Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06090 | A02 | 2592039 | G | A | missense_variant | MODERATE | c.14G>A|p.Arg5His |
S79 S91 |
2 | BAA02g06090 | A02 | 2592048 | C | T | missense_variant | MODERATE | c.23C>T|p.Pro8Leu |
S111 |
3 | BAA02g06090 | A02 | 2592315 | C | T | synonymous_variant | LOW | c.204C>T|p.Phe68Phe |
S84 S93 |
4 | BAA02g06090 | A02 | 2593566 | G | A | missense_variant | MODERATE | c.800G>A|p.Gly267Asp |
S259 |
5 | BAA02g06090 | A02 | 2593842 | C | T | missense_variant | MODERATE | c.905C>T|p.Ala302Val |
S183 S198 |
6 | BAA02g06090 | A02 | 2593866 | C | T | missense_variant | MODERATE | c.929C>T|p.Ser310Leu |
S244 |
7 | BAA02g06090 | A02 | 2593940 | G | A | missense_variant | MODERATE | c.1003G>A|p.Gly335Ser |
S256 |
8 | BAA02g06090 | A02 | 2594200 | G | A | synonymous_variant | LOW | c.1185G>A|p.Gln395Gln |
S210 |
9 | BAA02g06090 | A02 | 2594870 | C | T | missense_variant | MODERATE | c.1360C>T|p.Leu454Phe |
S64 |