Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11090 | A10 | 12771708 | C | T | missense_variant | MODERATE | c.1249G>A|p.Asp417Asn |
S286 |
2 | BAA10g11090 | A10 | 12772670 | C | T | missense_variant | MODERATE | c.611G>A|p.Gly204Glu |
S143 |
3 | BAA10g11090 | A10 | 12773093 | G | A | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S234 |
4 | BAA10g11090 | A10 | 12778058 | G | A | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S202 |
5 | BAA10g11090 | A10 | 12778780 | C | T | upstream_gene_variant | MODIFIER | c.-4940G>A| |
S166 |