Annotation Detail
Information
- Associated Genes
- KCNE1
- Associated Variants
-
KCNE1 p.Thr7Ile (p.T7I)
(
ENST00000337385.7,
ENST00000399284.1,
ENST00000399286.3,
ENST00000399289.7,
ENST00000416357.6,
ENST00000432085.5,
ENST00000611936.1,
ENST00000621601.4 )
KCNE1 p.Thr7Ile (p.T7I) ( ENST00000337385.7, ENST00000399284.1, ENST00000399286.3, ENST00000399289.7, ENST00000416357.6, ENST00000432085.5, ENST00000611936.1, ENST00000621601.4 ) - Associated Disease
- Congenital long QT syndrome
- Source Database
- ClinVar
- Description
- NM_000219.6(KCNE1):c.20C>T (p.Thr7Ile) AND Congenital long QT syndrome
- ClinVar Allele ID
- 28515
- ClinVar RefSeq Alternation Syntax
- NM_001127669.4:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127670.4:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001270402.3:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001270403.2:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127668.4:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001270404.3:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_000219.6:c.20C>T
- ClinVar RefSeq Alternation Syntax
- NM_001270405.3:c.20C>T
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000119076
- ClinVar Disease
- Congenital long QT syndrome
- Observed Origin Sample
- germline
Drugs