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
169601 BAA02g14690 A02 6864488 G A downstream_gene_variant MODIFIER c.*90G>A| S303
169602 BAA02g14690 A02 6865161 G A downstream_gene_variant MODIFIER c.*763G>A| S59
169603 BAA02g14690 A02 6865909 C T downstream_gene_variant MODIFIER c.*1511C>T| S268
169604 BAA02g14690 A02 6866359 C T downstream_gene_variant MODIFIER c.*1961C>T| S306
169605 BAA02g14700 A02 6869588 C T downstream_gene_variant MODIFIER c.*1403G>A| S114
169606 BAA02g14700 A02 6869611 C T downstream_gene_variant MODIFIER c.*1380G>A| S13
169607 BAA02g14700 A02 6870364 G A downstream_gene_variant MODIFIER c.*627C>T| S119
S305
169608 BAA02g14700 A02 6872317 G A missense_variant MODERATE c.943C>T|p.Pro315Ser S11
169609 BAA02g14710 A02 6872393 C T downstream_gene_variant MODIFIER c.*2442G>A| S107
169610 BAA02g14700 A02 6873821 C T upstream_gene_variant MODIFIER c.-29G>A| S301
S304
169611 BAA02g14710 A02 6875563 G A synonymous_variant LOW c.540C>T|p.His180His S91
169612 BAA02g14700 A02 6875759 G A upstream_gene_variant MODIFIER c.-1967C>T| S176
169613 BAA02g14710 A02 6876304 C T synonymous_variant LOW c.180G>A|p.Pro60Pro S47
169614 BAA02g14710 A02 6876453 C T missense_variant MODERATE c.31G>A|p.Ala11Thr S33
169615 BAA02g14720 A02 6877224 G A synonymous_variant LOW c.624C>T|p.Ile208Ile S50
169616 BAA02g14700 A02 6877860 C T upstream_gene_variant MODIFIER c.-4068G>A| S216
169617 BAA02g14700 A02 6878048 G A upstream_gene_variant MODIFIER c.-4256C>T| S23
169618 BAA02g14710 A02 6879005 C T upstream_gene_variant MODIFIER c.-2522G>A| S289
S290
169619 BAA02g14730 A02 6879258 C T missense_variant MODERATE c.895G>A|p.Asp299Asn S221
S71
169620 BAA02g14730 A02 6879558 G A missense_variant MODERATE c.595C>T|p.Leu199Phe S153
S213
169621 BAA02g14730 A02 6880422 G A synonymous_variant LOW c.321C>T|p.His107His S169
169622 BAA02g14730 A02 6880506 C T stop_gained HIGH c.237G>A|p.Trp79* S131
169623 BAA02g14730 A02 6880554 G A synonymous_variant LOW c.189C>T|p.Leu63Leu S61
169624 BAA02g14720 A02 6881977 G A upstream_gene_variant MODIFIER c.-4130C>T| S205
169625 BAA02g14720 A02 6882160 G A upstream_gene_variant MODIFIER c.-4313C>T| S237