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
163301 BAA02g10080 A02 4449530 C T upstream_gene_variant MODIFIER c.-803G>A| S116
163302 BAA02g10080 A02 4449571 C T upstream_gene_variant MODIFIER c.-844G>A| S142
163303 BAA02g10090 A02 4451177 G A missense_variant&splice_region_variant MODERATE c.550G>A|p.Glu184Lys S173
163304 BAA02g10090 A02 4451516 C T missense_variant MODERATE c.725C>T|p.Ala242Val S144
163305 BAA02g10090 A02 4451542 G A missense_variant MODERATE c.751G>A|p.Asp251Asn S146
163306 BAA02g10090 A02 4453885 G A downstream_gene_variant MODIFIER c.*788G>A| S45
163307 BAA02g10090 A02 4454567 C T downstream_gene_variant MODIFIER c.*1470C>T| S77
S82
163308 BAA02g10090 A02 4455340 C T downstream_gene_variant MODIFIER c.*2243C>T| S272
163309 BAA02g10090 A02 4456312 G A downstream_gene_variant MODIFIER c.*3215G>A| S51
163310 BAA02g10100 A02 4456794 C T upstream_gene_variant MODIFIER c.-4702C>T| S25
163311 BAA02g10100 A02 4456822 C T upstream_gene_variant MODIFIER c.-4674C>T| S6
163312 BAA02g10100 A02 4459134 G A upstream_gene_variant MODIFIER c.-2362G>A| S84
S93
163313 BAA02g10100 A02 4461498 G A start_lost HIGH c.3G>A|p.Met1? S37
163314 BAA02g10100 A02 4461612 C T synonymous_variant LOW c.117C>T|p.Cys39Cys S179
163315 BAA02g10100 A02 4461703 G A missense_variant MODERATE c.208G>A|p.Asp70Asn S188
163316 BAA02g10100 A02 4463437 G A missense_variant MODERATE c.1208G>A|p.Gly403Glu S131
163317 BAA02g10100 A02 4463564 G A intron_variant MODIFIER c.1244+91G>A| S282
163318 BAA02g10100 A02 4463615 G A intron_variant MODIFIER c.1244+142G>A| S187
163319 BAA02g10100 A02 4463787 C T intron_variant MODIFIER c.1244+314C>T| S234
163320 BAA02g10100 A02 4464432 G A intron_variant MODIFIER c.1245-13G>A| S247
163321 BAA02g10100 A02 4464715 C T synonymous_variant LOW c.1515C>T|p.Ile505Ile S32
163322 BAA02g10100 A02 4467322 G A downstream_gene_variant MODIFIER c.*2568G>A| S166
163323 BAA02g10100 A02 4468787 C T downstream_gene_variant MODIFIER c.*4033C>T| S272
163324 BAA02g10100 A02 4469103 C T downstream_gene_variant MODIFIER c.*4349C>T| S180
163325 BAA02g10100 A02 4469617 C T downstream_gene_variant MODIFIER c.*4863C>T| S305