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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g00160 A10 68847 C T missense_variant MODERATE c.1069G>A|p.Gly357Arg S246
2 BAA10g00160 A10 68956 C T synonymous_variant LOW c.960G>A|p.Ala320Ala S108
3 BAA10g00160 A10 69056 C T missense_variant MODERATE c.860G>A|p.Arg287His S56
4 BAA10g00160 A10 69122 C T missense_variant MODERATE c.794G>A|p.Gly265Glu S206
S26
5 BAA10g00160 A10 69688 C T missense_variant MODERATE c.297G>A|p.Met99Ile S139
6 BAA10g00160 A10 70889 C T upstream_gene_variant MODIFIER c.-905G>A| S108
7 BAA10g00160 A10 71762 G A upstream_gene_variant MODIFIER c.-1778C>T| S82
S92
8 BAA10g00160 A10 72499 G A upstream_gene_variant MODIFIER c.-2515C>T| S217
9 BAA10g00160 A10 72808 G A upstream_gene_variant MODIFIER c.-2824C>T| S205
10 BAA10g00160 A10 73093 G A upstream_gene_variant MODIFIER c.-3109C>T| S148
S30
11 BAA10g00160 A10 74318 G A upstream_gene_variant MODIFIER c.-4334C>T| S4
12 BAA10g00160 A10 74341 C T upstream_gene_variant MODIFIER c.-4357G>A| S174
13 BAA10g00160 A10 74545 G A upstream_gene_variant MODIFIER c.-4561C>T| S41
14 BAA10g00160 A10 74641 C T upstream_gene_variant MODIFIER c.-4657G>A| S275