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
134451 BAA10g20620 A10 18481095 G A upstream_gene_variant MODIFIER c.-504C>T| S166
134452 BAA10g20620 A10 18481186 C T upstream_gene_variant MODIFIER c.-595G>A| S250
134453 BAA10g20620 A10 18481916 G A upstream_gene_variant MODIFIER c.-1325C>T| S65
134454 BAA10g20620 A10 18482562 C T upstream_gene_variant MODIFIER c.-1971G>A| S119
134455 BAA10g20630 A10 18483359 G A missense_variant MODERATE c.443C>T|p.Ser148Phe S17
S218
S268
S269
134456 BAA10g20640 A10 18484045 C T synonymous_variant LOW c.396G>A|p.Pro132Pro S232
134457 BAA10g20640 A10 18484414 G A synonymous_variant LOW c.27C>T|p.Leu9Leu S67
134458 BAA10g20620 A10 18485430 C T upstream_gene_variant MODIFIER c.-4839G>A| S34
134459 BAA10g20660 A10 18487271 C T synonymous_variant LOW c.51C>T|p.Leu17Leu S143
134460 BAA10g20630 A10 18488073 G A upstream_gene_variant MODIFIER c.-4272C>T| S67
134461 BAA10g20630 A10 18488784 C T upstream_gene_variant MODIFIER c.-4983G>A| S56
134462 BAA10g20670 A10 18489490 G A missense_variant MODERATE c.301G>A|p.Ala101Thr S77
S82
134463 BAA10g20680 A10 18490435 G A upstream_gene_variant MODIFIER c.-284G>A| S16
134464 BAA10g20680 A10 18490573 C T upstream_gene_variant MODIFIER c.-146C>T| S257
134465 BAA10g20680 A10 18491047 G A stop_gained HIGH c.249G>A|p.Trp83* S270
134466 BAA10g20690 A10 18492731 C T upstream_gene_variant MODIFIER c.-2586C>T| S67
134467 BAA10g20690 A10 18492872 C T upstream_gene_variant MODIFIER c.-2445C>T| S168
134468 BAA10g20690 A10 18493634 C T upstream_gene_variant MODIFIER c.-1683C>T| S201
134469 BAA10g20690 A10 18494247 C T upstream_gene_variant MODIFIER c.-1070C>T| S203
134470 BAA10g20690 A10 18495556 C T synonymous_variant LOW c.240C>T|p.Leu80Leu S221
134471 BAA10g20690 A10 18495644 G A missense_variant MODERATE c.328G>A|p.Glu110Lys S240
134472 BAA10g20690 A10 18496298 G A missense_variant MODERATE c.982G>A|p.Asp328Asn S198
134473 BAA10g20680 A10 18496893 C T downstream_gene_variant MODIFIER c.*4469C>T| S40
S49
134474 BAA10g20700 A10 18498871 G A upstream_gene_variant MODIFIER c.-3724G>A| S112
134475 BAA10g20690 A10 18499463 G A missense_variant MODERATE c.2545G>A|p.Glu849Lys S39