Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Thr322Lys (p.T322K)
(
ENST00000713725.1,
ENST00000646564.2,
ENST00000335475.6,
ENST00000155840.12,
ENST00000496887.7 )
KCNQ1 p.Thr322Lys (p.T322K) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Associated Disease
- Congenital long QT syndrome
- Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.965C>A (p.Thr322Lys) AND Congenital long QT syndrome
- ClinVar Allele ID
- 67818
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.521C>A
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.584C>A
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.965C>A
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.965C>A
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.695C>A
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000057830
- ClinVar Disease
- Congenital long QT syndrome
- Observed Origin Sample
- germline
Drugs