RGD:407462878 Rat Genome Database

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Variant: RGD:407462878 -  Homo sapiens

RGD ID: 407462878
ClinVar ID: CV3488551
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF202  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 123,597,028
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301779.2:c.1624T>A
NM_001301780.2:c.1624T>A
NM_003455.4:c.1624T>A
NM_001301819.1:c.952T>A
More... 		04/04/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004688114 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ZNF202 CLINVAR
OMIM 603430 CLINVAR