Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43830 | A09 | 49795865 | G | A | missense_variant | MODERATE | c.2935C>T|p.Leu979Phe |
S23 |
2 | BAA09g43830 | A09 | 49796222 | C | T | missense_variant | MODERATE | c.2578G>A|p.Gly860Arg |
S100 |
3 | BAA09g43830 | A09 | 49797562 | C | T | missense_variant | MODERATE | c.1747G>A|p.Gly583Arg |
S206 S26 |
4 | BAA09g43830 | A09 | 49797675 | G | A | intron_variant | MODIFIER | c.1719+27C>T| |
S128 S157 |
5 | BAA09g43830 | A09 | 49798693 | G | A | missense_variant | MODERATE | c.1034C>T|p.Pro345Leu |
S218 |
6 | BAA09g43830 | A09 | 49798909 | C | T | missense_variant | MODERATE | c.818G>A|p.Arg273Lys |
S104 S52 |
7 | BAA09g43830 | A09 | 49798918 | C | T | missense_variant | MODERATE | c.809G>A|p.Gly270Glu |
S261 |
8 | BAA09g43830 | A09 | 49803638 | C | T | upstream_gene_variant | MODIFIER | c.-2893G>A| |
S182 |