Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13960 | A09 | 8035241 | G | A | missense_variant | MODERATE | c.835C>T|p.Leu279Phe |
S95 |
2 | BAA09g13960 | A09 | 8036155 | C | T | splice_region_variant&intron_variant | LOW | c.499+5G>A| |
S200 S261 S274 |
3 | BAA09g13960 | A09 | 8036229 | G | A | missense_variant | MODERATE | c.430C>T|p.Pro144Ser |
S79 S84 |
4 | BAA09g13960 | A09 | 8036496 | G | A | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S281 |
5 | BAA09g13960 | A09 | 8038886 | G | T | upstream_gene_variant | MODIFIER | c.-2228C>A| |
S166 |
6 | BAA09g13960 | A09 | 8040437 | G | A | upstream_gene_variant | MODIFIER | c.-3779C>T| |
S60 |