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
171451 BAA02g15640 A02 7561072 C T upstream_gene_variant MODIFIER c.-2826G>A| S144
171452 BAA02g15640 A02 7561926 G A upstream_gene_variant MODIFIER c.-3680C>T| S172
S217
171453 BAA02g15640 A02 7562752 G A upstream_gene_variant MODIFIER c.-4506C>T| S153
S213
171454 BAA02g15640 A02 7562802 G A upstream_gene_variant MODIFIER c.-4556C>T| S289
171455 BAA02g15640 A02 7563112 C T upstream_gene_variant MODIFIER c.-4866G>A| S270
171456 BAA02g15640-BAA02g15650 A02 7564225 C T intergenic_region MODIFIER n.7564225C>T| S1
S90
171457 BAA02g15640-BAA02g15650 A02 7565270 G A intergenic_region MODIFIER n.7565270G>A| S80
171458 BAA02g15650 A02 7566147 A T downstream_gene_variant MODIFIER c.*4824T>A| S54
171459 BAA02g15650 A02 7566422 G A downstream_gene_variant MODIFIER c.*4549C>T| S148
S30
S31
171460 BAA02g15650 A02 7568435 G A downstream_gene_variant MODIFIER c.*2536C>T| S125
171461 BAA02g15650 A02 7570608 G A downstream_gene_variant MODIFIER c.*363C>T| S176
171462 BAA02g15650 A02 7570984 G A missense_variant MODERATE c.824C>T|p.Ala275Val S113
171463 BAA02g15650 A02 7571003 C T missense_variant MODERATE c.805G>A|p.Glu269Lys S202
171464 BAA02g15650 A02 7571295 G A missense_variant MODERATE c.695C>T|p.Ser232Phe S85
171465 BAA02g15650 A02 7572950 C T upstream_gene_variant MODIFIER c.-727G>A| S32
171466 BAA02g15650 A02 7574167 G A upstream_gene_variant MODIFIER c.-1944C>T| S59
171467 BAA02g15670 A02 7577892 G A upstream_gene_variant MODIFIER c.-3152G>A| S150
171468 BAA02g15670 A02 7577910 C T upstream_gene_variant MODIFIER c.-3134C>T| S276
171469 BAA02g15660 A02 7578647 C T missense_variant MODERATE c.439C>T|p.His147Tyr S210
171470 BAA02g15660 A02 7578756 G A missense_variant MODERATE c.548G>A|p.Gly183Glu S246
171471 BAA02g15660 A02 7579742 G A missense_variant MODERATE c.1169G>A|p.Ser390Asn S67
171472 BAA02g15670 A02 7581134 C T missense_variant MODERATE c.91C>T|p.Arg31Cys S112
171473 BAA02g15670 A02 7581432 G A stop_gained HIGH c.300G>A|p.Trp100* S296
171474 BAA02g15670 A02 7581678 G A synonymous_variant LOW c.468G>A|p.Leu156Leu S183
171475 BAA02g15670 A02 7582112 G A missense_variant MODERATE c.902G>A|p.Arg301His S57