Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02990 | A02 | 1326894 | C | T | upstream_gene_variant | MODIFIER | c.-1693C>T| |
S109 S77 S82 |
2 | BAA02g02990 | A02 | 1329208 | C | T | splice_region_variant&intron_variant | LOW | c.317-3C>T| |
S42 |
3 | BAA02g02990 | A02 | 1329522 | G | A | missense_variant | MODERATE | c.547G>A|p.Gly183Arg |
S172 S217 |
4 | BAA02g02990 | A02 | 1329939 | G | A | missense_variant&splice_region_variant | MODERATE | c.805G>A|p.Glu269Lys |
S11 |
5 | BAA02g02990 | A02 | 1330463 | G | A | splice_region_variant&intron_variant | LOW | c.991-4G>A| |
S198 |
6 | BAA02g02990 | A02 | 1331286 | G | A | synonymous_variant | LOW | c.1476G>A|p.Lys492Lys |
S38 |