Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14980 | A02 | 7140002 | G | A | synonymous_variant | LOW | c.840C>T|p.Ser280Ser |
S139 |
2 | BAA02g14980 | A02 | 7140107 | G | A | missense_variant | MODERATE | c.797C>T|p.Thr266Ile |
S61 |
3 | BAA02g14980 | A02 | 7140431 | T | A | missense_variant | MODERATE | c.473A>T|p.Asp158Val |
S33 |
4 | BAA02g14980 | A02 | 7140659 | G | A | missense_variant | MODERATE | c.245C>T|p.Thr82Ile |
S148 S210 |
5 | BAA02g14980 | A02 | 7142123 | G | A | upstream_gene_variant | MODIFIER | c.-551C>T| |
S122 |
6 | BAA02g14980 | A02 | 7142325 | C | T | upstream_gene_variant | MODIFIER | c.-753G>A| |
S216 |
7 | BAA02g14980 | A02 | 7143740 | C | T | upstream_gene_variant | MODIFIER | c.-2168G>A| |
S202 |
8 | BAA02g14980 | A02 | 7144364 | C | T | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S216 |