Product Details

SNP ID

rs4429388

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:62331259 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAATAAATAAATAAGACACGGCAG[A/C]TGTCAGGACAAAAAAGCTGGCTGTT

Phenotype

MIM: 603499

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

TNFRSF11A PubMed Links

Additional Information

For this assay, SNP(s) [rs201843759] are located under a primer 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

TNFRSF11A

Gene Name

TNF receptor superfamily member 11a

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270949.1		Intron			NP_001257878.1
NM_001270950.1		Intron			NP_001257879.1
NM_001270951.1		Intron			NP_001257880.1
NM_001278268.1		Intron			NP_001265197.1
NM_003839.3		Intron			NP_003830.1
XM_011526244.2		Intron			XP_011524546.1
XM_011526245.2		Intron			XP_011524547.1
XM_017026064.1		Intron			XP_016881553.1
XM_017026065.1		Intron			XP_016881554.1
XM_017026066.1		Intron			XP_016881555.1

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