Product Details

SNP ID
rs140402087
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:73322743 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACCCCCAGCCCTGGGGAAGAGC[A/G]GGAAGGCAGCCATGGACTCCCCTGA
Phenotype
MIM: 605206
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HCN4 PubMed Links

Gene Details

Gene
HCN4
Gene Name
hyperpolarization activated cyclic nucleotide gated potassium channel 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005477.2 4344 Missense Mutation CCG,CTG P1117L NP_005468.1
XM_011521148.2 4344 Missense Mutation CCG,CTG P711L XP_011519450.1

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