Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34090 | A10 | 24075995 | G | A | missense_variant | MODERATE | c.799C>T|p.Leu267Phe |
S197 |
2 | BAA10g34090 | A10 | 24076022 | G | A | missense_variant | MODERATE | c.772C>T|p.Pro258Ser |
S298 |
3 | BAA10g34090 | A10 | 24076127 | C | T | missense_variant | MODERATE | c.667G>A|p.Asp223Asn |
S206 S26 |
4 | BAA10g34090 | A10 | 24076317 | C | T | synonymous_variant | LOW | c.477G>A|p.Thr159Thr |
S221 |
5 | BAA10g34090 | A10 | 24076550 | G | A | missense_variant | MODERATE | c.244C>T|p.Leu82Phe |
S1 S90 |
6 | BAA10g34090 | A10 | 24079058 | G | A | upstream_gene_variant | MODIFIER | c.-2265C>T| |
S88 |