Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44590 | A01 | 29691409 | G | A | upstream_gene_variant | MODIFIER | c.-33G>A| |
S278 |
2 | BAA01g44590 | A01 | 29692697 | G | A | synonymous_variant | LOW | c.609G>A|p.Lys203Lys |
S232 |
3 | BAA01g44590 | A01 | 29693036 | G | A | synonymous_variant | LOW | c.735G>A|p.Ala245Ala |
S302 S68 |
4 | BAA01g44590 | A01 | 29693144 | C | T | synonymous_variant | LOW | c.843C>T|p.Ser281Ser |
S60 |
5 | BAA01g44590 | A01 | 29693446 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ser382Phe |
S77 S82 |
6 | BAA01g44590 | A01 | 29694487 | C | T | missense_variant | MODERATE | c.1867C>T|p.Pro623Ser |
S260 |
7 | BAA01g44590 | A01 | 29695606 | C | T | missense_variant | MODERATE | c.2714C>T|p.Ala905Val |
S115 |
8 | BAA01g44590 | A01 | 29695658 | G | A | synonymous_variant | LOW | c.2766G>A|p.Arg922Arg |
S217 S248 |
9 | BAA01g44590 | A01 | 29695899 | G | A | missense_variant | MODERATE | c.3007G>A|p.Glu1003Lys |
S117 |