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Variant : CV479305 (NM_005359.5(SMAD4):c.9T>C (p.Asn3=)) Homo sapiens

Symbol: CV479305
Name: NM_005359.5(SMAD4):c.9T>C (p.Asn3=)
Condition: Hereditary cancer-predisposing syndrome [RCV000567859]|Juvenile polyposis syndrome [RCV000635514]
Clinical Significance: likely benign
Last Evaluated: 09/20/2017
Review Status: criteria provided, multiple submitters, no conflicts|criteria provided, single submitter
Related Genes: SMAD4  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_005359.5:c.9T>C
LRG_318t1:c.9T>C
NC_000018.9:g.48573425T>C
NP_005350.1:p.Asn3=
LRG_318:g.84016T>C
LRG_318p1:p.Asn3=
NG_013013.2:g.84016T>C
NC_000018.10:g.51047055T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381851,047,055 - 51,047,055CLINVAR
GRCh371848,573,425 - 48,573,425CLINVAR
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: 13485234
Created: 2018-01-09
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.