Product Details

SNP ID: rs182823354
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:4278826 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGCAGCTGTCACTCCTCATGACTTC[A/G]TTGAGCACATCTTGCGCAAGCTGCC
Phenotype: MIM: 123833
Polymorphism: A/G, 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	783	Missense Mutation	ATT,GTT	I160V	NP_001750.1

There are no transcripts associated with this gene.