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
166801 BAA02g12760 A02 5721503 G A upstream_gene_variant MODIFIER c.-4918C>T| S167
166802 BAA02g12780 A02 5721878 C T upstream_gene_variant MODIFIER c.-2071G>A| S275
166803 BAA02g12780 A02 5722216 G T upstream_gene_variant MODIFIER c.-2409C>A| S33
166804 BAA02g12780 A02 5722285 G A upstream_gene_variant MODIFIER c.-2478C>T| S135
166805 BAA02g12790 A02 5730826 G A upstream_gene_variant MODIFIER c.-534G>A| S50
166806 BAA02g12790 A02 5734419 C T downstream_gene_variant MODIFIER c.*1681C>T| S219
S72
166807 BAA02g12800 A02 5735547 G A synonymous_variant LOW c.78C>T|p.Asp26Asp S162
166808 BAA02g12800 A02 5737296 G A upstream_gene_variant MODIFIER c.-1672C>T| S57
166809 BAA02g12800 A02 5739527 C T upstream_gene_variant MODIFIER c.-3903G>A| S77
S82
166810 BAA02g12800 A02 5739537 C T upstream_gene_variant MODIFIER c.-3913G>A| S161
166811 BAA02g12800 A02 5740381 G A upstream_gene_variant MODIFIER c.-4757C>T| S155
S211
166812 BAA02g12810 A02 5740536 G A missense_variant MODERATE c.628G>A|p.Ala210Thr S17
166813 BAA02g12810 A02 5741270 G A missense_variant MODERATE c.1180G>A|p.Ala394Thr S126
166814 BAA02g12810 A02 5741434 G A synonymous_variant LOW c.1344G>A|p.Arg448Arg S159
S243
166815 BAA02g12810 A02 5741946 G A missense_variant MODERATE c.1856G>A|p.Arg619Lys S69
166816 BAA02g12810 A02 5742553 G A missense_variant MODERATE c.2260G>A|p.Asp754Asn S168
166817 BAA02g12810 A02 5742607 G A missense_variant MODERATE c.2314G>A|p.Gly772Arg S61
166818 BAA02g12820 A02 5743619 C T synonymous_variant LOW c.315C>T|p.Phe105Phe S241
166819 BAA02g12820 A02 5743732 G A synonymous_variant LOW c.345G>A|p.Glu115Glu S239
166820 BAA02g12810 A02 5744485 C T downstream_gene_variant MODIFIER c.*1604C>T| S212
166821 BAA02g12810 A02 5744522 C T downstream_gene_variant MODIFIER c.*1641C>T| S8
166822 BAA02g12820 A02 5745519 C T synonymous_variant LOW c.1114C>T|p.Leu372Leu S115
166823 BAA02g12810 A02 5745557 C T downstream_gene_variant MODIFIER c.*2676C>T| S249
166824 BAA02g12810 A02 5745613 C T downstream_gene_variant MODIFIER c.*2732C>T| S104
166825 BAA02g12810 A02 5745809 C T downstream_gene_variant MODIFIER c.*2928C>T| S289
S290