Product Details

SNP ID

rs12522231

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:168300068 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACTTGGACAGGGCTGAGGGCTAG[A/G]TCTGGGCAAAAAACTCCCGTCTTGC

Phenotype

MIM: 610533

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WWC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs114626878] 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

WWC1

Gene Name

WW and C2 domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161661.1		Intron			NP_001155133.1
NM_001161662.1		Intron			NP_001155134.1
NM_015238.2		Intron			NP_056053.1
XM_005265850.1		Intron			XP_005265907.1
XM_005265853.2		Intron			XP_005265910.1
XM_011534485.1		Intron			XP_011532787.1
XM_011534486.1		Intron			XP_011532788.1
XM_011534487.1		Intron			XP_011532789.1
XM_011534488.1		Intron			XP_011532790.1
XM_011534489.1		Intron			XP_011532791.1
XM_011534490.1		Intron			XP_011532792.1
XM_011534491.1		Intron			XP_011532793.1
XM_017009276.1		Intron			XP_016864765.1
XM_017009277.1		Intron			XP_016864766.1
XM_017009278.1		Intron			XP_016864767.1

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