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
150151 BAA10g34200 A10 24113766 C T missense_variant MODERATE c.422C>T|p.Ser141Leu S48
150152 BAA10g34180 A10 24114369 G A upstream_gene_variant MODIFIER c.-2950C>T| S100
150153 BAA10g34210 A10 24114952 C T missense_variant MODERATE c.194G>A|p.Gly65Glu S110
150154 BAA10g34180 A10 24115950 G A upstream_gene_variant MODIFIER c.-4531C>T| S181
150155 BAA10g34190 A10 24117283 C T upstream_gene_variant MODIFIER c.-4982G>A| S194
150156 BAA10g34210 A10 24117786 C T upstream_gene_variant MODIFIER c.-2641G>A| S308
150157 BAA10g34210 A10 24117864 C T upstream_gene_variant MODIFIER c.-2719G>A| S28
150158 BAA10g34210 A10 24117911 G A upstream_gene_variant MODIFIER c.-2766C>T| S294
150159 BAA10g34230 A10 24119281 T A missense_variant MODERATE c.1166A>T|p.Tyr389Phe S111
150160 BAA10g34230 A10 24119475 G A synonymous_variant LOW c.972C>T|p.Leu324Leu S174
S27
150161 BAA10g34230 A10 24120424 C T missense_variant MODERATE c.445G>A|p.Asp149Asn S161
150162 BAA10g34230 A10 24120747 G A synonymous_variant LOW c.192C>T|p.Tyr64Tyr S268
150163 BAA10g34230 A10 24120932 C T missense_variant MODERATE c.7G>A|p.Glu3Lys S274
150164 BAA10g34230 A10 24121564 G A upstream_gene_variant MODIFIER c.-626C>T| S185
150165 BAA10g34230 A10 24122957 C T upstream_gene_variant MODIFIER c.-2019G>A| S67
150166 BAA10g34240 A10 24123226 G A stop_gained HIGH c.58C>T|p.Gln20* S179
150167 BAA10g34250 A10 24124257 G A synonymous_variant LOW c.225G>A|p.Lys75Lys S95
150168 BAA10g34240 A10 24126644 C T upstream_gene_variant MODIFIER c.-3280G>A| S33
150169 BAA10g34240 A10 24126862 C T upstream_gene_variant MODIFIER c.-3498G>A| S282
150170 BAA10g34240 A10 24127885 G A upstream_gene_variant MODIFIER c.-4521C>T| S203
150171 BAA10g34240 A10 24128271 G A upstream_gene_variant MODIFIER c.-4907C>T| S189
150172 BAA10g34260 A10 24131911 G A upstream_gene_variant MODIFIER c.-4042C>T| S56
150173 BAA10g34280 A10 24138542 A G upstream_gene_variant MODIFIER c.-874T>C| S302
150174 BAA10g34280 A10 24138853 C T upstream_gene_variant MODIFIER c.-1185G>A| S122
150175 BAA10g34280 A10 24139381 G A upstream_gene_variant MODIFIER c.-1713C>T| S288