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
127651 BAA10g16070 A10 16094806 C T synonymous_variant LOW c.75C>T|p.Asn25Asn S173
127652 BAA10g16060 A10 16096062 C T upstream_gene_variant MODIFIER c.-1651G>A| S142
127653 BAA10g16060 A10 16096380 G A upstream_gene_variant MODIFIER c.-1969C>T| S126
127654 BAA10g16060 A10 16097013 G A upstream_gene_variant MODIFIER c.-2602C>T| S159
S243
127655 BAA10g16060 A10 16097072 C T upstream_gene_variant MODIFIER c.-2661G>A| S123
127656 BAA10g16060 A10 16097227 G A upstream_gene_variant MODIFIER c.-2816C>T| S53
127657 BAA10g16080 A10 16097697 G A stop_gained HIGH c.141G>A|p.Trp47* S288
127658 BAA10g16080 A10 16097729 C T missense_variant MODERATE c.173C>T|p.Ser58Phe S183
127659 BAA10g16080 A10 16098012 G A synonymous_variant LOW c.384G>A|p.Gln128Gln S176
127660 BAA10g16080 A10 16098041 G A missense_variant MODERATE c.413G>A|p.Gly138Asp S125
127661 BAA10g16080 A10 16099359 C T synonymous_variant LOW c.1407C>T|p.Asn469Asn S204
127662 BAA10g16080 A10 16099448 G A missense_variant MODERATE c.1496G>A|p.Arg499Lys S67
127663 BAA10g16090 A10 16100662 G A missense_variant MODERATE c.125C>T|p.Pro42Leu S186
127664 BAA10g16100 A10 16102393 C T missense_variant MODERATE c.452C>T|p.Ala151Val S42
127665 BAA10g16090 A10 16103360 C T upstream_gene_variant MODIFIER c.-2574G>A| S133
127666 BAA10g16090 A10 16104267 C T upstream_gene_variant MODIFIER c.-3481G>A| S117
127667 BAA10g16110 A10 16104977 C T missense_variant MODERATE c.94C>T|p.Leu32Phe S152
127668 BAA10g16110 A10 16105048 C T splice_region_variant&intron_variant LOW c.162+3C>T| S168
127669 BAA10g16110 A10 16105130 C T missense_variant MODERATE c.173C>T|p.Ala58Val S259
127670 BAA10g16110 A10 16105139 C T missense_variant MODERATE c.182C>T|p.Ser61Phe S8
127671 BAA10g16120 A10 16105794 C T missense_variant MODERATE c.1210G>A|p.Glu404Lys S196
127672 BAA10g16120 A10 16106468 G A missense_variant MODERATE c.536C>T|p.Ala179Val S293
127673 BAA10g16120 A10 16107113 C T upstream_gene_variant MODIFIER c.-110G>A| S123
127674 BAA10g16120 A10 16107281 C T upstream_gene_variant MODIFIER c.-278G>A| S169
127675 BAA10g16120 A10 16108487 G A upstream_gene_variant MODIFIER c.-1484C>T| S50