Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41350 | A05 | 39524568 | C | T | missense_variant | MODERATE | c.82C>T|p.Leu28Phe |
S207 |
2 | BAA05g41350 | A05 | 39524679 | C | T | stop_gained | HIGH | c.193C>T|p.Arg65* |
S156 |
3 | BAA05g41350 | A05 | 39525941 | C | T | missense_variant | MODERATE | c.1379C>T|p.Ser460Leu |
S262 |
4 | BAA05g41350 | A05 | 39526164 | C | T | splice_region_variant&intron_variant | LOW | c.1597+5C>T| |
S295 |
5 | BAA05g41350 | A05 | 39526437 | G | A | synonymous_variant | LOW | c.1794G>A|p.Arg598Arg |
S180 |