RGD:405254223 Rat Genome Database

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Variant: RGD:405254223 -  Homo sapiens

RGD ID: 405254223
ClinVar ID: CV3055132
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF10  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 1,905,059
GRCh38 8 1,956,893
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_234t1:c.3665C>A
NM_001308152.2:c.3551C>A
NM_014629.4:c.3665C>A
NM_001308153.2:c.3737C>A
More... 		07/30/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003722909 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARHGEF10 CLINVAR
OMIM 608136 CLINVAR