Product Details

SNP ID
rs200425698
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:43769443 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGTGCATACAAAGCGGCCCTCACG[C/T]GTTGATGGCGGCCAGCAGCTTGCGC
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 1444 Missense Mutation ACG,GCG T350A NP_002241.1
XM_005258882.2 1444 Missense Mutation ACG,GCG T318A XP_005258939.1
XM_005258883.2 1444 Missense Mutation ACG,GCG T287A XP_005258940.1
XM_011526938.1 1444 Intron XP_011525240.1

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