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SNP ID

rs201015865

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:84222333 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAGTTCACATTCACTGGCTGGAC[C/T]GGTGTTTTGGAGGTGGCGGAGGCGG

Phenotype

MIM: 607603

Polymorphism

C/T, Transition 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	1565	Missense Mutation	AGT,GGT	S482G	NP_758857.1

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