Product Details

SNP ID

rs116370050

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108135088 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCATGTCACAGAAGTGGGAATTGT[C/T]TATTTGAATGTGGTGAGATTTCTTC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

WSCD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs147219663] 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

WSCD2

Gene Name

WSC domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304447.1		Intron			NP_001291376.1
NM_014653.3		Intron			NP_055468.2
XM_017020243.1		Intron			XP_016875732.1
XM_017020244.1		Intron			XP_016875733.1
XM_017020245.1		Intron			XP_016875734.1
XM_017020246.1		Intron			XP_016875735.1
XM_017020247.1		Intron			XP_016875736.1
XM_017020248.1		Intron			XP_016875737.1
XM_017020249.1		Intron			XP_016875738.1
XM_017020250.1		Intron			XP_016875739.1
XM_017020251.1		Intron			XP_016875740.1
XM_017020252.1		Intron			XP_016875741.1

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