RGD:407487813 Rat Genome Database

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Variant: RGD:407487813 -  Homo sapiens

RGD ID: 407487813
ClinVar ID: CV3476163
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RPP30  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 92,654,596
GRCh38 10 90,894,839
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001104546.2:c.497G>A
NM_006413.5:c.497G>A
NC_000010.11:g.90894839G>A
NC_000010.10:g.92654596G>A
More... 		04/19/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004665764 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RPP30 CLINVAR
OMIM 606115 CLINVAR