Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45970 | A09 | 50946833 | C | T | missense_variant | MODERATE | c.182C>T|p.Ser61Phe |
S30 S31 |
2 | BAA09g45970 | A09 | 50946973 | C | T | stop_gained | HIGH | c.322C>T|p.Gln108* |
S152 |
3 | BAA09g45970 | A09 | 50947190 | G | A | missense_variant | MODERATE | c.539G>A|p.Arg180Lys |
S281 |
4 | BAA09g45970 | A09 | 50947402 | C | T | missense_variant | MODERATE | c.751C>T|p.Pro251Ser |
S37 |
5 | BAA09g45970 | A09 | 50948015 | G | A | synonymous_variant | LOW | c.990G>A|p.Lys330Lys |
S207 |
6 | BAA09g45970 | A09 | 50948050 | G | A | missense_variant | MODERATE | c.1025G>A|p.Arg342Lys |
S23 |
7 | BAA09g45970 | A09 | 50948158 | G | A | missense_variant | MODERATE | c.1133G>A|p.Gly378Asp |
S271 |
8 | BAA09g45970 | A09 | 50948645 | C | T | missense_variant | MODERATE | c.1463C>T|p.Ser488Phe |
S96 |
9 | BAA09g45970 | A09 | 50949603 | G | A | synonymous_variant | LOW | c.1986G>A|p.Lys662Lys |
S15 S3 |
10 | BAA09g45970 | A09 | 50954322 | C | T | downstream_gene_variant | MODIFIER | c.*4587C>T| |
S69 |