Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g20240 A02 10670544 G A upstream_gene_variant MODIFIER c.-4925G>A| S28
2 BAA02g20240 A02 10671574 C T upstream_gene_variant MODIFIER c.-3895C>T| S163
3 BAA02g20240 A02 10671726 C T upstream_gene_variant MODIFIER c.-3743C>T| S183
S198
4 BAA02g20240 A02 10672827 G A upstream_gene_variant MODIFIER c.-2642G>A| S274
5 BAA02g20240 A02 10673253 G A upstream_gene_variant MODIFIER c.-2216G>A| S67
6 BAA02g20240 A02 10673627 G A upstream_gene_variant MODIFIER c.-1842G>A| S284
7 BAA02g20240 A02 10673773 G A upstream_gene_variant MODIFIER c.-1696G>A| S40
S49
8 BAA02g20240 A02 10673855 C T upstream_gene_variant MODIFIER c.-1614C>T| S160
9 BAA02g20240 A02 10674544 C T upstream_gene_variant MODIFIER c.-925C>T| S25
10 BAA02g20240 A02 10675688 G A missense_variant MODERATE c.220G>A|p.Val74Ile S37
11 BAA02g20240 A02 10675716 G A missense_variant MODERATE c.248G>A|p.Ser83Asn S4
12 BAA02g20240 A02 10675773 C T missense_variant MODERATE c.305C>T|p.Ser102Phe S134
13 BAA02g20240 A02 10676321 C T missense_variant MODERATE c.775C>T|p.Pro259Ser S164
14 BAA02g20240 A02 10676974 C T stop_gained HIGH c.1165C>T|p.Gln389* S65
15 BAA02g20240 A02 10678518 G A downstream_gene_variant MODIFIER c.*1110G>A| S144
16 BAA02g20240 A02 10679112 G A downstream_gene_variant MODIFIER c.*1704G>A| S150