Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05110 | A09 | 2977569 | C | T | upstream_gene_variant | MODIFIER | c.-4117C>T| |
S249 |
2 | BAA09g05110 | A09 | 2979024 | C | T | upstream_gene_variant | MODIFIER | c.-2662C>T| |
S169 |
3 | BAA09g05110 | A09 | 2979983 | C | T | upstream_gene_variant | MODIFIER | c.-1703C>T| |
S37 |
4 | BAA09g05110 | A09 | 2980604 | C | T | upstream_gene_variant | MODIFIER | c.-1082C>T| |
S95 |
5 | BAA09g05110 | A09 | 2982986 | C | T | missense_variant | MODERATE | c.688C>T|p.Pro230Ser |
S59 |
6 | BAA09g05110 | A09 | 2983461 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.883-1G>A| |
S252 |