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
75451 BAA01g39750 A01 26406186 G A downstream_gene_variant MODIFIER c.*2027G>A| S262
75452 BAA01g39750 A01 26406878 C T downstream_gene_variant MODIFIER c.*2719C>T| S288
75453 BAA01g39750 A01 26407528 C T downstream_gene_variant MODIFIER c.*3369C>T| S279
75454 BAA01g39750 A01 26408195 G A downstream_gene_variant MODIFIER c.*4036G>A| S38
75455 BAA01g39750 A01 26408211 C T downstream_gene_variant MODIFIER c.*4052C>T| S10
75456 BAA01g39750 A01 26408999 C T downstream_gene_variant MODIFIER c.*4840C>T| S279
75457 BAA01g39750-BAA01g39760 A01 26410894 G A intergenic_region MODIFIER n.26410894G>A| S83
S88
75458 BAA01g39750-BAA01g39760 A01 26410979 C T intergenic_region MODIFIER n.26410979C>T| S107
75459 BAA01g39750-BAA01g39760 A01 26411001 C T intergenic_region MODIFIER n.26411001C>T| S201
75460 BAA01g39750-BAA01g39760 A01 26411344 G A intergenic_region MODIFIER n.26411344G>A| S238
75461 BAA01g39760 A01 26411695 C T downstream_gene_variant MODIFIER c.*4952G>A| S275
75462 BAA01g39760 A01 26412000 G A downstream_gene_variant MODIFIER c.*4647C>T| S60
75463 BAA01g39760 A01 26412294 C T downstream_gene_variant MODIFIER c.*4353G>A| S260
75464 BAA01g39760 A01 26412458 G A downstream_gene_variant MODIFIER c.*4189C>T| S212
75465 BAA01g39760 A01 26412703 C T downstream_gene_variant MODIFIER c.*3944G>A| S92
75466 BAA01g39760 A01 26413347 C T downstream_gene_variant MODIFIER c.*3300G>A| S183
S198
75467 BAA01g39760 A01 26413620 C T downstream_gene_variant MODIFIER c.*3027G>A| S56
75468 BAA01g39760 A01 26413705 G A downstream_gene_variant MODIFIER c.*2942C>T| S117
75469 BAA01g39760 A01 26415183 C T downstream_gene_variant MODIFIER c.*1464G>A| S210
S225
75470 BAA01g39760 A01 26416007 C T downstream_gene_variant MODIFIER c.*640G>A| S72
S78
75471 BAA01g39760 A01 26416221 C T downstream_gene_variant MODIFIER c.*426G>A| S183
S198
75472 BAA01g39760 A01 26416791 C T stop_gained HIGH c.1092G>A|p.Trp364* S162
75473 BAA01g39760 A01 26417123 C G intron_variant MODIFIER c.1073-313G>C| S54
75474 BAA01g39760 A01 26417164 G A intron_variant MODIFIER c.1073-354C>T| S116
75475 BAA01g39760 A01 26418705 C T missense_variant MODERATE c.943G>A|p.Glu315Lys S174
S27