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
105951 BAA10g08160-BAA10g08170 A10 5770623 C T intergenic_region MODIFIER n.5770623C>T| S185
105952 BAA10g08160-BAA10g08170 A10 5771365 C T intergenic_region MODIFIER n.5771365C>T| S193
105953 BAA10g08160-BAA10g08170 A10 5771477 C T intergenic_region MODIFIER n.5771477C>T| S192
105954 BAA10g08160-BAA10g08170 A10 5774616 C T intergenic_region MODIFIER n.5774616C>T| S113
105955 BAA10g08180 A10 5803070 G A upstream_gene_variant MODIFIER c.-4091G>A| S164
105956 BAA10g08180 A10 5804795 G A upstream_gene_variant MODIFIER c.-2366G>A| S17
105957 BAA10g08180 A10 5805019 T C upstream_gene_variant MODIFIER c.-2142T>C| S292
105958 BAA10g08180 A10 5805220 G A upstream_gene_variant MODIFIER c.-1941G>A| S245
105959 BAA10g08180 A10 5805401 G A upstream_gene_variant MODIFIER c.-1760G>A| S53
105960 BAA10g08180 A10 5805886 G A upstream_gene_variant MODIFIER c.-1275G>A| S59
105961 BAA10g08180 A10 5807089 G A upstream_gene_variant MODIFIER c.-72G>A| S120
105962 BAA10g08180 A10 5808309 G A intron_variant MODIFIER c.836+232G>A| S148
S30
S31
105963 BAA10g08180 A10 5809544 C T intron_variant MODIFIER c.1433+20C>T| S10
105964 BAA10g08180 A10 5809725 C T intron_variant MODIFIER c.1434-9C>T| S259
105965 BAA10g08180 A10 5810082 C T intron_variant MODIFIER c.1719-16C>T| S152
S289
105966 BAA10g08180 A10 5810713 G A stop_gained HIGH c.2268G>A|p.Trp756* S69
105967 BAA10g08180 A10 5811590 C T intron_variant MODIFIER c.2937+28C>T| S200
105968 BAA10g08180 A10 5811699 G A missense_variant MODERATE c.2995G>A|p.Ala999Thr S295
105969 BAA10g08180 A10 5812762 G A missense_variant MODERATE c.3763G>A|p.Asp1255Asn S293
105970 BAA10g08180 A10 5813014 G A intron_variant MODIFIER c.3931-39G>A| S172
S217
105971 BAA10g08180 A10 5813071 C T missense_variant MODERATE c.3949C>T|p.Leu1317Phe S162
105972 BAA10g08180 A10 5813664 C T missense_variant MODERATE c.4346C>T|p.Pro1449Leu S256
105973 BAA10g08180-BAA10g08190 A10 5838601 G A intergenic_region MODIFIER n.5838601G>A| S245
105974 BAA10g08180-BAA10g08190 A10 5839252 C T intergenic_region MODIFIER n.5839252C>T| S187
105975 BAA10g08180-BAA10g08190 A10 5839312 G A intergenic_region MODIFIER n.5839312G>A| S18