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
140651 BAA10g25750 A10 20681404 C T upstream_gene_variant MODIFIER c.-4785G>A| S171
S44
140652 BAA10g25760 A10 20681638 C T upstream_gene_variant MODIFIER c.-1839C>T| S123
140653 BAA10g25760 A10 20682390 G A upstream_gene_variant MODIFIER c.-1087G>A| S64
140654 BAA10g25760 A10 20682782 G A upstream_gene_variant MODIFIER c.-695G>A| S278
140655 BAA10g25760 A10 20682821 A T upstream_gene_variant MODIFIER c.-656A>T| S50
140656 BAA10g25770 A10 20684296 C T downstream_gene_variant MODIFIER c.*2355G>A| S286
140657 BAA10g25770 A10 20685016 C T downstream_gene_variant MODIFIER c.*1635G>A| S142
140658 BAA10g25770 A10 20685855 G A downstream_gene_variant MODIFIER c.*796C>T| S228
140659 BAA10g25760 A10 20686040 C T synonymous_variant LOW c.795C>T|p.Ile265Ile S20
140660 BAA10g25760 A10 20686288 G A downstream_gene_variant MODIFIER c.*152G>A| S279
140661 BAA10g25760 A10 20686541 C T downstream_gene_variant MODIFIER c.*405C>T| S56
140662 BAA10g25770 A10 20687214 C T missense_variant MODERATE c.850G>A|p.Ala284Thr S96
140663 BAA10g25760 A10 20687531 A T downstream_gene_variant MODIFIER c.*1395A>T| S184
140664 BAA10g25760 A10 20687780 G A downstream_gene_variant MODIFIER c.*1644G>A| S241
140665 BAA10g25770 A10 20688288 G A missense_variant MODERATE c.187C>T|p.Pro63Ser S128
140666 BAA10g25770 A10 20688859 G A upstream_gene_variant MODIFIER c.-385C>T| S128
140667 BAA10g25780 A10 20691424 G A synonymous_variant LOW c.381C>T|p.Phe127Phe S223
140668 BAA10g25780 A10 20691585 G A missense_variant MODERATE c.220C>T|p.Pro74Ser S130
140669 BAA10g25780 A10 20691621 C T missense_variant MODERATE c.184G>A|p.Glu62Lys S206
S26
140670 BAA10g25790 A10 20693657 C T missense_variant MODERATE c.101C>T|p.Pro34Leu S265
S39
140671 BAA10g25790 A10 20695891 G A synonymous_variant LOW c.2148G>A|p.Arg716Arg S278
140672 BAA10g25790 A10 20695924 C T synonymous_variant LOW c.2181C>T|p.Leu727Leu S294
140673 BAA10g25790 A10 20695950 C T splice_region_variant&intron_variant LOW c.2200+7C>T| S44
140674 BAA10g25790 A10 20696538 C T missense_variant MODERATE c.2710C>T|p.Pro904Ser S168
140675 BAA10g25790 A10 20696997 G A missense_variant MODERATE c.3169G>A|p.Glu1057Lys S39