Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12930 | A02 | 5772279 | C | T | missense_variant | MODERATE | c.1837G>A|p.Val613Met |
S185 |
2 | BAA02g12930 | A02 | 5772776 | G | A | synonymous_variant | LOW | c.1527C>T|p.Tyr509Tyr |
S148 S30 S31 |
3 | BAA02g12930 | A02 | 5773403 | G | A | splice_region_variant&intron_variant | LOW | c.1122+8C>T| |
S166 |
4 | BAA02g12930 | A02 | 5775284 | G | A | synonymous_variant | LOW | c.321C>T|p.Tyr107Tyr |
S62 |
5 | BAA02g12930 | A02 | 5775559 | G | A | missense_variant | MODERATE | c.154C>T|p.Leu52Phe |
S72 |
6 | BAA02g12930 | A02 | 5776034 | G | A | upstream_gene_variant | MODIFIER | c.-206C>T| |
S79 S91 |
7 | BAA02g12930 | A02 | 5776541 | C | T | upstream_gene_variant | MODIFIER | c.-713G>A| |
S54 |
8 | BAA02g12930 | A02 | 5778832 | C | T | upstream_gene_variant | MODIFIER | c.-3004G>A| |
S115 |
9 | BAA02g12930 | A02 | 5780053 | G | A | upstream_gene_variant | MODIFIER | c.-4225C>T| |
S133 S202 |