Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18690 | A05 | 10802620 | C | T | missense_variant | MODERATE | c.617C>T|p.Ser206Phe |
S103 |
2 | BAA05g18690 | A05 | 10802941 | G | A | missense_variant | MODERATE | c.839G>A|p.Gly280Asp |
S11 |
3 | BAA05g18690 | A05 | 10803603 | G | A | missense_variant | MODERATE | c.1138G>A|p.Glu380Lys |
S173 |
4 | BAA05g18690 | A05 | 10803706 | C | T | missense_variant | MODERATE | c.1241C>T|p.Ser414Phe |
S118 |
5 | BAA05g18690 | A05 | 10804247 | G | A | synonymous_variant | LOW | c.1578G>A|p.Leu526Leu |
S3 |
6 | BAA05g18690 | A05 | 10804276 | G | A | missense_variant | MODERATE | c.1607G>A|p.Gly536Glu |
S274 |
7 | BAA05g18690 | A05 | 10804692 | C | T | missense_variant | MODERATE | c.1817C>T|p.Ser606Phe |
S202 |
8 | BAA05g18690 | A05 | 10804707 | G | A | missense_variant | MODERATE | c.1832G>A|p.Gly611Asp |
S179 |
9 | BAA05g18690 | A05 | 10804947 | G | A | missense_variant | MODERATE | c.1990G>A|p.Glu664Lys |
S148 S210 |