Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08570 | A09 | 4797643 | C | T | missense_variant | MODERATE | c.664G>A|p.Asp222Asn |
S2 |
2 | BAA09g08570 | A09 | 4799017 | G | A | upstream_gene_variant | MODIFIER | c.-128C>T| |
S86 |
3 | BAA09g08570 | A09 | 4799456 | C | T | upstream_gene_variant | MODIFIER | c.-567G>A| |
S156 |
4 | BAA09g08570 | A09 | 4800297 | G | A | upstream_gene_variant | MODIFIER | c.-1408C>T| |
S46 |
5 | BAA09g08570 | A09 | 4800334 | G | A | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S32 |
6 | BAA09g08570 | A09 | 4800720 | G | A | upstream_gene_variant | MODIFIER | c.-1831C>T| |
S36 |
7 | BAA09g08570 | A09 | 4803530 | C | T | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S133 |