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SNP ID

rs143905141

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:24255758 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGAGGGAGCGCCAGAGTGCGCT[A/G]CGGGCTTCGCTCCCCTTCCCCTTTC

Phenotype

MIM: 606403

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CACNG3 PubMed Links

Gene Details

Gene

CACNG3

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006539.3	206	UTR 5			NP_006530.1

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