Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59090 | A09 | 57408952 | C | T | synonymous_variant | LOW | c.189C>T|p.Ala63Ala |
S153 S213 |
2 | BAA09g59090 | A09 | 57409291 | C | T | missense_variant | MODERATE | c.461C>T|p.Ala154Val |
S63 |
3 | BAA09g59090 | A09 | 57410941 | C | T | splice_region_variant&synonymous_variant | LOW | c.504C>T|p.Ser168Ser |
S306 S308 |
4 | BAA09g59090 | A09 | 57411009 | C | T | missense_variant | MODERATE | c.572C>T|p.Thr191Ile |
S124 S99 |
5 | BAA09g59090 | A09 | 57411224 | C | T | missense_variant | MODERATE | c.787C>T|p.Arg263Cys |
S65 |
6 | BAA09g59090 | A09 | 57415050 | G | A | downstream_gene_variant | MODIFIER | c.*3800G>A| |
S291 |