Product Details

SNP ID: rs61737594
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:95027042 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCAAGGCCACAGGCCTCAGCTCCC[G/T]CTTGCCAATGATTTGATGACAAATC
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	1785	Silent Mutation	CCG,CCT	P495P	NP_001155102.1