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
89801 BAA01g47420-CHR_END A01 32538717 C T intergenic_region MODIFIER n.32538717C>T| S172
S217
89802 BAA01g47420-CHR_END A01 32539896 C T intergenic_region MODIFIER n.32539896C>T| S302
89803 BAA01g47420-CHR_END A01 32540004 C G intergenic_region MODIFIER n.32540004C>G| S216
89804 BAA01g47420-CHR_END A01 32540358 G A intergenic_region MODIFIER n.32540358G>A| S1
S90
89805 BAA01g47420-CHR_END A01 32542068 C T intergenic_region MODIFIER n.32542068C>T| S74
89806 BAA01g47420-CHR_END A01 32560345 G A intergenic_region MODIFIER n.32560345G>A| S261
89807 BAA01g47420-CHR_END A01 32560348 G A intergenic_region MODIFIER n.32560348G>A| S148
S30
S31
89808 BAA10g00010 A10 4508 C T upstream_gene_variant MODIFIER c.-2068G>A| S40
S49
89809 BAA10g00010 A10 4987 G A upstream_gene_variant MODIFIER c.-2547C>T| S223
89810 BAA10g00010 A10 6635 C T upstream_gene_variant MODIFIER c.-4195G>A| S264
89811 BAA10g00010 A10 7427 C T upstream_gene_variant MODIFIER c.-4987G>A| S249
89812 BAA10g00020 A10 7522 C T upstream_gene_variant MODIFIER c.-3052C>T| S6
89813 BAA10g00020 A10 8097 C T upstream_gene_variant MODIFIER c.-2477C>T| S42
89814 BAA10g00020 A10 8856 G A upstream_gene_variant MODIFIER c.-1718G>A| S223
89815 BAA10g00020 A10 8889 G A upstream_gene_variant MODIFIER c.-1685G>A| S262
89816 BAA10g00020 A10 9263 G A upstream_gene_variant MODIFIER c.-1311G>A| S192
89817 BAA10g00020 A10 9640 G A upstream_gene_variant MODIFIER c.-934G>A| S94
89818 BAA10g00020 A10 9820 G A upstream_gene_variant MODIFIER c.-754G>A| S290
89819 BAA10g00020 A10 9844 G A upstream_gene_variant MODIFIER c.-730G>A| S212
89820 BAA10g00020 A10 10231 C T upstream_gene_variant MODIFIER c.-343C>T| S204
89821 BAA10g00020 A10 10454 G A upstream_gene_variant MODIFIER c.-120G>A| S217
89822 BAA10g00020 A10 11783 G A downstream_gene_variant MODIFIER c.*330G>A| S9
89823 BAA10g00040 A10 13709 C T missense_variant MODERATE c.667G>A|p.Asp223Asn S143
89824 BAA10g00040 A10 13932 G A synonymous_variant LOW c.444C>T|p.Val148Val S134
89825 BAA10g00040 A10 14401 G A missense_variant MODERATE c.41C>T|p.Ala14Val S278