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
166751 BAA02g12720 A02 5708181 C T missense_variant MODERATE c.146G>A|p.Arg49Lys S137
S249
166752 BAA02g12720 A02 5708355 C T upstream_gene_variant MODIFIER c.-29G>A| S245
166753 BAA02g12720 A02 5709086 G A upstream_gene_variant MODIFIER c.-760C>T| S303
166754 BAA02g12730 A02 5709801 G A missense_variant MODERATE c.302G>A|p.Gly101Glu S197
166755 BAA02g12720 A02 5710689 C T upstream_gene_variant MODIFIER c.-2363G>A| S114
166756 BAA02g12740 A02 5710859 C T missense_variant MODERATE c.479G>A|p.Ser160Asn S130
166757 BAA02g12720 A02 5711307 G A upstream_gene_variant MODIFIER c.-2981C>T| S126
166758 BAA02g12720 A02 5711745 G A upstream_gene_variant MODIFIER c.-3419C>T| S293
166759 BAA02g12720 A02 5712091 G A upstream_gene_variant MODIFIER c.-3765C>T| S89
166760 BAA02g12720 A02 5712986 C T upstream_gene_variant MODIFIER c.-4660G>A| S16
166761 BAA02g12750 A02 5713185 C T missense_variant MODERATE c.83C>T|p.Thr28Met S172
S217
166762 BAA02g12750 A02 5713992 C T missense_variant MODERATE c.599C>T|p.Pro200Leu S163
166763 BAA02g12750 A02 5714209 C T synonymous_variant LOW c.816C>T|p.Pro272Pro S46
166764 BAA02g12750 A02 5715138 G A missense_variant MODERATE c.1496G>A|p.Gly499Glu S144
166765 BAA02g12750 A02 5715422 C T missense_variant MODERATE c.1780C>T|p.His594Tyr S261
166766 BAA02g12770 A02 5718152 G A synonymous_variant LOW c.537G>A|p.Leu179Leu S59
166767 BAA02g12760 A02 5718363 C T upstream_gene_variant MODIFIER c.-1778G>A| S90
166768 BAA02g12760 A02 5718714 C T upstream_gene_variant MODIFIER c.-2129G>A| S178
166769 BAA02g12780 A02 5718759 A G stop_lost&splice_region_variant HIGH c.976T>C|p.Ter326Argext*? S178
166770 BAA02g12780 A02 5718968 G A missense_variant MODERATE c.767C>T|p.Ala256Val S23
166771 BAA02g12780 A02 5719433 G A synonymous_variant LOW c.375C>T|p.Ala125Ala S197
166772 BAA02g12780 A02 5719561 C T missense_variant MODERATE c.247G>A|p.Gly83Arg S172
S217
166773 BAA02g12780 A02 5719599 G A missense_variant MODERATE c.209C>T|p.Pro70Leu S82
S92
166774 BAA02g12760 A02 5720615 C T upstream_gene_variant MODIFIER c.-4030G>A| S121
166775 BAA02g12760 A02 5721482 C T upstream_gene_variant MODIFIER c.-4897G>A| S210
S225