Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04730 | A02 | 2049603 | C | T | missense_variant | MODERATE | c.1015G>A|p.Asp339Asn |
S255 |
2 | BAA02g04730 | A02 | 2049866 | G | A | missense_variant | MODERATE | c.752C>T|p.Thr251Ile |
S192 |
3 | BAA02g04730 | A02 | 2051377 | C | T | missense_variant | MODERATE | c.364G>A|p.Glu122Lys |
S103 |
4 | BAA02g04730 | A02 | 2051470 | C | T | missense_variant | MODERATE | c.271G>A|p.Gly91Arg |
S243 S299 |
5 | BAA02g04730 | A02 | 2052548 | G | A | upstream_gene_variant | MODIFIER | c.-808C>T| |
S273 |
6 | BAA02g04730 | A02 | 2052641 | G | A | upstream_gene_variant | MODIFIER | c.-901C>T| |
S76 |
7 | BAA02g04730 | A02 | 2053686 | C | T | upstream_gene_variant | MODIFIER | c.-1946G>A| |
S288 |
8 | BAA02g04730 | A02 | 2055776 | G | A | upstream_gene_variant | MODIFIER | c.-4036C>T| |
S259 |
9 | BAA02g04730 | A02 | 2055912 | G | A | upstream_gene_variant | MODIFIER | c.-4172C>T| |
S43 |