Annotation Detail

Information
Associated Genes
DYNC2LI1 ABCG5
Associated Variants
ABCG5 p.Gln604Glu (p.Q604E) ( ENST00000405322.8 )
ABCG5 p.Gln604Glu (p.Q604E) ( ENST00000405322.8 )
Associated Disease
not specified
Source Database
ClinVar
Description
NM_022436.3(ABCG5):c.1810C>G (p.Gln604Glu) AND not specified
ClinVar Allele ID
286312
ClinVar RefSeq Alternation Syntax
NM_001348912.2:c.*15+2738G>C
ClinVar RefSeq Alternation Syntax
NM_022436.3:c.1810C>G
ClinVar RefSeq Alternation Syntax
NM_001348913.2:c.*15+2738G>C
Clinical Significance Description
Benign/Likely benign
Clinical Significance Last Update
2023-04-04
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000591475
ClinVar Disease
not specified
Observed Origin Sample
germline
Drugs