Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44770 | A06 | 28635275 | G | A | missense_variant | MODERATE | c.2185C>T|p.Leu729Phe |
S79 S91 |
2 | BAA06g44770 | A06 | 28636161 | C | T | missense_variant | MODERATE | c.1541G>A|p.Gly514Asp |
S172 S217 |
3 | BAA06g44770 | A06 | 28637306 | G | A | synonymous_variant | LOW | c.724C>T|p.Leu242Leu |
S263 |
4 | BAA06g44770 | A06 | 28637519 | C | T | missense_variant | MODERATE | c.511G>A|p.Gly171Ser |
S105 S106 |
5 | BAA06g44770 | A06 | 28641501 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S28 |
6 | BAA06g44770 | A06 | 28642474 | C | T | upstream_gene_variant | MODIFIER | c.-4276G>A| |
S159 S243 |