Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29190 | A08 | 20116464 | C | T | missense_variant | MODERATE | c.440G>A|p.Gly147Asp |
S53 |
2 | BAA08g29190 | A08 | 20116604 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.301-1G>A| |
S169 |
3 | BAA08g29190 | A08 | 20117584 | G | A | upstream_gene_variant | MODIFIER | c.-156C>T| |
S77 S82 |
4 | BAA08g29190 | A08 | 20118037 | G | A | upstream_gene_variant | MODIFIER | c.-609C>T| |
S217 S248 |
5 | BAA08g29190 | A08 | 20121271 | G | A | upstream_gene_variant | MODIFIER | c.-3843C>T| |
S282 |