Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46370 | A02 | 37702971 | C | T | missense_variant | MODERATE | c.1396G>A|p.Val466Ile |
S176 |
2 | BAA02g46370 | A02 | 37703534 | G | A | missense_variant | MODERATE | c.833C>T|p.Ser278Phe |
S67 |
3 | BAA02g46370 | A02 | 37703605 | C | T | synonymous_variant | LOW | c.762G>A|p.Lys254Lys |
S289 S290 |
4 | BAA02g46370 | A02 | 37703791 | G | A | synonymous_variant | LOW | c.576C>T|p.Cys192Cys |
S96 |
5 | BAA02g46370 | A02 | 37703803 | G | A | synonymous_variant | LOW | c.564C>T|p.Phe188Phe |
S221 |
6 | BAA02g46370 | A02 | 37704027 | C | T | missense_variant | MODERATE | c.340G>A|p.Asp114Asn |
S98 |
7 | BAA02g46370 | A02 | 37704030 | C | T | missense_variant | MODERATE | c.337G>A|p.Gly113Arg |
S172 S217 |
8 | BAA02g46370 | A02 | 37704196 | G | A | synonymous_variant | LOW | c.171C>T|p.Leu57Leu |
S170 |
9 | BAA02g46370 | A02 | 37709093 | G | A | upstream_gene_variant | MODIFIER | c.-4727C>T| |
S268 |
10 | BAA02g46370 | A02 | 37709167 | G | A | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S103 |
11 | BAA02g46370 | A02 | 37709189 | G | A | upstream_gene_variant | MODIFIER | c.-4823C>T| |
S207 |