Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05080 | A07 | 4398216 | G | A | synonymous_variant | LOW | c.2118C>T|p.Tyr706Tyr |
S98 |
2 | BAA07g05080 | A07 | 4398312 | C | T | missense_variant | MODERATE | c.2022G>A|p.Met674Ile |
S302 |
3 | BAA07g05080 | A07 | 4399208 | G | A | missense_variant | MODERATE | c.1573C>T|p.Pro525Ser |
S225 S73 |
4 | BAA07g05080 | A07 | 4399240 | C | T | missense_variant | MODERATE | c.1541G>A|p.Arg514Gln |
S293 |
5 | BAA07g05080 | A07 | 4400072 | C | T | missense_variant | MODERATE | c.709G>A|p.Glu237Lys |
S261 S274 S303 |
6 | BAA07g05080 | A07 | 4400078 | C | T | missense_variant | MODERATE | c.703G>A|p.Glu235Lys |
S162 |
7 | BAA07g05080 | A07 | 4400500 | C | T | missense_variant | MODERATE | c.368G>A|p.Gly123Glu |
S281 |
8 | BAA07g05080 | A07 | 4402402 | C | T | upstream_gene_variant | MODIFIER | c.-664G>A| |
S63 |
9 | BAA07g05080 | A07 | 4404788 | A | G | upstream_gene_variant | MODIFIER | c.-3050T>C| |
S129 |