RGD:150417833 Rat Genome Database

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Variant: RGD:150417833 -  Homo sapiens

RGD ID: 150417833
RS ID: rs112416850
ClinVar ID: CV1194033
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 22,051,279
GRCh38 8 22,193,766
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.1181-292A>G
NM_006129.5:c.1181-292A>G
NG_029659.1:g.33627A>G
NC_000008.11:g.22193766A>G
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 RCV001568942 CLINVAR
dbSNP (RS) rs112416850 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP1 CLINVAR
OMIM 112264 CLINVAR