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Variant : CV347279 (NM_005359.5(SMAD4):c.*2461C>T) Homo sapiens

Symbol: CV347279
Name: NM_005359.5(SMAD4):c.*2461C>T
Condition: Juvenile Polyposis [RCV000391785]|Myhre syndrome [RCV000362188]|Osler hemorrhagic telangiectasia syndrome [RCV000307595]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: SMAD4  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): LRG_318t1:c.*2461C>T
LRG_318:g.117889C>T
NG_013013.2:g.117889C>T
NC_000018.10:g.51080928C>T
NC_000018.9:g.48607298C>T
NM_005359.5:c.*2461C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381851,080,928 - 51,080,928CLINVAR
GRCh371848,607,298 - 48,607,298CLINVAR
Cytogenetic Map1818q21.2CLINVAR
Trait Synonyms: Laryngotracheal stenosis, progressive, with short stature and arthropathy; TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1
Age Of Onset: childhood
Prevalence: 1:10,000|<1 / 1 000 000



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11652849
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.