Product Details

SNP ID

rs201808409

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:154708002 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGCAACTGCTTGAACTTGTGTACG[C/G]GGTCGGGAAGGAGGTGGAGCTGACC

Phenotype

MIM: 602983

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

KCNN3 PubMed Links

Gene Details

Gene

KCNN3

Gene Name

potassium calcium-activated channel subfamily N member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204087.1	2484	Missense Mutation	CCG,GCG	P739A	NP_001191016.1
NM_002249.5	2484	Missense Mutation	CCG,GCG	P724A	NP_002240.3
NM_170782.2	2484	Missense Mutation	CCG,GCG	P419A	NP_740752.1

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