Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14450 | A02 | 6749224 | G | A | upstream_gene_variant | MODIFIER | c.-4543G>A| |
S282 |
2 | BAA02g14450 | A02 | 6749262 | G | A | upstream_gene_variant | MODIFIER | c.-4505G>A| |
S288 |
3 | BAA02g14450 | A02 | 6749285 | C | T | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S167 |
4 | BAA02g14450 | A02 | 6750959 | G | A | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S251 |
5 | BAA02g14450 | A02 | 6752806 | C | T | upstream_gene_variant | MODIFIER | c.-961C>T| |
S131 |
6 | BAA02g14450 | A02 | 6753183 | G | A | upstream_gene_variant | MODIFIER | c.-584G>A| |
S187 |
7 | BAA02g14450 | A02 | 6753487 | C | T | upstream_gene_variant | MODIFIER | c.-280C>T| |
S206 S26 |
8 | BAA02g14450 | A02 | 6755982 | G | A | missense_variant | MODERATE | c.1486G>A|p.Asp496Asn |
S67 |
9 | BAA02g14450 | A02 | 6756098 | C | T | synonymous_variant | LOW | c.1602C>T|p.Ile534Ile |
S139 |