Product Details

SNP ID: rs62001000
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:56989440 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTCTGCAAGTCCAATAGCATCAATC[A/G]CTTTTTCTGTGATGTTCCCCCTATT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OR5AK2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005323.1	527	Missense Mutation	CAC,CGC	H176R	NP_001005323.1