Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01150 | A09 | 833826 | G | A | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S236 |
2 | BAA09g01150 | A09 | 833893 | C | T | missense_variant | MODERATE | c.115G>A|p.Gly39Ser |
S206 S26 |
3 | BAA09g01150 | A09 | 834341 | G | A | upstream_gene_variant | MODIFIER | c.-334C>T| |
S54 |
4 | BAA09g01150 | A09 | 835220 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S25 S264 |
5 | BAA09g01150 | A09 | 836705 | C | T | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S260 |
6 | BAA09g01150 | A09 | 837708 | G | A | upstream_gene_variant | MODIFIER | c.-3701C>T| |
S281 |