Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g56970 | A09 | 56383728 | C | T | synonymous_variant | LOW | c.1443G>A|p.Lys481Lys |
S206 |
2 | BAA09g56970 | A09 | 56384269 | G | A | missense_variant | MODERATE | c.902C>T|p.Pro301Leu |
S79 S84 |
3 | BAA09g56970 | A09 | 56384354 | G | A | missense_variant | MODERATE | c.817C>T|p.Leu273Phe |
S167 |
4 | BAA09g56970 | A09 | 56385084 | G | A | splice_region_variant&intron_variant | LOW | c.175-4C>T| |
S255 |
5 | BAA09g56970 | A09 | 56386250 | G | A | upstream_gene_variant | MODIFIER | c.-246C>T| |
S58 |
6 | BAA09g56970 | A09 | 56386657 | G | A | upstream_gene_variant | MODIFIER | c.-653C>T| |
S241 |