Product Details

SNP ID: rs56377228
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:45261953 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTTGAAGCAAATCGTGGCTTTTCTG[C/T]GTCTGGGTCTGTGTTTAAGACTGAG
Phenotype: MIM: 602780
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: HCN1 PubMed Links

Gene Details

Gene: HCN1
Gene Name: hyperpolarization activated cyclic nucleotide gated potassium channel 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021072.3	2666	Missense Mutation	ACA,GCA	T881A	NP_066550.2