Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21700 | A10 | 18988599 | G | A | missense_variant | MODERATE | c.1052C>T|p.Thr351Ile |
S75 S81 |
2 | BAA10g21700 | A10 | 18989667 | G | A | synonymous_variant | LOW | c.420C>T|p.Phe140Phe |
S233 |
3 | BAA10g21700 | A10 | 18989764 | C | T | missense_variant&splice_region_variant | MODERATE | c.405G>A|p.Met135Ile |
S133 |
4 | BAA10g21700 | A10 | 18991572 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S251 |
5 | BAA10g21700 | A10 | 18993513 | C | T | upstream_gene_variant | MODIFIER | c.-2715G>A| |
S18 |
6 | BAA10g21700 | A10 | 18994623 | G | A | upstream_gene_variant | MODIFIER | c.-3825C>T| |
S293 |