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
161001 BAA02g08120 A02 3499302 G A upstream_gene_variant MODIFIER c.-2899C>T| S133
161002 BAA02g08120 A02 3499386 C T upstream_gene_variant MODIFIER c.-2983G>A| S95
161003 BAA02g08120 A02 3499429 G A upstream_gene_variant MODIFIER c.-3026C>T| S256
161004 BAA02g08120 A02 3499456 C T upstream_gene_variant MODIFIER c.-3053G>A| S301
S304
161005 BAA02g08140 A02 3502505 C T missense_variant MODERATE c.2782G>A|p.Val928Met S63
161006 BAA02g08130 A02 3502584 C T upstream_gene_variant MODIFIER c.-4878G>A| S183
S198
161007 BAA02g08140 A02 3503127 G A missense_variant MODERATE c.2242C>T|p.Leu748Phe S205
161008 BAA02g08140 A02 3503560 G A synonymous_variant LOW c.1809C>T|p.Phe603Phe S82
S92
161009 BAA02g08140 A02 3503710 G A synonymous_variant LOW c.1659C>T|p.Leu553Leu S4
161010 BAA02g08140 A02 3504390 C T missense_variant MODERATE c.979G>A|p.Glu327Lys S6
161011 BAA02g08140 A02 3505230 G A synonymous_variant LOW c.243C>T|p.Cys81Cys S84
S93
161012 BAA02g08140 A02 3505692 C T upstream_gene_variant MODIFIER c.-139G>A| S249
161013 BAA02g08150 A02 3507132 G T missense_variant MODERATE c.40C>A|p.His14Asn S18
161014 BAA02g08140 A02 3507412 C T upstream_gene_variant MODIFIER c.-1859G>A| S46
161015 BAA02g08170 A02 3508286 C T synonymous_variant LOW c.267G>A|p.Glu89Glu S218
161016 BAA02g08140 A02 3508617 C T upstream_gene_variant MODIFIER c.-3064G>A| S280
161017 BAA02g08140 A02 3509571 G A upstream_gene_variant MODIFIER c.-4018C>T| S198
161018 BAA02g08140 A02 3509599 G A upstream_gene_variant MODIFIER c.-4046C>T| S294
161019 BAA02g08150 A02 3511009 C T upstream_gene_variant MODIFIER c.-3838G>A| S108
161020 BAA02g08150 A02 3511091 C T upstream_gene_variant MODIFIER c.-3920G>A| S240
161021 BAA02g08150 A02 3511552 A T upstream_gene_variant MODIFIER c.-4381T>A| S203
161022 BAA02g08190 A02 3512664 C T synonymous_variant LOW c.702G>A|p.Pro234Pro S179
161023 BAA02g08190 A02 3512713 C T missense_variant MODERATE c.653G>A|p.Gly218Glu S178
161024 BAA02g08180 A02 3514666 C T upstream_gene_variant MODIFIER c.-3787G>A| S270
161025 BAA02g08180 A02 3514935 C T upstream_gene_variant MODIFIER c.-4056G>A| S9