Product Details

SNP ID: rs17031981
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:154744668 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCAGCATCCGCGTGGACACAGTGGA[A/G]GACTTCGCCTACGGAGCTAACATCC
Phenotype: MIM: 604863
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LRAT PubMed Links

Gene Details

Gene: LRAT
Gene Name: lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301645.1	401	Silent Mutation	GAA,GAG	E114E	NP_001288574.1
NM_004744.4	401	Silent Mutation	GAA,GAG	E114E	NP_004735.2