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
187851 BAA02g24650 A02 13457119 T A downstream_gene_variant MODIFIER c.*2062T>A| S169
187852 BAA02g24660 A02 13457625 C T missense_variant MODERATE c.140G>A|p.Arg47Lys S33
187853 BAA02g24660 A02 13457992 G A upstream_gene_variant MODIFIER c.-228C>T| S199
187854 BAA02g24660 A02 13458023 G A upstream_gene_variant MODIFIER c.-259C>T| S37
187855 BAA02g24660 A02 13458177 G A upstream_gene_variant MODIFIER c.-413C>T| S103
187856 BAA02g24660 A02 13458747 C T upstream_gene_variant MODIFIER c.-983G>A| S107
187857 BAA02g24660 A02 13458922 G A upstream_gene_variant MODIFIER c.-1158C>T| S211
187858 BAA02g24660 A02 13459242 C T upstream_gene_variant MODIFIER c.-1478G>A| S165
187859 BAA02g24660 A02 13460822 G A upstream_gene_variant MODIFIER c.-3058C>T| S48
187860 BAA02g24670 A02 13463705 G A upstream_gene_variant MODIFIER c.-30G>A| S38
187861 BAA02g24670 A02 13463901 C T missense_variant MODERATE c.167C>T|p.Thr56Ile S283
187862 BAA02g24680 A02 13465259 C T upstream_gene_variant MODIFIER c.-1945C>T| S267
187863 BAA02g24680 A02 13465469 C T upstream_gene_variant MODIFIER c.-1735C>T| S192
187864 BAA02g24680 A02 13465887 C T upstream_gene_variant MODIFIER c.-1317C>T| S194
187865 BAA02g24670 A02 13466758 G A splice_acceptor_variant&intron_variant HIGH c.497-1G>A| S144
187866 BAA02g24680 A02 13466800 C T upstream_gene_variant MODIFIER c.-404C>T| S308
187867 BAA02g24670 A02 13467063 C T synonymous_variant LOW c.672C>T|p.Phe224Phe S283
187868 BAA02g24680 A02 13467321 G A missense_variant MODERATE c.118G>A|p.Glu40Lys S122
187869 BAA02g24670 A02 13468096 C T downstream_gene_variant MODIFIER c.*1006C>T| S289
S290
187870 BAA02g24690 A02 13468287 C T missense_variant MODERATE c.1183G>A|p.Gly395Arg S168
187871 BAA02g24670 A02 13468519 C T downstream_gene_variant MODIFIER c.*1429C>T| S221
187872 BAA02g24690 A02 13468864 G A missense_variant MODERATE c.962C>T|p.Ala321Val S60
187873 BAA02g24690 A02 13469285 C T missense_variant MODERATE c.541G>A|p.Glu181Lys S51
187874 BAA02g24690 A02 13469822 C T missense_variant MODERATE c.4G>A|p.Ala2Thr S171
187875 BAA02g24690 A02 13473911 G A upstream_gene_variant MODIFIER c.-4086C>T| S217
S248