Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44660 | A01 | 29718566 | G | A | synonymous_variant | LOW | c.465C>T|p.Phe155Phe |
S121 |
2 | BAA01g44660 | A01 | 29718778 | G | A | missense_variant | MODERATE | c.253C>T|p.Pro85Ser |
S169 |
3 | BAA01g44660 | A01 | 29719594 | C | T | upstream_gene_variant | MODIFIER | c.-353G>A| |
S146 |
4 | BAA01g44660 | A01 | 29719622 | C | A | upstream_gene_variant | MODIFIER | c.-381G>T| |
S20 |
5 | BAA01g44660 | A01 | 29719919 | C | T | upstream_gene_variant | MODIFIER | c.-678G>A| |
S178 |
6 | BAA01g44660 | A01 | 29720210 | G | A | upstream_gene_variant | MODIFIER | c.-969C>T| |
S185 |
7 | BAA01g44660 | A01 | 29721752 | C | T | upstream_gene_variant | MODIFIER | c.-2511G>A| |
S288 |
8 | BAA01g44660 | A01 | 29721972 | C | T | upstream_gene_variant | MODIFIER | c.-2731G>A| |
S281 |
9 | BAA01g44660 | A01 | 29722129 | C | T | upstream_gene_variant | MODIFIER | c.-2888G>A| |
S206 S26 |
10 | BAA01g44660 | A01 | 29723949 | C | T | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S281 |
11 | BAA01g44660 | A01 | 29724067 | G | A | upstream_gene_variant | MODIFIER | c.-4826C>T| |
S252 |