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 BAA10g10460 A10 12191301 G A upstream_gene_variant MODIFIER c.-4713G>A| S264
2 BAA10g10460 A10 12191636 G A upstream_gene_variant MODIFIER c.-4378G>A| S35
3 BAA10g10460 A10 12191728 G A upstream_gene_variant MODIFIER c.-4286G>A| S36
4 BAA10g10460 A10 12191814 C T upstream_gene_variant MODIFIER c.-4200C>T| S176
5 BAA10g10460 A10 12194346 G A upstream_gene_variant MODIFIER c.-1668G>A| S302
6 BAA10g10460 A10 12194535 C T upstream_gene_variant MODIFIER c.-1479C>T| S97
7 BAA10g10460 A10 12194812 C T upstream_gene_variant MODIFIER c.-1202C>T| S247
8 BAA10g10460 A10 12195258 C T upstream_gene_variant MODIFIER c.-756C>T| S19
9 BAA10g10460 A10 12195283 C T upstream_gene_variant MODIFIER c.-731C>T| S28
10 BAA10g10460 A10 12195506 G A upstream_gene_variant MODIFIER c.-508G>A| S296
11 BAA10g10460 A10 12196289 C T synonymous_variant LOW c.276C>T|p.Phe92Phe S259
12 BAA10g10460 A10 12196474 C T missense_variant MODERATE c.461C>T|p.Ala154Val S162
13 BAA10g10460 A10 12196771 G A missense_variant MODERATE c.758G>A|p.Gly253Asp S172
S217
14 BAA10g10460 A10 12197376 C T downstream_gene_variant MODIFIER c.*46C>T| S272