Product Details

SNP ID: rs185614631
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:95026579 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGAAACACAGGCAAGACTTGGCCA[C/T]TGTGGAACACACAGAGCCCAGGGTT
Phenotype: MIM: 616581
Polymorphism: C/T, Transition 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	1322	Missense Mutation	ACT,ATT	T341I	NP_001155102.1