RGD:150425500 Rat Genome Database

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Variant: RGD:150425500 -  Homo sapiens

RGD ID: 150425500
RS ID: rs5745673
ClinVar ID: CV1184016
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HGF  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 81,373,001
GRCh38 7 81,743,685
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001010932.3:c.732-214T>C
NM_001010933.3:c.732-214T>C
NM_000601.6:c.747-214T>C
NM_001010931.3:c.747-214T>C
More... 		02/02/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HGF
Accession:NM_001010933
Location:INTRON

Gene Symbol:HGF
Accession:XM_047420293
Location:INTRON

Gene Symbol:HGF
Accession:NM_000601
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010932
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010934
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010931
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001558073 CLINVAR
dbSNP (RS) rs5745673 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HGF CLINVAR
OMIM 142409 CLINVAR