Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09000 | A09 | 5017165 | C | T | missense_variant | MODERATE | c.190C>T|p.Pro64Ser |
S256 |
2 | BAA09g09000 | A09 | 5017705 | G | A | synonymous_variant | LOW | c.561G>A|p.Pro187Pro |
S15 S3 |
3 | BAA09g09000 | A09 | 5018343 | C | T | synonymous_variant | LOW | c.1002C>T|p.Tyr334Tyr |
S18 |
4 | BAA09g09000 | A09 | 5018346 | G | A | synonymous_variant | LOW | c.1005G>A|p.Leu335Leu |
S152 |
5 | BAA09g09000 | A09 | 5020420 | G | A | splice_region_variant&synonymous_variant | LOW | c.2124G>A|p.Gly708Gly |
S176 |
6 | BAA09g09000 | A09 | 5021869 | G | A | missense_variant | MODERATE | c.3233G>A|p.Cys1078Tyr |
S234 |
7 | BAA09g09000 | A09 | 5022817 | C | T | downstream_gene_variant | MODIFIER | c.*929C>T| |
S136 |
8 | BAA09g09000 | A09 | 5022885 | G | A | downstream_gene_variant | MODIFIER | c.*997G>A| |
S221 |
9 | BAA09g09000 | A09 | 5023071 | G | A | downstream_gene_variant | MODIFIER | c.*1183G>A| |
S164 |