Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38150 | A05 | 37718367 | C | T | missense_variant | MODERATE | c.1273G>A|p.Gly425Arg |
S174 |
2 | BAA05g38150 | A05 | 37719031 | G | A | synonymous_variant | LOW | c.609C>T|p.Phe203Phe |
S33 |
3 | BAA05g38150 | A05 | 37719500 | C | T | synonymous_variant | LOW | c.315G>A|p.Gly105Gly |
S38 |
4 | BAA05g38150 | A05 | 37719501 | C | T | missense_variant | MODERATE | c.314G>A|p.Gly105Glu |
S192 |
5 | BAA05g38150 | A05 | 37719554 | G | A | synonymous_variant | LOW | c.261C>T|p.Phe87Phe |
S281 S288 |
6 | BAA05g38150 | A05 | 37719579 | G | A | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S98 |
7 | BAA05g38150 | A05 | 37719682 | C | T | missense_variant | MODERATE | c.133G>A|p.Gly45Arg |
S208 S93 |
8 | BAA05g38150 | A05 | 37720164 | C | T | upstream_gene_variant | MODIFIER | c.-256G>A| |
S32 |
9 | BAA05g38150 | A05 | 37721256 | C | T | upstream_gene_variant | MODIFIER | c.-1348G>A| |
S287 |
10 | BAA05g38150 | A05 | 37721286 | G | A | upstream_gene_variant | MODIFIER | c.-1378C>T| |
S295 |