Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41320 | A02 | 34659933 | G | A | missense_variant | MODERATE | c.1328C>T|p.Ala443Val |
S166 |
2 | BAA02g41320 | A02 | 34660738 | C | T | missense_variant | MODERATE | c.1015G>A|p.Asp339Asn |
S80 |
3 | BAA02g41320 | A02 | 34660907 | C | T | missense_variant | MODERATE | c.940G>A|p.Val314Met |
S233 |
4 | BAA02g41320 | A02 | 34665694 | G | A | upstream_gene_variant | MODIFIER | c.-2680C>T| |
S286 |
5 | BAA02g41320 | A02 | 34667078 | G | A | upstream_gene_variant | MODIFIER | c.-4064C>T| |
S197 |
6 | BAA02g41320 | A02 | 34667531 | G | A | upstream_gene_variant | MODIFIER | c.-4517C>T| |
S209 |
7 | BAA02g41320 | A02 | 34668014 | C | T | upstream_gene_variant | MODIFIER | c.-5000G>A| |
S3 |