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
54751 BAA01g29890-BAA01g29900 A01 18983941 C T intergenic_region MODIFIER n.18983941C>T| S275
54752 BAA01g29890-BAA01g29900 A01 18983959 C G intergenic_region MODIFIER n.18983959C>G| S204
54753 BAA01g29900 A01 18985682 C T upstream_gene_variant MODIFIER c.-3477C>T| S192
54754 BAA01g29900 A01 18987216 C T upstream_gene_variant MODIFIER c.-1943C>T| S136
54755 BAA01g29900 A01 18987587 C T upstream_gene_variant MODIFIER c.-1572C>T| S277
54756 BAA01g29900 A01 18987979 C T upstream_gene_variant MODIFIER c.-1180C>T| S166
54757 BAA01g29900 A01 18988377 G A upstream_gene_variant MODIFIER c.-782G>A| S149
54758 BAA01g29900 A01 18988386 C T upstream_gene_variant MODIFIER c.-773C>T| S57
54759 BAA01g29900 A01 18988431 G A upstream_gene_variant MODIFIER c.-728G>A| S188
54760 BAA01g29900 A01 18988682 G A upstream_gene_variant MODIFIER c.-477G>A| S306
S308
54761 BAA01g29900 A01 18988974 C T upstream_gene_variant MODIFIER c.-185C>T| S164
54762 BAA01g29910 A01 18990189 G A upstream_gene_variant MODIFIER c.-3836G>A| S174
54763 BAA01g29910 A01 18990308 G A upstream_gene_variant MODIFIER c.-3717G>A| S144
54764 BAA01g29900 A01 18990437 C T synonymous_variant LOW c.552C>T|p.Asn184Asn S104
S52
54765 BAA01g29910 A01 18990792 C T upstream_gene_variant MODIFIER c.-3233C>T| S177
54766 BAA01g29910 A01 18992114 G A upstream_gene_variant MODIFIER c.-1911G>A| S58
54767 BAA01g29910 A01 18992579 G A upstream_gene_variant MODIFIER c.-1446G>A| S67
54768 BAA01g29910 A01 18992635 G A upstream_gene_variant MODIFIER c.-1390G>A| S38
54769 BAA01g29910 A01 18992731 G A upstream_gene_variant MODIFIER c.-1294G>A| S55
54770 BAA01g29910 A01 18995435 G A missense_variant MODERATE c.1411G>A|p.Glu471Lys S297
54771 BAA01g29900 A01 18995823 G A downstream_gene_variant MODIFIER c.*3588G>A| S281
54772 BAA01g29900 A01 18995976 G A downstream_gene_variant MODIFIER c.*3741G>A| S105
S106
54773 BAA01g29930 A01 18996695 C T missense_variant MODERATE c.104G>A|p.Ser35Asn S120
54774 BAA01g29920 A01 18996941 G A upstream_gene_variant MODIFIER c.-392C>T| S99
54775 BAA01g29920 A01 18997181 G A upstream_gene_variant MODIFIER c.-632C>T| S216