Product Details

SNP ID

rs41294792

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:54139569 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAATAGTGGAAACAAGCGGGAGCC[A/G]TACCGTCCAGTCTTAGGGGTCCCGA

Phenotype

MIM: 612320

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CDCP2 PubMed Links

Gene Details

Gene

CDCP2

Gene Name

CUB domain containing protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_201546.3	1385	Missense Mutation	ACG,ATG	T434M	NP_963840.2

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