Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15850 | A01 | 7701733 | C | T | upstream_gene_variant | MODIFIER | c.-2876C>T| |
S278 |
2 | BAA01g15850 | A01 | 7704313 | C | T | upstream_gene_variant | MODIFIER | c.-296C>T| |
S210 |
3 | BAA01g15850 | A01 | 7705042 | C | T | missense_variant | MODERATE | c.434C>T|p.Ser145Leu |
S138 |
4 | BAA01g15850 | A01 | 7706753 | G | A | missense_variant | MODERATE | c.1273G>A|p.Gly425Arg |
S289 S290 |
5 | BAA01g15850 | A01 | 7706978 | C | T | synonymous_variant | LOW | c.1498C>T|p.Leu500Leu |
S144 |
6 | BAA01g15850 | A01 | 7707155 | G | A | missense_variant | MODERATE | c.1675G>A|p.Asp559Asn |
S105 S106 |
7 | BAA01g15850 | A01 | 7707422 | C | T | missense_variant | MODERATE | c.1942C>T|p.Leu648Phe |
S153 |