RGD:150405292 Rat Genome Database

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Variant: RGD:150405292 -  Homo sapiens

RGD ID: 150405292
RS ID: rs115481770
ClinVar ID: CV1190761
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP1  LOC113788269  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 22,052,658
GRCh38 8 22,195,145
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.10:g.22052658T>G
NM_001199.4:c.1639+226T>G
NM_006129.5:c.1639+226T>G
NG_029659.1:g.35006T>G
More... 		07/10/2018 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 RCV001564216 CLINVAR
dbSNP (RS) rs115481770 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP1 CLINVAR
  LOC113788269 CLINVAR
OMIM 112264 CLINVAR