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
147801 BAA10g32220 A10 23231880 G A upstream_gene_variant MODIFIER c.-2171C>T| S160
147802 BAA10g32220 A10 23233057 C T upstream_gene_variant MODIFIER c.-3348G>A| S301
S304
147803 BAA10g32240 A10 23235513 C T synonymous_variant LOW c.609G>A|p.Glu203Glu S296
147804 BAA10g32240 A10 23236108 C T missense_variant MODERATE c.254G>A|p.Gly85Glu S277
147805 BAA10g32240 A10 23236303 G A missense_variant MODERATE c.59C>T|p.Ser20Phe S192
147806 BAA10g32230 A10 23236372 C T upstream_gene_variant MODIFIER c.-4525G>A| S94
147807 BAA10g32230 A10 23236503 G A upstream_gene_variant MODIFIER c.-4656C>T| S85
147808 BAA10g32240 A10 23237147 G A upstream_gene_variant MODIFIER c.-786C>T| S100
147809 BAA10g32240 A10 23238422 C T upstream_gene_variant MODIFIER c.-2061G>A| S104
147810 BAA10g32240 A10 23239270 G A upstream_gene_variant MODIFIER c.-2909C>T| S255
147811 BAA10g32250 A10 23240229 C T missense_variant MODERATE c.1960G>A|p.Glu654Lys S166
147812 BAA10g32250 A10 23240460 G A stop_gained HIGH c.1729C>T|p.Gln577* S278
147813 BAA10g32250 A10 23240770 G A missense_variant MODERATE c.1507C>T|p.Pro503Ser S180
147814 BAA10g32250 A10 23241886 C A missense_variant MODERATE c.474G>T|p.Glu158Asp S196
147815 BAA10g32250 A10 23241940 C T synonymous_variant LOW c.420G>A|p.Leu140Leu S268
147816 BAA10g32260 A10 23244765 C T missense_variant MODERATE c.730G>A|p.Val244Met S190
147817 BAA10g32260 A10 23245082 G A missense_variant MODERATE c.413C>T|p.Ser138Phe S128
147818 BAA10g32260 A10 23245325 G A missense_variant MODERATE c.170C>T|p.Thr57Ile S265
147819 BAA10g32260 A10 23245380 C T missense_variant MODERATE c.115G>A|p.Asp39Asn S187
147820 BAA10g32250 A10 23245809 G A upstream_gene_variant MODIFIER c.-3450C>T| S164
147821 BAA10g32250 A10 23246852 C T upstream_gene_variant MODIFIER c.-4493G>A| S257
147822 BAA10g32250 A10 23247240 C T upstream_gene_variant MODIFIER c.-4881G>A| S189
147823 BAA10g32250 A10 23247307 C T upstream_gene_variant MODIFIER c.-4948G>A| S282
147824 BAA10g32260 A10 23248645 C T upstream_gene_variant MODIFIER c.-3151G>A| S36
147825 BAA10g32260 A10 23249007 G A upstream_gene_variant MODIFIER c.-3513C>T| S271