Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37280 | A02 | 31985779 | C | T | synonymous_variant | LOW | c.87C>T|p.Phe29Phe |
S262 |
2 | BAA02g37280 | A02 | 31985998 | G | A | synonymous_variant | LOW | c.222G>A|p.Gln74Gln |
S110 |
3 | BAA02g37280 | A02 | 31986448 | G | A | synonymous_variant | LOW | c.672G>A|p.Arg224Arg |
S153 S213 |
4 | BAA02g37280 | A02 | 31987365 | C | T | missense_variant | MODERATE | c.1063C>T|p.Leu355Phe |
S73 S91 |
5 | BAA02g37280 | A02 | 31987638 | G | A | synonymous_variant | LOW | c.1248G>A|p.Leu416Leu |
S197 |
6 | BAA02g37280 | A02 | 31988123 | C | T | missense_variant | MODERATE | c.1664C>T|p.Thr555Ile |
S178 |
7 | BAA02g37280 | A02 | 31988758 | G | A | missense_variant | MODERATE | c.2147G>A|p.Arg716Lys |
S256 |
8 | BAA02g37280 | A02 | 31989015 | G | A | missense_variant | MODERATE | c.2404G>A|p.Gly802Arg |
S287 |
9 | BAA02g37280 | A02 | 31991094 | C | T | downstream_gene_variant | MODIFIER | c.*1705C>T| |
S124 S127 S149 S170 S176 S280 S287 S58 S59 |