RGD:405240641 Rat Genome Database

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Variant: RGD:405240641 -  Homo sapiens

RGD ID: 405240641
ClinVar ID: CV3176778
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF10  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 1,900,940
GRCh38 8 1,952,774
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008480.1:g.133792G>C
NC_000008.11:g.1952774G>C
NC_000008.10:g.1900940G>C
NM_014629.2:c.3467G>C
More... 		01/21/2024 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003867216 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARHGEF10 CLINVAR
OMIM 608136 CLINVAR