Product Details

SNP ID

rs142248522

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:119342601 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGGGGCAGGCTTCTCACCTGGG[G/T]GTGGGAACAAGGGGCCGCTGCAGTT

Phenotype

MIM: 608752 MIM: 606227 MIM: 606130

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

C1QTNF5 PubMed Links

Additional Information

For this assay, SNP(s) [rs11217241] 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

C1QTNF5

Gene Name

C1q and tumor necrosis factor related protein 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001278431.1	1542	Intron			NP_001265360.1
NM_015645.4	1542	UTR 5			NP_056460.1

Gene

MFRP

Gene Name

membrane frizzled-related protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031433.3	1542	Missense Mutation	CAC,CCC	H461P	NP_113621.1

Gene

RNF26

Gene Name

ring finger protein 26

There are no transcripts associated with this gene.

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