Annotation Detail
Information
- Associated Genes
- KCNE1
- Associated Variants
-
KCNE1 p.Arg67His (p.R67H)
(
ENST00000337385.7,
ENST00000399284.1,
ENST00000399286.3,
ENST00000399289.7,
ENST00000416357.6,
ENST00000432085.5,
ENST00000611936.1,
ENST00000621601.4 )
KCNE1 p.Arg67His (p.R67H) ( 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.200G>A (p.Arg67His) AND Congenital long QT syndrome
- ClinVar Allele ID
- 136409
- ClinVar RefSeq Alternation Syntax
- NM_001127669.4:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270405.3:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127668.4:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270403.2:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_000219.6:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127670.4:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270404.3:c.200G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270402.3:c.200G>A
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000119073
- ClinVar Disease
- Congenital long QT syndrome
- Observed Origin Sample
- germline
Drugs