Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02190 | A10 | 1049990 | G | A | stop_gained | HIGH | c.970C>T|p.Gln324* |
S295 |
2 | BAA10g02190 | A10 | 1050636 | G | A | missense_variant | MODERATE | c.622C>T|p.Pro208Ser |
S257 |
3 | BAA10g02190 | A10 | 1050846 | C | T | missense_variant | MODERATE | c.493G>A|p.Asp165Asn |
S182 |
4 | BAA10g02190 | A10 | 1050905 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S257 |
5 | BAA10g02190 | A10 | 1051058 | C | T | missense_variant | MODERATE | c.281G>A|p.Arg94Lys |
S143 S68 |
6 | BAA10g02190 | A10 | 1051433 | C | T | upstream_gene_variant | MODIFIER | c.-95G>A| |
S56 |
7 | BAA10g02190 | A10 | 1056133 | C | T | upstream_gene_variant | MODIFIER | c.-4795G>A| |
S142 |