Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42990 | A05 | 40522783 | G | T | missense_variant | MODERATE | c.766C>A|p.Pro256Thr |
S94 |
2 | BAA05g42990 | A05 | 40522801 | G | A | splice_region_variant&intron_variant | LOW | c.754-6C>T| |
S87 |
3 | BAA05g42990 | A05 | 40527156 | C | T | upstream_gene_variant | MODIFIER | c.-3185G>A| |
S136 |
4 | BAA05g42990 | A05 | 40528411 | C | T | upstream_gene_variant | MODIFIER | c.-4440G>A| |
S247 |