Product Details

SNP ID: rs113235723
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:79916872 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACAGTGCCGTGTGCCCAATGGTCAC[A/G]TGGAATTGAATCTGAAAAACAGAAA
Phenotype: MIM: 605512
Polymorphism: A/G, Transition 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	1000	Silent Mutation	CAC,CAT	H227H	NP_073563.1