Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20990 | A10 | 18632977 | C | T | missense_variant | MODERATE | c.419G>A|p.Ser140Asn |
S84 S93 |
2 | BAA10g20990 | A10 | 18635032 | C | T | upstream_gene_variant | MODIFIER | c.-1461G>A| |
S23 |
3 | BAA10g20990 | A10 | 18635097 | G | A | upstream_gene_variant | MODIFIER | c.-1526C>T| |
S105 S106 |
4 | BAA10g20990 | A10 | 18638220 | C | T | upstream_gene_variant | MODIFIER | c.-4649G>A| |
S132 S137 S215 |