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
147701 BAA10g32080 A10 23189471 C T missense_variant MODERATE c.836G>A|p.Arg279Lys S82
S92
147702 BAA10g32090 A10 23189619 G A upstream_gene_variant MODIFIER c.-1969G>A| S240
147703 BAA10g32080 A10 23189763 C T missense_variant MODERATE c.670G>A|p.Glu224Lys S169
147704 BAA10g32080 A10 23190299 C T missense_variant MODERATE c.412G>A|p.Ala138Thr S2
147705 BAA10g32090 A10 23190645 G A upstream_gene_variant MODIFIER c.-943G>A| S298
147706 BAA10g32080 A10 23190798 C T synonymous_variant LOW c.162G>A|p.Gly54Gly S242
147707 BAA10g32080 A10 23191085 A C upstream_gene_variant MODIFIER c.-30T>G| S165
147708 BAA10g32080 A10 23194231 G A upstream_gene_variant MODIFIER c.-3176C>T| S263
147709 BAA10g32080 A10 23194523 G A upstream_gene_variant MODIFIER c.-3468C>T| S193
147710 BAA10g32100 A10 23196244 G A upstream_gene_variant MODIFIER c.-2579C>T| S180
147711 BAA10g32110 A10 23196905 G A splice_region_variant&intron_variant LOW c.473-6C>T| S156
147712 BAA10g32100 A10 23197422 C T upstream_gene_variant MODIFIER c.-3757G>A| S236
147713 BAA10g32100 A10 23197812 G A upstream_gene_variant MODIFIER c.-4147C>T| S50
147714 BAA10g32100 A10 23198276 C T upstream_gene_variant MODIFIER c.-4611G>A| S299
147715 BAA10g32120 A10 23199233 G A upstream_gene_variant MODIFIER c.-1745G>A| S180
147716 BAA10g32110 A10 23199630 C T missense_variant MODERATE c.149G>A|p.Gly50Asp S282
147717 BAA10g32130 A10 23203099 G A synonymous_variant LOW c.93C>T|p.Ile31Ile S68
147718 BAA10g32140 A10 23205538 C T missense_variant MODERATE c.731C>T|p.Pro244Leu S111
147719 BAA10g32130 A10 23207307 C T upstream_gene_variant MODIFIER c.-4038G>A| S234
147720 BAA10g32130 A10 23207650 T C upstream_gene_variant MODIFIER c.-4381A>G| S225
S73
147721 BAA10g32150 A10 23208275 C T synonymous_variant LOW c.468C>T|p.Cys156Cys S296
147722 BAA10g32150 A10 23208366 C T synonymous_variant LOW c.559C>T|p.Leu187Leu S51
147723 BAA10g32160 A10 23210903 C T missense_variant MODERATE c.362C>T|p.Ser121Phe S44
147724 BAA10g32160 A10 23211060 C T synonymous_variant LOW c.519C>T|p.Ser173Ser S130
147725 BAA10g32160 A10 23211096 G A synonymous_variant LOW c.555G>A|p.Lys185Lys S76