Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00980 | A08 | 723960 | C | T | upstream_gene_variant | MODIFIER | c.-3155C>T| |
S142 |
2 | BAA08g00980 | A08 | 724888 | C | T | upstream_gene_variant | MODIFIER | c.-2227C>T| |
S267 |
3 | BAA08g00980 | A08 | 727499 | C | T | missense_variant | MODERATE | c.385C>T|p.Pro129Ser |
S28 |
4 | BAA08g00980 | A08 | 727501 | G | A | synonymous_variant | LOW | c.387G>A|p.Pro129Pro |
S58 |