Product Details

SNP ID: rs146355392
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:617822 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGCTGCGTGAGTCCAGTAACAGTC[A/G]TGCACAGAGACGAAGGTCAGGCCCT
Phenotype: MIM: 602781 MIM: 601778
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: HCN2 PubMed Links

Gene Details

Gene: HCN2
Gene Name: hyperpolarization activated cyclic nucleotide gated potassium channel 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001194.3		Intron			NP_001185.3

Gene: POLRMT
Gene Name: RNA polymerase mitochondrial

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005035.3		Intron			NP_005026.3
XM_005259580.3		Intron			XP_005259637.2

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