RGD:152074349 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:152074349 -  Homo sapiens

RGD ID: 152074349
RS ID: rs765238501
ClinVar ID: CV1647482
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT3A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 228,238,439
GRCh38 1 228,050,738
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.396G>A
NC_000001.11:g.228050738G>A
NC_000001.10:g.228238439G>A
NP_149122.1:p.Thr132=
07/26/2021 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WNT3A
Accession:NM_033131
Location:EXON
Amino Acid Prediction: T to T (synonymous)
Amino Acid Position: 132
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAPLGYFLLLCSLKQALGSYPIWWSLAVGPQYSSLGSQPILCASIPGLVPKQLRFCRNYVEIMPSVAEGIKIGIQECQHQ
FRGRRWNCTTVHDSLAIFGPVLDKATRESAFVHAIASAGVAFAVTRSCAEGTAAICGCSSRHQGSPGKGWKWGGCSEDIE
FGGMVSREFADARENRPDARSAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDFLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVSSHGIDGCDLLCCGRGHNARA
ERRREKCRCVFHWCCYVSCQECTRVYDVHTCK*

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002210393 CLINVAR
dbSNP (RS) rs765238501 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WNT3A CLINVAR
OMIM 606359 CLINVAR