Product Details

SNP ID: rs3828952
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:6166051 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGATGACACAACCGCGCTACAATTC[A/G]CTTCCTGGGAGAGTTAGTGGGATGG
Phenotype: MIM: 605081
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CYTH3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004227.3		Intron			NP_004218.1

There are no transcripts associated with this gene.