Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02190 | A02 | 985246 | G | A | missense_variant | MODERATE | c.3158C>T|p.Ala1053Val |
S20 |
2 | BAA02g02190 | A02 | 986605 | G | A | missense_variant | MODERATE | c.2680C>T|p.Leu894Phe |
S273 |
3 | BAA02g02190 | A02 | 988251 | C | T | splice_region_variant&intron_variant | LOW | c.2031+5G>A| |
S73 S91 |
4 | BAA02g02190 | A02 | 988740 | G | A | missense_variant | MODERATE | c.1906C>T|p.His636Tyr |
S107 |
5 | BAA02g02190 | A02 | 988886 | G | A | intron_variant | MODIFIER | c.1834-74C>T| |
S246 |
6 | BAA02g02190 | A02 | 991778 | G | A | missense_variant | MODERATE | c.665C>T|p.Pro222Leu |
S143 |