Product Details

SNP ID

rs202045319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:60523907 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTTTTATATCCAGTTTATCATTG[A/C]AGGAGTCTTCCTAATAAGAGTAACA

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

MS4A13 PubMed Links

Additional Information

For this assay, SNP(s) [rs6591595] 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

MS4A13

Gene Name

membrane spanning 4-domains A13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012417.2	463	Missense Mutation	GAA,GCA	E47A	NP_001012417.2
NM_001100909.1	463	Missense Mutation	GAA,GCA	E47A	NP_001094379.1
NM_001278320.1	463	Intron			NP_001265249.1

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