RGD:150428704 Rat Genome Database

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Variant: RGD:150428704 -  Homo sapiens

RGD ID: 150428704
RS ID: rs111475221
ClinVar ID: CV1187332
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 22,036,989
GRCh38 8 22,179,476
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.837-229G>A
NM_006129.5:c.837-229G>A
NG_029659.1:g.19337G>A
NC_000008.11:g.22179476G>A
More... 		02/04/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BMP1
Accession:NM_006129
Location:INTRON

Gene Symbol:BMP1
Accession:NM_001199
Location:INTRON

Gene Symbol:BMP1
Accession:NR_033403
Location:INTRON;NON-CODING

Gene Symbol:BMP1
Accession:NR_033404
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001562613 CLINVAR
dbSNP (RS) rs111475221 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP1 CLINVAR
OMIM 112264 CLINVAR