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
84301 BAA01g44750 A01 29752324 G A upstream_gene_variant MODIFIER c.-1097C>T| S53
84302 BAA01g44750 A01 29752475 C T upstream_gene_variant MODIFIER c.-1248G>A| S4
84303 BAA01g44750 A01 29752635 G A upstream_gene_variant MODIFIER c.-1408C>T| S5
84304 BAA01g44750 A01 29752775 G A upstream_gene_variant MODIFIER c.-1548C>T| S262
84305 BAA01g44750 A01 29753109 C T upstream_gene_variant MODIFIER c.-1882G>A| S305
84306 BAA01g44750 A01 29753430 G A upstream_gene_variant MODIFIER c.-2203C>T| S38
84307 BAA01g44750 A01 29753465 C T upstream_gene_variant MODIFIER c.-2238G>A| S290
84308 BAA01g44760 A01 29754516 G A missense_variant MODERATE c.419G>A|p.Arg140Lys S151
84309 BAA01g44760 A01 29755821 C T splice_region_variant&intron_variant LOW c.978+7C>T| S4
84310 BAA01g44760 A01 29756745 G A synonymous_variant LOW c.1677G>A|p.Gln559Gln S110
84311 BAA01g44780 A01 29758039 G A upstream_gene_variant MODIFIER c.-3761G>A| S13
84312 BAA01g44780 A01 29758804 G A upstream_gene_variant MODIFIER c.-2996G>A| S117
84313 BAA01g44770 A01 29759339 C T synonymous_variant LOW c.459G>A|p.Arg153Arg S305
84314 BAA01g44770 A01 29760064 G A upstream_gene_variant MODIFIER c.-267C>T| S229
84315 BAA01g44770 A01 29760956 C T upstream_gene_variant MODIFIER c.-1159G>A| S148
S30
S31
84316 BAA01g44770 A01 29761567 C T upstream_gene_variant MODIFIER c.-1770G>A| S120
84317 BAA01g44780 A01 29761835 C T synonymous_variant LOW c.36C>T|p.Ile12Ile S273
84318 BAA01g44780 A01 29761915 G A missense_variant MODERATE c.116G>A|p.Gly39Glu S70
84319 BAA01g44770 A01 29762136 G A upstream_gene_variant MODIFIER c.-2339C>T| S86
84320 BAA01g44770 A01 29763671 C T upstream_gene_variant MODIFIER c.-3874G>A| S46
84321 BAA01g44780 A01 29763754 G A missense_variant MODERATE c.925G>A|p.Val309Met S194
84322 BAA01g44780 A01 29763862 G A splice_region_variant&intron_variant LOW c.946-8G>A| S208
S219
84323 BAA01g44780 A01 29766016 C T synonymous_variant LOW c.2226C>T|p.Phe742Phe S18
84324 BAA01g44780 A01 29766753 C T downstream_gene_variant MODIFIER c.*79C>T| S269
84325 BAA01g44780 A01 29767694 C T downstream_gene_variant MODIFIER c.*1020C>T| S142