Product Details

SNP ID

hCV86368519

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:71810798 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCACAGTGGCTGCAGCTGCGCCT[C/G]CAGCTGGGGCTGCCTCCAGGAAGGA

Phenotype

MIM: 604485

Polymorphism

C/G, Transversion 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	251	Missense Mutation	CCA,GCA	P19A	NP_055064.1
NM_016346.3	251	Missense Mutation	CCA,GCA	P19A	NP_057430.1

View Full Product Details