Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29150 | A10 | 22052374 | C | T | missense_variant | MODERATE | c.1346G>A|p.Gly449Asp |
S11 |
2 | BAA10g29150 | A10 | 22054309 | G | A | missense_variant | MODERATE | c.184C>T|p.Pro62Ser |
S122 |
3 | BAA10g29150 | A10 | 22054420 | G | A | missense_variant | MODERATE | c.73C>T|p.Arg25Cys |
S230 |
4 | BAA10g29150 | A10 | 22054485 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S79 S84 |
5 | BAA10g29150 | A10 | 22054702 | G | A | upstream_gene_variant | MODIFIER | c.-210C>T| |
S228 |