Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59260 | A09 | 57494681 | C | T | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S261 |
2 | BAA09g59260 | A09 | 57495148 | G | A | synonymous_variant | LOW | c.1017C>T|p.Phe339Phe |
S79 S91 |
3 | BAA09g59260 | A09 | 57495913 | G | A | missense_variant | MODERATE | c.622C>T|p.Arg208Cys |
S148 S210 S30 S31 |
4 | BAA09g59260 | A09 | 57496398 | C | T | synonymous_variant | LOW | c.300G>A|p.Lys100Lys |
S7 |
5 | BAA09g59260 | A09 | 57497407 | A | T | upstream_gene_variant | MODIFIER | c.-710T>A| |
S125 |
6 | BAA09g59260 | A09 | 57497972 | C | T | upstream_gene_variant | MODIFIER | c.-1275G>A| |
S176 |
7 | BAA09g59260 | A09 | 57500090 | C | T | upstream_gene_variant | MODIFIER | c.-3393G>A| |
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