Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01700 | A02 | 756855 | C | T | synonymous_variant | LOW | c.2487G>A|p.Gly829Gly |
S117 |
2 | BAA02g01700 | A02 | 758127 | C | T | missense_variant | MODERATE | c.1603G>A|p.Val535Ile |
S119 |
3 | BAA02g01700 | A02 | 758868 | G | A | synonymous_variant | LOW | c.1104C>T|p.Tyr368Tyr |
S169 |
4 | BAA02g01700 | A02 | 758912 | G | A | missense_variant | MODERATE | c.1060C>T|p.Leu354Phe |
S279 |
5 | BAA02g01700 | A02 | 759265 | G | A | synonymous_variant | LOW | c.807C>T|p.Ile269Ile |
S226 |
6 | BAA02g01700 | A02 | 760369 | G | A | synonymous_variant | LOW | c.69C>T|p.Cys23Cys |
S139 |
7 | BAA02g01700 | A02 | 760576 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S122 |
8 | BAA02g01700 | A02 | 760806 | C | T | upstream_gene_variant | MODIFIER | c.-223G>A| |
S83 S88 |
9 | BAA02g01700 | A02 | 762995 | G | A | upstream_gene_variant | MODIFIER | c.-2412C>T| |
S125 |
10 | BAA02g01700 | A02 | 763035 | G | A | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S17 |
11 | BAA02g01700 | A02 | 763762 | C | T | upstream_gene_variant | MODIFIER | c.-3179G>A| |
S121 |
12 | BAA02g01700 | A02 | 764605 | G | A | upstream_gene_variant | MODIFIER | c.-4022C>T| |
S209 |
13 | BAA02g01700 | A02 | 764771 | G | A | upstream_gene_variant | MODIFIER | c.-4188C>T| |
S246 |