Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Thr322Met (p.T322M)
(
ENST00000335475.6,
ENST00000155840.12,
ENST00000496887.7,
ENST00000646564.2,
ENST00000713725.1 )
KCNQ1 p.Thr322Met (p.T322M) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.965C>T (p.Thr322Met) AND Cardiovascular phenotype
- ClinVar Allele ID
- 67819
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.521C>T
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.584C>T
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.965C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.965C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.695C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-04-05
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000247480
- Observed Origin Sample
- germline
Drugs