Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13320 | A02 | 6059597 | T | A | synonymous_variant | LOW | c.51T>A|p.Ala17Ala |
S226 S238 S91 |
2 | BAA02g13320 | A02 | 6059609 | G | A | synonymous_variant | LOW | c.63G>A|p.Glu21Glu |
S226 S238 S257 S91 |
3 | BAA02g13320 | A02 | 6059615 | C | T | synonymous_variant | LOW | c.69C>T|p.Asp23Asp |
S226 S238 S246 S257 S91 |
4 | BAA02g13320 | A02 | 6059618 | C | T | synonymous_variant | LOW | c.72C>T|p.Leu24Leu |
S226 S238 S257 S91 |
5 | BAA02g13320 | A02 | 6059623 | G | C | missense_variant | MODERATE | c.77G>C|p.Gly26Ala |
S226 S238 S257 S91 |
6 | BAA02g13320 | A02 | 6059624 | C | T | synonymous_variant | LOW | c.78C>T|p.Gly26Gly |
S226 S238 S257 S91 |
7 | BAA02g13320 | A02 | 6059627 | C | A | synonymous_variant | LOW | c.81C>A|p.Ser27Ser |
S226 S238 S257 S91 |
8 | BAA02g13320 | A02 | 6059731 | C | T | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S18 |
9 | BAA02g13320 | A02 | 6060035 | G | A | missense_variant | MODERATE | c.316G>A|p.Glu106Lys |
S293 |
10 | BAA02g13320 | A02 | 6060073 | C | T | synonymous_variant | LOW | c.354C>T|p.Leu118Leu |
S238 |