RGD:12838840 Rat Genome Database

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Variant: RGD:12838840 -  Homo sapiens

RGD ID: 12838840
RS ID: rs371529512
ClinVar ID: CV373274
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCND2  LOC129663087  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 4,388,105
GRCh38 12 4,278,939
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_034254.1:g.10204G>A
NC_000012.12:g.4278939G>A
NC_000012.11:g.4388105G>A
NM_001759.4:c.571+20G>A
More... 		04/02/2016 intron variant likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:CCND2
Accession:NM_001759
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000427712 CLINVAR
  RCV003766294 CLINVAR
dbSNP (RS) rs371529512 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene CCND2 CLINVAR
OMIM 123833 CLINVAR