RGD:14709077 Rat Genome Database

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Variant: RGD:14709077 -  Homo sapiens

RGD ID: 14709077
RS ID: rs1380761384
ClinVar ID: CV666156
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 68,170,940
GRCh38 11 68,403,472
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002335.4:c.1585-11C>T
NM_001291902.2:c.-353-11C>T
NG_015835.2:g.95833C>T
NC_000011.10:g.68403472C>T
More... 		10/24/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LRP5
Accession:NM_001291902
Location:5UTRS;INTRON

Gene Symbol:LRP5
Accession:XM_047426948
Location:INTRON

Gene Symbol:LRP5
Accession:XM_047426949
Location:INTRON

Gene Symbol:LRP5
Accession:NM_002335
Location:INTRON

Gene Symbol:LRP5
Accession:XM_011545029
Location:INTRON

Gene Symbol:LRP5
Accession:XM_011545031
Location:INTRON

Gene Symbol:LRP5
Accession:XM_047426950
Location:INTRON

Gene Symbol:LRP5
Accession:XM_005273994
Location:INTRON

Gene Symbol:LRP5
Accession:XM_017017735
Location:INTRON

Gene Symbol:LRP5
Accession:XM_017017736
Location:INTRON

Gene Symbol:LRP5
Accession:XM_011545030
Location:INTRON

Gene Symbol:LRP5
Accession:XR_001747874
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000827339 CLINVAR
dbSNP (RS) rs1380761384 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRP5 CLINVAR
OMIM 603506 CLINVAR