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
174901 BAA02g17580 A02 8766943 G A missense_variant MODERATE c.418C>T|p.Arg140Cys S4
174902 BAA02g17570 A02 8768035 C A upstream_gene_variant MODIFIER c.-4527G>T| S119
S123
S256
S270
174903 BAA02g17570 A02 8768216 G A upstream_gene_variant MODIFIER c.-4708C>T| S59
174904 BAA02g17580 A02 8769459 C T upstream_gene_variant MODIFIER c.-2099G>A| S32
174905 BAA02g17580 A02 8771137 C T upstream_gene_variant MODIFIER c.-3777G>A| S96
174906 BAA02g17590 A02 8771699 G A missense_variant MODERATE c.359C>T|p.Ser120Phe S95
174907 BAA02g17590 A02 8771947 G A synonymous_variant LOW c.111C>T|p.Ile37Ile S296
174908 BAA02g17580 A02 8772221 C T upstream_gene_variant MODIFIER c.-4861G>A| S246
174909 BAA02g17590 A02 8773162 C T upstream_gene_variant MODIFIER c.-1105G>A| S262
174910 BAA02g17590 A02 8773426 C T upstream_gene_variant MODIFIER c.-1369G>A| S275
174911 BAA02g17590 A02 8773744 G A upstream_gene_variant MODIFIER c.-1687C>T| S259
174912 BAA02g17590 A02 8773789 C A upstream_gene_variant MODIFIER c.-1732G>T| S11
S255
S271
S62
S82
174913 BAA02g17590 A02 8774023 C T upstream_gene_variant MODIFIER c.-1966G>A| S105
S106
174914 BAA02g17600 A02 8774171 C T missense_variant MODERATE c.143C>T|p.Pro48Leu S273
174915 BAA02g17600 A02 8774377 G A missense_variant MODERATE c.349G>A|p.Val117Ile S223
174916 BAA02g17600 A02 8774681 C T missense_variant MODERATE c.524C>T|p.Ser175Phe S84
S93
174917 BAA02g17600 A02 8774835 C T missense_variant MODERATE c.584C>T|p.Ala195Val S255
174918 BAA02g17600 A02 8775186 C T synonymous_variant LOW c.700C>T|p.Leu234Leu S234
174919 BAA02g17590 A02 8775469 C T upstream_gene_variant MODIFIER c.-3412G>A| S200
174920 BAA02g17600 A02 8775628 G A missense_variant MODERATE c.823G>A|p.Val275Ile S205
174921 BAA02g17600 A02 8777124 C T synonymous_variant LOW c.1540C>T|p.Leu514Leu S201
174922 BAA02g17600 A02 8777176 G A missense_variant MODERATE c.1592G>A|p.Ser531Asn S50
174923 BAA02g17600 A02 8777447 C T downstream_gene_variant MODIFIER c.*252C>T| S163
174924 BAA02g17600 A02 8778384 C T downstream_gene_variant MODIFIER c.*1189C>T| S9
174925 BAA02g17610 A02 8778524 G A splice_region_variant&intron_variant LOW c.695-3C>T| S289
S290