Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43360 | A02 | 35938801 | C | T | missense_variant | MODERATE | c.1681G>A|p.Asp561Asn |
S64 |
2 | BAA02g43360 | A02 | 35940257 | G | A | missense_variant | MODERATE | c.748C>T|p.Leu250Phe |
S44 |
3 | BAA02g43360 | A02 | 35942200 | G | A | synonymous_variant | LOW | c.429C>T|p.Ile143Ile |
S148 S30 |
4 | BAA02g43360 | A02 | 35942408 | C | T | missense_variant | MODERATE | c.317G>A|p.Gly106Asp |
S224 |
5 | BAA02g43360 | A02 | 35945462 | C | T | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S271 |
6 | BAA02g43360 | A02 | 35945627 | G | A | upstream_gene_variant | MODIFIER | c.-2903C>T| |
S143 |
7 | BAA02g43360 | A02 | 35947220 | G | A | upstream_gene_variant | MODIFIER | c.-4496C>T| |
S134 |