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
145351 BAA10g29900 A10 22337189 G A missense_variant MODERATE c.358G>A|p.Glu120Lys S62
145352 BAA10g29890 A10 22337643 G C upstream_gene_variant MODIFIER c.-4844C>G| S172
S217
145353 BAA10g29910 A10 22338076 G A upstream_gene_variant MODIFIER c.-490G>A| S284
145354 BAA10g29910 A10 22338257 C T upstream_gene_variant MODIFIER c.-309C>T| S188
145355 BAA10g29910 A10 22338683 G A missense_variant MODERATE c.118G>A|p.Gly40Ser S209
145356 BAA10g29910 A10 22338821 C T missense_variant MODERATE c.256C>T|p.His86Tyr S301
S304
145357 BAA10g29910 A10 22338910 C T synonymous_variant LOW c.345C>T|p.Leu115Leu S38
145358 BAA10g29900 A10 22340511 C T downstream_gene_variant MODIFIER c.*2498C>T| S308
145359 BAA10g29900 A10 22340609 C T downstream_gene_variant MODIFIER c.*2596C>T| S74
145360 BAA10g29900 A10 22342074 C T downstream_gene_variant MODIFIER c.*4061C>T| S287
145361 BAA10g29900 A10 22342421 C T downstream_gene_variant MODIFIER c.*4408C>T| S204
145362 BAA10g29900 A10 22342733 C T downstream_gene_variant MODIFIER c.*4720C>T| S140
145363 BAA10g29920 A10 22343080 C T missense_variant MODERATE c.796G>A|p.Asp266Asn S18
145364 BAA10g29920 A10 22343240 C T synonymous_variant LOW c.636G>A|p.Ser212Ser S221
145365 BAA10g29920 A10 22343334 G A missense_variant MODERATE c.542C>T|p.Ser181Phe S251
145366 BAA10g29920 A10 22343434 C T missense_variant MODERATE c.442G>A|p.Glu148Lys S295
145367 BAA10g29920 A10 22343484 G A missense_variant MODERATE c.392C>T|p.Thr131Ile S209
145368 BAA10g29920 A10 22347188 G A upstream_gene_variant MODIFIER c.-3313C>T| S1
S90
145369 BAA10g29930 A10 22351066 G A downstream_gene_variant MODIFIER c.*3779C>T| S264
145370 BAA10g29930 A10 22355814 C T synonymous_variant LOW c.1251G>A|p.Lys417Lys S28
145371 BAA10g29940 A10 22357975 G A missense_variant MODERATE c.560C>T|p.Pro187Leu S193
145372 BAA10g29930 A10 22358232 G A upstream_gene_variant MODIFIER c.-1168C>T| S255
145373 BAA10g29930 A10 22360085 C T upstream_gene_variant MODIFIER c.-3021G>A| S19
145374 BAA10g29950 A10 22361703 G A missense_variant MODERATE c.1190C>T|p.Ala397Val S125
145375 BAA10g29930 A10 22361969 C T upstream_gene_variant MODIFIER c.-4905G>A| S161