RGD:405151144 Rat Genome Database

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Variant: RGD:405151144 -  Homo sapiens

RGD ID: 405151144
ClinVar ID: CV3063476
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP1  LOC113788269  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 22,053,069
GRCh38 8 22,195,556
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001199.4:c.1734C>T
NM_006129.5:c.1734C>T
NG_062562.2:g.1281C>T
NG_029659.1:g.35417C>T
More... 		08/09/2023 non-coding transcript variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003726264 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP1 CLINVAR
  LOC113788269 CLINVAR
OMIM 112264 CLINVAR