Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18980 | A02 | 9813373 | C | T | missense_variant | MODERATE | c.989G>A|p.Gly330Glu |
S94 |
2 | BAA02g18980 | A02 | 9814445 | G | A | missense_variant | MODERATE | c.422C>T|p.Ser141Phe |
S47 |
3 | BAA02g18980 | A02 | 9815077 | G | A | upstream_gene_variant | MODIFIER | c.-211C>T| |
S70 |
4 | BAA02g18980 | A02 | 9816086 | C | T | upstream_gene_variant | MODIFIER | c.-1220G>A| |
S277 |
5 | BAA02g18980 | A02 | 9816163 | G | A | upstream_gene_variant | MODIFIER | c.-1297C>T| |
S92 |
6 | BAA02g18980 | A02 | 9817068 | C | T | upstream_gene_variant | MODIFIER | c.-2202G>A| |
S277 |
7 | BAA02g18980 | A02 | 9817317 | G | A | upstream_gene_variant | MODIFIER | c.-2451C>T| |
S168 |