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
97901 BAA10g05660 A10 2905589 G A upstream_gene_variant MODIFIER c.-3019C>T| S48
97902 BAA10g05660 A10 2905701 C T upstream_gene_variant MODIFIER c.-3131G>A| S269
97903 BAA10g05660 A10 2905868 C T upstream_gene_variant MODIFIER c.-3298G>A| S177
97904 BAA10g05660 A10 2905919 G A upstream_gene_variant MODIFIER c.-3349C>T| S182
97905 BAA10g05660 A10 2906283 G A upstream_gene_variant MODIFIER c.-3713C>T| S68
97906 BAA10g05660 A10 2906428 C T upstream_gene_variant MODIFIER c.-3858G>A| S114
S25
97907 BAA10g05660 A10 2906591 C T upstream_gene_variant MODIFIER c.-4021G>A| S42
97908 BAA10g05660 A10 2907459 A G upstream_gene_variant MODIFIER c.-4889T>C| S215
97909 BAA10g05680 A10 2911993 G A missense_variant MODERATE c.403C>T|p.Leu135Phe S221
97910 BAA10g05670 A10 2912721 C T downstream_gene_variant MODIFIER c.*2931C>T| S35
97911 BAA10g05670 A10 2912745 G A downstream_gene_variant MODIFIER c.*2955G>A| S274
97912 BAA10g05680 A10 2912982 C T missense_variant MODERATE c.28G>A|p.Gly10Arg S71
97913 BAA10g05680 A10 2913486 G A upstream_gene_variant MODIFIER c.-477C>T| S262
97914 BAA10g05680 A10 2914012 C T upstream_gene_variant MODIFIER c.-1003G>A| S232
97915 BAA10g05690 A10 2914167 C T synonymous_variant LOW c.3192G>A|p.Gln1064Gln S260
97916 BAA10g05690 A10 2915744 G A missense_variant MODERATE c.2222C>T|p.Pro741Leu S233
97917 BAA10g05690 A10 2915784 G A missense_variant MODERATE c.2182C>T|p.Leu728Phe S20
97918 BAA10g05690 A10 2916679 G A splice_region_variant&intron_variant LOW c.1561+8C>T| S208
S219
97919 BAA10g05690 A10 2916716 G A missense_variant MODERATE c.1532C>T|p.Ala511Val S284
97920 BAA10g05680 A10 2917766 G A upstream_gene_variant MODIFIER c.-4757C>T| S202
97921 BAA10g05690 A10 2917886 G A stop_gained HIGH c.853C>T|p.Gln285* S255
97922 BAA10g05700 A10 2920919 C T synonymous_variant LOW c.138C>T|p.Phe46Phe S272
97923 BAA10g05700 A10 2921037 C T missense_variant MODERATE c.256C>T|p.Arg86Cys S204
97924 BAA10g05700 A10 2921194 C T missense_variant MODERATE c.413C>T|p.Ser138Phe S92
97925 BAA10g05690 A10 2921322 C T upstream_gene_variant MODIFIER c.-1709G>A| S177