Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38290 | A02 | 32626428 | C | T | splice_region_variant&intron_variant | LOW | c.505-7G>A| |
S183 S198 |
2 | BAA02g38290 | A02 | 32626555 | C | T | missense_variant | MODERATE | c.482G>A|p.Gly161Glu |
S263 |
3 | BAA02g38290 | A02 | 32627111 | G | A | missense_variant | MODERATE | c.146C>T|p.Ser49Phe |
S158 |
4 | BAA02g38290 | A02 | 32630117 | G | A | upstream_gene_variant | MODIFIER | c.-1320C>T| |
S166 |
5 | BAA02g38290 | A02 | 32631496 | C | T | upstream_gene_variant | MODIFIER | c.-2699G>A| |
S2 |
6 | BAA02g38290 | A02 | 32632657 | C | T | upstream_gene_variant | MODIFIER | c.-3860G>A| |
S185 S202 |
7 | BAA02g38290 | A02 | 32632682 | C | T | upstream_gene_variant | MODIFIER | c.-3885G>A| |
S16 |