RGD:13833991 Rat Genome Database

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Variant: RGD:13833991 -  Homo sapiens

RGD ID: 13833991
RS ID: rs374104266
ClinVar ID: CV585231
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 68,216,542
GRCh38 11 68,449,074
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001291902.2:c.*4C>T
NM_002335.4:c.*4C>T
NG_015835.2:g.141435C>T
NC_000011.10:g.68449074C>T
More... 		10/06/2017 3 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:LRP5
Accession:XM_005273994
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_011545030
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_011545031
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:NM_001291902
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_011545029
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_017017735
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:NM_002335
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_017017736
Location:3UTRS;EXON

Gene Symbol:LRP5
Accession:XM_047426948
Location:INTRON

Gene Symbol:LRP5
Accession:XM_047426950
Location:INTRON

Gene Symbol:LRP5
Accession:XM_047426949
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000729392 CLINVAR
dbSNP (RS) rs374104266 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRP5 CLINVAR
OMIM 603506 CLINVAR