Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16220 | A08 | 13506012 | C | T | missense_variant | MODERATE | c.1289G>A|p.Gly430Asp |
S271 |
2 | BAA08g16220 | A08 | 13506230 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1072-1G>A| |
S59 |
3 | BAA08g16220 | A08 | 13506426 | G | A | missense_variant | MODERATE | c.956C>T|p.Ser319Phe |
S266 |
4 | BAA08g16220 | A08 | 13512699 | C | T | upstream_gene_variant | MODIFIER | c.-3671G>A| |
S18 |