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
178001 BAA02g19090 A02 9895486 C T missense_variant MODERATE c.247C>T|p.Arg83Cys S170
178002 BAA02g19090 A02 9895630 G A missense_variant MODERATE c.391G>A|p.Val131Ile S149
178003 BAA02g19100 A02 9896196 G A downstream_gene_variant MODIFIER c.*1727C>T| S79
S91
178004 BAA02g19100 A02 9896232 C T downstream_gene_variant MODIFIER c.*1691G>A| S183
S198
178005 BAA02g19100 A02 9896367 G A downstream_gene_variant MODIFIER c.*1556C>T| S137
S215
178006 BAA02g19100 A02 9896471 C T downstream_gene_variant MODIFIER c.*1452G>A| S2
178007 BAA02g19090 A02 9896586 C T missense_variant MODERATE c.707C>T|p.Pro236Leu S249
178008 BAA02g19090 A02 9896746 G A synonymous_variant LOW c.867G>A|p.Leu289Leu S272
178009 BAA02g19100 A02 9898318 C T missense_variant MODERATE c.208G>A|p.Ala70Thr S302
178010 BAA02g19100 A02 9899785 C T upstream_gene_variant MODIFIER c.-1260G>A| S32
178011 BAA02g19100 A02 9900135 G A upstream_gene_variant MODIFIER c.-1610C>T| S293
178012 BAA02g19100 A02 9900771 G A upstream_gene_variant MODIFIER c.-2246C>T| S86
178013 BAA02g19100 A02 9900780 G A upstream_gene_variant MODIFIER c.-2255C>T| S295
178014 BAA02g19100 A02 9901268 C T upstream_gene_variant MODIFIER c.-2743G>A| S216
S241
S265
S39
178015 BAA02g19100 A02 9902209 C T upstream_gene_variant MODIFIER c.-3684G>A| S165
178016 BAA02g19100 A02 9902541 G A upstream_gene_variant MODIFIER c.-4016C>T| S4
178017 BAA02g19100 A02 9902926 G A upstream_gene_variant MODIFIER c.-4401C>T| S269
178018 BAA02g19100 A02 9903156 C T upstream_gene_variant MODIFIER c.-4631G>A| S270
178019 BAA02g19100 A02 9903184 C T upstream_gene_variant MODIFIER c.-4659G>A| S131
178020 BAA02g19110 A02 9903559 C T upstream_gene_variant MODIFIER c.-578C>T| S224
178021 BAA02g19110 A02 9904171 G A missense_variant MODERATE c.35G>A|p.Gly12Glu S237
178022 BAA02g19110 A02 9904318 G A stop_gained HIGH c.182G>A|p.Trp61* S99
178023 BAA02g19110 A02 9905829 C T missense_variant MODERATE c.937C>T|p.Leu313Phe S18
178024 BAA02g19110 A02 9906281 C T downstream_gene_variant MODIFIER c.*93C>T| S271
178025 BAA02g19110 A02 9907882 C T downstream_gene_variant MODIFIER c.*1694C>T| S62