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
13751 BAA01g10740 A01 4948340 C T upstream_gene_variant MODIFIER c.-4773C>T| S301
13752 BAA01g10740 A01 4949876 G A upstream_gene_variant MODIFIER c.-3237G>A| S208
S219
13753 BAA01g10740 A01 4953547 G A synonymous_variant LOW c.360G>A|p.Lys120Lys S177
13754 BAA01g10740 A01 4954215 G A splice_acceptor_variant&intron_variant HIGH c.685-1G>A| S153
13755 BAA01g10750 A01 4954923 G A missense_variant MODERATE c.232G>A|p.Val78Met S256
13756 BAA01g10730 A01 4955060 C T upstream_gene_variant MODIFIER c.-3464G>A| S198
13757 BAA01g10730 A01 4955409 C T upstream_gene_variant MODIFIER c.-3813G>A| S249
13758 BAA01g10730 A01 4955545 C T upstream_gene_variant MODIFIER c.-3949G>A| S77
13759 BAA01g10760 A01 4956245 A C missense_variant MODERATE c.17A>C|p.Lys6Thr S184
13760 BAA01g10760 A01 4956691 G A missense_variant MODERATE c.463G>A|p.Val155Ile S247
13761 BAA01g10760 A01 4956761 C T missense_variant MODERATE c.533C>T|p.Ser178Phe S139
13762 BAA01g10760 A01 4957590 C T synonymous_variant LOW c.1176C>T|p.Asn392Asn S305
13763 BAA01g10760 A01 4957612 G A missense_variant MODERATE c.1198G>A|p.Gly400Arg S281
13764 BAA01g10770 A01 4958146 C T upstream_gene_variant MODIFIER c.-3124C>T| S136
13765 BAA01g10760 A01 4958403 C T synonymous_variant LOW c.1662C>T|p.Ser554Ser S50
13766 BAA01g10760 A01 4958408 C T missense_variant MODERATE c.1667C>T|p.Thr556Ile S268
13767 BAA01g10770 A01 4959087 C T upstream_gene_variant MODIFIER c.-2183C>T| S130
13768 BAA01g10770 A01 4959853 G A upstream_gene_variant MODIFIER c.-1417G>A| S216
13769 BAA01g10770 A01 4959957 G A upstream_gene_variant MODIFIER c.-1313G>A| S229
13770 BAA01g10770 A01 4961966 G A missense_variant MODERATE c.697G>A|p.Gly233Arg S226
13771 BAA01g10770 A01 4962000 C T missense_variant MODERATE c.731C>T|p.Ser244Phe S155
S211
13772 BAA01g10760 A01 4962947 G A downstream_gene_variant MODIFIER c.*4445G>A| S119
13773 BAA01g10770 A01 4963872 C T downstream_gene_variant MODIFIER c.*1469C>T| S47
13774 BAA01g10770 A01 4963892 G A downstream_gene_variant MODIFIER c.*1489G>A| S191
13775 BAA01g10770 A01 4966216 G A downstream_gene_variant MODIFIER c.*3813G>A| S263