Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13730 | A10 | 14690852 | C | T | missense_variant | MODERATE | c.809G>A|p.Gly270Asp |
S142 |
2 | BAA10g13730 | A10 | 14691243 | G | A | missense_variant | MODERATE | c.418C>T|p.Leu140Phe |
S82 S92 |
3 | BAA10g13730 | A10 | 14693771 | G | A | upstream_gene_variant | MODIFIER | c.-2111C>T| |
S34 |
4 | BAA10g13730 | A10 | 14693866 | G | A | upstream_gene_variant | MODIFIER | c.-2206C>T| |
S241 |
5 | BAA10g13730 | A10 | 14694868 | C | T | upstream_gene_variant | MODIFIER | c.-3208G>A| |
S161 |
6 | BAA10g13730 | A10 | 14695229 | G | A | upstream_gene_variant | MODIFIER | c.-3569C>T| |
S284 |