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
143651 BAA10g28440 A10 21781568 G A upstream_gene_variant MODIFIER c.-96G>A| S100
143652 BAA10g28440 A10 21781807 C T synonymous_variant LOW c.144C>T|p.Val48Val S129
143653 BAA10g28440 A10 21782987 G A intron_variant MODIFIER c.185+1139G>A| S57
143654 BAA10g28440 A10 21784551 C T intron_variant MODIFIER c.243+177C>T| S295
143655 BAA10g28440 A10 21785525 C T intron_variant MODIFIER c.489+100C>T| S295
143656 BAA10g28440 A10 21785641 C T intron_variant MODIFIER c.489+216C>T| S68
143657 BAA10g28440 A10 21787527 G A intron_variant MODIFIER c.570+1574G>A| S217
143658 BAA10g28440 A10 21788865 G A intron_variant MODIFIER c.571-252G>A| S88
143659 BAA10g28440 A10 21789116 G A splice_acceptor_variant&intron_variant HIGH c.571-1G>A| S134
143660 BAA10g28440 A10 21789253 G A missense_variant MODERATE c.707G>A|p.Gly236Glu S136
143661 BAA10g28440 A10 21789649 G A synonymous_variant LOW c.774G>A|p.Val258Val S127
143662 BAA10g28440 A10 21789764 C T missense_variant MODERATE c.889C>T|p.Pro297Ser S18
143663 BAA10g28440 A10 21790159 C T downstream_gene_variant MODIFIER c.*207C>T| S157
143664 BAA10g28440 A10 21790450 G A downstream_gene_variant MODIFIER c.*498G>A| S233
143665 BAA10g28440 A10 21791000 G A downstream_gene_variant MODIFIER c.*1048G>A| S132
S137
S215
S89
143666 BAA10g28440 A10 21794201 C T downstream_gene_variant MODIFIER c.*4249C>T| S51
143667 BAA10g28450 A10 21795035 G A downstream_gene_variant MODIFIER c.*2758C>T| S255
143668 BAA10g28450 A10 21796026 C T downstream_gene_variant MODIFIER c.*1767G>A| S167
143669 BAA10g28450 A10 21796848 G A downstream_gene_variant MODIFIER c.*945C>T| S94
143670 BAA10g28450 A10 21797218 C T downstream_gene_variant MODIFIER c.*575G>A| S161
143671 BAA10g28450 A10 21797432 G A downstream_gene_variant MODIFIER c.*361C>T| S249
143672 BAA10g28450 A10 21797982 G A intron_variant MODIFIER c.1027-133C>T| S271
143673 BAA10g28450 A10 21798456 A T intron_variant MODIFIER c.1026+100T>A| S174
S216
S241
S27
143674 BAA10g28450 A10 21800557 C T missense_variant MODERATE c.19G>A|p.Glu7Lys S129
143675 BAA10g28450 A10 21800855 G A upstream_gene_variant MODIFIER c.-178C>T| S205