Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Arg397Trp (p.R397W)
(
ENST00000155840.12,
ENST00000496887.7,
ENST00000646564.2,
ENST00000335475.6,
ENST00000713725.1 )
KCNQ1 p.Arg397Trp (p.R397W) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Associated Disease
- long QT syndrome 1
- Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.1189C>T (p.Arg397Trp) AND Long QT syndrome 1
- ClinVar Allele ID
- 67638
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.808C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.1093C>T
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.1189C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.649C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.919C>T
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-09-04
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000203070
- ClinVar Disease
- Long QT syndrome 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs