Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23660 | A08 | 17420856 | C | T | missense_variant | MODERATE | c.1402G>A|p.Ala468Thr |
S167 |
2 | BAA08g23660 | A08 | 17423925 | C | T | splice_region_variant&synonymous_variant | LOW | c.150G>A|p.Lys50Lys |
S236 |
3 | BAA08g23660 | A08 | 17424925 | C | T | upstream_gene_variant | MODIFIER | c.-609G>A| |
S173 |
4 | BAA08g23660 | A08 | 17425661 | G | A | upstream_gene_variant | MODIFIER | c.-1345C>T| |
S204 |