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
43851 BAA01g26770 A01 15049317 G A upstream_gene_variant MODIFIER c.-1426G>A| S157
43852 BAA01g26770 A01 15049476 C T upstream_gene_variant MODIFIER c.-1267C>T| S51
43853 BAA01g26770 A01 15049484 G A upstream_gene_variant MODIFIER c.-1259G>A| S46
43854 BAA01g26770 A01 15049555 G A upstream_gene_variant MODIFIER c.-1188G>A| S280
43855 BAA01g26770 A01 15049743 C T upstream_gene_variant MODIFIER c.-1000C>T| S176
43856 BAA01g26770 A01 15049868 G A upstream_gene_variant MODIFIER c.-875G>A| S122
43857 BAA01g26770 A01 15049922 G A upstream_gene_variant MODIFIER c.-821G>A| S232
43858 BAA01g26770 A01 15050143 G A upstream_gene_variant MODIFIER c.-600G>A| S14
S140
43859 BAA01g26770 A01 15052097 G A missense_variant MODERATE c.1057G>A|p.Asp353Asn S292
43860 BAA01g26770 A01 15052226 C T missense_variant MODERATE c.1186C>T|p.Leu396Phe S99
43861 BAA01g26770 A01 15053091 C T downstream_gene_variant MODIFIER c.*74C>T| S75
43862 BAA01g26770 A01 15053443 C T downstream_gene_variant MODIFIER c.*426C>T| S148
S30
S31
43863 BAA01g26770 A01 15053914 G A downstream_gene_variant MODIFIER c.*897G>A| S209
43864 BAA01g26770 A01 15054254 C T downstream_gene_variant MODIFIER c.*1237C>T| S28
43865 BAA01g26770 A01 15054432 C T downstream_gene_variant MODIFIER c.*1415C>T| S20
43866 BAA01g26770 A01 15054619 G A downstream_gene_variant MODIFIER c.*1602G>A| S149
43867 BAA01g26770 A01 15054641 G A downstream_gene_variant MODIFIER c.*1624G>A| S244
43868 BAA01g26770 A01 15055517 G A downstream_gene_variant MODIFIER c.*2500G>A| S281
43869 BAA01g26770 A01 15057234 C T downstream_gene_variant MODIFIER c.*4217C>T| S111
43870 BAA01g26770 A01 15057497 G A downstream_gene_variant MODIFIER c.*4480G>A| S302
43871 BAA01g26770 A01 15057865 C A downstream_gene_variant MODIFIER c.*4848C>A| S78
43872 BAA01g26770 A01 15057971 C T downstream_gene_variant MODIFIER c.*4954C>T| S302
43873 BAA01g26780 A01 15058293 C T downstream_gene_variant MODIFIER c.*648G>A| S203
43874 BAA01g26780 A01 15058489 G A downstream_gene_variant MODIFIER c.*452C>T| S244
43875 BAA01g26780 A01 15058539 G A downstream_gene_variant MODIFIER c.*402C>T| S191
S235