Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01170 | A02 | 550895 | C | T | synonymous_variant | LOW | c.12C>T|p.Val4Val |
S207 |
2 | BAA02g01170 | A02 | 550942 | C | T | missense_variant | MODERATE | c.59C>T|p.Ser20Leu |
S262 |
3 | BAA02g01170 | A02 | 551019 | G | A | missense_variant | MODERATE | c.136G>A|p.Gly46Arg |
S265 |
4 | BAA02g01170 | A02 | 551079 | G | A | missense_variant | MODERATE | c.196G>A|p.Glu66Lys |
S25 |
5 | BAA02g01170 | A02 | 551178 | G | A | missense_variant | MODERATE | c.295G>A|p.Gly99Arg |
S111 S129 |
6 | BAA02g01170 | A02 | 551191 | C | T | missense_variant | MODERATE | c.308C>T|p.Thr103Ile |
S211 |
7 | BAA02g01170 | A02 | 552476 | C | T | missense_variant | MODERATE | c.907C>T|p.Leu303Phe |
S82 S92 |
8 | BAA02g01170 | A02 | 553413 | G | A | synonymous_variant | LOW | c.1434G>A|p.Glu478Glu |
S4 |