Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43040 | A05 | 40536789 | G | A | synonymous_variant | LOW | c.939C>T|p.Phe313Phe |
S1 S90 |
2 | BAA05g43040 | A05 | 40537471 | C | T | missense_variant | MODERATE | c.257G>A|p.Cys86Tyr |
S302 |
3 | BAA05g43040 | A05 | 40537482 | C | T | synonymous_variant | LOW | c.246G>A|p.Arg82Arg |
S54 |
4 | BAA05g43040 | A05 | 40538367 | G | A | upstream_gene_variant | MODIFIER | c.-640C>T| |
S308 |
5 | BAA05g43040 | A05 | 40538956 | C | T | upstream_gene_variant | MODIFIER | c.-1229G>A| |
S126 |
6 | BAA05g43040 | A05 | 40539367 | C | T | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S33 |
7 | BAA05g43040 | A05 | 40539554 | C | T | upstream_gene_variant | MODIFIER | c.-1827G>A| |
S15 S3 |
8 | BAA05g43040 | A05 | 40542029 | G | A | upstream_gene_variant | MODIFIER | c.-4302C>T| |
S229 |
9 | BAA05g43040 | A05 | 40542112 | C | T | upstream_gene_variant | MODIFIER | c.-4385G>A| |
S162 |