Product Details

SNP ID

rs767828150

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:71812015 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGTCCACCTGGACAGCATGGAGT[C/T]CAACACTGAGTCCCGGCCGGAGTCC

Phenotype

MIM: 604485

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NR2E3 PubMed Links

Gene Details

Gene

NR2E3

Gene Name

nuclear receptor subfamily 2 group E member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014249.3	606	Missense Mutation	TCC,TTC	S137F	NP_055064.1
NM_016346.3	606	Missense Mutation	TCC,TTC	S137F	NP_057430.1

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