RGD:407528842 Rat Genome Database

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Variant: RGD:407528842 -  Homo sapiens

RGD ID: 407528842
ClinVar ID: CV3487626
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: USP4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 49,365,130
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001251877.2:c.349A>G
NM_003363.4:c.349A>G
NM_199443.3:c.349A>G
NG_030370.1:g.17407A>G
More...
04/17/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004680595 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene USP4 CLINVAR
OMIM 603486 CLINVAR