Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45190 | A02 | 37073517 | C | T | missense_variant | MODERATE | c.1789G>A|p.Gly597Arg |
S192 S32 |
2 | BAA02g45190 | A02 | 37073544 | G | A | missense_variant | MODERATE | c.1762C>T|p.Arg588Cys |
S278 |
3 | BAA02g45190 | A02 | 37073805 | C | T | missense_variant | MODERATE | c.1594G>A|p.Glu532Lys |
S167 |
4 | BAA02g45190 | A02 | 37074046 | G | A | missense_variant | MODERATE | c.1433C>T|p.Ser478Leu |
S30 |
5 | BAA02g45190 | A02 | 37074543 | G | A | missense_variant | MODERATE | c.1355C>T|p.Pro452Leu |
S35 |
6 | BAA02g45190 | A02 | 37075913 | C | T | missense_variant | MODERATE | c.478G>A|p.Glu160Lys |
S53 |
7 | BAA02g45190 | A02 | 37077091 | G | A | missense_variant | MODERATE | c.121C>T|p.His41Tyr |
S146 |
8 | BAA02g45190 | A02 | 37078171 | C | T | upstream_gene_variant | MODIFIER | c.-960G>A| |
S295 |
9 | BAA02g45190 | A02 | 37078195 | G | A | upstream_gene_variant | MODIFIER | c.-984C>T| |
S139 |
10 | BAA02g45190 | A02 | 37082169 | G | A | upstream_gene_variant | MODIFIER | c.-4958C>T| |
S269 |