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
150751 BAA10g34750 A10 24321543 T C downstream_gene_variant MODIFIER c.*30T>C| S278
150752 BAA10g34750 A10 24322326 G A downstream_gene_variant MODIFIER c.*813G>A| S303
150753 BAA10g34760 A10 24324775 G A upstream_gene_variant MODIFIER c.-205C>T| S240
150754 BAA10g34760 A10 24325546 G A upstream_gene_variant MODIFIER c.-976C>T| S62
150755 BAA10g34760 A10 24325553 C T upstream_gene_variant MODIFIER c.-983G>A| S262
150756 BAA10g34760 A10 24325992 C T upstream_gene_variant MODIFIER c.-1422G>A| S42
150757 BAA10g34760 A10 24326218 C T upstream_gene_variant MODIFIER c.-1648G>A| S89
150758 BAA10g34760 A10 24326284 C T upstream_gene_variant MODIFIER c.-1714G>A| S124
150759 BAA10g34760 A10 24327063 G A upstream_gene_variant MODIFIER c.-2493C>T| S262
150760 BAA10g34760 A10 24327671 G A upstream_gene_variant MODIFIER c.-3101C>T| S172
S217
150761 BAA10g34760 A10 24328799 C T upstream_gene_variant MODIFIER c.-4229G>A| S302
150762 BAA10g34760 A10 24328907 G A upstream_gene_variant MODIFIER c.-4337C>T| S205
150763 BAA10g34760 A10 24329391 C T upstream_gene_variant MODIFIER c.-4821G>A| S33
150764 BAA10g34760 A10 24329533 C T upstream_gene_variant MODIFIER c.-4963G>A| S116
150765 BAA10g34770 A10 24329929 C T upstream_gene_variant MODIFIER c.-4801C>T| S156
150766 BAA10g34770 A10 24332619 C T upstream_gene_variant MODIFIER c.-2111C>T| S266
150767 BAA10g34770 A10 24336300 C T missense_variant MODERATE c.1571C>T|p.Ser524Phe S97
150768 BAA10g34780 A10 24337375 G A upstream_gene_variant MODIFIER c.-98G>A| S111
150769 BAA10g34770 A10 24338464 G A downstream_gene_variant MODIFIER c.*1780G>A| S57
150770 BAA10g34780 A10 24338542 G A synonymous_variant LOW c.690G>A|p.Glu230Glu S182
150771 BAA10g34780 A10 24338873 C T missense_variant MODERATE c.922C>T|p.Leu308Phe S291
150772 BAA10g34770 A10 24339478 C T downstream_gene_variant MODIFIER c.*2794C>T| S169
150773 BAA10g34770 A10 24340132 G A downstream_gene_variant MODIFIER c.*3448G>A| S185
150774 BAA10g34770 A10 24340177 G A downstream_gene_variant MODIFIER c.*3493G>A| S298
150775 BAA10g34770 A10 24340206 C T downstream_gene_variant MODIFIER c.*3522C>T| S51