Product Details

SNP ID

rs144507683

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:183100562 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCAGGGATAACTTCGACATTTGG[A/G]CTTTTGTCATTTCTGAAAATTATAA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WWC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs146320791] 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

WWC2

Gene Name

WW and C2 domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024949.5		Intron			NP_079225.5
XM_011532269.2		Intron			XP_011530571.1

Gene

WWC2-AS2

Gene Name

WWC2 antisense RNA 2

There are no transcripts associated with this gene.

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