RGD:407426850 Rat Genome Database

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Variant: RGD:407426850 -  Homo sapiens

RGD ID: 407426850
ClinVar ID: CV3411650
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RLIM  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 73,812,446
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_016120.4:c.704T>G
NM_183353.3:c.704T>G
NG_013258.1:g.27016T>G
NC_000023.11:g.74592611A>C
More... 		12/10/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004590828 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RLIM CLINVAR
OMIM 300379 CLINVAR