RGD:11600090 Rat Genome Database

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Variant: RGD:11600090 -  Homo sapiens

RGD ID: 11600090
RS ID: rs529020970
ClinVar ID: CV316346
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDKN1B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 12,874,288
GRCh38 12 12,721,354
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016341.1:g.8987C>T
NC_000012.12:g.12721354C>T
NC_000012.11:g.12874288C>T
NM_004064.3:c.*327C>T
More... 		06/14/2016 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CDKN1B
Accession:NM_004064
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000270820 CLINVAR
dbSNP (RS) rs529020970 CLINVAR
MedGen C0027662 CLINVAR
NCBI Gene CDKN1B CLINVAR
OMIM 600778 CLINVAR
SNOMED CT 46724008 CLINVAR