Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42750 | A02 | 35584889 | G | A | upstream_gene_variant | MODIFIER | c.-4940G>A| |
S37 |
2 | BAA02g42750 | A02 | 35585428 | G | A | upstream_gene_variant | MODIFIER | c.-4401G>A| |
S8 |
3 | BAA02g42750 | A02 | 35585619 | C | T | upstream_gene_variant | MODIFIER | c.-4210C>T| |
S17 |
4 | BAA02g42750 | A02 | 35586089 | C | T | upstream_gene_variant | MODIFIER | c.-3740C>T| |
S266 |
5 | BAA02g42750 | A02 | 35589849 | C | T | synonymous_variant | LOW | c.21C>T|p.Phe7Phe |
S171 |
6 | BAA02g42750 | A02 | 35590884 | G | A | missense_variant | MODERATE | c.523G>A|p.Asp175Asn |
S148 S30 S31 |
7 | BAA02g42750 | A02 | 35590983 | G | A | missense_variant | MODERATE | c.622G>A|p.Asp208Asn |
S164 |
8 | BAA02g42750 | A02 | 35591447 | G | A | missense_variant | MODERATE | c.949G>A|p.Asp317Asn |
S166 S167 S262 |
9 | BAA02g42750 | A02 | 35591710 | A | T | synonymous_variant | LOW | c.1128A>T|p.Arg376Arg |
S237 |
10 | BAA02g42750 | A02 | 35595899 | C | T | downstream_gene_variant | MODIFIER | c.*3869C>T| |
S266 |
11 | BAA02g42750 | A02 | 35596411 | C | T | downstream_gene_variant | MODIFIER | c.*4381C>T| |
S18 |