Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g10150 A10 11917144 C T upstream_gene_variant MODIFIER c.-3268C>T| S135
2 BAA10g10150 A10 11917640 C T upstream_gene_variant MODIFIER c.-2772C>T| S79
S91
3 BAA10g10150 A10 11917699 G A upstream_gene_variant MODIFIER c.-2713G>A| S278
4 BAA10g10150 A10 11918240 G A upstream_gene_variant MODIFIER c.-2172G>A| S16
5 BAA10g10150 A10 11918317 G A upstream_gene_variant MODIFIER c.-2095G>A| S303
6 BAA10g10150 A10 11918423 C T upstream_gene_variant MODIFIER c.-1989C>T| S114
7 BAA10g10150 A10 11918837 C T upstream_gene_variant MODIFIER c.-1575C>T| S123
8 BAA10g10150 A10 11919100 C T upstream_gene_variant MODIFIER c.-1312C>T| S287
9 BAA10g10150 A10 11920462 C T synonymous_variant LOW c.51C>T|p.Ile17Ile S286
10 BAA10g10150 A10 11922832 C T synonymous_variant LOW c.1611C>T|p.Val537Val S98
11 BAA10g10150 A10 11922868 C T synonymous_variant LOW c.1647C>T|p.Phe549Phe S210
S225
12 BAA10g10150 A10 11922871 C T synonymous_variant LOW c.1650C>T|p.Ser550Ser S19
13 BAA10g10150 A10 11923734 G A missense_variant MODERATE c.2513G>A|p.Arg838Lys S262
14 BAA10g10150 A10 11923802 G A missense_variant MODERATE c.2581G>A|p.Gly861Arg S288
15 BAA10g10150 A10 11926589 C T downstream_gene_variant MODIFIER c.*2491C>T| S38
16 BAA10g10150 A10 11926605 G A downstream_gene_variant MODIFIER c.*2507G>A| S255