RGD:405219347 Rat Genome Database

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Variant: RGD:405219347 -  Homo sapiens

RGD ID: 405219347
ClinVar ID: CV3034979
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP1  LOC127458870  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 22,069,191
GRCh38 8 22,211,678
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006129.5:c.2911C>T
NG_113639.1:g.233C>T
NG_029659.1:g.51539C>T
NC_000008.11:g.22211678C>T
More... 		10/18/2023 non-coding transcript variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003709690 CLINVAR
  RCV003966586 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP1 CLINVAR
OMIM 112264 CLINVAR