Annotation Detail

Information
Associated Genes
DSP DSP-AS1
Associated Variants
DSP p.Cys3= (p.C3=) ( ENST00000379802.8, ENST00000418664.3, ENST00000683682.2, ENST00000710359.2, ENST00000713909.1, ENST00000713910.1, ENST00000713918.1 )
DSP p.Cys3= (p.C3=) ( ENST00000379802.8, ENST00000418664.3, ENST00000683682.2, ENST00000710359.2, ENST00000713909.1, ENST00000713910.1, ENST00000713918.1 )
Source Database
ClinVar
Description
NM_004415.4(DSP):c.9C>T (p.Cys3=) AND Cardiovascular phenotype
ClinVar Allele ID
304013
ClinVar RefSeq Alternation Syntax
NM_004415.4:c.9C>T
ClinVar RefSeq Alternation Syntax
NM_001008844.3:c.9C>T
ClinVar RefSeq Alternation Syntax
NM_001319034.2:c.9C>T
Clinical Significance Description
Likely benign
Clinical Significance Last Update
2016-06-08
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000620987
Observed Origin Sample
germline
Drugs