Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41660 | A01 | 27709692 | G | A | missense_variant | MODERATE | c.83G>A|p.Gly28Glu |
S284 |
2 | BAA01g41660 | A01 | 27709735 | C | T | synonymous_variant | LOW | c.126C>T|p.Asn42Asn |
S146 |
3 | BAA01g41660 | A01 | 27710387 | C | T | missense_variant | MODERATE | c.548C>T|p.Ser183Phe |
S168 |
4 | BAA01g41660 | A01 | 27710681 | C | T | missense_variant | MODERATE | c.842C>T|p.Pro281Leu |
S211 S227 |
5 | BAA01g41660 | A01 | 27710748 | C | T | synonymous_variant | LOW | c.909C>T|p.Phe303Phe |
S239 |
6 | BAA01g41660 | A01 | 27710760 | G | A | missense_variant | MODERATE | c.921G>A|p.Met307Ile |
S1 S90 |