Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45780 | A01 | 30528252 | C | T | missense_variant | MODERATE | c.32C>T|p.Ser11Leu |
S67 |
2 | BAA01g45780 | A01 | 30528285 | C | T | missense_variant | MODERATE | c.65C>T|p.Pro22Leu |
S260 |
3 | BAA01g45780 | A01 | 30528411 | C | T | missense_variant | MODERATE | c.191C>T|p.Ala64Val |
S182 |
4 | BAA01g45780 | A01 | 30528962 | G | A | synonymous_variant | LOW | c.507G>A|p.Arg169Arg |
S5 |
5 | BAA01g45780 | A01 | 30529236 | G | T | splice_acceptor_variant&intron_variant | HIGH | c.603-1G>T| |
S292 |
6 | BAA01g45780 | A01 | 30529819 | C | T | missense_variant | MODERATE | c.886C>T|p.Leu296Phe |
S127 |
7 | BAA01g45780 | A01 | 30530186 | G | A | synonymous_variant | LOW | c.1017G>A|p.Arg339Arg |
S70 |
8 | BAA01g45780 | A01 | 30530572 | G | A | splice_region_variant&intron_variant | LOW | c.1311+8G>A| |
S292 |
9 | BAA01g45780 | A01 | 30530737 | C | T | missense_variant | MODERATE | c.1394C>T|p.Ala465Val |
S294 |
10 | BAA01g45780 | A01 | 30531718 | C | T | missense_variant | MODERATE | c.1967C>T|p.Ala656Val |
S221 |