Product Details

SNP ID

rs6699979

Assay Type

Functionally tested

NCBI dbSNP Submissions

41

Location

Chr.1:154702018 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAACTTTTATTAAACTGGCTTTGCA[C/G]AGCTACTAAAGGAGTGATGGCTTTT

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	8468	UTR 3			NP_001191016.1
NM_002249.5	8468	UTR 3			NP_002240.3
NM_170782.2	8468	UTR 3			NP_740752.1

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