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
190601 BAA02g25950 A02 14387838 C T missense_variant MODERATE c.335C>T|p.Ser112Phe S233
190602 BAA02g25950 A02 14387906 G A missense_variant MODERATE c.403G>A|p.Asp135Asn S5
190603 BAA02g25950 A02 14388034 G A synonymous_variant LOW c.531G>A|p.Thr177Thr S210
190604 BAA02g25940 A02 14388280 C T upstream_gene_variant MODIFIER c.-1944G>A| S157
S163
190605 BAA02g25940 A02 14388345 C T upstream_gene_variant MODIFIER c.-2009G>A| S120
190606 BAA02g25940 A02 14389325 G A upstream_gene_variant MODIFIER c.-2989C>T| S17
190607 BAA02g25940 A02 14389927 C T upstream_gene_variant MODIFIER c.-3591G>A| S180
190608 BAA02g25960 A02 14390241 C T missense_variant MODERATE c.191C>T|p.Ala64Val S9
190609 BAA02g25960 A02 14390547 C T missense_variant MODERATE c.338C>T|p.Pro113Leu S183
S198
190610 BAA02g25960 A02 14390588 C T missense_variant MODERATE c.379C>T|p.His127Tyr S242
190611 BAA02g25970 A02 14392307 C T upstream_gene_variant MODIFIER c.-701C>T| S240
190612 BAA02g25970 A02 14392525 G A upstream_gene_variant MODIFIER c.-483G>A| S105
190613 BAA02g25970 A02 14392991 C T upstream_gene_variant MODIFIER c.-17C>T| S83
190614 BAA02g25980 A02 14394112 G A upstream_gene_variant MODIFIER c.-2430G>A| S247
190615 BAA02g25980 A02 14394571 G A upstream_gene_variant MODIFIER c.-1971G>A| S293
190616 BAA02g25980 A02 14394666 G A upstream_gene_variant MODIFIER c.-1876G>A| S259
190617 BAA02g25970 A02 14394747 G A missense_variant MODERATE c.475G>A|p.Ala159Thr S231
190618 BAA02g25980 A02 14395194 G A upstream_gene_variant MODIFIER c.-1348G>A| S187
190619 BAA02g25980 A02 14395534 C T upstream_gene_variant MODIFIER c.-1008C>T| S25
S264
190620 BAA02g25980 A02 14395722 C T upstream_gene_variant MODIFIER c.-820C>T| S195
190621 BAA02g25980 A02 14396554 G A missense_variant MODERATE c.13G>A|p.Gly5Arg S294
190622 BAA02g25980 A02 14396623 C T missense_variant MODERATE c.82C>T|p.Leu28Phe S135
190623 BAA02g25980 A02 14396894 C T missense_variant MODERATE c.278C>T|p.Ala93Val S112
190624 BAA02g25980 A02 14396972 C T missense_variant MODERATE c.356C>T|p.Pro119Leu S100
S104
190625 BAA02g25970 A02 14397507 G A downstream_gene_variant MODIFIER c.*2509G>A| S122