Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40500 | A01 | 26825115 | C | T | synonymous_variant | LOW | c.207C>T|p.Leu69Leu |
S115 |
2 | BAA01g40500 | A01 | 26825499 | C | T | missense_variant | MODERATE | c.512C>T|p.Ser171Phe |
S135 S262 |
3 | BAA01g40500 | A01 | 26825917 | G | A | missense_variant | MODERATE | c.596G>A|p.Gly199Glu |
S121 |
4 | BAA01g40500 | A01 | 26826013 | G | A | missense_variant | MODERATE | c.692G>A|p.Gly231Asp |
S125 |
5 | BAA01g40500 | A01 | 26826338 | G | A | missense_variant | MODERATE | c.940G>A|p.Val314Met |
S34 |
6 | BAA01g40500 | A01 | 26826406 | C | T | synonymous_variant | LOW | c.1008C>T|p.Asp336Asp |
S292 |
7 | BAA01g40500 | A01 | 26827275 | C | T | missense_variant | MODERATE | c.1474C>T|p.Pro492Ser |
S73 S91 |
8 | BAA01g40500 | A01 | 26827478 | C | T | synonymous_variant | LOW | c.1677C>T|p.Pro559Pro |
S161 |