Product Details

SNP ID

rs200026820

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53963199 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGCCTCTGGTGCGAGAAGGGGGT[G/T]CAGGTGCTGCTGACGACGGTGGGCG

Phenotype

MIM: 606900

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CACNG8 PubMed Links

Gene Details

Gene

CACNG8

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031895.5	164	Silent Mutation	GTG,GTT	V19V	NP_114101.4

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