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
74251 BAA01g39020 A01 25975601 G A missense_variant MODERATE c.293G>A|p.Cys98Tyr S70
74252 BAA01g39020 A01 25976081 C T missense_variant MODERATE c.773C>T|p.Ser258Phe S183
S198
74253 BAA01g39020 A01 25977607 G A missense_variant MODERATE c.1984G>A|p.Glu662Lys S271
74254 BAA01g39030 A01 25980024 C T missense_variant MODERATE c.1129G>A|p.Glu377Lys S11
74255 BAA01g39030 A01 25980099 C T missense_variant MODERATE c.1054G>A|p.Asp352Asn S130
74256 BAA01g39030 A01 25980270 C T missense_variant MODERATE c.1003G>A|p.Glu335Lys S157
74257 BAA01g39030 A01 25980388 C T missense_variant MODERATE c.970G>A|p.Val324Ile S134
74258 BAA01g39030 A01 25980412 C T missense_variant MODERATE c.946G>A|p.Glu316Lys S153
74259 BAA01g39030 A01 25980449 C T stop_gained HIGH c.909G>A|p.Trp303* S240
74260 BAA01g39020 A01 25980787 G A downstream_gene_variant MODIFIER c.*2754G>A| S172
S217
74261 BAA01g39030 A01 25980939 C T missense_variant MODERATE c.599G>A|p.Arg200His S62
74262 BAA01g39030 A01 25981025 G A synonymous_variant LOW c.513C>T|p.Ser171Ser S157
S163
74263 BAA01g39030 A01 25981616 G A missense_variant MODERATE c.106C>T|p.Leu36Phe S223
74264 BAA01g39030 A01 25981763 G A upstream_gene_variant MODIFIER c.-42C>T| S209
74265 BAA01g39030 A01 25981954 G T upstream_gene_variant MODIFIER c.-233C>A| S212
S69
74266 BAA01g39030 A01 25982494 G A upstream_gene_variant MODIFIER c.-773C>T| S207
74267 BAA01g39030 A01 25984321 C T upstream_gene_variant MODIFIER c.-2600G>A| S270
74268 BAA01g39030 A01 25984329 C T upstream_gene_variant MODIFIER c.-2608G>A| S274
74269 BAA01g39030 A01 25986373 C T upstream_gene_variant MODIFIER c.-4652G>A| S56
74270 BAA01g39040 A01 25989639 G A synonymous_variant LOW c.483C>T|p.Ile161Ile S218
74271 BAA01g39040 A01 25989750 G A synonymous_variant LOW c.372C>T|p.Ile124Ile S100
74272 BAA01g39040 A01 25990629 C T upstream_gene_variant MODIFIER c.-508G>A| S233
74273 BAA01g39040 A01 25991484 C T upstream_gene_variant MODIFIER c.-1363G>A| S255
74274 BAA01g39040 A01 25991561 C T upstream_gene_variant MODIFIER c.-1440G>A| S65
74275 BAA01g39040 A01 25992068 C T upstream_gene_variant MODIFIER c.-1947G>A| S130