RGD:405151301 Rat Genome Database

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Variant: RGD:405151301 -  Homo sapiens

RGD ID: 405151301
ClinVar ID: CV3079252
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABCC9  LOC105369689  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 21,981,964
GRCh38 12 21,829,030
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_377t1:c.3597G>A
LRG_377t2:c.3597G>A
NM_001377274.1:c.2730G>A
NM_001377273.1:c.3597G>A
More... 		10/08/2023 synonymous variant likely benign CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003620387 CLINVAR
MedGen C1837839 CLINVAR
NCBI Gene ABCC9 CLINVAR
OMIM 601439 CLINVAR
  608569 CLINVAR