Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01070 | A10 | 529377 | C | T | missense_variant | MODERATE | c.479G>A|p.Gly160Asp |
S116 |
2 | BAA10g01070 | A10 | 529766 | G | A | missense_variant | MODERATE | c.179C>T|p.Pro60Leu |
S38 |
3 | BAA10g01070 | A10 | 529802 | C | T | missense_variant | MODERATE | c.143G>A|p.Arg48Lys |
S162 |
4 | BAA10g01070 | A10 | 529979 | C | T | missense_variant | MODERATE | c.37G>A|p.Ala13Thr |
S282 |
5 | BAA10g01070 | A10 | 530144 | C | T | upstream_gene_variant | MODIFIER | c.-129G>A| |
S84 S93 |