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
185501 BAA02g23100 A02 12580961 C T intron_variant MODIFIER c.483-702C>T| S94
185502 BAA02g23100 A02 12580989 G A intron_variant MODIFIER c.483-674G>A| S279
185503 BAA02g23100 A02 12582147 G A missense_variant MODERATE c.967G>A|p.Glu323Lys S44
185504 BAA02g23100 A02 12582303 C T missense_variant MODERATE c.1123C>T|p.Leu375Phe S112
185505 BAA02g23100 A02 12583290 G A downstream_gene_variant MODIFIER c.*505G>A| S70
185506 BAA02g23100 A02 12583900 G A downstream_gene_variant MODIFIER c.*1115G>A| S37
185507 BAA02g23110 A02 12585280 C T upstream_gene_variant MODIFIER c.-4927C>T| S182
185508 BAA02g23110 A02 12585290 G A upstream_gene_variant MODIFIER c.-4917G>A| S187
185509 BAA02g23110 A02 12585297 G A upstream_gene_variant MODIFIER c.-4910G>A| S229
185510 BAA02g23110 A02 12585305 C T upstream_gene_variant MODIFIER c.-4902C>T| S192
185511 BAA02g23110 A02 12586713 C T upstream_gene_variant MODIFIER c.-3494C>T| S261
185512 BAA02g23110 A02 12588223 G A upstream_gene_variant MODIFIER c.-1984G>A| S173
185513 BAA02g23110 A02 12589253 C T upstream_gene_variant MODIFIER c.-954C>T| S289
S290
185514 BAA02g23110 A02 12589762 C T upstream_gene_variant MODIFIER c.-445C>T| S178
185515 BAA02g23110 A02 12590253 G A missense_variant MODERATE c.47G>A|p.Ser16Asn S64
185516 BAA02g23110 A02 12590855 G A intron_variant MODIFIER c.456-29G>A| S50
185517 BAA02g23110 A02 12591860 C T synonymous_variant LOW c.1432C>T|p.Leu478Leu S296
185518 BAA02g23110 A02 12591905 C T missense_variant MODERATE c.1477C>T|p.Pro493Ser S97
185519 BAA02g23110 A02 12591963 C T missense_variant MODERATE c.1535C>T|p.Pro512Leu S94
185520 BAA02g23110 A02 12592055 C T downstream_gene_variant MODIFIER c.*25C>T| S178
185521 BAA02g23110 A02 12592883 C T downstream_gene_variant MODIFIER c.*853C>T| S164
185522 BAA02g23110 A02 12593201 C T downstream_gene_variant MODIFIER c.*1171C>T| S262
185523 BAA02g23110 A02 12593288 C T downstream_gene_variant MODIFIER c.*1258C>T| S268
185524 BAA02g23110 A02 12593408 C T downstream_gene_variant MODIFIER c.*1378C>T| S245
185525 BAA02g23110 A02 12593432 G A downstream_gene_variant MODIFIER c.*1402G>A| S4