Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20280 | A01 | 9955284 | C | T | missense_variant | MODERATE | c.1070G>A|p.Gly357Glu |
S128 |
2 | BAA01g20280 | A01 | 9955524 | C | T | missense_variant | MODERATE | c.830G>A|p.Ser277Asn |
S233 |
3 | BAA01g20280 | A01 | 9955915 | C | A | missense_variant | MODERATE | c.439G>T|p.Val147Leu |
S195 |
4 | BAA01g20280 | A01 | 9956006 | G | A | synonymous_variant | LOW | c.348C>T|p.Leu116Leu |
S240 |
5 | BAA01g20280 | A01 | 9957672 | C | T | upstream_gene_variant | MODIFIER | c.-1319G>A| |
S11 |
6 | BAA01g20280 | A01 | 9957990 | C | T | upstream_gene_variant | MODIFIER | c.-1637G>A| |
S159 S243 |
7 | BAA01g20280 | A01 | 9959060 | C | T | upstream_gene_variant | MODIFIER | c.-2707G>A| |
S267 |