Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38230 | A06 | 25075287 | C | T | missense_variant | MODERATE | c.1912G>A|p.Glu638Lys |
S45 |
2 | BAA06g38230 | A06 | 25075659 | G | A | missense_variant | MODERATE | c.1540C>T|p.His514Tyr |
S126 |
3 | BAA06g38230 | A06 | 25075741 | C | T | synonymous_variant | LOW | c.1458G>A|p.Arg486Arg |
S87 |
4 | BAA06g38230 | A06 | 25075921 | C | T | synonymous_variant | LOW | c.1278G>A|p.Glu426Glu |
S46 |
5 | BAA06g38230 | A06 | 25076172 | C | T | missense_variant | MODERATE | c.1027G>A|p.Glu343Lys |
S278 |
6 | BAA06g38230 | A06 | 25076660 | G | A | missense_variant | MODERATE | c.539C>T|p.Ser180Phe |
S183 S198 |
7 | BAA06g38230 | A06 | 25076985 | G | A | missense_variant | MODERATE | c.214C>T|p.Leu72Phe |
S228 |
8 | BAA06g38230 | A06 | 25079661 | G | A | upstream_gene_variant | MODIFIER | c.-2463C>T| |
S71 |