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
90851 BAA10g00900 A10 418900 C T upstream_gene_variant MODIFIER c.-1028C>T| S286
90852 BAA10g00900 A10 419619 C T upstream_gene_variant MODIFIER c.-309C>T| S165
90853 BAA10g00900 A10 420027 C T missense_variant MODERATE c.100C>T|p.His34Tyr S12
90854 BAA10g00890 A10 421000 C T downstream_gene_variant MODIFIER c.*2214C>T| S225
S73
90855 BAA10g00890 A10 421052 G A downstream_gene_variant MODIFIER c.*2266G>A| S148
S30
90856 BAA10g00890 A10 421335 C T downstream_gene_variant MODIFIER c.*2549C>T| S287
90857 BAA10g00890 A10 421397 G A downstream_gene_variant MODIFIER c.*2611G>A| S46
90858 BAA10g00910 A10 421911 C T synonymous_variant LOW c.1767G>A|p.Glu589Glu S287
90859 BAA10g00910 A10 422153 G A missense_variant MODERATE c.1525C>T|p.Pro509Ser S267
90860 BAA10g00910 A10 422864 G A missense_variant MODERATE c.961C>T|p.Pro321Ser S99
90861 BAA10g00910 A10 423105 G A synonymous_variant LOW c.720C>T|p.Asp240Asp S219
S72
90862 BAA10g00910 A10 423133 C T missense_variant MODERATE c.692G>A|p.Gly231Glu S177
90863 BAA10g00910 A10 423378 C T synonymous_variant LOW c.447G>A|p.Glu149Glu S233
90864 BAA10g00910 A10 423396 C T synonymous_variant LOW c.429G>A|p.Gln143Gln S260
90865 BAA10g00910 A10 423936 G A missense_variant MODERATE c.43C>T|p.Leu15Phe S2
90866 BAA10g00920 A10 424248 G A missense_variant MODERATE c.3527C>T|p.Ala1176Val S245
90867 BAA10g00920 A10 424344 C T missense_variant MODERATE c.3431G>A|p.Arg1144Lys S182
90868 BAA10g00910 A10 425572 C T upstream_gene_variant MODIFIER c.-1594G>A| S298
90869 BAA10g00920 A10 425729 G A missense_variant MODERATE c.2360C>T|p.Pro787Leu S133
90870 BAA10g00920 A10 425737 G A synonymous_variant LOW c.2352C>T|p.Asp784Asp S186
90871 BAA10g00920 A10 425834 C T missense_variant MODERATE c.2255G>A|p.Arg752Lys S165
90872 BAA10g00920 A10 426951 C T missense_variant MODERATE c.1472G>A|p.Gly491Glu S275
90873 BAA10g00920 A10 427473 G A synonymous_variant LOW c.1041C>T|p.His347His S262
90874 BAA10g00920 A10 427703 C T missense_variant MODERATE c.811G>A|p.Val271Met S231
90875 BAA10g00920 A10 427719 G A synonymous_variant LOW c.795C>T|p.Val265Val S242