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
162851 BAA02g09710 A02 4276308 C T upstream_gene_variant MODIFIER c.-1431G>A| S14
162852 BAA02g09710 A02 4277765 C T upstream_gene_variant MODIFIER c.-2888G>A| S249
162853 BAA02g09710 A02 4277957 C T upstream_gene_variant MODIFIER c.-3080G>A| S116
162854 BAA02g09710 A02 4278039 C T upstream_gene_variant MODIFIER c.-3162G>A| S183
S198
162855 BAA02g09710 A02 4278311 G A upstream_gene_variant MODIFIER c.-3434C>T| S82
S92
162856 BAA02g09710 A02 4278336 G A upstream_gene_variant MODIFIER c.-3459C>T| S5
162857 BAA02g09710 A02 4278797 G A upstream_gene_variant MODIFIER c.-3920C>T| S288
162858 BAA02g09710 A02 4278936 G A upstream_gene_variant MODIFIER c.-4059C>T| S41
162859 BAA02g09720 A02 4280627 G A upstream_gene_variant MODIFIER c.-325G>A| S177
162860 BAA02g09720 A02 4280709 C T upstream_gene_variant MODIFIER c.-243C>T| S242
162861 BAA02g09720 A02 4286256 G A downstream_gene_variant MODIFIER c.*4114G>A| S43
162862 BAA02g09730 A02 4286719 C T missense_variant MODERATE c.3109G>A|p.Asp1037Asn S270
162863 BAA02g09730 A02 4287168 C T missense_variant MODERATE c.2660G>A|p.Gly887Glu S63
162864 BAA02g09730 A02 4287205 C T missense_variant MODERATE c.2623G>A|p.Gly875Ser S241
162865 BAA02g09730 A02 4287685 G A missense_variant MODERATE c.2143C>T|p.His715Tyr S210
S225
162866 BAA02g09730 A02 4288486 G A missense_variant MODERATE c.1342C>T|p.Pro448Ser S107
162867 BAA02g09730 A02 4288619 C T synonymous_variant LOW c.1209G>A|p.Glu403Glu S40
S49
162868 BAA02g09730 A02 4289695 G A synonymous_variant LOW c.664C>T|p.Leu222Leu S155
S211
162869 BAA02g09730 A02 4289737 G A intron_variant MODIFIER c.645-23C>T| S291
162870 BAA02g09730 A02 4290010 C T missense_variant MODERATE c.511G>A|p.Asp171Asn S272
162871 BAA02g09730 A02 4290310 C T intron_variant MODIFIER c.313-16G>A| S183
S198
162872 BAA02g09730 A02 4292875 G A upstream_gene_variant MODIFIER c.-1621C>T| S68
162873 BAA02g09730 A02 4293481 G A upstream_gene_variant MODIFIER c.-2227C>T| S188
162874 BAA02g09730 A02 4294805 C T upstream_gene_variant MODIFIER c.-3551G>A| S152
162875 BAA02g09730 A02 4295607 C T upstream_gene_variant MODIFIER c.-4353G>A| S299