RGD:405167900 Rat Genome Database

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Variant: RGD:405167900 -  Homo sapiens

RGD ID: 405167900
ClinVar ID: CV3070938
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFATC1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 18 77,211,730
GRCh38 18 79,451,730
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_765977.1:p.Tyr593Cys
NP_001265598.1:p.Tyr606Cys
NP_001265599.1:p.Tyr606Cys
NP_006153.2:p.Tyr606Cys
More... 		05/19/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003727550 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFATC1 CLINVAR
OMIM 600489 CLINVAR