Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03490 | A02 | 1538324 | C | T | synonymous_variant | LOW | c.144C>T|p.Asp48Asp |
S82 S92 |
2 | BAA02g03490 | A02 | 1538374 | C | T | missense_variant | MODERATE | c.194C>T|p.Ser65Phe |
S117 |
3 | BAA02g03490 | A02 | 1538502 | C | T | missense_variant | MODERATE | c.322C>T|p.Pro108Ser |
S289 S290 |
4 | BAA02g03490 | A02 | 1539460 | C | T | missense_variant&splice_region_variant | MODERATE | c.611C>T|p.Ala204Val |
S216 |
5 | BAA02g03490 | A02 | 1540990 | G | A | missense_variant | MODERATE | c.1126G>A|p.Glu376Lys |
S180 |