Product Details

SNP ID
rs147651812
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:49541010 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTCCCGGGCTGAGGTCATGCAGC[A/G]GGGCTGTGCCTGCTCCTTCCTTTAT
Phenotype
MIM: 604527
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
KCNH3 PubMed Links

Gene Details

Gene
KCNH3
Gene Name
potassium voltage-gated channel subfamily H member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001314030.1 1064 Missense Mutation CAG,CGG Q3R NP_001300959.1
NM_012284.2 1064 Missense Mutation CAG,CGG Q63R NP_036416.1
XM_011538085.2 1064 Missense Mutation CAG,CGG Q63R XP_011536387.1
XM_011538086.2 1064 Missense Mutation CAG,CGG Q3R XP_011536388.1
XM_017019096.1 1064 Intron XP_016874585.1
XM_017019097.1 1064 Intron XP_016874586.1

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