RGD:407523744 Rat Genome Database

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Variant: RGD:407523744 -  Homo sapiens

RGD ID: 407523744
ClinVar ID: CV3489710
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WDR20  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 102,675,209
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001353681.2:c.*2-13958C>A
NM_001242414.2:c.*271C>A
NM_001353675.2:c.-70C>A
NM_001353676.2:c.-70C>A
More... 		05/08/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004678168 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene WDR20 CLINVAR
OMIM 617741 CLINVAR