RGD:405149137 Rat Genome Database

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Variant: RGD:405149137 -  Homo sapiens

RGD ID: 405149137
ClinVar ID: CV3142005
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF113A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 119,005,206
GRCh38 X 119,871,243
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006978.3:c.371C>T
NG_009381.1:g.4473G>A
NG_021227.1:g.5586C>T
NC_000023.11:g.119871243G>A
More... 		09/08/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003839927 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RNF113A CLINVAR
OMIM 300951 CLINVAR