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
57751 BAA01g31150-BAA01g31160 A01 20198831 G A intergenic_region MODIFIER n.20198831G>A| S71
57752 BAA01g31150-BAA01g31160 A01 20200110 G A intergenic_region MODIFIER n.20200110G>A| S163
57753 BAA01g31150-BAA01g31160 A01 20201236 G A intergenic_region MODIFIER n.20201236G>A| S287
57754 BAA01g31150-BAA01g31160 A01 20201712 G A intergenic_region MODIFIER n.20201712G>A| S278
57755 BAA01g31150-BAA01g31160 A01 20201881 G A intergenic_region MODIFIER n.20201881G>A| S225
57756 BAA01g31150-BAA01g31160 A01 20202649 G A intergenic_region MODIFIER n.20202649G>A| S138
57757 BAA01g31150-BAA01g31160 A01 20203622 C T intergenic_region MODIFIER n.20203622C>T| S270
57758 BAA01g31150-BAA01g31160 A01 20203784 G A intergenic_region MODIFIER n.20203784G>A| S267
57759 BAA01g31160 A01 20210694 C T downstream_gene_variant MODIFIER c.*277G>A| S136
57760 BAA01g31160 A01 20210881 G A downstream_gene_variant MODIFIER c.*90C>T| S246
57761 BAA01g31160 A01 20210979 C T missense_variant MODERATE c.1828G>A|p.Val610Ile S255
57762 BAA01g31160 A01 20210991 C T missense_variant MODERATE c.1816G>A|p.Asp606Asn S41
57763 BAA01g31160 A01 20211001 G A synonymous_variant LOW c.1806C>T|p.Arg602Arg S284
57764 BAA01g31160 A01 20211096 C T missense_variant MODERATE c.1711G>A|p.Asp571Asn S120
57765 BAA01g31160 A01 20211133 G A synonymous_variant LOW c.1674C>T|p.Ser558Ser S260
57766 BAA01g31160 A01 20211237 C T missense_variant MODERATE c.1570G>A|p.Asp524Asn S8
57767 BAA01g31160 A01 20211281 G A missense_variant MODERATE c.1526C>T|p.Ala509Val S271
57768 BAA01g31160 A01 20211294 C T missense_variant MODERATE c.1513G>A|p.Val505Met S171
57769 BAA01g31160 A01 20211465 C T missense_variant MODERATE c.1342G>A|p.Glu448Lys S164
57770 BAA01g31160 A01 20211698 C T missense_variant MODERATE c.1109G>A|p.Arg370Lys S166
57771 BAA01g31160 A01 20211943 C T synonymous_variant LOW c.864G>A|p.Thr288Thr S232
57772 BAA01g31160 A01 20212033 C T synonymous_variant LOW c.774G>A|p.Lys258Lys S9
57773 BAA01g31160 A01 20212218 C T missense_variant MODERATE c.662G>A|p.Gly221Asp S69
57774 BAA01g31160 A01 20212286 C T synonymous_variant LOW c.594G>A|p.Glu198Glu S153
57775 BAA01g31160 A01 20212773 G A missense_variant MODERATE c.107C>T|p.Ser36Leu S263