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
146301 BAA10g30740 A10 22684206 C T missense_variant MODERATE c.254C>T|p.Pro85Leu S12
146302 BAA10g30740 A10 22684391 G A missense_variant MODERATE c.439G>A|p.Glu147Lys S274
146303 BAA10g30720 A10 22685702 C T upstream_gene_variant MODIFIER c.-4945G>A| S247
146304 BAA10g30750 A10 22687392 C T missense_variant MODERATE c.437G>A|p.Arg146Lys S244
146305 BAA10g30750 A10 22687592 G A missense_variant MODERATE c.316C>T|p.His106Tyr S283
146306 BAA10g30750 A10 22687912 G A upstream_gene_variant MODIFIER c.-5C>T| S252
146307 BAA10g30750 A10 22690567 C T upstream_gene_variant MODIFIER c.-2660G>A| S234
146308 BAA10g30750 A10 22691167 C T upstream_gene_variant MODIFIER c.-3260G>A| S19
146309 BAA10g30750 A10 22692074 G A upstream_gene_variant MODIFIER c.-4167C>T| S19
146310 BAA10g30750 A10 22692196 G A upstream_gene_variant MODIFIER c.-4289C>T| S173
146311 BAA10g30760 A10 22693442 C T missense_variant MODERATE c.71C>T|p.Ser24Leu S152
146312 BAA10g30760 A10 22693461 G A synonymous_variant LOW c.90G>A|p.Lys30Lys S202
146313 BAA10g30760 A10 22693515 C T synonymous_variant LOW c.144C>T|p.Ile48Ile S148
S210
S30
S31
146314 BAA10g30770 A10 22694617 C T upstream_gene_variant MODIFIER c.-1237C>T| S135
146315 BAA10g30770 A10 22694692 C T upstream_gene_variant MODIFIER c.-1162C>T| S23
146316 BAA10g30770 A10 22694936 C T upstream_gene_variant MODIFIER c.-918C>T| S281
146317 BAA10g30770 A10 22695300 C T upstream_gene_variant MODIFIER c.-554C>T| S229
146318 BAA10g30770 A10 22696278 G A missense_variant MODERATE c.259G>A|p.Val87Ile S183
S198
146319 BAA10g30770 A10 22696544 C T synonymous_variant LOW c.447C>T|p.Ser149Ser S295
146320 BAA10g30780 A10 22697235 G A upstream_gene_variant MODIFIER c.-1124G>A| S172
S217
146321 BAA10g30790 A10 22699069 G A upstream_gene_variant MODIFIER c.-812G>A| S262
146322 BAA10g30790 A10 22699429 G A upstream_gene_variant MODIFIER c.-452G>A| S35
146323 BAA10g30770 A10 22701244 G A downstream_gene_variant MODIFIER c.*3564G>A| S219
S72
146324 BAA10g30790 A10 22701351 G A missense_variant MODERATE c.991G>A|p.Glu331Lys S274
146325 BAA10g30770 A10 22701651 C T downstream_gene_variant MODIFIER c.*3971C>T| S5