Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14640 | A02 | 6841199 | G | A | missense_variant | MODERATE | c.833C>T|p.Ser278Phe |
S95 |
2 | BAA02g14640 | A02 | 6841727 | G | A | synonymous_variant | LOW | c.519C>T|p.Ser173Ser |
S245 |
3 | BAA02g14640 | A02 | 6843001 | G | A | synonymous_variant | LOW | c.111C>T|p.Ser37Ser |
S79 S91 |
4 | BAA02g14640 | A02 | 6843572 | G | A | upstream_gene_variant | MODIFIER | c.-398C>T| |
S67 |
5 | BAA02g14640 | A02 | 6846111 | G | A | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S143 |
6 | BAA02g14640 | A02 | 6846854 | C | T | upstream_gene_variant | MODIFIER | c.-3680G>A| |
S18 |
7 | BAA02g14640 | A02 | 6847998 | G | A | upstream_gene_variant | MODIFIER | c.-4824C>T| |
S67 |