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
90001 BAA10g00140 A10 68435 C T upstream_gene_variant MODIFIER c.-2896G>A| S294
90002 BAA10g00160 A10 68847 C T missense_variant MODERATE c.1069G>A|p.Gly357Arg S246
90003 BAA10g00160 A10 68956 C T synonymous_variant LOW c.960G>A|p.Ala320Ala S108
90004 BAA10g00160 A10 69056 C T missense_variant MODERATE c.860G>A|p.Arg287His S56
90005 BAA10g00160 A10 69122 C T missense_variant MODERATE c.794G>A|p.Gly265Glu S206
S26
90006 BAA10g00160 A10 69688 C T missense_variant MODERATE c.297G>A|p.Met99Ile S139
90007 BAA10g00140 A10 70009 G A upstream_gene_variant MODIFIER c.-4470C>T| S211
S227
90008 BAA10g00140 A10 70140 C T upstream_gene_variant MODIFIER c.-4601G>A| S135
90009 BAA10g00140 A10 70539 C T upstream_gene_variant MODIFIER c.-5000G>A| S203
90010 BAA10g00160 A10 70889 C T upstream_gene_variant MODIFIER c.-905G>A| S108
90011 BAA10g00160 A10 71762 G A upstream_gene_variant MODIFIER c.-1778C>T| S82
S92
90012 BAA10g00160 A10 72499 G A upstream_gene_variant MODIFIER c.-2515C>T| S217
90013 BAA10g00160 A10 72808 G A upstream_gene_variant MODIFIER c.-2824C>T| S205
90014 BAA10g00160 A10 73093 G A upstream_gene_variant MODIFIER c.-3109C>T| S148
S30
90015 BAA10g00160 A10 74318 G A upstream_gene_variant MODIFIER c.-4334C>T| S4
90016 BAA10g00160 A10 74341 C T upstream_gene_variant MODIFIER c.-4357G>A| S174
90017 BAA10g00160 A10 74545 G A upstream_gene_variant MODIFIER c.-4561C>T| S41
90018 BAA10g00160 A10 74641 C T upstream_gene_variant MODIFIER c.-4657G>A| S275
90019 BAA10g00170 A10 76607 C T downstream_gene_variant MODIFIER c.*907G>A| S28
90020 BAA10g00170 A10 76684 G A downstream_gene_variant MODIFIER c.*830C>T| S64
90021 BAA10g00170 A10 77062 G A downstream_gene_variant MODIFIER c.*452C>T| S283
90022 BAA10g00170 A10 78418 C T intron_variant MODIFIER c.2520+37G>A| S124
S259
90023 BAA10g00170 A10 78442 C T intron_variant MODIFIER c.2520+13G>A| S62
90024 BAA10g00170 A10 78484 C T missense_variant MODERATE c.2491G>A|p.Ala831Thr S202
90025 BAA10g00180 A10 78791 C T downstream_gene_variant MODIFIER c.*4920G>A| S152