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
184601 BAA02g22670 A02 12296656 C T upstream_gene_variant MODIFIER c.-1856G>A| S164
184602 BAA02g22670 A02 12296810 G A upstream_gene_variant MODIFIER c.-2010C>T| S265
184603 BAA02g22670 A02 12296981 G A upstream_gene_variant MODIFIER c.-2181C>T| S69
184604 BAA02g22670 A02 12297195 G A upstream_gene_variant MODIFIER c.-2395C>T| S247
184605 BAA02g22670 A02 12297502 C T upstream_gene_variant MODIFIER c.-2702G>A| S125
184606 BAA02g22670 A02 12297536 G A upstream_gene_variant MODIFIER c.-2736C>T| S132
S215
S89
184607 BAA02g22670 A02 12298275 G A upstream_gene_variant MODIFIER c.-3475C>T| S132
S215
184608 BAA02g22670 A02 12299364 C T upstream_gene_variant MODIFIER c.-4564G>A| S42
184609 BAA02g22670 A02 12299707 C T upstream_gene_variant MODIFIER c.-4907G>A| S155
184610 BAA02g22680 A02 12299976 G A upstream_gene_variant MODIFIER c.-159G>A| S92
184611 BAA02g22690 A02 12300271 C T downstream_gene_variant MODIFIER c.*4371G>A| S299
184612 BAA02g22690 A02 12300544 C T downstream_gene_variant MODIFIER c.*4098G>A| S33
184613 BAA02g22690 A02 12300793 C T downstream_gene_variant MODIFIER c.*3849G>A| S64
184614 BAA02g22690 A02 12300848 C T downstream_gene_variant MODIFIER c.*3794G>A| S301
S304
184615 BAA02g22690 A02 12301253 C T downstream_gene_variant MODIFIER c.*3389G>A| S267
184616 BAA02g22690 A02 12301645 G A downstream_gene_variant MODIFIER c.*2997C>T| S4
184617 BAA02g22690 A02 12301751 C T downstream_gene_variant MODIFIER c.*2891G>A| S242
184618 BAA02g22680 A02 12302532 C T missense_variant MODERATE c.503C>T|p.Pro168Leu S267
184619 BAA02g22680 A02 12304195 G A downstream_gene_variant MODIFIER c.*1656G>A| S173
184620 BAA02g22680 A02 12304269 G A downstream_gene_variant MODIFIER c.*1730G>A| S303
184621 BAA02g22680 A02 12304494 G A downstream_gene_variant MODIFIER c.*1955G>A| S297
184622 BAA02g22690 A02 12304748 C T missense_variant MODERATE c.542G>A|p.Arg181His S209
184623 BAA02g22690 A02 12304754 C T missense_variant MODERATE c.536G>A|p.Ser179Asn S53
184624 BAA02g22690 A02 12304763 G A missense_variant MODERATE c.527C>T|p.Ala176Val S81
S85
184625 BAA02g22690 A02 12305142 C T synonymous_variant LOW c.327G>A|p.Thr109Thr S15
S156
S3
S34