Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26120 | A04 | 26896590 | C | T | upstream_gene_variant | MODIFIER | c.-4836C>T| |
S306 S308 |
2 | BAA04g26120 | A04 | 26898363 | G | A | upstream_gene_variant | MODIFIER | c.-3063G>A| |
S202 |
3 | BAA04g26120 | A04 | 26898643 | C | T | upstream_gene_variant | MODIFIER | c.-2783C>T| |
S2 S4 S6 |
4 | BAA04g26120 | A04 | 26900265 | G | A | upstream_gene_variant | MODIFIER | c.-1161G>A| |
S19 |
5 | BAA04g26120 | A04 | 26901634 | C | T | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S2 S4 S6 |
6 | BAA04g26120 | A04 | 26901964 | C | T | missense_variant | MODERATE | c.539C>T|p.Ala180Val |
S165 |
7 | BAA04g26120 | A04 | 26902094 | G | A | synonymous_variant | LOW | c.669G>A|p.Glu223Glu |
S235 |
8 | BAA04g26120 | A04 | 26902297 | C | T | missense_variant | MODERATE | c.872C>T|p.Ser291Phe |
S1 |
9 | BAA04g26120 | A04 | 26902335 | G | A | missense_variant | MODERATE | c.910G>A|p.Gly304Ser |
S218 |