Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64120 | A09 | 59646160 | C | T | missense_variant | MODERATE | c.1504G>A|p.Glu502Lys |
S52 |
2 | BAA09g64120 | A09 | 59648558 | G | A | synonymous_variant | LOW | c.753C>T|p.Pro251Pro |
S216 S241 S39 |
3 | BAA09g64120 | A09 | 59648774 | C | T | missense_variant | MODERATE | c.625G>A|p.Asp209Asn |
S204 |
4 | BAA09g64120 | A09 | 59649443 | C | T | synonymous_variant | LOW | c.387G>A|p.Glu129Glu |
S303 |
5 | BAA09g64120 | A09 | 59651183 | G | A | upstream_gene_variant | MODIFIER | c.-1354C>T| |
S10 |
6 | BAA09g64120 | A09 | 59651306 | C | T | upstream_gene_variant | MODIFIER | c.-1477G>A| |
S292 |
7 | BAA09g64120 | A09 | 59651735 | C | T | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S28 |
8 | BAA09g64120 | A09 | 59652548 | C | T | upstream_gene_variant | MODIFIER | c.-2719G>A| |
S152 |
9 | BAA09g64120 | A09 | 59652761 | C | T | upstream_gene_variant | MODIFIER | c.-2932G>A| |
S171 |