Product Details

SNP ID: rs200399862
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:73322873 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCTGGGTGAGGCGGCCGGGGGTGA[A/G]CGGGGGTGTGCCCCGGCGCTGGGGG
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	4214	Missense Mutation	CTC,TTC	L1074F	NP_005468.1
XM_011521148.2	4214	Missense Mutation	CTC,TTC	L668F	XP_011519450.1