Product Details

SNP ID

rs114839477

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:165403596 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTCAAAAGCCTCCAGTGGTAAAG[A/C]CCCTGAAAGCATTTGAGTGGCATCA

Phenotype

MIM: 180247

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

RXRG PubMed Links

Gene Details

Gene

RXRG

Gene Name

retinoid X receptor gamma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256570.1		Intron			NP_001243499.1
NM_001256571.1		Intron			NP_001243500.1
NM_006917.4		Intron			NP_008848.1

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