Annotation Detail
Information
- Associated Genes
- KCNE1
- Associated Variants
-
KCNE1 p.Asp85Asn (p.D85N)
(
ENST00000416357.6,
ENST00000399284.1,
ENST00000399286.3,
ENST00000337385.7,
ENST00000399289.7,
ENST00000432085.5,
ENST00000611936.1,
ENST00000621601.4 )
KCNE1 p.Asp85Asn (p.D85N) ( ENST00000337385.7, ENST00000399284.1, ENST00000399286.3, ENST00000399289.7, ENST00000416357.6, ENST00000432085.5, ENST00000611936.1, ENST00000621601.4 ) - Associated Disease
- Long QT syndrome 5, acquired, susceptibility to
- Source Database
- ClinVar
- Description
- NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn) AND Long QT syndrome 5, acquired, susceptibility to
- ClinVar Allele ID
- 28518
- ClinVar RefSeq Alternation Syntax
- NM_001127670.4:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270404.3:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270402.3:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_000219.6:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270405.3:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001270403.2:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127668.4:c.253G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127669.4:c.253G>A
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2006-08-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014422
- ClinVar Disease
- Long QT syndrome 5, acquired, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 14760488
- Pubmed
- 16823764
- Pubmed
- 8899564
- Pubmed
- 15051636
Drugs