Product Details

SNP ID: rs1049606
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:4273870 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCGCCCACCACCCAATCCTCGCCTC[C/T]CTTCTGCTCCACCTTCTCTCTCTGC
Phenotype: MIM: 123833
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CCND2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001759.3	135	UTR 5			NP_001750.1

There are no transcripts associated with this gene.