Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22670 | A01 | 11456343 | G | A | missense_variant | MODERATE | c.2771C>T|p.Thr924Ile |
S178 |
2 | BAA01g22670 | A01 | 11456792 | C | T | missense_variant | MODERATE | c.2491G>A|p.Glu831Lys |
S203 |
3 | BAA01g22670 | A01 | 11457412 | C | T | missense_variant | MODERATE | c.2305G>A|p.Gly769Arg |
S104 S52 |
4 | BAA01g22670 | A01 | 11459157 | C | T | missense_variant | MODERATE | c.1435G>A|p.Gly479Arg |
S53 |
5 | BAA01g22670 | A01 | 11460763 | C | T | synonymous_variant | LOW | c.192G>A|p.Lys64Lys |
S54 |
6 | BAA01g22670 | A01 | 11460923 | G | A | missense_variant | MODERATE | c.32C>T|p.Ala11Val |
S138 |
7 | BAA01g22670 | A01 | 11461803 | G | A | upstream_gene_variant | MODIFIER | c.-849C>T| |
S63 |
8 | BAA01g22670 | A01 | 11461904 | G | A | upstream_gene_variant | MODIFIER | c.-950C>T| |
S252 |
9 | BAA01g22670 | A01 | 11462778 | G | A | upstream_gene_variant | MODIFIER | c.-1824C>T| |
S244 |