Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11770 | A07 | 20384706 | C | T | missense_variant | MODERATE | c.1045G>A|p.Val349Ile |
S275 |
2 | BAA07g11770 | A07 | 20384754 | C | T | missense_variant | MODERATE | c.997G>A|p.Glu333Lys |
S293 |
3 | BAA07g11770 | A07 | 20385929 | G | A | splice_region_variant&synonymous_variant | LOW | c.399C>T|p.Leu133Leu |
S160 |
4 | BAA07g11770 | A07 | 20388830 | C | T | upstream_gene_variant | MODIFIER | c.-2503G>A| |
S297 |