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
133651 BAA10g20050 A10 18195853 G A synonymous_variant LOW c.1290C>T|p.Ile430Ile S132
S137
S215
S89
133652 BAA10g20040 A10 18196611 G A upstream_gene_variant MODIFIER c.-2222C>T| S125
133653 BAA10g20040 A10 18197880 G A upstream_gene_variant MODIFIER c.-3491C>T| S164
133654 BAA10g20040 A10 18198635 G A upstream_gene_variant MODIFIER c.-4246C>T| S62
133655 BAA10g20040 A10 18198807 C T upstream_gene_variant MODIFIER c.-4418G>A| S210
S225
133656 BAA10g20050 A10 18200281 C T upstream_gene_variant MODIFIER c.-2252G>A| S10
133657 BAA10g20050 A10 18201034 C T upstream_gene_variant MODIFIER c.-3005G>A| S296
133658 BAA10g20050 A10 18202188 C T upstream_gene_variant MODIFIER c.-4159G>A| S142
133659 BAA10g20050 A10 18202998 G A upstream_gene_variant MODIFIER c.-4969C>T| S50
133660 BAA10g20060 A10 18203128 G A synonymous_variant LOW c.99G>A|p.Glu33Glu S216
133661 BAA10g20060 A10 18203199 C T missense_variant MODERATE c.170C>T|p.Ala57Val S195
133662 BAA10g20070 A10 18204319 C T upstream_gene_variant MODIFIER c.-1585C>T| S224
133663 BAA10g20070 A10 18204624 C T upstream_gene_variant MODIFIER c.-1280C>T| S14
133664 BAA10g20070 A10 18205823 C T upstream_gene_variant MODIFIER c.-81C>T| S18
133665 BAA10g20060 A10 18206605 G A downstream_gene_variant MODIFIER c.*3117G>A| S67
133666 BAA10g20060 A10 18207516 C T downstream_gene_variant MODIFIER c.*4028C>T| S292
133667 BAA10g20060 A10 18207544 C T downstream_gene_variant MODIFIER c.*4056C>T| S133
133668 BAA10g20060 A10 18207645 G A downstream_gene_variant MODIFIER c.*4157G>A| S298
133669 BAA10g20060 A10 18207764 C T downstream_gene_variant MODIFIER c.*4276C>T| S230
133670 BAA10g20060 A10 18207831 C T downstream_gene_variant MODIFIER c.*4343C>T| S298
133671 BAA10g20060 A10 18208465 C T downstream_gene_variant MODIFIER c.*4977C>T| S68
133672 BAA10g20070 A10 18208513 C T downstream_gene_variant MODIFIER c.*2175C>T| S209
133673 BAA10g20080 A10 18208641 C T stop_gained HIGH c.396G>A|p.Trp132* S46
133674 BAA10g20080 A10 18208672 C T missense_variant MODERATE c.365G>A|p.Cys122Tyr S26
133675 BAA10g20090 A10 18208809 C T upstream_gene_variant MODIFIER c.-4713C>T| S25