Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15040 | A01 | 7174729 | C | T | missense_variant | MODERATE | c.899G>A|p.Gly300Asp |
S40 S49 |
2 | BAA01g15040 | A01 | 7175176 | G | A | stop_gained | HIGH | c.616C>T|p.Gln206* |
S262 |
3 | BAA01g15040 | A01 | 7175513 | G | A | synonymous_variant | LOW | c.279C>T|p.Leu93Leu |
S45 |
4 | BAA01g15040 | A01 | 7176844 | C | T | upstream_gene_variant | MODIFIER | c.-1053G>A| |
S18 |
5 | BAA01g15040 | A01 | 7176996 | G | A | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S207 |
6 | BAA01g15040 | A01 | 7179168 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S198 |