Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08740 | A02 | 3865569 | C | T | missense_variant | MODERATE | c.1355G>A|p.Ser452Asn |
S127 |
2 | BAA02g08740 | A02 | 3865596 | G | A | missense_variant | MODERATE | c.1328C>T|p.Ala443Val |
S197 |
3 | BAA02g08740 | A02 | 3866542 | C | T | missense_variant | MODERATE | c.746G>A|p.Gly249Asp |
S111 |
4 | BAA02g08740 | A02 | 3866589 | C | T | synonymous_variant | LOW | c.699G>A|p.Glu233Glu |
S66 |
5 | BAA02g08740 | A02 | 3866715 | G | A | synonymous_variant | LOW | c.573C>T|p.Asn191Asn |
S80 |
6 | BAA02g08740 | A02 | 3866752 | G | A | missense_variant | MODERATE | c.536C>T|p.Ser179Phe |
S80 |
7 | BAA02g08740 | A02 | 3868818 | C | T | upstream_gene_variant | MODIFIER | c.-1531G>A| |
S270 |
8 | BAA02g08740 | A02 | 3869934 | G | A | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S187 |
9 | BAA02g08740 | A02 | 3871916 | G | A | upstream_gene_variant | MODIFIER | c.-4629C>T| |
S37 |