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
139751 BAA10g24950 A10 20365323 C T missense_variant MODERATE c.157G>A|p.Glu53Lys S155
S211
139752 BAA10g24950 A10 20365599 G A synonymous_variant LOW c.60C>T|p.Tyr20Tyr S176
139753 BAA10g24950 A10 20365894 C T upstream_gene_variant MODIFIER c.-236G>A| S23
139754 BAA10g24950 A10 20367444 G A upstream_gene_variant MODIFIER c.-1786C>T| S240
139755 BAA10g24950 A10 20368199 G A upstream_gene_variant MODIFIER c.-2541C>T| S239
139756 BAA10g24950 A10 20368228 C T upstream_gene_variant MODIFIER c.-2570G>A| S47
139757 BAA10g24950 A10 20369269 G A upstream_gene_variant MODIFIER c.-3611C>T| S202
139758 BAA10g24950 A10 20369808 C T upstream_gene_variant MODIFIER c.-4150G>A| S11
139759 BAA10g24960 A10 20371264 C T downstream_gene_variant MODIFIER c.*454C>T| S19
139760 BAA10g24960 A10 20371382 G A downstream_gene_variant MODIFIER c.*572G>A| S151
139761 BAA10g24960 A10 20371533 C T downstream_gene_variant MODIFIER c.*723C>T| S275
139762 BAA10g24960 A10 20371710 G A downstream_gene_variant MODIFIER c.*900G>A| S4
139763 BAA10g24960 A10 20371996 G A downstream_gene_variant MODIFIER c.*1186G>A| S289
S290
139764 BAA10g24970 A10 20374079 G A missense_variant MODERATE c.403C>T|p.Pro135Ser S179
139765 BAA10g24970 A10 20374292 C T missense_variant MODERATE c.190G>A|p.Glu64Lys S281
139766 BAA10g24970 A10 20376138 C T upstream_gene_variant MODIFIER c.-1657G>A| S107
139767 BAA10g24970 A10 20377963 G A upstream_gene_variant MODIFIER c.-3482C>T| S83
139768 BAA10g24970 A10 20378296 G A upstream_gene_variant MODIFIER c.-3815C>T| S70
139769 BAA10g24970 A10 20378862 C T upstream_gene_variant MODIFIER c.-4381G>A| S38
139770 BAA10g24980 A10 20379979 C T upstream_gene_variant MODIFIER c.-3938G>A| S45
139771 BAA10g24990 A10 20380905 A G missense_variant MODERATE c.329A>G|p.Glu110Gly S172
S217
139772 BAA10g25000 A10 20382299 G A downstream_gene_variant MODIFIER c.*2870C>T| S164
139773 BAA10g25000 A10 20382664 C T downstream_gene_variant MODIFIER c.*2505G>A| S153
S213
139774 BAA10g24990 A10 20382744 G A missense_variant MODERATE c.1228G>A|p.Ala410Thr S286
139775 BAA10g24990 A10 20383023 G A missense_variant MODERATE c.1291G>A|p.Asp431Asn S303