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SNP ID

rs143617158

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53971592 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCAGGGATTTCAGCCACACCC[C/T]GAGGTCTTCTCTCAGGACTCAAGAG

Phenotype

MIM: 606900

Polymorphism

C/T, Transition 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		Intron			NP_114101.4

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