Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17460 | A09 | 10427703 | C | T | missense_variant | MODERATE | c.2165G>A|p.Ser722Asn |
S157 |
2 | BAA09g17460 | A09 | 10428916 | C | T | missense_variant | MODERATE | c.1069G>A|p.Gly357Arg |
S10 |
3 | BAA09g17460 | A09 | 10429048 | G | A | synonymous_variant | LOW | c.937C>T|p.Leu313Leu |
S267 |
4 | BAA09g17460 | A09 | 10429439 | C | T | stop_gained | HIGH | c.546G>A|p.Trp182* |
S270 |
5 | BAA09g17460 | A09 | 10431524 | G | A | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S105 S106 |
6 | BAA09g17460 | A09 | 10432389 | C | T | upstream_gene_variant | MODIFIER | c.-2294G>A| |
S143 |
7 | BAA09g17460 | A09 | 10432745 | C | T | upstream_gene_variant | MODIFIER | c.-2650G>A| |
S62 |
8 | BAA09g17460 | A09 | 10432828 | G | A | upstream_gene_variant | MODIFIER | c.-2733C>T| |
S198 |