Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17130 | A02 | 8534628 | C | T | upstream_gene_variant | MODIFIER | c.-3181C>T| |
S160 |
2 | BAA02g17130 | A02 | 8534754 | C | T | upstream_gene_variant | MODIFIER | c.-3055C>T| |
S267 |
3 | BAA02g17130 | A02 | 8536158 | C | T | upstream_gene_variant | MODIFIER | c.-1651C>T| |
S283 |
4 | BAA02g17130 | A02 | 8536514 | C | T | upstream_gene_variant | MODIFIER | c.-1295C>T| |
S182 |
5 | BAA02g17130 | A02 | 8536554 | G | A | upstream_gene_variant | MODIFIER | c.-1255G>A| |
S122 |
6 | BAA02g17130 | A02 | 8536750 | G | A | upstream_gene_variant | MODIFIER | c.-1059G>A| |
S208 S93 |
7 | BAA02g17130 | A02 | 8537080 | G | A | upstream_gene_variant | MODIFIER | c.-729G>A| |
S308 |
8 | BAA02g17130 | A02 | 8538432 | G | A | missense_variant | MODERATE | c.467G>A|p.Gly156Glu |
S207 |
9 | BAA02g17130 | A02 | 8540454 | C | T | synonymous_variant | LOW | c.1815C>T|p.Leu605Leu |
S25 |
10 | BAA02g17130 | A02 | 8540460 | C | T | synonymous_variant | LOW | c.1821C>T|p.Asn607Asn |
S205 |
11 | BAA02g17130 | A02 | 8541098 | C | T | synonymous_variant | LOW | c.2364C>T|p.Phe788Phe |
S211 S227 |
12 | BAA02g17130 | A02 | 8541105 | G | A | missense_variant | MODERATE | c.2371G>A|p.Glu791Lys |
S161 |