Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13170 | A10 | 14401447 | C | T | missense_variant | MODERATE | c.772G>A|p.Gly258Arg |
S229 |
2 | BAA10g13170 | A10 | 14402177 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S264 |
3 | BAA10g13170 | A10 | 14403365 | C | T | upstream_gene_variant | MODIFIER | c.-1073G>A| |
S191 |
4 | BAA10g13170 | A10 | 14403441 | G | A | upstream_gene_variant | MODIFIER | c.-1149C>T| |
S262 |