Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29990 | A10 | 22373938 | C | T | synonymous_variant | LOW | c.828G>A|p.Arg276Arg |
S206 S26 |
2 | BAA10g29990 | A10 | 22374138 | G | A | missense_variant | MODERATE | c.628C>T|p.Leu210Phe |
S125 |
3 | BAA10g29990 | A10 | 22378225 | C | T | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S277 |
4 | BAA10g29990 | A10 | 22378474 | C | T | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S42 |
5 | BAA10g29990 | A10 | 22379669 | C | T | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S186 S301 S304 |