RGD:407450994 Rat Genome Database

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Variant: RGD:407450994 -  Homo sapiens

RGD ID: 407450994
ClinVar ID: CV3491725
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WASHC2A  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 51,853,055
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001005751.3:c.1031C>G
NM_001291398.2:c.1031C>G
NM_001330102.2:c.1031C>G
NC_000010.11:g.50093295C>G
More... 		04/30/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004683504 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene WASHC2A CLINVAR