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
112601 BAA10g08590-BAA10g08600 A10 10412659 G A intergenic_region MODIFIER n.10412659G>A| S216
112602 BAA10g08590-BAA10g08600 A10 10412741 G A intergenic_region MODIFIER n.10412741G>A| S136
112603 BAA10g08590-BAA10g08600 A10 10413241 C T intergenic_region MODIFIER n.10413241C>T| S181
112604 BAA10g08590-BAA10g08600 A10 10413862 G A intergenic_region MODIFIER n.10413862G>A| S18
112605 BAA10g08590-BAA10g08600 A10 10413926 G A intergenic_region MODIFIER n.10413926G>A| S262
112606 BAA10g08590-BAA10g08600 A10 10415195 G A intergenic_region MODIFIER n.10415195G>A| S1
112607 BAA10g08600 A10 10417055 C T downstream_gene_variant MODIFIER c.*3707G>A| S38
112608 BAA10g08600 A10 10417377 G A downstream_gene_variant MODIFIER c.*3385C>T| S107
112609 BAA10g08600 A10 10417511 G A downstream_gene_variant MODIFIER c.*3251C>T| S291
112610 BAA10g08600 A10 10417737 G A downstream_gene_variant MODIFIER c.*3025C>T| S245
112611 BAA10g08600 A10 10418178 G A downstream_gene_variant MODIFIER c.*2584C>T| S202
112612 BAA10g08600 A10 10418268 C T downstream_gene_variant MODIFIER c.*2494G>A| S301
S304
112613 BAA10g08600 A10 10419010 G A downstream_gene_variant MODIFIER c.*1752C>T| S4
112614 BAA10g08600 A10 10419100 G A downstream_gene_variant MODIFIER c.*1662C>T| S3
112615 BAA10g08600 A10 10419733 G A downstream_gene_variant MODIFIER c.*1029C>T| S48
112616 BAA10g08600 A10 10420032 G A downstream_gene_variant MODIFIER c.*730C>T| S294
112617 BAA10g08600 A10 10420066 G A downstream_gene_variant MODIFIER c.*696C>T| S118
112618 BAA10g08600 A10 10420787 G A missense_variant MODERATE c.1235C>T|p.Pro412Leu S289
112619 BAA10g08600 A10 10421477 C T intron_variant MODIFIER c.883-338G>A| S162
112620 BAA10g08600 A10 10422486 G A intron_variant MODIFIER c.883-1347C>T| S1
S90
112621 BAA10g08600 A10 10422895 G A intron_variant MODIFIER c.882+1080C>T| S171
S296
112622 BAA10g08600 A10 10423302 G A intron_variant MODIFIER c.882+673C>T| S128
112623 BAA10g08600 A10 10423540 C T intron_variant MODIFIER c.882+435G>A| S164
112624 BAA10g08600 A10 10425469 G A intron_variant MODIFIER c.516+21C>T| S62
112625 BAA10g08600 A10 10426490 G A upstream_gene_variant MODIFIER c.-93C>T| S94