Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13960 | A05 | 7307049 | G | A | missense_variant | MODERATE | c.532G>A|p.Asp178Asn |
S134 |
2 | BAA05g13960 | A05 | 7307379 | C | T | missense_variant | MODERATE | c.761C>T|p.Ala254Val |
S47 |
3 | BAA05g13960 | A05 | 7307640 | G | A | missense_variant | MODERATE | c.917G>A|p.Cys306Tyr |
S239 |
4 | BAA05g13960 | A05 | 7308393 | G | A | missense_variant | MODERATE | c.1342G>A|p.Glu448Lys |
S282 |
5 | BAA05g13960 | A05 | 7309022 | G | A | synonymous_variant | LOW | c.1887G>A|p.Lys629Lys |
S34 |
6 | BAA05g13960 | A05 | 7309163 | C | T | missense_variant | MODERATE | c.1954C>T|p.Pro652Ser |
S286 |
7 | BAA05g13960 | A05 | 7309709 | C | T | missense_variant | MODERATE | c.2314C>T|p.Leu772Phe |
S284 |
8 | BAA05g13960 | A05 | 7311095 | C | T | downstream_gene_variant | MODIFIER | c.*169C>T| |
S146 |