Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Thr312Ile (p.T312I)
(
ENST00000496887.7,
ENST00000155840.12,
ENST00000646564.2,
ENST00000335475.6,
ENST00000713725.1 )
KCNQ1 p.Thr312Ile (p.T312I) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.935C>T (p.Thr312Ile) AND Cardiovascular phenotype
- ClinVar Allele ID
- 18155
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.935C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.491C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.665C>T
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.554C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.935C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2020-06-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002444417
- Observed Origin Sample
- germline
Drugs