Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16790 | A10 | 16444792 | G | A | downstream_gene_variant | MODIFIER | c.*1498C>T| |
S234 |
2 | BAA10g16790 | A10 | 16444904 | C | T | downstream_gene_variant | MODIFIER | c.*1386G>A| |
S210 |
3 | BAA10g16790 | A10 | 16445324 | G | A | downstream_gene_variant | MODIFIER | c.*966C>T| |
S292 |
4 | BAA10g16790 | A10 | 16445833 | G | A | downstream_gene_variant | MODIFIER | c.*457C>T| |
S239 |
5 | BAA10g16790 | A10 | 16446578 | T | C | synonymous_variant | LOW | c.1593A>G|p.Arg531Arg |
S195 |
6 | BAA10g16790 | A10 | 16446589 | G | A | synonymous_variant | LOW | c.1582C>T|p.Leu528Leu |
S217 S248 |
7 | BAA10g16790 | A10 | 16447368 | G | A | missense_variant | MODERATE | c.1105C>T|p.Pro369Ser |
S132 S137 S89 |
8 | BAA10g16790 | A10 | 16448272 | C | T | synonymous_variant | LOW | c.687G>A|p.Leu229Leu |
S210 S225 |
9 | BAA10g16790 | A10 | 16450148 | C | T | upstream_gene_variant | MODIFIER | c.-173G>A| |
S296 |