Product Details

SNP ID: rs200880354
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:4276103 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGTCCCGACTCCGAAGTCCCATCT[G/T]CAACTCCTGGGTGCTGTCTGCATGT
Phenotype: MIM: 123833
Polymorphism: G/T, Transversion 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	599	Silent Mutation	CTG,CTT	L98L	NP_001750.1

There are no transcripts associated with this gene.