Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44660 | A03 | 21257680 | G | A | missense_variant | MODERATE | c.2498C>T|p.Pro833Leu |
S67 |
2 | BAA03g44660 | A03 | 21258169 | G | A | missense_variant | MODERATE | c.2009C>T|p.Pro670Leu |
S297 |
3 | BAA03g44660 | A03 | 21258536 | G | A | missense_variant | MODERATE | c.1642C>T|p.Pro548Ser |
S7 |
4 | BAA03g44660 | A03 | 21259060 | C | T | missense_variant | MODERATE | c.1118G>A|p.Arg373Lys |
S18 |
5 | BAA03g44660 | A03 | 21259949 | C | T | missense_variant | MODERATE | c.229G>A|p.Ala77Thr |
S223 |
6 | BAA03g44660 | A03 | 21262541 | G | A | upstream_gene_variant | MODIFIER | c.-2364C>T| |
S247 |
7 | BAA03g44660 | A03 | 21263291 | C | T | upstream_gene_variant | MODIFIER | c.-3114G>A| |
S119 S230 |
8 | BAA03g44660 | A03 | 21263866 | G | A | upstream_gene_variant | MODIFIER | c.-3689C>T| |
S303 |
9 | BAA03g44660 | A03 | 21264686 | C | T | upstream_gene_variant | MODIFIER | c.-4509G>A| |
S223 |