Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17460 | A02 | 8691316 | C | T | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S219 |
2 | BAA02g17460 | A02 | 8691374 | G | A | synonymous_variant | LOW | c.186G>A|p.Ala62Ala |
S28 |
3 | BAA02g17460 | A02 | 8691380 | G | A | synonymous_variant | LOW | c.192G>A|p.Ala64Ala |
S48 |
4 | BAA02g17460 | A02 | 8691869 | C | T | missense_variant | MODERATE | c.418C>T|p.Pro140Ser |
S262 |
5 | BAA02g17460 | A02 | 8692178 | C | T | missense_variant | MODERATE | c.727C>T|p.Leu243Phe |
S128 |
6 | BAA02g17460 | A02 | 8692302 | G | A | missense_variant | MODERATE | c.851G>A|p.Gly284Glu |
S136 |
7 | BAA02g17460 | A02 | 8697585 | G | A | downstream_gene_variant | MODIFIER | c.*15G>A| |
S37 |