Product Details

SNP ID

rs2343849

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:32404660 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTATCTCTCCATGTATGGAAAGC[A/C]GTCTCCCACACTAGCCCACCATGGT

Phenotype

MIM: 607890

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

CMTM7 PubMed Links

Additional Information

For this assay, SNP(s) [rs347129] 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

CMTM7

Gene Name

CKLF like MARVEL transmembrane domain containing 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138410.3		Intron			NP_612419.1
NM_181472.2		Intron			NP_852137.1
XM_011533319.2		Intron			XP_011531621.1
XM_017005646.1		Intron			XP_016861135.1

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