Annotation Detail
Information
- Associated Genes
- ABCC8
- Associated Variants
-
ABCC8 p.Ile1478Met (p.I1478M)
(
ENST00000389817.8,
ENST00000684571.1,
ENST00000643260.1,
ENST00000646902.1,
ENST00000644772.1,
ENST00000302539.9,
ENST00000642271.1,
ENST00000647015.1,
ENST00000683136.1 )
ABCC8 p.Ile1478Met (p.I1478M) ( ENST00000302539.9, ENST00000389817.8, ENST00000642271.1, ENST00000643260.1, ENST00000644772.1, ENST00000646902.1, ENST00000647015.1, ENST00000683136.1, ENST00000684571.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000352.6(ABCC8):c.4368C>G (p.Ile1456Met) AND not specified
- ClinVar Allele ID
- 44283
- ClinVar RefSeq Alternation Syntax
- NM_001351295.2:c.4434C>G
- ClinVar RefSeq Alternation Syntax
- NM_001351297.2:c.4365C>G
- ClinVar RefSeq Alternation Syntax
- NM_001287174.3:c.4371C>G
- ClinVar RefSeq Alternation Syntax
- NR_147094.2:n.4663C>G
- ClinVar RefSeq Alternation Syntax
- NM_000352.6:c.4368C>G
- ClinVar RefSeq Alternation Syntax
- NM_001351296.2:c.4368C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-05-04
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003234920
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs