RGD:28910995 Rat Genome Database

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Variant: RGD:28910995 -  Homo sapiens

RGD ID: 28910995
RS ID: rs935518014
ClinVar ID: CV869556
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MGP  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 15,034,897
GRCh38 12 14,881,963
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000900.5:c.*176C>G
NM_001190839.3:c.*176C>G
NG_023331.2:g.8957C>G
NC_000012.12:g.14881963G>C
More... 		04/27/2017 3 prime utr variant uncertain significance Pulmonic stenosis brachytelephalangism and calcification of cartilages
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MGP
Accession:NM_001190839
Location:3UTRS;EXON

Gene Symbol:MGP
Accession:NM_000900
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001109761 CLINVAR
dbSNP (RS) rs935518014 CLINVAR
MedGen C1855607 CLINVAR
NCBI Gene MGP CLINVAR
OMIM 154870 CLINVAR
  245150 CLINVAR