Product Details

SNP ID

rs355938

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:66609273 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGCTGGCAAGGCAGCAGAGGCACC[G/T]CGGGGGTGGGACAAGGGCCTAGGCA

Phenotype

MIM: 607886 MIM: 607887

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CMTM3 PubMed Links

Additional Information

For this assay, SNP(s) [rs146088650] 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

CMTM3

Gene Name

CKLF like MARVEL transmembrane domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144601.3		Intron			NP_653202.1
NM_181553.2		Intron			NP_853531.1
XM_006721131.1		Intron			XP_006721194.1
XM_011522861.1		Intron			XP_011521163.1

Gene

CMTM4

Gene Name

CKLF like MARVEL transmembrane domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178818.2		Intron			NP_848933.1
NM_181521.2		Intron			NP_852662.1
XM_011522882.1		Intron			XP_011521184.1
XM_017022954.1		Intron			XP_016878443.1

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