Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44740 | A01 | 29747144 | C | T | missense_variant | MODERATE | c.1051C>T|p.Pro351Ser |
S183 S198 |
2 | BAA01g44740 | A01 | 29747310 | C | T | missense_variant | MODERATE | c.1217C>T|p.Thr406Ile |
S16 |
3 | BAA01g44740 | A01 | 29747427 | C | T | missense_variant | MODERATE | c.1334C>T|p.Ala445Val |
S74 |
4 | BAA01g44740 | A01 | 29747566 | C | T | synonymous_variant | LOW | c.1473C>T|p.Phe491Phe |
S166 |
5 | BAA01g44740 | A01 | 29747581 | G | A | synonymous_variant | LOW | c.1488G>A|p.Lys496Lys |
S283 |
6 | BAA01g44740 | A01 | 29747629 | G | A | synonymous_variant | LOW | c.1536G>A|p.Gln512Gln |
S5 |
7 | BAA01g44740 | A01 | 29747648 | G | A | missense_variant | MODERATE | c.1555G>A|p.Val519Met |
S95 |