Product Details

SNP ID: rs7999481
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:53031025 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AACCAGCATTTGGGTAAGATTATCA[A/G]CTATAATAATAGAAAATAAAATACA
Phenotype: MIM: 614061
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OLFM4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006418.4		Intron			NP_006409.3