Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10270 | A02 | 4565473 | C | T | synonymous_variant | LOW | c.1335G>A|p.Gln445Gln |
S83 S88 |
2 | BAA02g10270 | A02 | 4566024 | C | T | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S218 |
3 | BAA02g10270 | A02 | 4566123 | C | T | missense_variant | MODERATE | c.685G>A|p.Asp229Asn |
S277 |
4 | BAA02g10270 | A02 | 4566356 | C | T | missense_variant | MODERATE | c.452G>A|p.Gly151Asp |
S127 |
5 | BAA02g10270 | A02 | 4566422 | C | T | missense_variant | MODERATE | c.386G>A|p.Arg129Lys |
S90 |
6 | BAA02g10270 | A02 | 4569427 | C | T | upstream_gene_variant | MODIFIER | c.-2620G>A| |
S32 |
7 | BAA02g10270 | A02 | 4570140 | G | A | upstream_gene_variant | MODIFIER | c.-3333C>T| |
S25 |
8 | BAA02g10270 | A02 | 4570372 | G | A | upstream_gene_variant | MODIFIER | c.-3565C>T| |
S305 |
9 | BAA02g10270 | A02 | 4570378 | C | T | upstream_gene_variant | MODIFIER | c.-3571G>A| |
S270 |
10 | BAA02g10270 | A02 | 4571014 | C | T | upstream_gene_variant | MODIFIER | c.-4207G>A| |
S243 |