Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09890 | A05 | 5048761 | C | T | missense_variant | MODERATE | c.22C>T|p.Arg8Trp |
S250 |
2 | BAA05g09890 | A05 | 5048805 | C | T | synonymous_variant | LOW | c.66C>T|p.Ile22Ile |
S262 |
3 | BAA05g09890 | A05 | 5050622 | C | T | splice_region_variant&intron_variant | LOW | c.1250+7C>T| |
S25 |
4 | BAA05g09890 | A05 | 5052061 | C | T | synonymous_variant | LOW | c.1683C>T|p.Asn561Asn |
S270 |
5 | BAA05g09890 | A05 | 5056702 | C | T | downstream_gene_variant | MODIFIER | c.*3233C>T| |
S259 |