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VARIANT - TERM ANNOTATION REPORT

RGD ID: 25317161
Species: Homo sapiens
RGD Object: Variant
Symbol: CV805125
Name: NM_003413.4(ZIC3):c.958C>T (p.Arg320Ter)
Acc ID: DOID:9003587
Term: Congenital Heart Defects, Multiple Types, 1, X-Linked
Definition: null
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
CV805125 IAGP 8554872ClinVarClinVar Annotator: match by term: Heterotaxy, visceral, X-linkedPMID:25741868
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