Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41500 | A09 | 48235860 | C | T | missense_variant | MODERATE | c.403G>A|p.Gly135Arg |
S119 |
2 | BAA09g41500 | A09 | 48235970 | G | A | missense_variant | MODERATE | c.293C>T|p.Ala98Val |
S216 |
3 | BAA09g41500 | A09 | 48236796 | C | T | upstream_gene_variant | MODIFIER | c.-534G>A| |
S292 |
4 | BAA09g41500 | A09 | 48236903 | G | A | upstream_gene_variant | MODIFIER | c.-641C>T| |
S197 |
5 | BAA09g41500 | A09 | 48237792 | C | T | upstream_gene_variant | MODIFIER | c.-1530G>A| |
S61 |
6 | BAA09g41500 | A09 | 48239977 | C | T | upstream_gene_variant | MODIFIER | c.-3715G>A| |
S120 |