Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48650 | A09 | 52383339 | C | T | missense_variant | MODERATE | c.1552G>A|p.Gly518Arg |
S25 |
2 | BAA09g48650 | A09 | 52384146 | G | A | missense_variant | MODERATE | c.908C>T|p.Pro303Leu |
S270 |
3 | BAA09g48650 | A09 | 52386074 | G | A | synonymous_variant | LOW | c.12C>T|p.His4His |
S165 |
4 | BAA09g48650 | A09 | 52388070 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S244 |
5 | BAA09g48650 | A09 | 52389283 | G | A | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S113 |
6 | BAA09g48650 | A09 | 52389380 | G | A | upstream_gene_variant | MODIFIER | c.-3295C>T| |
S70 |