Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07600 | A02 | 3266765 | G | A | missense_variant | MODERATE | c.153G>A|p.Met51Ile |
S148 S210 S30 S31 |
2 | BAA02g07600 | A02 | 3268216 | C | T | missense_variant | MODERATE | c.737C>T|p.Ser246Phe |
S251 |
3 | BAA02g07600 | A02 | 3268455 | G | A | missense_variant | MODERATE | c.895G>A|p.Gly299Arg |
S266 |
4 | BAA02g07600 | A02 | 3268741 | C | T | stop_gained | HIGH | c.1024C>T|p.Gln342* |
S263 |
5 | BAA02g07600 | A02 | 3270164 | C | T | missense_variant | MODERATE | c.1817C>T|p.Ser606Phe |
S97 |
6 | BAA02g07600 | A02 | 3273804 | C | T | downstream_gene_variant | MODIFIER | c.*3612C>T| |
S196 |
7 | BAA02g07600 | A02 | 3274885 | C | T | downstream_gene_variant | MODIFIER | c.*4693C>T| |
S8 |
8 | BAA02g07600 | A02 | 3275162 | G | A | downstream_gene_variant | MODIFIER | c.*4970G>A| |
S176 |