Annotation Detail

Information
Associated Genes
AKAP9
Associated Variants
AKAP9 p.Met463Ile (p.M463I) ( ENST00000356239.8, ENST00000359028.7, ENST00000679521.1, ENST00000679821.1, ENST00000680072.1, ENST00000680181.1, ENST00000680513.1, ENST00000680534.1, ENST00000680766.1, ENST00000680952.1, ENST00000681412.1, ENST00000681722.1 )
AKAP9 p.Met463Ile (p.M463I) ( ENST00000356239.8, ENST00000359028.7, ENST00000679521.1, ENST00000679821.1, ENST00000680072.1, ENST00000680181.1, ENST00000680513.1, ENST00000680534.1, ENST00000680766.1, ENST00000680952.1, ENST00000681412.1, ENST00000681722.1 )
Associated Disease
not specified
Source Database
ClinVar
Description
NM_005751.5(AKAP9):c.1389G>T (p.Met463Ile) AND not specified
ClinVar Allele ID
140050
ClinVar RefSeq Alternation Syntax
NM_005751.5:c.1389G>T
ClinVar RefSeq Alternation Syntax
NM_147185.3:c.1389G>T
Clinical Significance Description
Benign
Clinical Significance Last Update
2019-08-12
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000123592
ClinVar Disease
not specified
Observed Origin Sample
germline
Drugs