Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53950 | A09 | 54888170 | C | T | missense_variant | MODERATE | c.1630G>A|p.Val544Met |
S18 |
2 | BAA09g53950 | A09 | 54889236 | C | T | missense_variant | MODERATE | c.698G>A|p.Gly233Glu |
S208 S219 |
3 | BAA09g53950 | A09 | 54889379 | C | T | synonymous_variant | LOW | c.555G>A|p.Lys185Lys |
S259 |
4 | BAA09g53950 | A09 | 54889811 | C | T | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S302 |
5 | BAA09g53950 | A09 | 54889914 | C | T | synonymous_variant | LOW | c.102G>A|p.Pro34Pro |
S230 |
6 | BAA09g53950 | A09 | 54889935 | T | C | synonymous_variant | LOW | c.81A>G|p.Arg27Arg |
S94 |
7 | BAA09g53950 | A09 | 54889942 | T | A | missense_variant | MODERATE | c.74A>T|p.Glu25Val |
S156 S213 S34 S4 S6 |
8 | BAA09g53950 | A09 | 54889979 | C | T | missense_variant | MODERATE | c.37G>A|p.Gly13Arg |
S50 |
9 | BAA09g53950 | A09 | 54890265 | C | T | upstream_gene_variant | MODIFIER | c.-250G>A| |
S208 S219 |
10 | BAA09g53950 | A09 | 54891247 | G | A | upstream_gene_variant | MODIFIER | c.-1232C>T| |
S204 |
11 | BAA09g53950 | A09 | 54893810 | C | T | upstream_gene_variant | MODIFIER | c.-3795G>A| |
S163 |
12 | BAA09g53950 | A09 | 54894294 | G | A | upstream_gene_variant | MODIFIER | c.-4279C>T| |
S249 |