Product Details

SNP ID

rs13060345

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:24834451 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACAGATTTTTTTGACAAAAAATAA[A/C]AATGAAAGCAAAATATTTGAGTGAG

Phenotype

MIM: 180220

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

RARB PubMed Links

Additional Information

For this assay, SNP(s) [rs79069309] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

RARB

Gene Name

retinoic acid receptor beta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000965.4		Intron			NP_000956.2
NM_001290216.2		Intron			NP_001277145.1
NM_001290217.1		Intron			NP_001277146.1
NM_001290266.1		Intron			NP_001277195.1
NM_001290276.1		Intron			NP_001277205.1
NM_001290277.1		Intron			NP_001277206.1
NM_001290300.1		Intron			NP_001277229.1
NM_016152.3		Intron			NP_057236.1

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