Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30770 | A02 | 18124019 | G | A | upstream_gene_variant | MODIFIER | c.-1724G>A| |
S223 |
2 | BAA02g30770 | A02 | 18124345 | C | T | upstream_gene_variant | MODIFIER | c.-1398C>T| |
S42 |
3 | BAA02g30770 | A02 | 18126102 | G | A | missense_variant | MODERATE | c.292G>A|p.Asp98Asn |
S34 |
4 | BAA02g30770 | A02 | 18126560 | G | A | synonymous_variant | LOW | c.663G>A|p.Leu221Leu |
S132 S137 S215 S89 |
5 | BAA02g30770 | A02 | 18127020 | G | A | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S96 |
6 | BAA02g30770 | A02 | 18127146 | C | T | intron_variant | MODIFIER | c.1113+46C>T| |
S244 |
7 | BAA02g30770 | A02 | 18128274 | G | A | intron_variant | MODIFIER | c.1756-10G>A| |
S186 |
8 | BAA02g30770 | A02 | 18128714 | G | A | missense_variant | MODERATE | c.2095G>A|p.Ala699Thr |
S188 |
9 | BAA02g30770 | A02 | 18129232 | G | A | missense_variant | MODERATE | c.2396G>A|p.Ser799Asn |
S41 |
10 | BAA02g30770 | A02 | 18129430 | C | T | missense_variant | MODERATE | c.2492C>T|p.Ala831Val |
S181 |