Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02030 | A02 | 900332 | G | A | missense_variant | MODERATE | c.712C>T|p.Pro238Ser |
S168 |
2 | BAA02g02030 | A02 | 900578 | C | T | synonymous_variant | LOW | c.588G>A|p.Lys196Lys |
S80 |
3 | BAA02g02030 | A02 | 900911 | C | T | missense_variant | MODERATE | c.332G>A|p.Ser111Asn |
S15 S3 |
4 | BAA02g02030 | A02 | 904134 | C | T | upstream_gene_variant | MODIFIER | c.-2309G>A| |
S263 |
5 | BAA02g02030 | A02 | 904294 | G | A | upstream_gene_variant | MODIFIER | c.-2469C>T| |
S23 |
6 | BAA02g02030 | A02 | 904519 | C | T | upstream_gene_variant | MODIFIER | c.-2694G>A| |
S71 |
7 | BAA02g02030 | A02 | 904799 | G | A | upstream_gene_variant | MODIFIER | c.-2974C>T| |
S225 |
8 | BAA02g02030 | A02 | 906742 | G | A | upstream_gene_variant | MODIFIER | c.-4917C>T| |
S17 |