RGD:14705858 Rat Genome Database

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Variant: RGD:14705858 -  Homo sapiens

RGD ID: 14705858
RS ID: rs7352741
ClinVar ID: CV670253
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 55,803,149
GRCh38 20 57,228,093
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001719.3:c.611+136G>A
NG_032771.1:g.43559G>A
NC_000020.11:g.57228093C>T
NC_000020.10:g.55803149C>T
More...
06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BMP7
Accession:NM_001719
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826334 CLINVAR
dbSNP (RS) rs7352741 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BMP7 CLINVAR
OMIM 112267 CLINVAR