Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10970 | A02 | 4932415 | C | T | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S172 S217 |
2 | BAA02g10970 | A02 | 4932734 | C | T | upstream_gene_variant | MODIFIER | c.-2327C>T| |
S305 |
3 | BAA02g10970 | A02 | 4932821 | C | T | upstream_gene_variant | MODIFIER | c.-2240C>T| |
S100 |
4 | BAA02g10970 | A02 | 4932934 | G | A | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S153 S213 |
5 | BAA02g10970 | A02 | 4933825 | G | A | upstream_gene_variant | MODIFIER | c.-1236G>A| |
S303 |
6 | BAA02g10970 | A02 | 4934339 | G | A | upstream_gene_variant | MODIFIER | c.-722G>A| |
S207 |
7 | BAA02g10970 | A02 | 4934400 | G | A | upstream_gene_variant | MODIFIER | c.-661G>A| |
S56 |
8 | BAA02g10970 | A02 | 4935236 | C | T | missense_variant | MODERATE | c.176C>T|p.Pro59Leu |
S267 |
9 | BAA02g10970 | A02 | 4935472 | G | A | missense_variant | MODERATE | c.412G>A|p.Glu138Lys |
S92 |
10 | BAA02g10970 | A02 | 4935604 | G | A | missense_variant | MODERATE | c.454G>A|p.Asp152Asn |
S282 |
11 | BAA02g10970 | A02 | 4936323 | G | A | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S283 |
12 | BAA02g10970 | A02 | 4943167 | G | A | downstream_gene_variant | MODIFIER | c.*4036G>A| |
S11 |