Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19800 | A09 | 12194579 | G | A | missense_variant | MODERATE | c.14G>A|p.Arg5Gln |
S165 |
2 | BAA09g19800 | A09 | 12194627 | C | T | missense_variant | MODERATE | c.62C>T|p.Pro21Leu |
S293 |
3 | BAA09g19800 | A09 | 12194782 | C | T | missense_variant | MODERATE | c.128C>T|p.Ala43Val |
S296 |
4 | BAA09g19800 | A09 | 12198427 | G | A | missense_variant&splice_region_variant | MODERATE | c.665G>A|p.Arg222Gln |
S47 |
5 | BAA09g19800 | A09 | 12198588 | G | A | missense_variant | MODERATE | c.826G>A|p.Ala276Thr |
S298 |
6 | BAA09g19800 | A09 | 12200482 | A | T | downstream_gene_variant | MODIFIER | c.*1865A>T| |
S205 |