Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11680 | A02 | 5278092 | C | T | missense_variant | MODERATE | c.2351G>A|p.Arg784Lys |
S177 S195 |
2 | BAA02g11680 | A02 | 5278107 | G | A | missense_variant | MODERATE | c.2336C>T|p.Ser779Phe |
S113 |
3 | BAA02g11680 | A02 | 5278682 | G | A | splice_region_variant&intron_variant | LOW | c.1948+4C>T| |
S170 |
4 | BAA02g11680 | A02 | 5278712 | A | T | missense_variant | MODERATE | c.1922T>A|p.Leu641Gln |
S120 |
5 | BAA02g11680 | A02 | 5280737 | G | A | synonymous_variant | LOW | c.855C>T|p.Ile285Ile |
S190 |
6 | BAA02g11680 | A02 | 5281030 | C | T | synonymous_variant | LOW | c.648G>A|p.Arg216Arg |
S182 |
7 | BAA02g11680 | A02 | 5281675 | C | T | missense_variant | MODERATE | c.149G>A|p.Arg50Lys |
S230 |
8 | BAA02g11680 | A02 | 5282592 | G | A | upstream_gene_variant | MODIFIER | c.-651C>T| |
S136 |
9 | BAA02g11680 | A02 | 5282793 | G | A | upstream_gene_variant | MODIFIER | c.-852C>T| |
S4 |