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
175001 BAA02g17620 A02 8792938 G A upstream_gene_variant MODIFIER c.-4915C>T| S177
175002 BAA02g17620 A02 8793005 C T upstream_gene_variant MODIFIER c.-4982G>A| S200
175003 BAA02g17630 A02 8793049 G A upstream_gene_variant MODIFIER c.-3128C>T| S68
175004 BAA02g17630 A02 8793167 C T upstream_gene_variant MODIFIER c.-3246G>A| S119
175005 BAA02g17630 A02 8793614 C T upstream_gene_variant MODIFIER c.-3693G>A| S208
175006 BAA02g17630 A02 8794206 C T upstream_gene_variant MODIFIER c.-4285G>A| S302
175007 BAA02g17630 A02 8794718 C T upstream_gene_variant MODIFIER c.-4797G>A| S295
175008 BAA02g17640 A02 8796026 G A upstream_gene_variant MODIFIER c.-1357C>T| S295
175009 BAA02g17650 A02 8796635 G A missense_variant MODERATE c.862G>A|p.Ala288Thr S296
175010 BAA02g17640 A02 8796738 G A upstream_gene_variant MODIFIER c.-2069C>T| S232
175011 BAA02g17640 A02 8796950 C T upstream_gene_variant MODIFIER c.-2281G>A| S152
175012 BAA02g17660 A02 8797646 G A splice_region_variant&intron_variant LOW c.3009+8C>T| S17
175013 BAA02g17660 A02 8797782 G A splice_region_variant&synonymous_variant LOW c.2881C>T|p.Leu961Leu S205
175014 BAA02g17660 A02 8800117 C T missense_variant MODERATE c.1232G>A|p.Cys411Tyr S18
175015 BAA02g17660 A02 8800530 C T stop_gained HIGH c.852G>A|p.Trp284* S79
175016 BAA02g17660 A02 8800717 C T missense_variant MODERATE c.665G>A|p.Gly222Glu S234
175017 BAA02g17660 A02 8801115 G A synonymous_variant LOW c.267C>T|p.Asn89Asn S37
175018 BAA02g17660 A02 8801787 G A upstream_gene_variant MODIFIER c.-406C>T| S256
175019 BAA02g17660 A02 8802619 C T upstream_gene_variant MODIFIER c.-1238G>A| S165
175020 BAA02g17670 A02 8803543 C T splice_region_variant&synonymous_variant LOW c.655C>T|p.Leu219Leu S175
175021 BAA02g17660 A02 8803887 G A upstream_gene_variant MODIFIER c.-2506C>T| S188
175022 BAA02g17660 A02 8803888 G A upstream_gene_variant MODIFIER c.-2507C>T| S33
175023 BAA02g17680 A02 8805590 C T missense_variant MODERATE c.2855G>A|p.Gly952Glu S175
175024 BAA02g17680 A02 8806352 C T missense_variant MODERATE c.2365G>A|p.Glu789Lys S123
175025 BAA02g17680 A02 8807060 G A missense_variant MODERATE c.2002C>T|p.Leu668Phe S197