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Variant : CV618923 (NM_005359.5(SMAD4):c.*1G>C) Homo sapiens

Symbol: CV618923
Name: NM_005359.5(SMAD4):c.*1G>C
Condition: Hereditary cancer-predisposing syndrome [RCV000776603]
Clinical Significance: likely benign
Last Evaluated: 09/22/2017
Review Status: criteria provided, single submitter
Related Genes: SMAD4  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): LRG_318t1:c.*1G>C
LRG_318:g.115429G>C
NG_013013.2:g.115429G>C
NC_000018.10:g.51078468G>C
NC_000018.9:g.48604838G>C
NM_005359.5:c.*1G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381851,078,468 - 51,078,468CLINVAR
GRCh371848,604,838 - 48,604,838CLINVAR
Cytogenetic Map1818q21.2CLINVAR
Trait Synonyms: Cancer predisposition; Neoplastic Syndromes, Hereditary; Tumor predisposition



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14694210
Created: 2019-06-11
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.