Product Details

SNP ID: rs143234858
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:95026776 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACTGATGCTGTGCCTGGATCCGCA[G/T]TCCAAAGCTCTGCATATCATACCCA
Phenotype: MIM: 616581
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: KDM4E PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161630.1	1519	Missense Mutation	GTC,TTC	V407F	NP_001155102.1