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
111851 BAA10g08390 A10 10135891 C T missense_variant MODERATE c.814G>A|p.Asp272Asn S131
111852 BAA10g08390 A10 10137192 G A upstream_gene_variant MODIFIER c.-488C>T| S221
111853 BAA10g08390 A10 10137497 C A upstream_gene_variant MODIFIER c.-793G>T| S146
111854 BAA10g08390 A10 10137872 G A upstream_gene_variant MODIFIER c.-1168C>T| S68
111855 BAA10g08390 A10 10138035 T A upstream_gene_variant MODIFIER c.-1331A>T| S108
111856 BAA10g08390 A10 10139103 G A upstream_gene_variant MODIFIER c.-2399C>T| S198
111857 BAA10g08390 A10 10139521 C T upstream_gene_variant MODIFIER c.-2817G>A| S155
S211
111858 BAA10g08390 A10 10139809 G A upstream_gene_variant MODIFIER c.-3105C>T| S13
111859 BAA10g08400 A10 10141247 C T missense_variant MODERATE c.1810G>A|p.Ala604Thr S155
S211
111860 BAA10g08400 A10 10141378 C T missense_variant MODERATE c.1679G>A|p.Arg560His S247
111861 BAA10g08390 A10 10141668 C T upstream_gene_variant MODIFIER c.-4964G>A| S287
111862 BAA10g08400 A10 10141741 G A intron_variant MODIFIER c.1459-143C>T| S221
111863 BAA10g08400 A10 10141797 G A intron_variant MODIFIER c.1458+92C>T| S66
111864 BAA10g08400 A10 10141969 C T missense_variant MODERATE c.1378G>A|p.Asp460Asn S249
111865 BAA10g08400 A10 10142339 G A intron_variant MODIFIER c.1150-17C>T| S158
111866 BAA10g08400 A10 10142526 G A synonymous_variant LOW c.1035C>T|p.Asn345Asn S259
111867 BAA10g08400 A10 10143135 G A missense_variant MODERATE c.515C>T|p.Pro172Leu S38
111868 BAA10g08400 A10 10143730 G A upstream_gene_variant MODIFIER c.-17C>T| S18
111869 BAA10g08400 A10 10145245 G A upstream_gene_variant MODIFIER c.-1532C>T| S126
111870 BAA10g08400 A10 10145882 G A upstream_gene_variant MODIFIER c.-2169C>T| S148
S30
S31
111871 BAA10g08400 A10 10147183 G A upstream_gene_variant MODIFIER c.-3470C>T| S284
111872 BAA10g08400 A10 10147652 T A upstream_gene_variant MODIFIER c.-3939A>T| S205
111873 BAA10g08400 A10 10148341 C T upstream_gene_variant MODIFIER c.-4628G>A| S37
111874 BAA10g08400-BAA10g08410 A10 10151100 G A intergenic_region MODIFIER n.10151100G>A| S274
111875 BAA10g08400-BAA10g08410 A10 10151430 C T intergenic_region MODIFIER n.10151430C>T| S197