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SNP ID

rs137917225

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:66965034 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTGTACTCCAGCGCGCACATCTG[C/T]AACGGCACCAACCTGACCATGGACG

Phenotype

MIM: 606404

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CACNG4 PubMed Links

Gene Details

Gene

CACNG4

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014405.3	171	Silent Mutation	TGC,TGT	C41C	NP_055220.1

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