Annotation Detail

Information
Associated Genes
ABCC8
Associated Variants
ABCC8 p.Arg1204Trp (p.R1204W) ( ENST00000643260.1, ENST00000389817.8, ENST00000684571.1, ENST00000302539.9, ENST00000646902.1, ENST00000644772.1, ENST00000642271.1, ENST00000683136.1, ENST00000647015.1 )
ABCC8 p.Arg1204Trp (p.R1204W) ( ENST00000302539.9, ENST00000389817.8, ENST00000642271.1, ENST00000643260.1, ENST00000644772.1, ENST00000646902.1, ENST00000647015.1, ENST00000683136.1, ENST00000684571.1 )
Associated Disease
Diabetes mellitus, transient neonatal, 2
Source Database
ClinVar
Description
NM_000352.6(ABCC8):c.3544C>T (p.Arg1182Trp) AND Diabetes mellitus, transient neonatal, 2
ClinVar Allele ID
207846
ClinVar RefSeq Alternation Syntax
NM_001351297.2:c.3541C>T
ClinVar RefSeq Alternation Syntax
NR_147094.2:n.3693C>T
ClinVar RefSeq Alternation Syntax
NM_001351295.2:c.3610C>T
ClinVar RefSeq Alternation Syntax
NM_001287174.3:c.3547C>T
ClinVar RefSeq Alternation Syntax
NM_000352.6:c.3544C>T
ClinVar RefSeq Alternation Syntax
NM_001351296.2:c.3544C>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2014-11-24
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000192916
ClinVar Disease
Diabetes mellitus, transient neonatal, 2
Observed Origin Sample
germline
Drugs