Product Details

SNP ID

rs199762590

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:124326365 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCCAGAGACCTTGGCCTTCCCGC[C/T]GCCACCTGCAGGGGGACAAGATGGG

Phenotype

MIM: 600848

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NCOR2 PubMed Links

Gene Details

Gene

NCOR2

Gene Name

nuclear receptor corepressor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077261.3	7342	Missense Mutation			NP_001070729.2
NM_001206654.1	7342	Missense Mutation			NP_001193583.1
NM_006312.5	7342	Missense Mutation			NP_006303.4

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