RGD:155964650 Rat Genome Database

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Variant: RGD:155964650 -  Homo sapiens

RGD ID: 155964650
ClinVar ID: CV2210025
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT3A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 228,210,567
GRCh38 1 228,022,866
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.271G>A
NC_000001.11:g.228022866G>A
NC_000001.10:g.228210567G>A
NM_033131.3:c.271G>A
More... 		05/20/2023 missense variant uncertain significance AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:WNT3A
Accession:NM_033131
Location:EXON
Amino Acid Prediction: V to I (nonsynonymous)
Amino Acid Position: 91
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAPLGYFLLLCSLKQALGSYPIWWSLAVGPQYSSLGSQPILCASIPGLVPKQLRFCRNYVEIMPSVAEGIKIGIQECQHQ
FRGRRWNCTTIHDSLAIFGPVLDKATRESAFVHAIASAGVAFAVTRSCAEGTAAICGCSSRHQGSPGKGWKWGGCSEDIE
FGGMVSREFADARENRPDARSAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDFLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVSSHGIDGCDLLCCGRGHNARA
ERRREKCRCVFHWCCYVSCQECTRVYDVHTCK*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003565573 CLINVAR
  RCV004076457 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene WNT3A CLINVAR
OMIM 606359 CLINVAR