Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37750 | A02 | 32264884 | C | T | missense_variant | MODERATE | c.488G>A|p.Gly163Glu |
S118 |
2 | BAA02g37750 | A02 | 32265568 | C | T | missense_variant | MODERATE | c.46G>A|p.Val16Ile |
S54 |
3 | BAA02g37750 | A02 | 32269366 | G | A | upstream_gene_variant | MODIFIER | c.-3753C>T| |
S188 |
4 | BAA02g37750 | A02 | 32269961 | G | A | upstream_gene_variant | MODIFIER | c.-4348C>T| |
S81 |
5 | BAA02g37750 | A02 | 32270572 | G | A | upstream_gene_variant | MODIFIER | c.-4959C>T| |
S212 |