Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19240 | A02 | 9988034 | G | A | missense_variant | MODERATE | c.622C>T|p.Leu208Phe |
S60 |
2 | BAA02g19240 | A02 | 9993321 | C | T | upstream_gene_variant | MODIFIER | c.-408G>A| |
S183 S198 |
3 | BAA02g19240 | A02 | 9995054 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S15 S3 |
4 | BAA02g19240 | A02 | 9995069 | C | T | upstream_gene_variant | MODIFIER | c.-2156G>A| |
S181 |
5 | BAA02g19240 | A02 | 9996242 | T | A | upstream_gene_variant | MODIFIER | c.-3329A>T| |
S38 |
6 | BAA02g19240 | A02 | 9997417 | C | T | upstream_gene_variant | MODIFIER | c.-4504G>A| |
S76 |
7 | BAA02g19240 | A02 | 9997430 | C | T | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S270 |