Annotation Detail

Information
Associated Genes
CCNH RASA1
Associated Variants
RASA1 p.Thr843Asn (p.T843N) ( ENST00000456692.6, ENST00000274376.11, ENST00000506290.1, ENST00000512763.5 )
RASA1 p.Thr843Asn (p.T843N) ( ENST00000512763.5, ENST00000274376.11, ENST00000456692.6, ENST00000506290.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_002890.3(RASA1):c.2528C>A (p.Thr843Asn) AND not provided
ClinVar Allele ID
239862
ClinVar RefSeq Alternation Syntax
NM_001364075.2:c.933+15269G>T
ClinVar RefSeq Alternation Syntax
NM_022650.3:c.1997C>A
ClinVar RefSeq Alternation Syntax
NM_002890.3:c.2528C>A
Clinical Significance Description
Benign/Likely benign
Clinical Significance Last Update
2023-03-27
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV001561210
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs