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
179001 BAA02g19680 A02 10241934 C T downstream_gene_variant MODIFIER c.*1751C>T| S262
179002 BAA02g19680 A02 10243533 C T downstream_gene_variant MODIFIER c.*3350C>T| S2
179003 BAA02g19680 A02 10244038 G A downstream_gene_variant MODIFIER c.*3855G>A| S177
179004 BAA02g19680 A02 10244712 G A downstream_gene_variant MODIFIER c.*4529G>A| S150
179005 BAA02g19680 A02 10245112 C T downstream_gene_variant MODIFIER c.*4929C>T| S6
179006 BAA02g19690 A02 10245721 C T intron_variant MODIFIER c.702+324G>A| S293
179007 BAA02g19690 A02 10248371 C T intron_variant MODIFIER c.386+1282G>A| S171
179008 BAA02g19690 A02 10249263 G A intron_variant MODIFIER c.386+390C>T| S35
179009 BAA02g19690 A02 10249668 G A missense_variant MODERATE c.371C>T|p.Pro124Leu S52
179010 BAA02g19690 A02 10250325 C T upstream_gene_variant MODIFIER c.-287G>A| S112
179011 BAA02g19690 A02 10252937 C T upstream_gene_variant MODIFIER c.-2899G>A| S284
179012 BAA02g19690-BAA02g19700 A02 10255620 G A intergenic_region MODIFIER n.10255620G>A| S62
179013 BAA02g19710 A02 10257778 G A upstream_gene_variant MODIFIER c.-4539G>A| S35
179014 BAA02g19710 A02 10258726 C T upstream_gene_variant MODIFIER c.-3591C>T| S270
179015 BAA02g19710 A02 10260145 C T upstream_gene_variant MODIFIER c.-2172C>T| S255
179016 BAA02g19700 A02 10260975 C T synonymous_variant LOW c.822G>A|p.Ala274Ala S80
179017 BAA02g19700 A02 10261308 G A synonymous_variant LOW c.489C>T|p.Val163Val S34
179018 BAA02g19700 A02 10261397 C T missense_variant MODERATE c.400G>A|p.Asp134Asn S46
179019 BAA02g19700 A02 10261451 G A missense_variant MODERATE c.346C>T|p.Pro116Ser S174
S27
179020 BAA02g19700 A02 10262893 C T upstream_gene_variant MODIFIER c.-1097G>A| S171
179021 BAA02g19700 A02 10262908 C T upstream_gene_variant MODIFIER c.-1112G>A| S279
179022 BAA02g19700 A02 10263354 C T upstream_gene_variant MODIFIER c.-1558G>A| S49
179023 BAA02g19700 A02 10264612 C T upstream_gene_variant MODIFIER c.-2816G>A| S119
179024 BAA02g19700 A02 10265401 G A upstream_gene_variant MODIFIER c.-3605C>T| S256
179025 BAA02g19720 A02 10265768 C G missense_variant MODERATE c.541G>C|p.Ala181Pro S278