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
127701 BAA10g16120 A10 16109693 G A upstream_gene_variant MODIFIER c.-2690C>T| S1
S228
S244
S251
S90
127702 BAA10g16120 A10 16109709 G A upstream_gene_variant MODIFIER c.-2706C>T| S132
S137
S215
127703 BAA10g16120 A10 16111153 C T upstream_gene_variant MODIFIER c.-4150G>A| S298
127704 BAA10g16120 A10 16111940 C T upstream_gene_variant MODIFIER c.-4937G>A| S283
127705 BAA10g16120 A10 16111952 C T upstream_gene_variant MODIFIER c.-4949G>A| S283
127706 BAA10g16140 A10 16112037 C T upstream_gene_variant MODIFIER c.-64C>T| S45
127707 BAA10g16130 A10 16112177 C T downstream_gene_variant MODIFIER c.*1239C>T| S170
127708 BAA10g16140 A10 16112581 C T missense_variant MODERATE c.247C>T|p.Leu83Phe S5
127709 BAA10g16140 A10 16112759 G A splice_acceptor_variant&intron_variant HIGH c.316-1G>A| S262
127710 BAA10g16140 A10 16112812 C T missense_variant MODERATE c.368C>T|p.Ser123Phe S10
127711 BAA10g16130 A10 16113079 C T downstream_gene_variant MODIFIER c.*2141C>T| S208
S93
127712 BAA10g16130 A10 16113180 G A downstream_gene_variant MODIFIER c.*2242G>A| S139
127713 BAA10g16140 A10 16113540 G A missense_variant MODERATE c.583G>A|p.Glu195Lys S1
127714 BAA10g16140 A10 16115208 G A missense_variant MODERATE c.2059G>A|p.Gly687Arg S219
127715 BAA10g16140 A10 16115658 C T missense_variant MODERATE c.2341C>T|p.Leu781Phe S237
127716 BAA10g16140 A10 16116189 G A missense_variant MODERATE c.2872G>A|p.Glu958Lys S262
127717 BAA10g16140 A10 16116949 G A missense_variant MODERATE c.3632G>A|p.Ser1211Asn S198
127718 BAA10g16140 A10 16117316 C T missense_variant MODERATE c.3782C>T|p.Pro1261Leu S53
127719 BAA10g16150 A10 16118243 C T upstream_gene_variant MODIFIER c.-1733C>T| S162
127720 BAA10g16140 A10 16118356 G A missense_variant MODERATE c.4736G>A|p.Gly1579Glu S289
127721 BAA10g16140 A10 16118704 G A missense_variant MODERATE c.5084G>A|p.Arg1695Lys S67
127722 BAA10g16140 A10 16118843 C T splice_region_variant&intron_variant LOW c.5128-3C>T| S281
127723 BAA10g16140 A10 16119235 C T synonymous_variant LOW c.5400C>T|p.Asn1800Asn S162
127724 BAA10g16140 A10 16119367 G A synonymous_variant LOW c.5532G>A|p.Lys1844Lys S198
127725 BAA10g16150 A10 16119902 G A upstream_gene_variant MODIFIER c.-74G>A| S159
S243