Annotation Detail

Information
Associated Genes
ACTB
Associated Variants
ACTB p.Ile75Thr (p.I75T) ( ENST00000432588.6, ENST00000473257.3, ENST00000493945.6, ENST00000642480.2, ENST00000646664.1, ENST00000674681.1, ENST00000675515.1, ENST00000676319.1, ENST00000676397.1 )
ACTB p.Ile75Thr (p.I75T) ( ENST00000432588.6, ENST00000473257.3, ENST00000493945.6, ENST00000642480.2, ENST00000646664.1, ENST00000674681.1, ENST00000675515.1, ENST00000676319.1, ENST00000676397.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_001101.5(ACTB):c.224T>C (p.Ile75Thr) AND not provided
ClinVar Allele ID
132662
ClinVar RefSeq Alternation Syntax
NM_001101.5:c.224T>C
Clinical Significance Description
Likely pathogenic
Clinical Significance Last Update
2017-10-19
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000519582
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs