Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g18770 | A04 | 22446709 | C | T | missense_variant | MODERATE | c.1171C>T|p.Leu391Phe |
S8 |
2 | BAA04g18770 | A04 | 22446811 | C | T | synonymous_variant | LOW | c.1273C>T|p.Leu425Leu |
S270 |
3 | BAA04g18770 | A04 | 22446815 | G | A | missense_variant | MODERATE | c.1277G>A|p.Arg426Lys |
S83 S88 |
4 | BAA04g18770 | A04 | 22446891 | T | C | synonymous_variant | LOW | c.1353T>C|p.Asp451Asp |
S63 |
5 | BAA04g18770 | A04 | 22448491 | G | A | missense_variant | MODERATE | c.2746G>A|p.Glu916Lys |
S86 |
6 | BAA04g18770 | A04 | 22448801 | G | A | missense_variant | MODERATE | c.3056G>A|p.Gly1019Glu |
S108 |
7 | BAA04g18770 | A04 | 22451318 | C | T | downstream_gene_variant | MODIFIER | c.*2279C>T| |
S294 |