Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38130 | A09 | 46143043 | C | T | missense_variant | MODERATE | c.125C>T|p.Ser42Phe |
S135 |
2 | BAA09g38130 | A09 | 46143089 | C | T | synonymous_variant | LOW | c.171C>T|p.Phe57Phe |
S301 S304 |
3 | BAA09g38130 | A09 | 46143228 | G | A | missense_variant | MODERATE | c.310G>A|p.Gly104Arg |
S280 |
4 | BAA09g38130 | A09 | 46143248 | C | T | synonymous_variant | LOW | c.330C>T|p.His110His |
S208 |
5 | BAA09g38130 | A09 | 46143280 | G | A | missense_variant | MODERATE | c.362G>A|p.Gly121Glu |
S156 |
6 | BAA09g38130 | A09 | 46143359 | C | T | synonymous_variant | LOW | c.441C>T|p.His147His |
S171 |
7 | BAA09g38130 | A09 | 46143612 | G | A | downstream_gene_variant | MODIFIER | c.*4G>A| |
S12 |
8 | BAA09g38130 | A09 | 46144227 | C | T | downstream_gene_variant | MODIFIER | c.*619C>T| |
S191 |
9 | BAA09g38130 | A09 | 46144691 | C | T | downstream_gene_variant | MODIFIER | c.*1083C>T| |
S150 |