RGD:405169583 Rat Genome Database

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Variant: RGD:405169583 -  Homo sapiens

RGD ID: 405169583
ClinVar ID: CV3156945
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 6,707,945
GRCh38 19 6,707,934
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000064.4:c.1846-5C>G
LRG_27:g.17718C>G
NG_009557.1:g.17718C>G
NC_000019.10:g.6707934G>C
More... 		03/27/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:C3
Accession:NM_000064
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003857649 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C3 CLINVAR
OMIM 120700 CLINVAR