Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05990 | A01 | 2685433 | C | T | upstream_gene_variant | MODIFIER | c.-185C>T| |
S221 |
2 | BAA01g05990 | A01 | 2687275 | C | T | missense_variant | MODERATE | c.1084C>T|p.Pro362Ser |
S67 |
3 | BAA01g05990 | A01 | 2687633 | G | A | missense_variant | MODERATE | c.1366G>A|p.Asp456Asn |
S308 |
4 | BAA01g05990 | A01 | 2687727 | G | A | missense_variant | MODERATE | c.1460G>A|p.Arg487Lys |
S156 |
5 | BAA01g05990 | A01 | 2687851 | C | T | splice_region_variant&intron_variant | LOW | c.1580+4C>T| |
S1 S90 |