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
116751 BAA10g10410 A10 12162350 G A missense_variant MODERATE c.472G>A|p.Val158Ile S218
116752 BAA10g10410 A10 12162365 G A missense_variant MODERATE c.487G>A|p.Gly163Arg S109
116753 BAA10g10410 A10 12163041 C T missense_variant MODERATE c.1163C>T|p.Thr388Ile S45
116754 BAA10g10410 A10 12163658 G A missense_variant MODERATE c.1780G>A|p.Gly594Ser S181
116755 BAA10g10420 A10 12163806 G A upstream_gene_variant MODIFIER c.-283G>A| S172
S217
116756 BAA10g10420 A10 12164154 C T synonymous_variant LOW c.66C>T|p.Leu22Leu S287
116757 BAA10g10420 A10 12164203 C T missense_variant MODERATE c.115C>T|p.Leu39Phe S210
S225
116758 BAA10g10420 A10 12164247 C T splice_region_variant&intron_variant LOW c.153+6C>T| S185
116759 BAA10g10430 A10 12165804 G A missense_variant&splice_region_variant MODERATE c.158C>T|p.Thr53Met S265
116760 BAA10g10430 A10 12166832 G A upstream_gene_variant MODIFIER c.-804C>T| S71
116761 BAA10g10430 A10 12166876 C T upstream_gene_variant MODIFIER c.-848G>A| S282
116762 BAA10g10430 A10 12167289 G A upstream_gene_variant MODIFIER c.-1261C>T| S202
116763 BAA10g10440 A10 12167772 C T missense_variant MODERATE c.382C>T|p.Arg128Trp S87
116764 BAA10g10440 A10 12167820 G A missense_variant MODERATE c.430G>A|p.Glu144Lys S192
116765 BAA10g10430 A10 12168512 C T upstream_gene_variant MODIFIER c.-2484G>A| S272
116766 BAA10g10430 A10 12168568 G A upstream_gene_variant MODIFIER c.-2540C>T| S16
116767 BAA10g10430 A10 12168575 C T upstream_gene_variant MODIFIER c.-2547G>A| S206
S26
116768 BAA10g10430 A10 12168647 G A upstream_gene_variant MODIFIER c.-2619C>T| S136
116769 BAA10g10430 A10 12169450 C T upstream_gene_variant MODIFIER c.-3422G>A| S180
116770 BAA10g10430 A10 12170441 C T upstream_gene_variant MODIFIER c.-4413G>A| S210
S225
116771 BAA10g10440 A10 12171190 C T downstream_gene_variant MODIFIER c.*3260C>T| S152
116772 BAA10g10440-BAA10g10450 A10 12173595 C T intergenic_region MODIFIER n.12173595C>T| S5
116773 BAA10g10440-BAA10g10450 A10 12173909 C T intergenic_region MODIFIER n.12173909C>T| S84
116774 BAA10g10440-BAA10g10450 A10 12173935 C T intergenic_region MODIFIER n.12173935C>T| S286
116775 BAA10g10440-BAA10g10450 A10 12173956 C T intergenic_region MODIFIER n.12173956C>T| S100