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
70101 BAA01g36740 A01 24555359 C T intron_variant MODIFIER c.1076-57G>A| S178
70102 BAA01g36740 A01 24555941 G A synonymous_variant LOW c.714C>T|p.Val238Val S188
70103 BAA01g36740 A01 24555991 C T missense_variant MODERATE c.664G>A|p.Glu222Lys S128
70104 BAA01g36750 A01 24556230 G A upstream_gene_variant MODIFIER c.-4996G>A| S223
70105 BAA01g36740 A01 24556339 C T missense_variant&splice_region_variant MODERATE c.398G>A|p.Gly133Glu S74
70106 BAA01g36750 A01 24556701 C T upstream_gene_variant MODIFIER c.-4525C>T| S193
70107 BAA01g36740 A01 24557465 C T upstream_gene_variant MODIFIER c.-376G>A| S183
S198
70108 BAA01g36740 A01 24558630 C T upstream_gene_variant MODIFIER c.-1541G>A| S255
S301
S304
70109 BAA01g36740 A01 24558933 C T upstream_gene_variant MODIFIER c.-1844G>A| S182
70110 BAA01g36740 A01 24559396 G A upstream_gene_variant MODIFIER c.-2307C>T| S263
70111 BAA01g36750 A01 24561678 C T missense_variant MODERATE c.355C>T|p.Leu119Phe S303
70112 BAA01g36750 A01 24562151 C T synonymous_variant LOW c.828C>T|p.Thr276Thr S88
70113 BAA01g36750 A01 24562227 C T missense_variant MODERATE c.904C>T|p.Pro302Ser S50
70114 BAA01g36750 A01 24562229 C T synonymous_variant LOW c.906C>T|p.Pro302Pro S299
70115 BAA01g36750 A01 24562237 C T missense_variant MODERATE c.914C>T|p.Ala305Val S94
70116 BAA01g36750 A01 24562297 C T missense_variant MODERATE c.974C>T|p.Pro325Leu S242
70117 BAA01g36750 A01 24562373 C T synonymous_variant LOW c.1050C>T|p.Pro350Pro S200
70118 BAA01g36760 A01 24562604 C T upstream_gene_variant MODIFIER c.-1426C>T| S90
70119 BAA01g36760 A01 24563569 C T upstream_gene_variant MODIFIER c.-461C>T| S50
70120 BAA01g36760 A01 24563852 C T upstream_gene_variant MODIFIER c.-178C>T| S295
70121 BAA01g36760 A01 24564007 C T upstream_gene_variant MODIFIER c.-23C>T| S236
70122 BAA01g36760 A01 24564517 C T synonymous_variant LOW c.408C>T|p.Phe136Phe S94
70123 BAA01g36760 A01 24564593 G A missense_variant MODERATE c.484G>A|p.Gly162Arg S197
70124 BAA01g36750 A01 24567918 G A downstream_gene_variant MODIFIER c.*4986G>A| S8
70125 BAA01g36760 A01 24568851 G A downstream_gene_variant MODIFIER c.*4124G>A| S149