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
71001 BAA01g37250-BAA01g37260 A01 24846099 C T intergenic_region MODIFIER n.24846099C>T| S219
S72
71002 BAA01g37260 A01 24846292 C T downstream_gene_variant MODIFIER c.*4839G>A| S174
S27
71003 BAA01g37260 A01 24846388 C T downstream_gene_variant MODIFIER c.*4743G>A| S134
71004 BAA01g37260 A01 24846390 C T downstream_gene_variant MODIFIER c.*4741G>A| S208
S93
71005 BAA01g37260 A01 24846441 C T downstream_gene_variant MODIFIER c.*4690G>A| S269
71006 BAA01g37260 A01 24846577 G A downstream_gene_variant MODIFIER c.*4554C>T| S221
71007 BAA01g37260 A01 24846847 G T downstream_gene_variant MODIFIER c.*4284C>A| S208
S93
71008 BAA01g37260 A01 24848225 C T downstream_gene_variant MODIFIER c.*2906G>A| S247
71009 BAA01g37260 A01 24849884 G A downstream_gene_variant MODIFIER c.*1247C>T| S8
71010 BAA01g37260 A01 24850096 C T downstream_gene_variant MODIFIER c.*1035G>A| S204
71011 BAA01g37260 A01 24851245 C T synonymous_variant LOW c.981G>A|p.Val327Val S275
71012 BAA01g37260 A01 24851399 G A intron_variant MODIFIER c.954+111C>T| S86
71013 BAA01g37260 A01 24851999 G A missense_variant MODERATE c.700C>T|p.Arg234Cys S20
71014 BAA01g37270 A01 24852468 C T upstream_gene_variant MODIFIER c.-3958C>T| S47
71015 BAA01g37260 A01 24852890 G A synonymous_variant LOW c.261C>T|p.Leu87Leu S175
71016 BAA01g37270 A01 24853104 C T upstream_gene_variant MODIFIER c.-3322C>T| S249
71017 BAA01g37260 A01 24853663 C T upstream_gene_variant MODIFIER c.-413G>A| S269
71018 BAA01g37260 A01 24853842 G A upstream_gene_variant MODIFIER c.-592C>T| S35
71019 BAA01g37260 A01 24855319 C T upstream_gene_variant MODIFIER c.-2069G>A| S270
71020 BAA01g37260 A01 24855829 G T upstream_gene_variant MODIFIER c.-2579C>A| S139
71021 BAA01g37260 A01 24855867 G A upstream_gene_variant MODIFIER c.-2617C>T| S129
71022 BAA01g37260 A01 24856127 C T upstream_gene_variant MODIFIER c.-2877G>A| S198
71023 BAA01g37260 A01 24856302 C T upstream_gene_variant MODIFIER c.-3052G>A| S171
71024 BAA01g37260 A01 24856315 G A upstream_gene_variant MODIFIER c.-3065C>T| S263
71025 BAA01g37260 A01 24856776 G A upstream_gene_variant MODIFIER c.-3526C>T| S306
S308