Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08630 | A01 | 3815332 | G | A | missense_variant | MODERATE | c.106G>A|p.Asp36Asn |
S146 |
2 | BAA01g08630 | A01 | 3815349 | G | A | synonymous_variant | LOW | c.123G>A|p.Lys41Lys |
S115 |
3 | BAA01g08630 | A01 | 3815865 | G | A | missense_variant | MODERATE | c.245G>A|p.Gly82Asp |
S124 |
4 | BAA01g08630 | A01 | 3816029 | G | A | missense_variant | MODERATE | c.409G>A|p.Asp137Asn |
S105 S106 |
5 | BAA01g08630 | A01 | 3816542 | G | A | missense_variant | MODERATE | c.761G>A|p.Gly254Glu |
S11 |
6 | BAA01g08630 | A01 | 3820123 | C | T | downstream_gene_variant | MODIFIER | c.*3082C>T| |
S182 |
7 | BAA01g08630 | A01 | 3821705 | G | A | downstream_gene_variant | MODIFIER | c.*4664G>A| |
S95 |
8 | BAA01g08630 | A01 | 3821756 | C | T | downstream_gene_variant | MODIFIER | c.*4715C>T| |
S278 |