Product Details

SNP ID
rs189457419
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:150946886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGCTGGAGCTTACCTGAGAAAG[C/T]GAGTCCAAGGTGAGGGTGGGGAGGG
Phenotype
MIM: 152427
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
KCNH2 PubMed Links

Gene Details

Gene
KCNH2
Gene Name
potassium voltage-gated channel subfamily H member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000238.3 3133 Silent Mutation NP_000229.1
NM_001204798.1 3133 Intron NP_001191727.1
NM_172056.2 3133 Intron NP_742053.1
NM_172057.2 3133 Silent Mutation NP_742054.1
XM_011516185.2 3133 Silent Mutation XP_011514487.1
XM_011516186.2 3133 Intron XP_011514488.1
XM_017012195.1 3133 Silent Mutation XP_016867684.1
XM_017012196.1 3133 Silent Mutation XP_016867685.1

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