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
174051 BAA02g17050 A02 8482715 C T upstream_gene_variant MODIFIER c.-4760C>T| S163
174052 BAA02g17050 A02 8482915 C T upstream_gene_variant MODIFIER c.-4560C>T| S264
174053 BAA02g17050 A02 8484053 G A upstream_gene_variant MODIFIER c.-3422G>A| S238
174054 BAA02g17050 A02 8485813 A G upstream_gene_variant MODIFIER c.-1662A>G| S206
174055 BAA02g17050 A02 8485914 C T upstream_gene_variant MODIFIER c.-1561C>T| S77
S82
174056 BAA02g17050 A02 8486063 G A upstream_gene_variant MODIFIER c.-1412G>A| S247
174057 BAA02g17050 A02 8486201 G A upstream_gene_variant MODIFIER c.-1274G>A| S35
174058 BAA02g17050 A02 8486382 G A upstream_gene_variant MODIFIER c.-1093G>A| S148
S30
S31
174059 BAA02g17050 A02 8486983 G A upstream_gene_variant MODIFIER c.-492G>A| S155
S211
174060 BAA02g17050 A02 8488381 G A missense_variant MODERATE c.655G>A|p.Gly219Ser S251
S66
174061 BAA02g17050 A02 8489285 C T synonymous_variant LOW c.1284C>T|p.Thr428Thr S70
174062 BAA02g17050 A02 8489522 G A intron_variant MODIFIER c.1429-57G>A| S174
S27
174063 BAA02g17050 A02 8489684 G A missense_variant MODERATE c.1534G>A|p.Asp512Asn S60
174064 BAA02g17050 A02 8491485 C A downstream_gene_variant MODIFIER c.*870C>A| S194
174065 BAA02g17060 A02 8492794 C T upstream_gene_variant MODIFIER c.-3846C>T| S179
174066 BAA02g17060 A02 8495092 G A upstream_gene_variant MODIFIER c.-1548G>A| S225
174067 BAA02g17060 A02 8496766 G A missense_variant MODERATE c.127G>A|p.Glu43Lys S170
174068 BAA02g17070 A02 8497111 C T downstream_gene_variant MODIFIER c.*1828G>A| S273
174069 BAA02g17060 A02 8497543 C T missense_variant MODERATE c.613C>T|p.Pro205Ser S264
174070 BAA02g17060 A02 8497938 G A downstream_gene_variant MODIFIER c.*222G>A| S35
174071 BAA02g17060 A02 8499361 G A downstream_gene_variant MODIFIER c.*1645G>A| S235
174072 BAA02g17070 A02 8499425 C T stop_gained HIGH c.1659G>A|p.Trp553* S1
S90
174073 BAA02g17070 A02 8502827 C T missense_variant MODERATE c.284G>A|p.Gly95Glu S164
174074 BAA02g17070 A02 8502834 C T missense_variant MODERATE c.277G>A|p.Asp93Asn S76
174075 BAA02g17070 A02 8502850 G A synonymous_variant LOW c.261C>T|p.Phe87Phe S228