Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08760 | A09 | 4898293 | G | A | missense_variant | MODERATE | c.788C>T|p.Ser263Phe |
S30 S31 |
2 | BAA09g08760 | A09 | 4898842 | G | A | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S74 |
3 | BAA09g08760 | A09 | 4898876 | C | T | missense_variant | MODERATE | c.205G>A|p.Ala69Thr |
S206 S26 |
4 | BAA09g08760 | A09 | 4899056 | G | A | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S165 |
5 | BAA09g08760 | A09 | 4899394 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S255 |
6 | BAA09g08760 | A09 | 4900025 | C | T | upstream_gene_variant | MODIFIER | c.-945G>A| |
S204 |
7 | BAA09g08760 | A09 | 4900245 | G | A | upstream_gene_variant | MODIFIER | c.-1165C>T| |
S240 |
8 | BAA09g08760 | A09 | 4902233 | C | T | upstream_gene_variant | MODIFIER | c.-3153G>A| |
S282 |
9 | BAA09g08760 | A09 | 4903912 | G | A | upstream_gene_variant | MODIFIER | c.-4832C>T| |
S30 S31 |
10 | BAA09g08760 | A09 | 4904022 | G | A | upstream_gene_variant | MODIFIER | c.-4942C>T| |
S163 |