Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28850 | A10 | 21954905 | G | A | missense_variant | MODERATE | c.425C>T|p.Ala142Val |
S139 |
2 | BAA10g28850 | A10 | 21955726 | G | A | missense_variant | MODERATE | c.41C>T|p.Pro14Leu |
S257 |
3 | BAA10g28850 | A10 | 21959503 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S125 |