RGD:405219448 Rat Genome Database

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Variant: RGD:405219448 -  Homo sapiens

RGD ID: 405219448
ClinVar ID: CV3063346
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC101927897  NFATC1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 18 77,221,339
GRCh38 18 79,461,339
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_172387.3:c.1893G>A
NM_172389.3:c.1893G>A
NM_001278669.2:c.1932G>A
NM_001278670.2:c.1932G>A
More... 		05/31/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003733089 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFATC1 CLINVAR
OMIM 600489 CLINVAR