Product Details

SNP ID

rs111786572

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:42444061 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAATGCCAATAGAACAATTCCACTG[A/G]CAACACAAACTCCTCCAAGAATTCT

Phenotype

MIM: 606767

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

KCNG3 PubMed Links

Gene Details

Gene

KCNG3

Gene Name

potassium voltage-gated channel modifier subfamily G member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_133329.5	1747	Missense Mutation	GCC,GTC	A395V	NP_579875.1
NM_172344.2	1747	Missense Mutation	GCC,GTC	A384V	NP_758847.1

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