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
162901 BAA02g09750 A02 4296428 G A upstream_gene_variant MODIFIER c.-4037G>A| S165
162902 BAA02g09750 A02 4296770 C T upstream_gene_variant MODIFIER c.-3695C>T| S182
162903 BAA02g09750 A02 4298282 T A upstream_gene_variant MODIFIER c.-2183T>A| S17
S18
S186
S267
S282
162904 BAA02g09740 A02 4299008 G A missense_variant MODERATE c.68C>T|p.Ser23Phe S36
162905 BAA02g09760 A02 4301840 C T missense_variant MODERATE c.386G>A|p.Gly129Glu S46
162906 BAA02g09760 A02 4302095 C T missense_variant MODERATE c.131G>A|p.Arg44Lys S218
162907 BAA02g09760 A02 4302186 C T missense_variant MODERATE c.40G>A|p.Glu14Lys S40
S49
162908 BAA02g09740 A02 4302410 G A upstream_gene_variant MODIFIER c.-3033C>T| S245
162909 BAA02g09740 A02 4303138 C T upstream_gene_variant MODIFIER c.-3761G>A| S293
162910 BAA02g09760 A02 4305265 G A upstream_gene_variant MODIFIER c.-3040C>T| S187
162911 BAA02g09760 A02 4306440 G A upstream_gene_variant MODIFIER c.-4215C>T| S70
162912 BAA02g09770 A02 4306767 G A missense_variant MODERATE c.253G>A|p.Ala85Thr S36
162913 BAA02g09770 A02 4307267 C T downstream_gene_variant MODIFIER c.*23C>T| S69
162914 BAA02g09780 A02 4309859 C T missense_variant MODERATE c.139G>A|p.Glu47Lys S156
S34
162915 BAA02g09780 A02 4310253 G A upstream_gene_variant MODIFIER c.-256C>T| S30
162916 BAA02g09780 A02 4311672 G A upstream_gene_variant MODIFIER c.-1675C>T| S208
162917 BAA02g09780 A02 4312171 G A upstream_gene_variant MODIFIER c.-2174C>T| S107
162918 BAA02g09780 A02 4312961 C T upstream_gene_variant MODIFIER c.-2964G>A| S135
162919 BAA02g09780 A02 4314154 G A upstream_gene_variant MODIFIER c.-4157C>T| S170
162920 BAA02g09790 A02 4315021 G A intron_variant MODIFIER c.2237+114C>T| S79
S91
162921 BAA02g09790 A02 4316206 C T missense_variant MODERATE c.1657G>A|p.Gly553Arg S167
162922 BAA02g09790 A02 4316544 G A intron_variant MODIFIER c.1638+86C>T| S45
162923 BAA02g09790 A02 4316840 C T synonymous_variant LOW c.1428G>A|p.Arg476Arg S200
162924 BAA02g09790 A02 4317220 G A intron_variant MODIFIER c.1286+57C>T| S291
162925 BAA02g09790 A02 4317316 G A missense_variant MODERATE c.1247C>T|p.Ala416Val S50