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
167751 BAA02g13380 A02 6092761 G A missense_variant MODERATE c.1067C>T|p.Pro356Leu S204
167752 BAA02g13380 A02 6092849 C T missense_variant MODERATE c.979G>A|p.Glu327Lys S121
167753 BAA02g13390 A02 6093613 G A downstream_gene_variant MODIFIER c.*2852C>T| S139
167754 BAA02g13380 A02 6094623 C T missense_variant MODERATE c.62G>A|p.Gly21Asp S263
167755 BAA02g13380 A02 6094681 C T missense_variant MODERATE c.4G>A|p.Gly2Arg S308
167756 BAA02g13380 A02 6095815 G A upstream_gene_variant MODIFIER c.-1131C>T| S43
167757 BAA02g13380 A02 6095940 G A upstream_gene_variant MODIFIER c.-1256C>T| S68
167758 BAA02g13380 A02 6096747 C T upstream_gene_variant MODIFIER c.-2063G>A| S272
167759 BAA02g13390 A02 6098515 G A synonymous_variant LOW c.225C>T|p.Leu75Leu S232
167760 BAA02g13380 A02 6099060 C T upstream_gene_variant MODIFIER c.-4376G>A| S44
167761 BAA02g13390 A02 6100996 G A upstream_gene_variant MODIFIER c.-2257C>T| S122
167762 BAA02g13390 A02 6102266 C T upstream_gene_variant MODIFIER c.-3527G>A| S94
167763 BAA02g13390 A02 6102421 C T upstream_gene_variant MODIFIER c.-3682G>A| S153
167764 BAA02g13400 A02 6102942 G A missense_variant MODERATE c.427G>A|p.Glu143Lys S139
S4
167765 BAA02g13400 A02 6106300 G A downstream_gene_variant MODIFIER c.*3218G>A| S157
167766 BAA02g13400 A02 6106418 C T downstream_gene_variant MODIFIER c.*3336C>T| S209
167767 BAA02g13400 A02 6106776 C T downstream_gene_variant MODIFIER c.*3694C>T| S284
167768 BAA02g13400 A02 6106779 A G downstream_gene_variant MODIFIER c.*3697A>G| S165
167769 BAA02g13400 A02 6106917 G A downstream_gene_variant MODIFIER c.*3835G>A| S28
167770 BAA02g13400 A02 6106919 G A downstream_gene_variant MODIFIER c.*3837G>A| S133
167771 BAA02g13400 A02 6107435 C T downstream_gene_variant MODIFIER c.*4353C>T| S65
167772 BAA02g13410 A02 6108560 C T downstream_gene_variant MODIFIER c.*1802C>T| S5
167773 BAA02g13410 A02 6110513 A T downstream_gene_variant MODIFIER c.*3755A>T| S174
167774 BAA02g13420 A02 6113235 G A upstream_gene_variant MODIFIER c.-576C>T| S62
167775 BAA02g13420 A02 6113304 C T upstream_gene_variant MODIFIER c.-645G>A| S130