Product Details

SNP ID: rs9366689
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:27308392 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CACAAAAACCTGAACATGAATGTTT[A/C]TGGTGACTTTATTTATTTTTGAGAA
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: LOC105375107 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033482.3		Intron			NP_258443.2