Product Details

SNP ID

rs201791412

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43767627 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCAGTCAGGGCATCCAGCTTCCC[C/T]GCCAGCGTGTCAATCTGTTTCTCCA

Phenotype

MIM: 602754

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

KCNN4 PubMed Links

Gene Details

Gene

KCNN4

Gene Name

potassium calcium-activated channel subfamily N member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002250.2	1596	Silent Mutation	GCA,GCG	A400A	NP_002241.1
XM_005258882.2	1596	Silent Mutation	GCA,GCG	A368A	XP_005258939.1
XM_005258883.2	1596	Silent Mutation	GCA,GCG	A337A	XP_005258940.1
XM_011526938.1	1596	Intron			XP_011525240.1

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