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
134251 BAA10g20460 A10 18409155 C T upstream_gene_variant MODIFIER c.-4648G>A| S262
134252 BAA10g20460 A10 18409281 G A upstream_gene_variant MODIFIER c.-4774C>T| S270
134253 BAA10g20480 A10 18411183 G A missense_variant MODERATE c.28C>T|p.Leu10Phe S163
134254 BAA10g20470 A10 18411567 C T upstream_gene_variant MODIFIER c.-2745G>A| S10
134255 BAA10g20470 A10 18411606 C T upstream_gene_variant MODIFIER c.-2784G>A| S277
134256 BAA10g20470 A10 18411645 C T upstream_gene_variant MODIFIER c.-2823G>A| S206
134257 BAA10g20470 A10 18412796 C T upstream_gene_variant MODIFIER c.-3974G>A| S135
134258 BAA10g20470 A10 18413150 T C upstream_gene_variant MODIFIER c.-4328A>G| S274
134259 BAA10g20470 A10 18413814 C T upstream_gene_variant MODIFIER c.-4992G>A| S291
134260 BAA10g20480 A10 18414022 G A upstream_gene_variant MODIFIER c.-2812C>T| S4
134261 BAA10g20480 A10 18414536 C T upstream_gene_variant MODIFIER c.-3326G>A| S8
134262 BAA10g20490 A10 18416457 G A upstream_gene_variant MODIFIER c.-3920G>A| S85
134263 BAA10g20490 A10 18416538 G A upstream_gene_variant MODIFIER c.-3839G>A| S75
S81
134264 BAA10g20490 A10 18416674 G A upstream_gene_variant MODIFIER c.-3703G>A| S9
134265 BAA10g20490 A10 18416718 C T upstream_gene_variant MODIFIER c.-3659C>T| S23
134266 BAA10g20490 A10 18418510 G A upstream_gene_variant MODIFIER c.-1867G>A| S191
134267 BAA10g20490 A10 18418679 C T upstream_gene_variant MODIFIER c.-1698C>T| S199
134268 BAA10g20490 A10 18420029 C T upstream_gene_variant MODIFIER c.-348C>T| S221
134269 BAA10g20490 A10 18421686 A C downstream_gene_variant MODIFIER c.*581A>C| S92
134270 BAA10g20490 A10 18422201 C T downstream_gene_variant MODIFIER c.*1096C>T| S152
134271 BAA10g20490 A10 18422270 C T downstream_gene_variant MODIFIER c.*1165C>T| S148
S30
S31
134272 BAA10g20500 A10 18423055 C T synonymous_variant LOW c.1161G>A|p.Arg387Arg S269
134273 BAA10g20510 A10 18423565 T C upstream_gene_variant MODIFIER c.-3949T>C| S90
134274 BAA10g20510 A10 18423863 G A upstream_gene_variant MODIFIER c.-3651G>A| S280
134275 BAA10g20500 A10 18424495 C T missense_variant&splice_region_variant MODERATE c.523G>A|p.Glu175Lys S302