Product Details

SNP ID: rs117112355
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:79918316 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTGCATCACCAAAAAGGGTGTGTA[G/T]AAGGGTGTGATTGGGTATGGCATCA
Phenotype: MIM: 605512
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: ELOVL4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022726.3		Intron			NP_073563.1