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
126151 BAA10g14970 A10 15547443 G A upstream_gene_variant MODIFIER c.-1011C>T| S226
126152 BAA10g14970 A10 15547574 C T upstream_gene_variant MODIFIER c.-1142G>A| S33
126153 BAA10g14980 A10 15550755 G A synonymous_variant LOW c.390G>A|p.Gln130Gln S234
126154 BAA10g14980 A10 15550891 G A missense_variant MODERATE c.526G>A|p.Val176Ile S64
126155 BAA10g14990 A10 15551843 G A upstream_gene_variant MODIFIER c.-3247G>A| S151
S263
126156 BAA10g14990 A10 15552112 G A upstream_gene_variant MODIFIER c.-2978G>A| S261
126157 BAA10g14980 A10 15553601 G A missense_variant MODERATE c.2239G>A|p.Asp747Asn S9
126158 BAA10g14980 A10 15553967 C T missense_variant MODERATE c.2605C>T|p.Arg869Trp S45
126159 BAA10g14980 A10 15554036 G A missense_variant MODERATE c.2674G>A|p.Val892Ile S94
126160 BAA10g14980 A10 15554222 G A missense_variant MODERATE c.2860G>A|p.Val954Met S303
126161 BAA10g14980 A10 15554237 G A missense_variant MODERATE c.2875G>A|p.Val959Ile S289
126162 BAA10g14990 A10 15554557 G A upstream_gene_variant MODIFIER c.-533G>A| S13
126163 BAA10g14990 A10 15554815 C T upstream_gene_variant MODIFIER c.-275C>T| S232
126164 BAA10g15000 A10 15555833 C T upstream_gene_variant MODIFIER c.-2195C>T| S8
126165 BAA10g15000 A10 15555860 G A upstream_gene_variant MODIFIER c.-2168G>A| S171
126166 BAA10g14990 A10 15556007 G A missense_variant MODERATE c.356G>A|p.Gly119Glu S195
126167 BAA10g14990 A10 15556885 G A missense_variant MODERATE c.1126G>A|p.Asp376Asn S53
126168 BAA10g15000 A10 15558331 C T synonymous_variant LOW c.207C>T|p.Leu69Leu S107
126169 BAA10g14990 A10 15560611 G A downstream_gene_variant MODIFIER c.*3667G>A| S289
S86
126170 BAA10g15010 A10 15561425 C T missense_variant MODERATE c.3616G>A|p.Asp1206Asn S117
126171 BAA10g15010 A10 15561911 G A missense_variant MODERATE c.3130C>T|p.Pro1044Ser S236
126172 BAA10g15000 A10 15562545 C T downstream_gene_variant MODIFIER c.*1725C>T| S12
126173 BAA10g15010 A10 15563001 C T missense_variant MODERATE c.2332G>A|p.Ala778Thr S297
126174 BAA10g15000 A10 15563063 C T downstream_gene_variant MODIFIER c.*2243C>T| S162
126175 BAA10g15010 A10 15563961 G A synonymous_variant LOW c.1815C>T|p.Gly605Gly S32