Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39700 | A01 | 26357058 | C | T | missense_variant | MODERATE | c.1250G>A|p.Gly417Asp |
S293 |
2 | BAA01g39700 | A01 | 26357594 | G | A | synonymous_variant | LOW | c.1176C>T|p.Ser392Ser |
S122 |
3 | BAA01g39700 | A01 | 26358402 | C | T | missense_variant | MODERATE | c.616G>A|p.Asp206Asn |
S41 |
4 | BAA01g39700 | A01 | 26358416 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.603-1G>A| |
S148 S210 |
5 | BAA01g39700 | A01 | 26359379 | C | T | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S48 |
6 | BAA01g39700 | A01 | 26360172 | G | A | upstream_gene_variant | MODIFIER | c.-441C>T| |
S201 |
7 | BAA01g39700 | A01 | 26361955 | G | A | upstream_gene_variant | MODIFIER | c.-2224C>T| |
S189 |