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
204501 BAA02g31830 A02 19553492 G A upstream_gene_variant MODIFIER c.-2418G>A| S128
204502 BAA02g31820 A02 19554090 C T upstream_gene_variant MODIFIER c.-105G>A| S42
204503 BAA02g31820 A02 19554199 C T upstream_gene_variant MODIFIER c.-214G>A| S239
204504 BAA02g31820 A02 19555657 C T upstream_gene_variant MODIFIER c.-1672G>A| S203
204505 BAA02g31820 A02 19556160 G A upstream_gene_variant MODIFIER c.-2175C>T| S127
204506 BAA02g31820 A02 19558128 C T upstream_gene_variant MODIFIER c.-4143G>A| S134
204507 BAA02g31820 A02 19558154 G A upstream_gene_variant MODIFIER c.-4169C>T| S136
204508 BAA02g31820 A02 19558717 C T upstream_gene_variant MODIFIER c.-4732G>A| S105
S106
204509 BAA02g31820 A02 19558791 G A upstream_gene_variant MODIFIER c.-4806C>T| S17
204510 BAA02g31840 A02 19559844 G A missense_variant MODERATE c.764C>T|p.Ser255Phe S20
204511 BAA02g31840 A02 19560482 G A missense_variant MODERATE c.305C>T|p.Ser102Phe S4
204512 BAA02g31840 A02 19562493 C T upstream_gene_variant MODIFIER c.-1627G>A| S84
S93
204513 BAA02g31840 A02 19562557 G A upstream_gene_variant MODIFIER c.-1691C>T| S126
204514 BAA02g31840 A02 19564727 G A upstream_gene_variant MODIFIER c.-3861C>T| S97
204515 BAA02g31840 A02 19565816 G A upstream_gene_variant MODIFIER c.-4950C>T| S13
204516 BAA02g31850 A02 19566732 G A downstream_gene_variant MODIFIER c.*1645C>T| S41
204517 BAA02g31860 A02 19567062 G A upstream_gene_variant MODIFIER c.-4700G>A| S278
204518 BAA02g31860 A02 19567078 G A upstream_gene_variant MODIFIER c.-4684G>A| S271
204519 BAA02g31860 A02 19567450 C T upstream_gene_variant MODIFIER c.-4312C>T| S138
204520 BAA02g31850 A02 19568467 G A synonymous_variant LOW c.2097C>T|p.Pro699Pro S282
204521 BAA02g31850 A02 19568860 G A synonymous_variant LOW c.1704C>T|p.Asp568Asp S99
204522 BAA02g31850 A02 19569964 G A synonymous_variant LOW c.600C>T|p.Ala200Ala S8
204523 BAA02g31850 A02 19570008 G A missense_variant MODERATE c.556C>T|p.Pro186Ser S13
204524 BAA02g31850 A02 19570054 C T stop_gained HIGH c.510G>A|p.Trp170* S246
204525 BAA02g31850 A02 19571433 G A upstream_gene_variant MODIFIER c.-782C>T| S256