Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14500 | A02 | 6780744 | C | T | splice_region_variant&intron_variant | LOW | c.1320+5G>A| |
S79 S84 |
2 | BAA02g14500 | A02 | 6782147 | G | A | missense_variant | MODERATE | c.409C>T|p.Pro137Ser |
S166 |
3 | BAA02g14500 | A02 | 6782507 | G | A | stop_gained | HIGH | c.214C>T|p.Arg72* |
S265 |
4 | BAA02g14500 | A02 | 6782518 | C | T | missense_variant | MODERATE | c.203G>A|p.Gly68Glu |
S230 S85 |
5 | BAA02g14500 | A02 | 6784563 | C | T | upstream_gene_variant | MODIFIER | c.-1843G>A| |
S212 |
6 | BAA02g14500 | A02 | 6787652 | C | T | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S40 S49 |
7 | BAA02g14500 | A02 | 6787673 | G | A | upstream_gene_variant | MODIFIER | c.-4953C>T| |
S59 |