show | 5 | HG02486.hp1 HG03041.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+5073delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171281 | ||||||
| chr14:75171336
|
G | A | 4 | a0001c0001t0014g0238a0001c0001t0014g0240a0001c0001t0014g0241others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+5019C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171336 | ||||||
| chr14:75171342
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+5013G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171342 | ||||||
| chr14:75171512
|
T | G | 1 | a0001c0001t0013g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225+4843A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171512 | ||||||
| chr14:75171592
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225+4763A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171592 | ||||||
| chr14:75171690
|
A | AGAAACAT others(32): Show |
113 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(110): Show | 114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.225+4626_225+4664d others(41): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171690 | ||||||
| chr14:75171929
|
C | CT | 9 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 9 | HG02622.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+4425dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171929 | ||||||
| chr14:75171958
|
T | C | 1 | a0001c0001t0005g0032 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.225+4397A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171958 | ||||||
| chr14:75172075
|
G | GGAAGAAC others(8): Show |
1 | a0001c0001t0005g0175 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.225+4265_225+4279d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172075 | ||||||
| chr14:75172311
|
C | CT | 6 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0009g0256others(3): Show | 6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+4043dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172311 | ||||||
| chr14:75172311
|
CT | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0176a0001c0001t0010g0233others(3): Show | 6 | HG02735.hp2 HG03195.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+4043delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172311 | ||||||
| chr14:75172393
|
C | T | 1 | a0001c0001t0013g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225+3962G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172393 | ||||||
| chr14:75172482
|
A | T | 1 | a0001c0001t0010g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225+3873T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172482 | ||||||
| chr14:75172519
|
A | G | 1 | a0001c0002t0001g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.225+3836T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172519 | ||||||
| chr14:75172543
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+3812G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172543 | ||||||
| chr14:75172642
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225+3713C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172642 | ||||||
| chr14:75172658
|
T | C | 1 | a0001c0001t0011g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+3697A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172658 | ||||||
| chr14:75172868
|
G | A | 136 | a0001c0001t0001g0010a0001c0001t0002g0001a0001c0001t0002g0012others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.225+3487C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172868 | ||||||
| chr14:75172893
|
A | AT | 5 | a0001c0001t0009g0251a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+3461dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172893 | ||||||
| chr14:75172893
|
AT | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0177a0001c0001t0004g0125others(2): Show | 5 | HG01943.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+3461delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172893 | ||||||
| chr14:75172991
|
G | C | 5 | a0001c0001t0002g0237a0001c0001t0014g0238a0001c0001t0014g0240others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+3364C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172991 | ||||||
| chr14:75173087
|
T | C | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+3268A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173087 | ||||||
| chr14:75173151
|
C | T | 120 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+3204G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173151 | ||||||
| chr14:75173243
|
C | T | 2 | a0001c0001t0006g0178a0001c0001t0011g0034 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.225+3112G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173243 | ||||||
| chr14:75173342
|
T | C | 5 | a0001c0001t0002g0237a0001c0001t0014g0238a0001c0001t0014g0240others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+3013A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173342 | ||||||
| chr14:75173380
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 7 | HG00558.hp1 NA18939.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+2975T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173380 | ||||||
| chr14:75173408
|
G | C | 1 | a0001c0001t0013g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.225+2947C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173408 | ||||||
| chr14:75173487
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+2868C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173487 | ||||||
| chr14:75173545
|
C | CT | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+2809dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173545 | ||||||
| chr14:75173556
|
A | T | 4 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0234others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2799T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173556 | ||||||
| chr14:75173651
|
C | G | 120 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+2704G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173651 | ||||||
| chr14:75173673
|
C | T | 5 | a0001c0001t0009g0251a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2682G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173673 | ||||||
| chr14:75173700
|
G | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.225+2655C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173700 | ||||||
| chr14:75173754
|
C | T | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+2601G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173754 | ||||||
| chr14:75173848
|
A | G | 1 | a0001c0001t0009g0250 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+2507T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173848 | ||||||
| chr14:75174209
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.225+2146A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174209 | ||||||
| chr14:75174374
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.225+1981A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174374 | ||||||
| chr14:75174544
|
T | C | 1 | a0001c0001t0004g0127 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.225+1811A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174544 | ||||||
| chr14:75174695
|
G | A | 1 | a0001c0001t0004g0127 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.225+1660C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174695 | ||||||
| chr14:75174827
|
G | A | 6 | a0001c0001t0010g0232a0001c0001t0010g0233a0001c0001t0010g0236others(3): Show | 6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1528C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174827 | ||||||
| chr14:75174838
|
C | G | 120 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+1517G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174838 | ||||||
| chr14:75175039
|
C | CA | 14 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(11): Show | 15 | HG01081.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+1315dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | ||||||
| chr14:75175039
|
C | CAA | 9 | a0001c0001t0002g0237a0001c0001t0010g0242a0001c0001t0010g0243others(6): Show | 9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+1314_225+1315d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | ||||||
| chr14:75175039
|
CAAAAAA | C | 7 | a0001c0001t0001g0182a0001c0001t0003g0183a0001c0001t0003g0184others(4): Show | 7 | HG00423.hp1 HG00735.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1310_225+1315d others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | ||||||
| chr14:75175039
|
CAAAAAAA | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(173): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.225+1309_225+1315d others(9): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | ||||||
| chr14:75175190
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1165A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175190 | ||||||
| chr14:75175291
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1064A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175291 | ||||||
| chr14:75175559
|
G | A | 3 | a0001c0001t0002g0247a0001c0001t0015g0246a0001c0001t0018g0248 | 3 | HG02615.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.225+796C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175559 | ||||||
| chr14:75175588
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.225+767A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175588 | ||||||
| chr14:75175632
|
C | A | 6 | a0001c0001t0009g0250a0001c0001t0009g0251a0001c0001t0009g0256others(3): Show | 6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+723G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175632 | ||||||
| chr14:75175647
|
G | A | 2 | a0001c0001t0003g0253a0001c0001t0005g0254 | 2 | HG02056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.225+708C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175647 | ||||||
| chr14:75175831
|
A | G | 7 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+524T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175831 | ||||||
| chr14:75175843
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+512C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175843 | ||||||
| chr14:75175860
|
A | G | 15 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(12): Show | 15 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+495T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175860 | ||||||
| chr14:75175974
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0005g0008a0001c0001t0005g0009others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+381G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175974 | ||||||
| chr14:75176085
|
T | C | 3 | a0001c0001t0009g0256a0001c0001t0009g0257a0001c0001t0019g0258 | 3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.225+270A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75176085 | ||||||
| chr14:75176123
|
A | G | 1 | a0001c0001t0001g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.225+232T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75176123 | ||||||
| chr14:75176142
|
C | T | 1 | a0001c0001t0008g0006 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.225+213G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75176142 |