Product Details

SNP ID

rs147207795

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:49543249 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTGCCAATATTCTTTCCTCTCT[C/G]CCTGGACCTGCCCTGCCTCACTCAG

Phenotype

MIM: 604527

Polymorphism

C/G, Transversion 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		Intron			NP_001300959.1
NM_012284.2		Intron			NP_036416.1
XM_011538085.2		Intron			XP_011536387.1
XM_011538086.2		Intron			XP_011536388.1
XM_017019096.1		Intron			XP_016874585.1
XM_017019097.1		Intron			XP_016874586.1

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