Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19660 | A06 | 10194367 | C | T | missense_variant | MODERATE | c.995G>A|p.Gly332Glu |
S6 |
2 | BAA06g19660 | A06 | 10195375 | G | A | missense_variant | MODERATE | c.241C>T|p.His81Tyr |
S202 |
3 | BAA06g19660 | A06 | 10195428 | G | A | missense_variant | MODERATE | c.188C>T|p.Pro63Leu |
S51 |
4 | BAA06g19660 | A06 | 10195481 | C | T | synonymous_variant | LOW | c.135G>A|p.Val45Val |
S87 |
5 | BAA06g19660 | A06 | 10197125 | C | T | upstream_gene_variant | MODIFIER | c.-874G>A| |
S156 |
6 | BAA06g19660 | A06 | 10199448 | G | A | upstream_gene_variant | MODIFIER | c.-3197C>T| |
S202 |