Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41900 | A01 | 27867547 | G | A | synonymous_variant | LOW | c.2622C>T|p.Val874Val |
S144 |
2 | BAA01g41900 | A01 | 27867781 | G | A | synonymous_variant | LOW | c.2388C>T|p.Phe796Phe |
S272 |
3 | BAA01g41900 | A01 | 27867807 | G | A | missense_variant | MODERATE | c.2362C>T|p.Pro788Ser |
S262 |
4 | BAA01g41900 | A01 | 27867957 | C | T | missense_variant | MODERATE | c.2212G>A|p.Glu738Lys |
S255 |
5 | BAA01g41900 | A01 | 27868925 | G | A | missense_variant | MODERATE | c.1244C>T|p.Ser415Leu |
S251 |
6 | BAA01g41900 | A01 | 27869902 | C | T | stop_gained | HIGH | c.267G>A|p.Trp89* |
S156 |
7 | BAA01g41900 | A01 | 27871286 | C | T | upstream_gene_variant | MODIFIER | c.-1118G>A| |
S155 S211 |
8 | BAA01g41900 | A01 | 27873397 | C | T | upstream_gene_variant | MODIFIER | c.-3229G>A| |
S153 |