Product Details

SNP ID

rs28640032

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:183643509 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAATAGTTTTGACCTTGTGTACCC[C/T]CTGAGAGAGTCTCAGGGACATCCCA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RWDD4 PubMed Links

Additional Information

For this assay, SNP(s) [rs201611593] 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

RWDD4

Gene Name

RWD domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001307922.1		Intron			NP_001294851.1
NM_152682.3		Intron			NP_689895.2

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