Annotation Detail
Information
- Associated Genes
- KCNJ11
- Associated Variants
-
KCNJ11 p.Phe333Ile (p.F333I)
(
ENST00000339994.5,
ENST00000682764.1,
ENST00000682350.1,
ENST00000528731.1 )
KCNJ11 p.Phe333Ile (p.F333I) ( ENST00000339994.5, ENST00000528731.1, ENST00000682350.1, ENST00000682764.1 ) - Source Database
- ClinVar
- Description
- NM_000525.4(KCNJ11):c.997T>A (p.Phe333Ile) AND Neonatal hypoglycemia
- ClinVar Allele ID
- 34057
- ClinVar RefSeq Alternation Syntax
- NM_001166290.2:c.736T>A
- ClinVar RefSeq Alternation Syntax
- NM_001377296.1:c.736T>A
- ClinVar RefSeq Alternation Syntax
- NM_001377297.1:c.736T>A
- ClinVar RefSeq Alternation Syntax
- NM_000525.4:c.997T>A
- Clinical Significance Description
- Benign
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002226653
- Observed Origin Sample
- somatic
Drugs