Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30990 | A08 | 20761441 | C | T | missense_variant | MODERATE | c.1168G>A|p.Val390Ile |
S215 |
2 | BAA08g30990 | A08 | 20762550 | C | T | missense_variant | MODERATE | c.763G>A|p.Val255Met |
S198 |
3 | BAA08g30990 | A08 | 20762877 | G | A | missense_variant | MODERATE | c.436C>T|p.Leu146Phe |
S242 |
4 | BAA08g30990 | A08 | 20763194 | G | A | missense_variant | MODERATE | c.119C>T|p.Ser40Phe |
S233 |
5 | BAA08g30990 | A08 | 20766826 | C | T | upstream_gene_variant | MODIFIER | c.-3402G>A| |
S262 |
6 | BAA08g30990 | A08 | 20766865 | G | A | upstream_gene_variant | MODIFIER | c.-3441C>T| |
S273 |
7 | BAA08g30990 | A08 | 20768226 | G | A | upstream_gene_variant | MODIFIER | c.-4802C>T| |
S55 |