Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05780 | A01 | 2574847 | A | C | missense_variant | MODERATE | c.172A>C|p.Ile58Leu |
S15 S156 S2 S3 S4 S6 |
2 | BAA01g05780 | A01 | 2575126 | G | A | synonymous_variant | LOW | c.294G>A|p.Arg98Arg |
S127 |
3 | BAA01g05780 | A01 | 2575201 | C | T | synonymous_variant | LOW | c.369C>T|p.Leu123Leu |
S94 |
4 | BAA01g05780 | A01 | 2575480 | G | A | synonymous_variant | LOW | c.648G>A|p.Gly216Gly |
S257 |
5 | BAA01g05780 | A01 | 2575557 | C | T | missense_variant | MODERATE | c.725C>T|p.Ala242Val |
S192 |
6 | BAA01g05780 | A01 | 2575854 | G | A | missense_variant | MODERATE | c.931G>A|p.Asp311Asn |
S180 S268 |
7 | BAA01g05780 | A01 | 2576358 | C | T | synonymous_variant | LOW | c.1362C>T|p.Pro454Pro |
S46 |
8 | BAA01g05780 | A01 | 2576946 | C | T | synonymous_variant | LOW | c.1842C>T|p.Asp614Asp |
S119 |
9 | BAA01g05780 | A01 | 2577640 | G | A | missense_variant | MODERATE | c.2282G>A|p.Gly761Glu |
S308 |