Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00800 | A04 | 428765 | C | T | missense_variant | MODERATE | c.835G>A|p.Gly279Ser |
S8 |
2 | BAA04g00800 | A04 | 428925 | C | T | synonymous_variant | LOW | c.675G>A|p.Arg225Arg |
S292 |
3 | BAA04g00800 | A04 | 429324 | G | A | synonymous_variant | LOW | c.276C>T|p.Ile92Ile |
S208 S219 |
4 | BAA04g00800 | A04 | 429401 | C | T | missense_variant | MODERATE | c.199G>A|p.Glu67Lys |
S50 |
5 | BAA04g00800 | A04 | 433078 | C | T | upstream_gene_variant | MODIFIER | c.-3479G>A| |
S19 |
6 | BAA04g00800 | A04 | 433892 | G | A | upstream_gene_variant | MODIFIER | c.-4293C>T| |
S305 |