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
149501 BAA10g33620 A10 23879795 G A missense_variant MODERATE c.1007G>A|p.Gly336Glu S180
149502 BAA10g33630 A10 23880712 G A upstream_gene_variant MODIFIER c.-305G>A| S43
149503 BAA10g33620 A10 23884792 G A downstream_gene_variant MODIFIER c.*4924G>A| S289
S290
149504 BAA10g33630 A10 23885886 G A downstream_gene_variant MODIFIER c.*2895G>A| S1
149505 BAA10g33630 A10 23885964 C T downstream_gene_variant MODIFIER c.*2973C>T| S143
149506 BAA10g33640 A10 23889570 C T upstream_gene_variant MODIFIER c.-2399G>A| S194
149507 BAA10g33640 A10 23889833 G A upstream_gene_variant MODIFIER c.-2662C>T| S193
149508 BAA10g33650 A10 23892724 C T missense_variant MODERATE c.1660G>A|p.Asp554Asn S279
149509 BAA10g33650 A10 23893139 C T synonymous_variant LOW c.1245G>A|p.Glu415Glu S18
149510 BAA10g33650 A10 23893459 C T missense_variant MODERATE c.925G>A|p.Glu309Lys S86
149511 BAA10g33650 A10 23893937 C T splice_region_variant&synonymous_variant LOW c.447G>A|p.Arg149Arg S247
149512 BAA10g33650 A10 23894357 C T intron_variant MODIFIER c.447-420G>A| S11
149513 BAA10g33650 A10 23894455 C T intron_variant MODIFIER c.447-518G>A| S302
149514 BAA10g33650 A10 23896796 C T upstream_gene_variant MODIFIER c.-1272G>A| S166
149515 BAA10g33650 A10 23898457 A T upstream_gene_variant MODIFIER c.-2933T>A| S180
149516 BAA10g33650 A10 23899680 T C upstream_gene_variant MODIFIER c.-4156A>G| S43
149517 BAA10g33650 A10 23899736 G A upstream_gene_variant MODIFIER c.-4212C>T| S207
149518 BAA10g33650 A10 23899937 G A upstream_gene_variant MODIFIER c.-4413C>T| S43
149519 BAA10g33650 A10 23900373 C T upstream_gene_variant MODIFIER c.-4849G>A| S244
149520 BAA10g33660 A10 23901028 G A downstream_gene_variant MODIFIER c.*1809C>T| S270
149521 BAA10g33660 A10 23902756 G A downstream_gene_variant MODIFIER c.*81C>T| S158
149522 BAA10g33660 A10 23903033 G A missense_variant MODERATE c.1325C>T|p.Ser442Leu S59
149523 BAA10g33660 A10 23903276 C T missense_variant MODERATE c.1082G>A|p.Arg361Lys S36
149524 BAA10g33660 A10 23904075 C T missense_variant MODERATE c.877G>A|p.Glu293Lys S291
149525 BAA10g33660 A10 23904160 G A intron_variant MODIFIER c.850-58C>T| S53