Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66330 | A09 | 60693030 | G | A | missense_variant | MODERATE | c.1808C>T|p.Thr603Met |
S13 |
2 | BAA09g66330 | A09 | 60694060 | C | T | missense_variant | MODERATE | c.1334G>A|p.Gly445Glu |
S117 |
3 | BAA09g66330 | A09 | 60694287 | G | A | synonymous_variant | LOW | c.1230C>T|p.Leu410Leu |
S110 |
4 | BAA09g66330 | A09 | 60694729 | C | T | missense_variant | MODERATE | c.979G>A|p.Gly327Ser |
S60 |
5 | BAA09g66330 | A09 | 60695339 | G | A | missense_variant | MODERATE | c.680C>T|p.Ala227Val |
S13 |
6 | BAA09g66330 | A09 | 60695578 | G | A | missense_variant | MODERATE | c.518C>T|p.Ala173Val |
S171 |
7 | BAA09g66330 | A09 | 60697247 | G | A | upstream_gene_variant | MODIFIER | c.-210C>T| |
S233 |
8 | BAA09g66330 | A09 | 60698471 | G | A | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S234 |
9 | BAA09g66330 | A09 | 60700604 | C | T | upstream_gene_variant | MODIFIER | c.-3567G>A| |
S192 |
10 | BAA09g66330 | A09 | 60701559 | A | G | upstream_gene_variant | MODIFIER | c.-4522T>C| |
S301 |