Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20750 | A10 | 18517336 | C | T | missense_variant | MODERATE | c.1792G>A|p.Asp598Asn |
S2 |
2 | BAA10g20750 | A10 | 18517862 | G | A | missense_variant | MODERATE | c.1429C>T|p.Pro477Ser |
S165 |
3 | BAA10g20750 | A10 | 18519382 | C | T | synonymous_variant | LOW | c.471G>A|p.Leu157Leu |
S45 |
4 | BAA10g20750 | A10 | 18519706 | G | A | synonymous_variant | LOW | c.147C>T|p.Arg49Arg |
S216 |
5 | BAA10g20750 | A10 | 18522122 | G | A | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S167 |
6 | BAA10g20750 | A10 | 18523536 | G | A | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S278 |
7 | BAA10g20750 | A10 | 18524767 | T | C | upstream_gene_variant | MODIFIER | c.-4915A>G| |
S19 |