Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44900 | A01 | 29902333 | C | T | intron_variant | MODIFIER | c.182+1719C>T| |
S234 |
2 | BAA01g44900 | A01 | 29904793 | C | T | missense_variant | MODERATE | c.233C>T|p.Ser78Phe |
S232 |
3 | BAA01g44900 | A01 | 29904807 | G | A | missense_variant | MODERATE | c.247G>A|p.Gly83Arg |
S61 |
4 | BAA01g44900 | A01 | 29905351 | C | T | missense_variant | MODERATE | c.593C>T|p.Ser198Phe |
S69 |
5 | BAA01g44900 | A01 | 29909490 | C | T | downstream_gene_variant | MODIFIER | c.*3435C>T| |
S171 |
6 | BAA01g44900 | A01 | 29910130 | G | A | downstream_gene_variant | MODIFIER | c.*4075G>A| |
S247 |