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
98751 BAA10g06140 A10 3181182 G A upstream_gene_variant MODIFIER c.-612C>T| S120
98752 BAA10g06140 A10 3181332 C T upstream_gene_variant MODIFIER c.-762G>A| S40
S49
98753 BAA10g06150 A10 3182282 C T missense_variant MODERATE c.106G>A|p.Gly36Arg S260
98754 BAA10g06150 A10 3182371 C T stop_gained HIGH c.17G>A|p.Trp6* S249
98755 BAA10g06140 A10 3183039 G A upstream_gene_variant MODIFIER c.-2469C>T| S136
98756 BAA10g06160 A10 3184475 G A synonymous_variant LOW c.81C>T|p.Ile27Ile S240
98757 BAA10g06160 A10 3184507 G A missense_variant MODERATE c.49C>T|p.Pro17Ser S296
98758 BAA10g06150 A10 3185592 G A upstream_gene_variant MODIFIER c.-3205C>T| S264
98759 BAA10g06170 A10 3186228 C T missense_variant MODERATE c.803G>A|p.Gly268Asp S177
98760 BAA10g06170 A10 3186635 C T synonymous_variant LOW c.396G>A|p.Lys132Lys S44
98761 BAA10g06170 A10 3186770 G A synonymous_variant LOW c.261C>T|p.Val87Val S100
98762 BAA10g06170 A10 3186948 C T missense_variant MODERATE c.83G>A|p.Gly28Glu S188
98763 BAA10g06180 A10 3187466 C T missense_variant MODERATE c.113C>T|p.Ser38Phe S256
98764 BAA10g06180 A10 3187610 C T missense_variant MODERATE c.257C>T|p.Ala86Val S40
S49
98765 BAA10g06180 A10 3187999 G A missense_variant MODERATE c.646G>A|p.Glu216Lys S172
S217
98766 BAA10g06180 A10 3188149 G A missense_variant MODERATE c.796G>A|p.Glu266Lys S198
98767 BAA10g06160 A10 3188526 G A upstream_gene_variant MODIFIER c.-3971C>T| S62
98768 BAA10g06160 A10 3188627 C T upstream_gene_variant MODIFIER c.-4072G>A| S305
98769 BAA10g06170 A10 3189724 C T upstream_gene_variant MODIFIER c.-2694G>A| S183
98770 BAA10g06170 A10 3189976 G A upstream_gene_variant MODIFIER c.-2946C>T| S81
98771 BAA10g06170 A10 3190054 G A upstream_gene_variant MODIFIER c.-3024C>T| S228
98772 BAA10g06170 A10 3190568 C T upstream_gene_variant MODIFIER c.-3538G>A| S96
98773 BAA10g06170 A10 3190753 C T upstream_gene_variant MODIFIER c.-3723G>A| S74
98774 BAA10g06170 A10 3191364 C T upstream_gene_variant MODIFIER c.-4334G>A| S286
S301
98775 BAA10g06200 A10 3193000 C T missense_variant MODERATE c.25G>A|p.Glu9Lys S91