Product Details

SNP ID

rs17854365

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:23954582 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTCTTCCAGCTCAGCCTCAAGCC[A/C]TGCCTCTTGTCACAGTGAGGGTTCT

Phenotype

MIM: 602304

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

NR1D2 PubMed Links

Gene Details

Gene

NR1D2

Gene Name

nuclear receptor subfamily 1 group D member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145425.1	381	UTR 5			NP_001138897.1
NM_005126.4	381	Missense Mutation	CAT,CCT	H21P	NP_005117.3
XM_006713451.3	381	Missense Mutation	CAT,CCT	H21P	XP_006713514.1

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