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
162751 BAA02g09640 A02 4239141 G A missense_variant MODERATE c.98C>T|p.Pro33Leu S84
S93
162752 BAA02g09640 A02 4240415 C T upstream_gene_variant MODIFIER c.-1177G>A| S144
162753 BAA02g09650 A02 4241103 C T missense_variant MODERATE c.190C>T|p.Leu64Phe S178
162754 BAA02g09640 A02 4242309 G A upstream_gene_variant MODIFIER c.-3071C>T| S171
162755 BAA02g09640 A02 4242369 C T upstream_gene_variant MODIFIER c.-3131G>A| S174
S216
S265
S39
162756 BAA02g09640 A02 4243254 C T upstream_gene_variant MODIFIER c.-4016G>A| S31
162757 BAA02g09640 A02 4243609 C T upstream_gene_variant MODIFIER c.-4371G>A| S123
162758 BAA02g09650 A02 4244740 G A downstream_gene_variant MODIFIER c.*2737G>A| S17
162759 BAA02g09650 A02 4245086 C T downstream_gene_variant MODIFIER c.*3083C>T| S128
162760 BAA02g09650 A02 4245577 G A downstream_gene_variant MODIFIER c.*3574G>A| S188
162761 BAA02g09650 A02 4246752 C T downstream_gene_variant MODIFIER c.*4749C>T| S70
162762 BAA02g09650 A02 4246886 C T downstream_gene_variant MODIFIER c.*4883C>T| S198
162763 BAA02g09660 A02 4247686 C T downstream_gene_variant MODIFIER c.*1161G>A| S266
162764 BAA02g09660 A02 4248864 G A missense_variant MODERATE c.415C>T|p.Pro139Ser S239
162765 BAA02g09660 A02 4249222 C T stop_gained HIGH c.57G>A|p.Trp19* S42
162766 BAA02g09660 A02 4249813 G A upstream_gene_variant MODIFIER c.-535C>T| S279
162767 BAA02g09660 A02 4251552 C T upstream_gene_variant MODIFIER c.-2274G>A| S226
162768 BAA02g09660 A02 4251652 C T upstream_gene_variant MODIFIER c.-2374G>A| S262
162769 BAA02g09660 A02 4251688 G A upstream_gene_variant MODIFIER c.-2410C>T| S12
162770 BAA02g09660 A02 4251983 G A upstream_gene_variant MODIFIER c.-2705C>T| S122
162771 BAA02g09660 A02 4252577 C T upstream_gene_variant MODIFIER c.-3299G>A| S8
162772 BAA02g09660 A02 4253409 G A upstream_gene_variant MODIFIER c.-4131C>T| S264
162773 BAA02g09670 A02 4253589 C T missense_variant MODERATE c.388G>A|p.Gly130Arg S18
162774 BAA02g09670 A02 4255628 G A upstream_gene_variant MODIFIER c.-1652C>T| S294
162775 BAA02g09670 A02 4255718 G A upstream_gene_variant MODIFIER c.-1742C>T| S10