RGD:407461755 Rat Genome Database

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Variant: RGD:407461755 -  Homo sapiens

RGD ID: 407461755
ClinVar ID: CV3480188
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC110599576  SCNN1D  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 1,223,058
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.1287678G>A
NC_000001.10:g.1223058G>A
NR_037668.3:n.1537G>A
NM_001130413.3:c.1405G>A
More... 		05/29/2024 missense variant likely benign AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004658826 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LOC110599576 CLINVAR
  SCNN1D CLINVAR
OMIM 601328 CLINVAR