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
118751 BAA10g11160 A10 12812664 G A synonymous_variant LOW c.6G>A|p.Glu2Glu S71
118752 BAA10g11160 A10 12813026 G A missense_variant MODERATE c.368G>A|p.Arg123Lys S81
S85
118753 BAA10g11160 A10 12813127 G A missense_variant MODERATE c.469G>A|p.Glu157Lys S205
118754 BAA10g11160 A10 12814020 C T missense_variant MODERATE c.1202C>T|p.Pro401Leu S110
118755 BAA10g11160 A10 12814196 G A splice_donor_variant&intron_variant HIGH c.1377+1G>A| S262
118756 BAA10g11160 A10 12814484 C T missense_variant MODERATE c.1580C>T|p.Ala527Val S23
118757 BAA10g11170 A10 12814953 C T upstream_gene_variant MODIFIER c.-2610C>T| S104
S52
118758 BAA10g11160 A10 12815096 G A missense_variant MODERATE c.1843G>A|p.Gly615Ser S129
118759 BAA10g11170 A10 12815576 C T upstream_gene_variant MODIFIER c.-1987C>T| S270
118760 BAA10g11170 A10 12815988 C T upstream_gene_variant MODIFIER c.-1575C>T| S297
118761 BAA10g11170 A10 12816496 C T upstream_gene_variant MODIFIER c.-1067C>T| S117
118762 BAA10g11170 A10 12817826 G A missense_variant MODERATE c.173G>A|p.Gly58Glu S75
S81
118763 BAA10g11180 A10 12818847 G A upstream_gene_variant MODIFIER c.-4605G>A| S221
118764 BAA10g11180 A10 12819019 G A upstream_gene_variant MODIFIER c.-4433G>A| S296
118765 BAA10g11180 A10 12820557 G A upstream_gene_variant MODIFIER c.-2895G>A| S155
S211
118766 BAA10g11180 A10 12821857 A T upstream_gene_variant MODIFIER c.-1595A>T| S33
118767 BAA10g11180 A10 12821958 C T upstream_gene_variant MODIFIER c.-1494C>T| S235
118768 BAA10g11180 A10 12822510 C T upstream_gene_variant MODIFIER c.-942C>T| S247
118769 BAA10g11180 A10 12823296 C T upstream_gene_variant MODIFIER c.-156C>T| S40
S49
118770 BAA10g11180 A10 12823538 C T synonymous_variant LOW c.87C>T|p.Leu29Leu S99
118771 BAA10g11180 A10 12823622 G A synonymous_variant LOW c.171G>A|p.Lys57Lys S74
118772 BAA10g11180 A10 12823792 C T missense_variant MODERATE c.341C>T|p.Ala114Val S282
118773 BAA10g11180 A10 12824461 G A intron_variant MODIFIER c.765+102G>A| S125
118774 BAA10g11180 A10 12824823 C T missense_variant MODERATE c.863C>T|p.Ala288Val S166
118775 BAA10g11180 A10 12824936 G A missense_variant MODERATE c.976G>A|p.Glu326Lys S209