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
4451 BAA01g03600 A01 1630219 C T downstream_gene_variant MODIFIER c.*1558C>T| S137
4452 BAA01g03610 A01 1633476 C T upstream_gene_variant MODIFIER c.-1065G>A| S171
4453 BAA01g03610 A01 1634105 G A upstream_gene_variant MODIFIER c.-1694C>T| S294
4454 BAA01g03610 A01 1634596 C T upstream_gene_variant MODIFIER c.-2185G>A| S192
4455 BAA01g03610 A01 1635424 C T upstream_gene_variant MODIFIER c.-3013G>A| S45
4456 BAA01g03610 A01 1636076 G A upstream_gene_variant MODIFIER c.-3665C>T| S177
4457 BAA01g03610 A01 1636581 C T upstream_gene_variant MODIFIER c.-4170G>A| S35
4458 BAA01g03610 A01 1636923 C T upstream_gene_variant MODIFIER c.-4512G>A| S194
4459 BAA01g03610 A01 1637061 C T upstream_gene_variant MODIFIER c.-4650G>A| S252
4460 BAA01g03620 A01 1638034 C T missense_variant MODERATE c.280C>T|p.Pro94Ser S302
4461 BAA01g03620 A01 1638155 C T missense_variant MODERATE c.401C>T|p.Pro134Leu S126
4462 BAA01g03620 A01 1639075 G A missense_variant MODERATE c.1321G>A|p.Glu441Lys S85
4463 BAA01g03620 A01 1639132 G A missense_variant MODERATE c.1378G>A|p.Asp460Asn S284
4464 BAA01g03620 A01 1639309 C T missense_variant MODERATE c.1555C>T|p.Leu519Phe S182
4465 BAA01g03620 A01 1639422 C T synonymous_variant LOW c.1668C>T|p.Thr556Thr S176
4466 BAA01g03620 A01 1639807 C T missense_variant MODERATE c.1973C>T|p.Pro658Leu S81
S85
4467 BAA01g03620 A01 1639868 C T synonymous_variant LOW c.2034C>T|p.Arg678Arg S113
4468 BAA01g03620 A01 1639885 C T missense_variant MODERATE c.2051C>T|p.Ser684Phe S206
S26
4469 BAA01g03620 A01 1639900 C T missense_variant MODERATE c.2066C>T|p.Ala689Val S152
4470 BAA01g03620 A01 1640123 C T synonymous_variant LOW c.2289C>T|p.Ile763Ile S32
4471 BAA01g03620 A01 1640737 C T missense_variant MODERATE c.2903C>T|p.Ala968Val S4
4472 BAA01g03620 A01 1640909 C T synonymous_variant LOW c.3075C>T|p.Arg1025Arg S242
4473 BAA01g03620 A01 1641128 C T intron_variant MODIFIER c.3141+153C>T| S97
4474 BAA01g03620 A01 1641132 C T intron_variant MODIFIER c.3141+157C>T| S203
4475 BAA01g03620 A01 1641498 C T intron_variant MODIFIER c.3142-264C>T| S107