Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01890 | A06 | 1159255 | C | T | synonymous_variant | LOW | c.294C>T|p.Tyr98Tyr |
S48 |
2 | BAA06g01890 | A06 | 1159567 | G | A | synonymous_variant | LOW | c.606G>A|p.Arg202Arg |
S61 |
3 | BAA06g01890 | A06 | 1159618 | C | T | synonymous_variant | LOW | c.657C>T|p.Arg219Arg |
S164 |
4 | BAA06g01890 | A06 | 1159632 | G | A | missense_variant | MODERATE | c.671G>A|p.Cys224Tyr |
S54 |
5 | BAA06g01890 | A06 | 1159749 | C | T | missense_variant | MODERATE | c.788C>T|p.Ala263Val |
S60 |
6 | BAA06g01890 | A06 | 1159799 | C | T | missense_variant | MODERATE | c.838C>T|p.Arg280Cys |
S296 |
7 | BAA06g01890 | A06 | 1159900 | G | A | synonymous_variant | LOW | c.939G>A|p.Gly313Gly |
S249 |
8 | BAA06g01890 | A06 | 1160131 | G | A | synonymous_variant | LOW | c.1170G>A|p.Thr390Thr |
S217 S248 |
9 | BAA06g01890 | A06 | 1160300 | G | A | missense_variant | MODERATE | c.1339G>A|p.Ala447Thr |
S166 |