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
142901 BAA10g27730 A10 21516369 C T missense_variant MODERATE c.779G>A|p.Gly260Glu S259
142902 BAA10g27730 A10 21517382 C T upstream_gene_variant MODIFIER c.-235G>A| S156
142903 BAA10g27730 A10 21517674 C T upstream_gene_variant MODIFIER c.-527G>A| S260
142904 BAA10g27730 A10 21517739 G A upstream_gene_variant MODIFIER c.-592C>T| S212
142905 BAA10g27730 A10 21518638 C T upstream_gene_variant MODIFIER c.-1491G>A| S283
142906 BAA10g27730 A10 21518886 C T upstream_gene_variant MODIFIER c.-1739G>A| S302
142907 BAA10g27730 A10 21519341 G A upstream_gene_variant MODIFIER c.-2194C>T| S298
142908 BAA10g27730 A10 21520074 C T upstream_gene_variant MODIFIER c.-2927G>A| S296
142909 BAA10g27730 A10 21520442 C T upstream_gene_variant MODIFIER c.-3295G>A| S62
142910 BAA10g27730 A10 21520588 C T upstream_gene_variant MODIFIER c.-3441G>A| S98
142911 BAA10g27740 A10 21524129 C T synonymous_variant LOW c.330C>T|p.Val110Val S195
142912 BAA10g27740 A10 21524312 C T synonymous_variant LOW c.438C>T|p.His146His S5
142913 BAA10g27740 A10 21524395 T C intron_variant MODIFIER c.463-14T>C| S244
142914 BAA10g27740 A10 21525117 G A missense_variant MODERATE c.896G>A|p.Ser299Asn S172
S217
142915 BAA10g27740 A10 21526660 G A missense_variant MODERATE c.1757G>A|p.Gly586Glu S205
142916 BAA10g27740 A10 21526871 G A synonymous_variant LOW c.1803G>A|p.Glu601Glu S278
142917 BAA10g27750 A10 21527985 G A upstream_gene_variant MODIFIER c.-4937G>A| S267
142918 BAA10g27750 A10 21528017 T C upstream_gene_variant MODIFIER c.-4905T>C| S212
142919 BAA10g27750 A10 21532589 C T upstream_gene_variant MODIFIER c.-333C>T| S306
S308
142920 BAA10g27750 A10 21532986 C T missense_variant MODERATE c.65C>T|p.Thr22Ile S169
142921 BAA10g27750 A10 21533421 A G missense_variant MODERATE c.500A>G|p.Asp167Gly S38
142922 BAA10g27750 A10 21534006 G A missense_variant MODERATE c.1085G>A|p.Gly362Glu S279
142923 BAA10g27750 A10 21534096 C T missense_variant MODERATE c.1175C>T|p.Ser392Leu S182
142924 BAA10g27750 A10 21534411 C T downstream_gene_variant MODIFIER c.*185C>T| S51
142925 BAA10g27750 A10 21535280 C T downstream_gene_variant MODIFIER c.*1054C>T| S157
S163