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
171251 BAA02g15540 A02 7504625 C T intron_variant MODIFIER c.599-29G>A| S114
171252 BAA02g15540 A02 7504857 C T splice_donor_variant&intron_variant HIGH c.514+1G>A| S130
171253 BAA02g15540 A02 7505830 G A intron_variant MODIFIER c.213-425C>T| S139
171254 BAA02g15540 A02 7505911 C T intron_variant MODIFIER c.212+355G>A| S211
S227
171255 BAA02g15540 A02 7506204 C T intron_variant MODIFIER c.212+62G>A| S127
171256 BAA02g15540 A02 7507007 G A upstream_gene_variant MODIFIER c.-530C>T| S245
171257 BAA02g15540 A02 7507911 C T upstream_gene_variant MODIFIER c.-1434G>A| S255
171258 BAA02g15540 A02 7507945 C T upstream_gene_variant MODIFIER c.-1468G>A| S77
S82
171259 BAA02g15550 A02 7512831 C T upstream_gene_variant MODIFIER c.-1030C>T| S183
S198
171260 BAA02g15550 A02 7513011 C T upstream_gene_variant MODIFIER c.-850C>T| S246
171261 BAA02g15550 A02 7513064 G A upstream_gene_variant MODIFIER c.-797G>A| S168
171262 BAA02g15550 A02 7513439 G A upstream_gene_variant MODIFIER c.-422G>A| S133
171263 BAA02g15550 A02 7513624 G A upstream_gene_variant MODIFIER c.-237G>A| S206
171264 BAA02g15550 A02 7513745 G A upstream_gene_variant MODIFIER c.-116G>A| S295
171265 BAA02g15550 A02 7514001 C T synonymous_variant LOW c.141C>T|p.Leu47Leu S117
171266 BAA02g15550 A02 7514036 C T missense_variant MODERATE c.176C>T|p.Thr59Ile S5
171267 BAA02g15570 A02 7514340 G A upstream_gene_variant MODIFIER c.-4279G>A| S155
S211
171268 BAA02g15550 A02 7515216 C T missense_variant MODERATE c.998C>T|p.Pro333Leu S112
171269 BAA02g15550 A02 7515560 C T missense_variant MODERATE c.1342C>T|p.Pro448Ser S156
S34
171270 BAA02g15550 A02 7515759 G A missense_variant MODERATE c.1541G>A|p.Arg514Gln S190
171271 BAA02g15570 A02 7516430 G A upstream_gene_variant MODIFIER c.-2189G>A| S148
S30
S31
171272 BAA02g15560 A02 7516857 C T synonymous_variant LOW c.207G>A|p.Arg69Arg S266
171273 BAA02g15560 A02 7517035 C T missense_variant MODERATE c.112G>A|p.Asp38Asn S1
S90
171274 BAA02g15570 A02 7517259 C T upstream_gene_variant MODIFIER c.-1360C>T| S128
171275 BAA02g15560 A02 7518223 G A upstream_gene_variant MODIFIER c.-869C>T| S57