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SNP ID

rs186685311

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:84222400 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCCTTCTTGAGCTCCAGGTAGGA[G/T]TGGGAGAAGGTGTGGAAGATAGACG

Phenotype

MIM: 607603

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

KCNG4 PubMed Links

Gene Details

Gene

KCNG4

Gene Name

potassium voltage-gated channel modifier subfamily G member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_172347.2	1498	Missense Mutation	CAA,CAC	Q459H	NP_758857.1

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