Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g54700 | A03 | 26997491 | C | T | missense_variant | MODERATE | c.142C>T|p.Leu48Phe |
S2 |
2 | BAA03g54700 | A03 | 26997525 | C | T | missense_variant | MODERATE | c.176C>T|p.Pro59Leu |
S251 |
3 | BAA03g54700 | A03 | 26999514 | G | A | missense_variant | MODERATE | c.680G>A|p.Gly227Glu |
S217 |
4 | BAA03g54700 | A03 | 27000008 | G | A | synonymous_variant | LOW | c.975G>A|p.Arg325Arg |
S223 |
5 | BAA03g54700 | A03 | 27000040 | C | T | missense_variant | MODERATE | c.1007C>T|p.Ala336Val |
S94 |
6 | BAA03g54700 | A03 | 27000414 | G | A | missense_variant | MODERATE | c.1265G>A|p.Arg422Lys |
S267 |
7 | BAA03g54700 | A03 | 27000624 | G | A | missense_variant | MODERATE | c.1475G>A|p.Ser492Asn |
S308 |
8 | BAA03g54700 | A03 | 27000626 | C | T | stop_gained | HIGH | c.1477C>T|p.Arg493* |
S200 S255 |
9 | BAA03g54700 | A03 | 27000929 | C | T | missense_variant | MODERATE | c.1780C>T|p.His594Tyr |
S100 |
10 | BAA03g54700 | A03 | 27000948 | C | T | missense_variant | MODERATE | c.1799C>T|p.Ala600Val |
S121 |
11 | BAA03g54700 | A03 | 27000955 | G | A | synonymous_variant | LOW | c.1806G>A|p.Ala602Ala |
S283 |