Product Details

SNP ID

rs201548399

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:31069010 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGTGTGATGGTGGCCAGCCCCCC[A/G]GCAGGATTCCGAGGTCTGGTGTCCT

Phenotype

MIM: 125645

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DSC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs61731921] 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

DSC2

Gene Name

desmocollin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004949.4	2853	Silent Mutation			NP_004940.1
NM_024422.4	2853	Silent Mutation			NP_077740.1
XM_005258206.4	2853	Missense Mutation			XP_005258263.1

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