Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09400 | A09 | 5217346 | C | T | missense_variant | MODERATE | c.26C>T|p.Thr9Ile |
S13 |
2 | BAA09g09400 | A09 | 5217401 | C | T | synonymous_variant | LOW | c.81C>T|p.His27His |
S256 |
3 | BAA09g09400 | A09 | 5218020 | G | A | missense_variant | MODERATE | c.700G>A|p.Ala234Thr |
S240 |
4 | BAA09g09400 | A09 | 5218266 | G | A | missense_variant | MODERATE | c.946G>A|p.Glu316Lys |
S172 S217 |
5 | BAA09g09400 | A09 | 5218292 | G | A | synonymous_variant | LOW | c.972G>A|p.Arg324Arg |
S167 |
6 | BAA09g09400 | A09 | 5218321 | G | A | missense_variant | MODERATE | c.1001G>A|p.Arg334Lys |
S274 |
7 | BAA09g09400 | A09 | 5218586 | C | T | synonymous_variant | LOW | c.1266C>T|p.Ala422Ala |
S206 S26 |
8 | BAA09g09400 | A09 | 5218593 | C | T | synonymous_variant | LOW | c.1273C>T|p.Leu425Leu |
S87 |
9 | BAA09g09400 | A09 | 5222510 | G | A | downstream_gene_variant | MODIFIER | c.*3816G>A| |
S65 |