RGD:407474377 Rat Genome Database

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Variant: RGD:407474377 -  Homo sapiens

RGD ID: 407474377
ClinVar ID: CV3472856
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF5  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 144,069,839
GRCh38 7 144,372,746
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005435.4:c.4039G>A
NC_000007.14:g.144372746G>A
NC_000007.13:g.144069839G>A
NM_005435.3:c.4039G>A
More... 		05/02/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004662984 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ARHGEF5 CLINVAR
OMIM 600888 CLINVAR