Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04810 | A01 | 2139812 | C | T | missense_variant | MODERATE | c.2248G>A|p.Glu750Lys |
S170 S176 |
2 | BAA01g04810 | A01 | 2140268 | G | A | synonymous_variant | LOW | c.2064C>T|p.Phe688Phe |
S186 |
3 | BAA01g04810 | A01 | 2140352 | C | T | synonymous_variant | LOW | c.1980G>A|p.Gln660Gln |
S58 |
4 | BAA01g04810 | A01 | 2140569 | G | A | synonymous_variant | LOW | c.1851C>T|p.Phe617Phe |
S40 |
5 | BAA01g04810 | A01 | 2141143 | C | T | synonymous_variant | LOW | c.1599G>A|p.Ser533Ser |
S166 |
6 | BAA01g04810 | A01 | 2141609 | C | T | splice_region_variant&intron_variant | LOW | c.1377+8G>A| |
S267 |
7 | BAA01g04810 | A01 | 2142187 | G | A | synonymous_variant | LOW | c.1056C>T|p.Leu352Leu |
S236 |
8 | BAA01g04810 | A01 | 2144540 | G | A | upstream_gene_variant | MODIFIER | c.-16C>T| |
S174 |
9 | BAA01g04810 | A01 | 2145750 | G | A | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S183 S198 |