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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
197951 BAA02g29530 A02 16900468 C T upstream_gene_variant MODIFIER c.-1612C>T| S185
197952 BAA02g29530 A02 16900667 C T upstream_gene_variant MODIFIER c.-1413C>T| S269
197953 BAA02g29530 A02 16901989 G A upstream_gene_variant MODIFIER c.-91G>A| S272
197954 BAA02g29530 A02 16902157 G A synonymous_variant LOW c.78G>A|p.Ala26Ala S191
197955 BAA02g29530 A02 16903511 G A missense_variant MODERATE c.1364G>A|p.Gly455Asp S90
197956 BAA02g29540 A02 16904145 G A upstream_gene_variant MODIFIER c.-4611G>A| S202
197957 BAA02g29540 A02 16904783 C T upstream_gene_variant MODIFIER c.-3973C>T| S180
197958 BAA02g29540 A02 16906595 G A upstream_gene_variant MODIFIER c.-2161G>A| S19
197959 BAA02g29540 A02 16908988 C T synonymous_variant LOW c.126C>T|p.His42His S42
197960 BAA02g29540 A02 16909244 G A splice_acceptor_variant&intron_variant HIGH c.190-1G>A| S45
197961 BAA02g29550 A02 16910530 C T upstream_gene_variant MODIFIER c.-1508C>T| S163
197962 BAA02g29550 A02 16911223 C T upstream_gene_variant MODIFIER c.-815C>T| S104
S52
197963 BAA02g29550 A02 16911226 T C upstream_gene_variant MODIFIER c.-812T>C| S133
197964 BAA02g29550 A02 16912072 G A missense_variant MODERATE c.35G>A|p.Cys12Tyr S36
197965 BAA02g29540 A02 16912872 C T downstream_gene_variant MODIFIER c.*2762C>T| S198
197966 BAA02g29540 A02 16913584 G A downstream_gene_variant MODIFIER c.*3474G>A| S67
S95
197967 BAA02g29540 A02 16913714 C T downstream_gene_variant MODIFIER c.*3604C>T| S241
197968 BAA02g29540 A02 16914634 C T downstream_gene_variant MODIFIER c.*4524C>T| S299
197969 BAA02g29540 A02 16915042 C T downstream_gene_variant MODIFIER c.*4932C>T| S206
197970 BAA02g29550 A02 16915435 C T downstream_gene_variant MODIFIER c.*2845C>T| S66
197971 BAA02g29550 A02 16916130 C T downstream_gene_variant MODIFIER c.*3540C>T| S282
197972 BAA02g29560 A02 16917387 C T upstream_gene_variant MODIFIER c.-1002G>A| S109
197973 BAA02g29570 A02 16917550 G A missense_variant MODERATE c.536C>T|p.Ser179Phe S132
S137
S215
S89
197974 BAA02g29570 A02 16917899 G A missense_variant MODERATE c.260C>T|p.Ser87Phe S199
197975 BAA02g29560 A02 16919242 C T upstream_gene_variant MODIFIER c.-2857G>A| S183
S198