Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43990 | A09 | 49885138 | G | A | upstream_gene_variant | MODIFIER | c.-3626G>A| |
S167 |
2 | BAA09g43990 | A09 | 49888832 | C | T | synonymous_variant | LOW | c.69C>T|p.Tyr23Tyr |
S51 |
3 | BAA09g43990 | A09 | 49889088 | C | T | missense_variant | MODERATE | c.325C>T|p.Pro109Ser |
S169 |
4 | BAA09g43990 | A09 | 49889157 | C | T | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S122 |
5 | BAA09g43990 | A09 | 49889320 | C | T | missense_variant | MODERATE | c.557C>T|p.Thr186Ile |
S206 S26 |
6 | BAA09g43990 | A09 | 49890835 | G | A | missense_variant | MODERATE | c.1549G>A|p.Glu517Lys |
S281 |
7 | BAA09g43990 | A09 | 49890972 | G | A | synonymous_variant | LOW | c.1686G>A|p.Lys562Lys |
S127 |
8 | BAA09g43990 | A09 | 49891078 | G | A | missense_variant | MODERATE | c.1792G>A|p.Gly598Arg |
S244 |
9 | BAA09g43990 | A09 | 49891152 | C | T | synonymous_variant | LOW | c.1866C>T|p.Asn622Asn |
S183 S198 |