Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16860 | A10 | 16485974 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S167 |
2 | BAA10g16860 | A10 | 16486165 | C | T | splice_donor_variant&intron_variant | HIGH | c.123+1G>A| |
S281 |
3 | BAA10g16860 | A10 | 16486267 | C | T | missense_variant | MODERATE | c.22G>A|p.Asp8Asn |
S144 |
4 | BAA10g16860 | A10 | 16491039 | G | A | upstream_gene_variant | MODIFIER | c.-4751C>T| |
S34 |