Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Lys526Gln (p.K526Q)
(
ENST00000496887.7,
ENST00000155840.12,
ENST00000713725.1,
ENST00000646564.2,
ENST00000335475.6 )
KCNQ1 p.Lys526Gln (p.K526Q) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Associated Disease
- long QT syndrome
- Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.1576A>C (p.Lys526Gln) AND Long QT syndrome
- ClinVar Allele ID
- 838247
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.1195A>C
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.1036A>C
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.1576A>C
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.1306A>C
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.1480A>C
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-08-15
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001058372
- ClinVar Disease
- Long QT syndrome
- Observed Origin Sample
- germline
Drugs