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
52651 BAA01g28930 A01 18230921 C T upstream_gene_variant MODIFIER c.-3079G>A| S132
S137
S138
S215
S237
S288
S89
52652 BAA01g28940 A01 18234785 G A upstream_gene_variant MODIFIER c.-2681C>T| S238
52653 BAA01g28940 A01 18236125 G A upstream_gene_variant MODIFIER c.-4021C>T| S176
52654 BAA01g28940 A01 18236553 G A upstream_gene_variant MODIFIER c.-4449C>T| S274
52655 BAA01g28940 A01 18236742 C T upstream_gene_variant MODIFIER c.-4638G>A| S296
52656 BAA01g28940 A01 18237089 G A upstream_gene_variant MODIFIER c.-4985C>T| S288
52657 BAA01g28940-BAA01g28950 A01 18237769 G A intergenic_region MODIFIER n.18237769G>A| S202
52658 BAA01g28940-BAA01g28950 A01 18237904 G A intergenic_region MODIFIER n.18237904G>A| S283
52659 BAA01g29080 A01 18320559 G A upstream_gene_variant MODIFIER c.-2888C>T| S178
52660 BAA01g29080 A01 18320926 C T upstream_gene_variant MODIFIER c.-3255G>A| S219
S72
52661 BAA01g29080 A01 18320999 G A upstream_gene_variant MODIFIER c.-3328C>T| S194
52662 BAA01g29100 A01 18326440 G A downstream_gene_variant MODIFIER c.*640G>A| S288
52663 BAA01g29100 A01 18328280 C T downstream_gene_variant MODIFIER c.*2480C>T| S289
S290
52664 BAA01g29100 A01 18329760 G A downstream_gene_variant MODIFIER c.*3960G>A| S197
52665 BAA01g29110 A01 18329920 C T splice_acceptor_variant&intron_variant HIGH c.618-1G>A| S131
52666 BAA01g29120 A01 18330740 C T upstream_gene_variant MODIFIER c.-4805C>T| S50
52667 BAA01g29120 A01 18331249 G A upstream_gene_variant MODIFIER c.-4296G>A| S181
52668 BAA01g29110 A01 18333848 A G upstream_gene_variant MODIFIER c.-1619T>C| S55
52669 BAA01g29110 A01 18335024 G A upstream_gene_variant MODIFIER c.-2795C>T| S187
52670 BAA01g29110 A01 18335457 G A upstream_gene_variant MODIFIER c.-3228C>T| S188
52671 BAA01g29110 A01 18335672 C T upstream_gene_variant MODIFIER c.-3443G>A| S251
52672 BAA01g29120 A01 18337209 C T missense_variant MODERATE c.880C>T|p.Leu294Phe S155
S211
52673 BAA01g29120 A01 18337525 C T synonymous_variant LOW c.996C>T|p.Ser332Ser S15
S2
S3
S34
S4
S6
52674 BAA01g29120 A01 18337979 G A intron_variant MODIFIER c.1335+115G>A| S252
52675 BAA01g29120 A01 18338112 A T intron_variant MODIFIER c.1336-90A>T| S86