Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25770 | A02 | 14187733 | G | A | missense_variant | MODERATE | c.1447C>T|p.His483Tyr |
S177 |
2 | BAA02g25770 | A02 | 14188672 | C | T | missense_variant | MODERATE | c.1073G>A|p.Gly358Asp |
S181 |
3 | BAA02g25770 | A02 | 14189299 | C | T | missense_variant | MODERATE | c.640G>A|p.Glu214Lys |
S2 |
4 | BAA02g25770 | A02 | 14189323 | C | T | missense_variant | MODERATE | c.616G>A|p.Gly206Arg |
S112 |
5 | BAA02g25770 | A02 | 14190030 | G | A | upstream_gene_variant | MODIFIER | c.-92C>T| |
S80 |
6 | BAA02g25770 | A02 | 14190592 | C | T | upstream_gene_variant | MODIFIER | c.-654G>A| |
S149 |