Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12150 | A10 | 13620026 | C | T | upstream_gene_variant | MODIFIER | c.-4146C>T| |
S144 |
2 | BAA10g12150 | A10 | 13621017 | C | T | upstream_gene_variant | MODIFIER | c.-3155C>T| |
S164 |
3 | BAA10g12150 | A10 | 13625320 | G | A | missense_variant | MODERATE | c.1051G>A|p.Ala351Thr |
S276 |
4 | BAA10g12150 | A10 | 13625615 | C | T | missense_variant | MODERATE | c.1346C>T|p.Ala449Val |
S122 |
5 | BAA10g12150 | A10 | 13627909 | G | A | downstream_gene_variant | MODIFIER | c.*2140G>A| |
S178 |
6 | BAA10g12150 | A10 | 13628224 | C | T | downstream_gene_variant | MODIFIER | c.*2455C>T| |
S197 |