Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18190 | A02 | 9162214 | G | A | synonymous_variant | LOW | c.87G>A|p.Glu29Glu |
S188 |
2 | BAA02g18190 | A02 | 9162256 | C | T | synonymous_variant | LOW | c.129C>T|p.Asp43Asp |
S299 |
3 | BAA02g18190 | A02 | 9163421 | C | T | splice_region_variant&intron_variant | LOW | c.1212+7C>T| |
S163 |
4 | BAA02g18190 | A02 | 9163686 | C | T | missense_variant | MODERATE | c.1412C>T|p.Ser471Phe |
S64 |
5 | BAA02g18190 | A02 | 9163910 | C | T | missense_variant | MODERATE | c.1636C>T|p.Leu546Phe |
S158 |
6 | BAA02g18190 | A02 | 9164078 | G | A | missense_variant | MODERATE | c.1804G>A|p.Gly602Ser |
S274 |