Annotation Detail

Information
Associated Genes
ANO5
Associated Variants
ANO5 p.His725Ter (p.H725*) ( ENST00000684663.1, ENST00000682266.1, ENST00000683197.1, ENST00000324559.9, ENST00000683411.1, ENST00000682341.1, ENST00000683437.1 )
ANO5 p.His725Ter (p.H725*) ( ENST00000324559.9, ENST00000682266.1, ENST00000682341.1, ENST00000683197.1, ENST00000683411.1, ENST00000683437.1, ENST00000684663.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_213599.3(ANO5):c.2172_2178del (p.Ala724_His725insTer) AND not provided
ClinVar Allele ID
192164
ClinVar RefSeq Alternation Syntax
NM_213599.3:c.2172_2178del
ClinVar RefSeq Alternation Syntax
NM_001142649.2:c.2169_2175del
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2015-06-03
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000175500
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs