Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43850 | A01 | 29035205 | G | A | missense_variant | MODERATE | c.440C>T|p.Thr147Met |
S259 |
2 | BAA01g43850 | A01 | 29035216 | C | T | synonymous_variant | LOW | c.429G>A|p.Ala143Ala |
S186 |
3 | BAA01g43850 | A01 | 29035284 | T | G | missense_variant | MODERATE | c.361A>C|p.Thr121Pro |
S128 S137 S252 S56 S59 S98 |
4 | BAA01g43850 | A01 | 29035328 | G | A | missense_variant | MODERATE | c.317C>T|p.Ala106Val |
S172 S217 |
5 | BAA01g43850 | A01 | 29037454 | G | A | upstream_gene_variant | MODIFIER | c.-1810C>T| |
S98 |
6 | BAA01g43850 | A01 | 29037899 | C | T | upstream_gene_variant | MODIFIER | c.-2255G>A| |
S165 |
7 | BAA01g43850 | A01 | 29038135 | C | T | upstream_gene_variant | MODIFIER | c.-2491G>A| |
S219 S72 |
8 | BAA01g43850 | A01 | 29038541 | C | T | upstream_gene_variant | MODIFIER | c.-2897G>A| |
S201 |
9 | BAA01g43850 | A01 | 29039909 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S293 |