Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09890 | A02 | 4358360 | G | A | upstream_gene_variant | MODIFIER | c.-2580G>A| |
S288 |
2 | BAA02g09890 | A02 | 4358810 | C | T | upstream_gene_variant | MODIFIER | c.-2130C>T| |
S185 |
3 | BAA02g09890 | A02 | 4360039 | C | T | upstream_gene_variant | MODIFIER | c.-901C>T| |
S54 |
4 | BAA02g09890 | A02 | 4361099 | G | A | synonymous_variant | LOW | c.84G>A|p.Lys28Lys |
S150 |
5 | BAA02g09890 | A02 | 4361447 | C | T | intron_variant | MODIFIER | c.109+323C>T| |
S301 S304 |
6 | BAA02g09890 | A02 | 4363415 | G | A | synonymous_variant | LOW | c.840G>A|p.Glu280Glu |
S162 |
7 | BAA02g09890 | A02 | 4363741 | G | A | stop_gained | HIGH | c.1166G>A|p.Trp389* |
S185 |
8 | BAA02g09890 | A02 | 4364208 | G | A | missense_variant | MODERATE | c.1633G>A|p.Ala545Thr |
S61 |
9 | BAA02g09890 | A02 | 4365104 | C | T | missense_variant | MODERATE | c.2303C>T|p.Pro768Leu |
S180 |
10 | BAA02g09890 | A02 | 4366193 | C | T | synonymous_variant | LOW | c.3240C>T|p.Gly1080Gly |
S183 S198 |