RGD:150462028 Rat Genome Database

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Variant: RGD:150462028 -  Homo sapiens

RGD ID: 150462028
RS ID: rs77211836
ClinVar ID: CV1214586
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT10B  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 49,359,693
GRCh38 12 48,965,910
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023347.1:g.10949A>G
NC_000012.12:g.48965910T>C
NM_003394.4:c.*185A>G
NC_000012.11:g.49359693T>C
 06/28/2020 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WNT10B
Accession:NM_003394
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001613579 CLINVAR
dbSNP (RS) rs77211836 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WNT10B CLINVAR
OMIM 601906 CLINVAR