Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28930 | A10 | 21982707 | C | A | missense_variant | MODERATE | c.1297G>T|p.Gly433Trp |
S181 |
2 | BAA10g28930 | A10 | 21984286 | C | T | missense_variant | MODERATE | c.350G>A|p.Gly117Glu |
S211 S227 |
3 | BAA10g28930 | A10 | 21986331 | G | A | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S180 |
4 | BAA10g28930 | A10 | 21986348 | G | A | upstream_gene_variant | MODIFIER | c.-1527C>T| |
S84 S93 |
5 | BAA10g28930 | A10 | 21987797 | G | A | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S223 |
6 | BAA10g28930 | A10 | 21988449 | C | T | upstream_gene_variant | MODIFIER | c.-3628G>A| |
S97 |