RGD:156008914 Rat Genome Database

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Variant: RGD:156008914 -  Homo sapiens

RGD ID: 156008914
ClinVar ID: CV2075378
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT3A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 228,246,680
GRCh38 1 228,058,979
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_033131.4:c.580-7C>T
NC_000001.11:g.228058979C>T
NC_000001.10:g.228246680C>T
 07/14/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WNT3A
Accession:NM_033131
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002843764 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WNT3A CLINVAR
OMIM 606359 CLINVAR