Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44620 | A09 | 50195256 | C | T | splice_region_variant&synonymous_variant | LOW | c.924G>A|p.Arg308Arg |
S10 |
2 | BAA09g44620 | A09 | 50195589 | C | T | synonymous_variant | LOW | c.807G>A|p.Glu269Glu |
S259 |
3 | BAA09g44620 | A09 | 50196017 | G | A | synonymous_variant | LOW | c.627C>T|p.Ser209Ser |
S210 |
4 | BAA09g44620 | A09 | 50196060 | C | T | missense_variant | MODERATE | c.584G>A|p.Gly195Glu |
S69 |
5 | BAA09g44620 | A09 | 50196384 | C | T | missense_variant | MODERATE | c.457G>A|p.Glu153Lys |
S295 |
6 | BAA09g44620 | A09 | 50199941 | C | T | upstream_gene_variant | MODIFIER | c.-2455G>A| |
S18 |
7 | BAA09g44620 | A09 | 50200245 | G | A | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S95 |
8 | BAA09g44620 | A09 | 50201332 | G | A | upstream_gene_variant | MODIFIER | c.-3846C>T| |
S151 S263 |
9 | BAA09g44620 | A09 | 50201509 | C | T | upstream_gene_variant | MODIFIER | c.-4023G>A| |
S30 S31 |
10 | BAA09g44620 | A09 | 50201793 | G | A | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S187 |
11 | BAA09g44620 | A09 | 50202196 | C | T | upstream_gene_variant | MODIFIER | c.-4710G>A| |
S302 |