Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09440 | A10 | 11424367 | G | A | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S81 |
2 | BAA10g09440 | A10 | 11424657 | G | A | missense_variant | MODERATE | c.196C>T|p.Pro66Ser |
S65 |
3 | BAA10g09440 | A10 | 11425240 | G | A | upstream_gene_variant | MODIFIER | c.-241C>T| |
S151 |
4 | BAA10g09440 | A10 | 11425649 | G | A | upstream_gene_variant | MODIFIER | c.-650C>T| |
S262 S265 |
5 | BAA10g09440 | A10 | 11425662 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S129 |
6 | BAA10g09440 | A10 | 11425701 | C | T | upstream_gene_variant | MODIFIER | c.-702G>A| |
S237 |