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
127201 BAA10g15650 A10 15959583 G A upstream_gene_variant MODIFIER c.-2318G>A| S174
S216
S241
S265
127202 BAA10g15650 A10 15959658 G A upstream_gene_variant MODIFIER c.-2243G>A| S59
127203 BAA10g15650 A10 15959675 C T upstream_gene_variant MODIFIER c.-2226C>T| S46
127204 BAA10g15650 A10 15960631 C T upstream_gene_variant MODIFIER c.-1270C>T| S299
127205 BAA10g15650 A10 15961598 G A upstream_gene_variant MODIFIER c.-303G>A| S295
127206 BAA10g15650 A10 15962090 C T missense_variant MODERATE c.190C>T|p.Leu64Phe S33
127207 BAA10g15660 A10 15962692 C T downstream_gene_variant MODIFIER c.*2583G>A| S183
127208 BAA10g15650 A10 15963400 G A missense_variant MODERATE c.775G>A|p.Gly259Arg S68
127209 BAA10g15650 A10 15964598 G A downstream_gene_variant MODIFIER c.*208G>A| S293
127210 BAA10g15660 A10 15965303 C T missense_variant MODERATE c.875G>A|p.Arg292Lys S225
S73
127211 BAA10g15660 A10 15966328 C T missense_variant MODERATE c.79G>A|p.Gly27Arg S189
127212 BAA10g15660 A10 15967678 G A upstream_gene_variant MODIFIER c.-1272C>T| S63
127213 BAA10g15680 A10 15968067 G A missense_variant MODERATE c.25C>T|p.Leu9Phe S283
127214 BAA10g15660 A10 15968431 C T upstream_gene_variant MODIFIER c.-2025G>A| S294
127215 BAA10g15660 A10 15969095 C T upstream_gene_variant MODIFIER c.-2689G>A| S185
127216 BAA10g15690 A10 15969434 C T stop_gained HIGH c.234G>A|p.Trp78* S157
127217 BAA10g15660 A10 15970099 C T upstream_gene_variant MODIFIER c.-3693G>A| S247
127218 BAA10g15660 A10 15970710 G A upstream_gene_variant MODIFIER c.-4304C>T| S43
127219 BAA10g15700 A10 15970930 G A synonymous_variant LOW c.48G>A|p.Lys16Lys S202
127220 BAA10g15700 A10 15970945 G A synonymous_variant LOW c.63G>A|p.Glu21Glu S120
127221 BAA10g15700 A10 15971452 G A missense_variant&splice_region_variant MODERATE c.307G>A|p.Gly103Ser S265
127222 BAA10g15700 A10 15971721 G A missense_variant MODERATE c.485G>A|p.Gly162Glu S35
127223 BAA10g15670 A10 15972620 C T upstream_gene_variant MODIFIER c.-4716G>A| S117
127224 BAA10g15690 A10 15973734 C T upstream_gene_variant MODIFIER c.-3308G>A| S189
127225 BAA10g15690 A10 15973838 C T upstream_gene_variant MODIFIER c.-3412G>A| S236