Product Details

SNP ID

rs113704375

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36564597 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTGGAGTGTGAGGGCTCCGTGGA[A/G]CGCGAGCTGGAGCGGCTGCGGCGCT

Phenotype

MIM: 602911

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CACNG2 PubMed Links

Gene Details

Gene

CACNG2

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006078.3	592	Silent Mutation			NP_006069.1
XM_017028531.1	592	Silent Mutation			XP_016884020.1

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