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
149801 BAA10g33880 A10 23999039 G A downstream_gene_variant MODIFIER c.*3382G>A| S184
149802 BAA10g33900 A10 24001108 C T upstream_gene_variant MODIFIER c.-4356C>T| S229
149803 BAA10g33890 A10 24001989 C T missense_variant MODERATE c.961G>A|p.Asp321Asn S262
149804 BAA10g33900 A10 24002601 C T upstream_gene_variant MODIFIER c.-2863C>T| S186
149805 BAA10g33900 A10 24003149 G A upstream_gene_variant MODIFIER c.-2315G>A| S259
149806 BAA10g33900 A10 24005485 C T missense_variant MODERATE c.22C>T|p.Leu8Phe S10
149807 BAA10g33890 A10 24006480 C T upstream_gene_variant MODIFIER c.-2949G>A| S37
149808 BAA10g33890 A10 24007115 C T upstream_gene_variant MODIFIER c.-3584G>A| S108
149809 BAA10g33890 A10 24007240 C T upstream_gene_variant MODIFIER c.-3709G>A| S282
149810 BAA10g33890 A10 24007388 G A upstream_gene_variant MODIFIER c.-3857C>T| S303
149811 BAA10g33890 A10 24007818 G A upstream_gene_variant MODIFIER c.-4287C>T| S1
S90
149812 BAA10g33910 A10 24008889 G A missense_variant MODERATE c.190C>T|p.Pro64Ser S298
149813 BAA10g33910 A10 24009254 C T upstream_gene_variant MODIFIER c.-176G>A| S44
149814 BAA10g33910 A10 24009637 C T upstream_gene_variant MODIFIER c.-559G>A| S210
S225
149815 BAA10g33910 A10 24009671 G A upstream_gene_variant MODIFIER c.-593C>T| S99
149816 BAA10g33920 A10 24010182 C T missense_variant MODERATE c.19C>T|p.Pro7Ser S45
149817 BAA10g33920 A10 24010204 G A missense_variant MODERATE c.41G>A|p.Arg14Lys S180
149818 BAA10g33910 A10 24010958 C T upstream_gene_variant MODIFIER c.-1880G>A| S218
149819 BAA10g33910 A10 24013712 G A upstream_gene_variant MODIFIER c.-4634C>T| S293
149820 BAA10g33930 A10 24017957 C T missense_variant MODERATE c.140C>T|p.Pro47Leu S116
149821 BAA10g33930 A10 24017989 C T stop_gained HIGH c.172C>T|p.Arg58* S301
S304
149822 BAA10g33930 A10 24019985 C T splice_region_variant&synonymous_variant LOW c.534C>T|p.Arg178Arg S18
149823 BAA10g33930 A10 24020082 G A missense_variant MODERATE c.631G>A|p.Val211Ile S185
149824 BAA10g33940 A10 24020262 C T upstream_gene_variant MODIFIER c.-734C>T| S204
149825 BAA10g33940 A10 24021124 C T synonymous_variant LOW c.129C>T|p.Ala43Ala S144