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
105501 BAA10g08140 A10 5559399 G A synonymous_variant LOW c.456C>T|p.Asp152Asp S181
105502 BAA10g08140 A10 5559480 C T missense_variant MODERATE c.375G>A|p.Met125Ile S123
105503 BAA10g08140 A10 5559692 G A missense_variant MODERATE c.163C>T|p.Pro55Ser S79
S84
105504 BAA10g08140 A10 5560167 G A upstream_gene_variant MODIFIER c.-313C>T| S290
105505 BAA10g08150 A10 5560254 C T missense_variant MODERATE c.412G>A|p.Glu138Lys S269
105506 BAA10g08150 A10 5560389 G A missense_variant MODERATE c.277C>T|p.Pro93Ser S245
105507 BAA10g08160 A10 5560873 G A synonymous_variant LOW c.6G>A|p.Glu2Glu S125
105508 BAA10g08140 A10 5561097 G A upstream_gene_variant MODIFIER c.-1243C>T| S159
S243
105509 BAA10g08140 A10 5561216 G A upstream_gene_variant MODIFIER c.-1362C>T| S7
105510 BAA10g08140 A10 5561540 C T upstream_gene_variant MODIFIER c.-1686G>A| S238
105511 BAA10g08140 A10 5561561 C T upstream_gene_variant MODIFIER c.-1707G>A| S224
105512 BAA10g08140 A10 5561692 C T upstream_gene_variant MODIFIER c.-1838G>A| S95
105513 BAA10g08140 A10 5561807 C T upstream_gene_variant MODIFIER c.-1953G>A| S146
105514 BAA10g08140 A10 5562059 C T upstream_gene_variant MODIFIER c.-2205G>A| S142
105515 BAA10g08140 A10 5562335 G A upstream_gene_variant MODIFIER c.-2481C>T| S85
105516 BAA10g08160 A10 5564378 G A synonymous_variant LOW c.453G>A|p.Glu151Glu S152
105517 BAA10g08160 A10 5565806 C T synonymous_variant LOW c.669C>T|p.Leu223Leu S142
105518 BAA10g08160 A10 5565915 G A missense_variant MODERATE c.778G>A|p.Ala260Thr S262
105519 BAA10g08160 A10 5565979 G A missense_variant MODERATE c.842G>A|p.Ser281Asn S76
105520 BAA10g08160 A10 5566661 G A splice_acceptor_variant&intron_variant HIGH c.971-1G>A| S64
105521 BAA10g08160 A10 5567000 G A missense_variant MODERATE c.1309G>A|p.Val437Met S120
S122
S266
S9
105522 BAA10g08160 A10 5567204 G A downstream_gene_variant MODIFIER c.*91G>A| S128
105523 BAA10g08160 A10 5567437 C T downstream_gene_variant MODIFIER c.*324C>T| S187
105524 BAA10g08160 A10 5567630 C T downstream_gene_variant MODIFIER c.*517C>T| S237
105525 BAA10g08160 A10 5567822 C T downstream_gene_variant MODIFIER c.*709C>T| S270