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
111651 BAA10g08320-BAA10g08330 A10 10027637 C T intergenic_region MODIFIER n.10027637C>T| S203
111652 BAA10g08330 A10 10043982 G A missense_variant MODERATE c.130G>A|p.Gly44Arg S228
111653 BAA10g08330 A10 10044481 G A downstream_gene_variant MODIFIER c.*314G>A| S9
111654 BAA10g08330 A10 10044607 C T downstream_gene_variant MODIFIER c.*440C>T| S204
111655 BAA10g08330 A10 10045017 C T downstream_gene_variant MODIFIER c.*850C>T| S256
111656 BAA10g08330 A10 10045300 G A downstream_gene_variant MODIFIER c.*1133G>A| S50
111657 BAA10g08330 A10 10048311 G A downstream_gene_variant MODIFIER c.*4144G>A| S64
111658 BAA10g08330 A10 10048744 G A downstream_gene_variant MODIFIER c.*4577G>A| S209
111659 BAA10g08330-BAA10g08340 A10 10049513 C T intergenic_region MODIFIER n.10049513C>T| S272
111660 BAA10g08330-BAA10g08340 A10 10052915 C T intergenic_region MODIFIER n.10052915C>T| S162
111661 BAA10g08330-BAA10g08340 A10 10053913 T A intergenic_region MODIFIER n.10053913T>A| S247
111662 BAA10g08340 A10 10062506 G A upstream_gene_variant MODIFIER c.-952G>A| S134
111663 BAA10g08340 A10 10062863 G A upstream_gene_variant MODIFIER c.-595G>A| S180
111664 BAA10g08340 A10 10063490 G A synonymous_variant LOW c.33G>A|p.Ser11Ser S155
S211
111665 BAA10g08340 A10 10064160 G A missense_variant MODERATE c.563G>A|p.Cys188Tyr S159
S243
111666 BAA10g08350 A10 10078952 G A downstream_gene_variant MODIFIER c.*3456C>T| S206
111667 BAA10g08350 A10 10079131 C T downstream_gene_variant MODIFIER c.*3277G>A| S193
111668 BAA10g08350 A10 10079325 G A downstream_gene_variant MODIFIER c.*3083C>T| S18
111669 BAA10g08350 A10 10079934 G A downstream_gene_variant MODIFIER c.*2474C>T| S66
111670 BAA10g08350 A10 10080617 C T downstream_gene_variant MODIFIER c.*1791G>A| S68
111671 BAA10g08350 A10 10081392 G A downstream_gene_variant MODIFIER c.*1016C>T| S251
111672 BAA10g08350 A10 10082342 G A downstream_gene_variant MODIFIER c.*66C>T| S15
S3
111673 BAA10g08350 A10 10082760 C T missense_variant MODERATE c.1052G>A|p.Gly351Glu S25
111674 BAA10g08350 A10 10083711 C T intron_variant MODIFIER c.902-801G>A| S270
111675 BAA10g08350 A10 10083987 C T intron_variant MODIFIER c.902-1077G>A| S169