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
137851 BAA10g23450 A10 19721153 G A synonymous_variant LOW c.738C>T|p.Leu246Leu S284
137852 BAA10g23440 A10 19721938 C T upstream_gene_variant MODIFIER c.-3636G>A| S129
S195
137853 BAA10g23450 A10 19722076 G A missense_variant MODERATE c.299C>T|p.Thr100Ile S219
S72
137854 BAA10g23450 A10 19722324 C T stop_gained HIGH c.51G>A|p.Trp17* S41
137855 BAA10g23440 A10 19722822 G A upstream_gene_variant MODIFIER c.-4520C>T| S128
137856 BAA10g23460 A10 19723308 G A missense_variant MODERATE c.2072C>T|p.Ala691Val S18
137857 BAA10g23460 A10 19723336 C T missense_variant MODERATE c.2044G>A|p.Glu682Lys S140
137858 BAA10g23460 A10 19724249 C T synonymous_variant LOW c.1680G>A|p.Ser560Ser S55
137859 BAA10g23450 A10 19724837 G A upstream_gene_variant MODIFIER c.-2463C>T| S182
137860 BAA10g23450 A10 19725072 C T upstream_gene_variant MODIFIER c.-2698G>A| S49
137861 BAA10g23460 A10 19725320 C T missense_variant MODERATE c.1436G>A|p.Arg479Lys S292
137862 BAA10g23450 A10 19726016 G A upstream_gene_variant MODIFIER c.-3642C>T| S37
137863 BAA10g23460 A10 19726505 G A missense_variant MODERATE c.932C>T|p.Ala311Val S295
137864 BAA10g23450 A10 19726986 G A upstream_gene_variant MODIFIER c.-4612C>T| S271
137865 BAA10g23460 A10 19729248 C T upstream_gene_variant MODIFIER c.-1249G>A| S201
137866 BAA10g23470 A10 19730204 G A missense_variant MODERATE c.43G>A|p.Gly15Ser S240
137867 BAA10g23470 A10 19730514 C T missense_variant MODERATE c.353C>T|p.Ser118Phe S234
137868 BAA10g23470 A10 19730738 C T missense_variant MODERATE c.577C>T|p.Pro193Ser S266
137869 BAA10g23470 A10 19731370 G A missense_variant MODERATE c.931G>A|p.Glu311Lys S83
S88
137870 BAA10g23460 A10 19731441 C T upstream_gene_variant MODIFIER c.-3442G>A| S150
137871 BAA10g23460 A10 19731838 G A upstream_gene_variant MODIFIER c.-3839C>T| S203
137872 BAA10g23470 A10 19731988 G A missense_variant MODERATE c.1330G>A|p.Asp444Asn S212
137873 BAA10g23470 A10 19732513 C T missense_variant MODERATE c.1754C>T|p.Ser585Phe S183
137874 BAA10g23470 A10 19733094 C T missense_variant MODERATE c.2335C>T|p.Pro779Ser S294
137875 BAA10g23480 A10 19733840 C T upstream_gene_variant MODIFIER c.-1730C>T| S146