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
122701 BAA10g12950 A10 14222996 C T upstream_gene_variant MODIFIER c.-30G>A| S17
122702 BAA10g12950 A10 14223497 G A upstream_gene_variant MODIFIER c.-531C>T| S250
122703 BAA10g12950 A10 14227453 C T upstream_gene_variant MODIFIER c.-4487G>A| S143
122704 BAA10g12950 A10 14227784 C T upstream_gene_variant MODIFIER c.-4818G>A| S5
122705 BAA10g12960 A10 14228024 C T upstream_gene_variant MODIFIER c.-3379C>T| S108
122706 BAA10g12960 A10 14228124 G A upstream_gene_variant MODIFIER c.-3279G>A| S155
S211
122707 BAA10g12960 A10 14228311 C T upstream_gene_variant MODIFIER c.-3092C>T| S98
122708 BAA10g12960 A10 14229785 G A upstream_gene_variant MODIFIER c.-1618G>A| S195
122709 BAA10g12960 A10 14232026 G A missense_variant MODERATE c.529G>A|p.Asp177Asn S128
122710 BAA10g12960 A10 14232174 G A missense_variant MODERATE c.677G>A|p.Gly226Asp S219
S72
122711 BAA10g12960 A10 14232465 C T missense_variant MODERATE c.968C>T|p.Thr323Met S61
122712 BAA10g12960 A10 14232680 G A missense_variant MODERATE c.1183G>A|p.Gly395Ser S15
122713 BAA10g12960 A10 14233765 C T downstream_gene_variant MODIFIER c.*582C>T| S38
122714 BAA10g12960 A10 14234600 C T downstream_gene_variant MODIFIER c.*1417C>T| S162
122715 BAA10g12960 A10 14234744 G A downstream_gene_variant MODIFIER c.*1561G>A| S212
122716 BAA10g12970 A10 14237245 G A upstream_gene_variant MODIFIER c.-3029G>A| S23
122717 BAA10g12970 A10 14239299 C T upstream_gene_variant MODIFIER c.-975C>T| S308
122718 BAA10g12970 A10 14239730 G A upstream_gene_variant MODIFIER c.-544G>A| S207
122719 BAA10g12970 A10 14239892 C T upstream_gene_variant MODIFIER c.-382C>T| S266
122720 BAA10g12970 A10 14240477 C T intron_variant MODIFIER c.73+38C>T| S191
122721 BAA10g12970 A10 14240527 G A intron_variant MODIFIER c.74-53G>A| S292
122722 BAA10g12970 A10 14243042 G A downstream_gene_variant MODIFIER c.*1326G>A| S71
122723 BAA10g12970 A10 14243454 C T downstream_gene_variant MODIFIER c.*1738C>T| S103
122724 BAA10g12980 A10 14244781 G A upstream_gene_variant MODIFIER c.-4327G>A| S68
122725 BAA10g12980 A10 14245098 C T upstream_gene_variant MODIFIER c.-4010C>T| S44