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Variant : CV331650 (NM_005359.5(SMAD4):c.*2989A>G) Homo sapiens

Symbol: CV331650
Name: NM_005359.5(SMAD4):c.*2989A>G
Condition: Juvenile Polyposis [RCV000336049]|Myhre syndrome [RCV000376546]|Osler hemorrhagic telangiectasia syndrome [RCV000285715]
Clinical Significance: likely benign
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.*2989A>G
LRG_318:g.118417A>G
NG_013013.2:g.118417A>G
NC_000018.10:g.51081456A>G
NC_000018.9:g.48607826A>G
NM_005359.5:c.*2989A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381851,081,456 - 51,081,456CLINVAR
GRCh371848,607,826 - 48,607,826CLINVAR
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: 11615463
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.