Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44350 | A09 | 50069340 | G | A | missense_variant | MODERATE | c.829G>A|p.Asp277Asn |
S4 |
2 | BAA09g44350 | A09 | 50069456 | C | T | synonymous_variant | LOW | c.945C>T|p.Leu315Leu |
S153 |
3 | BAA09g44350 | A09 | 50071134 | G | A | missense_variant | MODERATE | c.2446G>A|p.Glu816Lys |
S249 |
4 | BAA09g44350 | A09 | 50071142 | G | A | synonymous_variant | LOW | c.2454G>A|p.Leu818Leu |
S270 |
5 | BAA09g44350 | A09 | 50071158 | G | A | missense_variant | MODERATE | c.2470G>A|p.Gly824Ser |
S111 |
6 | BAA09g44350 | A09 | 50071461 | G | A | missense_variant | MODERATE | c.2773G>A|p.Asp925Asn |
S107 S288 |
7 | BAA09g44350 | A09 | 50073509 | C | T | downstream_gene_variant | MODIFIER | c.*952C>T| |
S278 |
8 | BAA09g44350 | A09 | 50073641 | C | T | downstream_gene_variant | MODIFIER | c.*1084C>T| |
S66 |
9 | BAA09g44350 | A09 | 50073888 | C | T | downstream_gene_variant | MODIFIER | c.*1331C>T| |
S273 |