RGD:150471038 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:150471038 -  Homo sapiens

RGD ID: 150471038
RS ID: rs5745767
ClinVar ID: CV1209459
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HGF  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 81,332,105
GRCh38 7 81,702,789
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.1996-32T>G
NM_000601.6:c.2011-32T>G
NG_016274.2:g.72348T>G
NC_000007.14:g.81702789A>C
More...
11/24/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HGF
Accession:NM_001010932
Location:INTRON

Gene Symbol:HGF
Accession:NM_000601
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010933
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010931
Location:INTRON

Gene Symbol:HGF
Accession:NM_001010934
Location:INTRON

Gene Symbol:HGF
Accession:XM_047420293
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001588570 CLINVAR
dbSNP (RS) rs5745767 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HGF CLINVAR
OMIM 142409 CLINVAR