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
134401 BAA10g20590 A10 18458555 C T downstream_gene_variant MODIFIER c.*2342C>T| S266
134402 BAA10g20590 A10 18458762 C T downstream_gene_variant MODIFIER c.*2549C>T| S194
134403 BAA10g20590 A10 18458958 C T downstream_gene_variant MODIFIER c.*2745C>T| S25
134404 BAA10g20600 A10 18459291 C T upstream_gene_variant MODIFIER c.-4730C>T| S238
134405 BAA10g20600 A10 18459301 C T upstream_gene_variant MODIFIER c.-4720C>T| S113
134406 BAA10g20600 A10 18460674 G A upstream_gene_variant MODIFIER c.-3347G>A| S136
134407 BAA10g20600 A10 18461046 C T upstream_gene_variant MODIFIER c.-2975C>T| S185
134408 BAA10g20600 A10 18461919 G A upstream_gene_variant MODIFIER c.-2102G>A| S191
134409 BAA10g20600 A10 18462205 A T upstream_gene_variant MODIFIER c.-1816A>T| S11
S207
S248
S40
S42
S49
S71
134410 BAA10g20600 A10 18463297 T C upstream_gene_variant MODIFIER c.-724T>C| S18
134411 BAA10g20600 A10 18463407 G A upstream_gene_variant MODIFIER c.-614G>A| S125
134412 BAA10g20600 A10 18463419 G A upstream_gene_variant MODIFIER c.-602G>A| S155
134413 BAA10g20600 A10 18464701 G A missense_variant&splice_region_variant MODERATE c.214G>A|p.Gly72Arg S288
134414 BAA10g20600 A10 18470114 C T synonymous_variant LOW c.1632C>T|p.Thr544Thr S260
134415 BAA10g20610 A10 18470935 C T upstream_gene_variant MODIFIER c.-4764C>T| S84
S93
134416 BAA10g20610 A10 18474615 C T upstream_gene_variant MODIFIER c.-1084C>T| S122
134417 BAA10g20610 A10 18475640 C T upstream_gene_variant MODIFIER c.-59C>T| S244
134418 BAA10g20620 A10 18476849 G A downstream_gene_variant MODIFIER c.*3371C>T| S4
134419 BAA10g20610 A10 18477455 G A missense_variant MODERATE c.842G>A|p.Gly281Glu S270
134420 BAA10g20610 A10 18477942 G A downstream_gene_variant MODIFIER c.*336G>A| S270
134421 BAA10g20610 A10 18478816 G A downstream_gene_variant MODIFIER c.*1210G>A| S112
134422 BAA10g20610 A10 18479271 C T downstream_gene_variant MODIFIER c.*1665C>T| S99
134423 BAA10g20610 A10 18479342 C T downstream_gene_variant MODIFIER c.*1736C>T| S25
134424 BAA10g20610 A10 18479358 C T downstream_gene_variant MODIFIER c.*1752C>T| S110
134425 BAA10g20620 A10 18480231 C T missense_variant MODERATE c.361G>A|p.Gly121Arg S271