Annotation Detail
Information
- Associated Genes
- SCN5A
- Associated Variants
-
SCN5A p.Arg1826His (p.R1826H)
(
ENST00000333535.9,
ENST00000413689.6,
ENST00000414099.6,
ENST00000423572.7,
ENST00000449557.6,
ENST00000450102.6,
ENST00000455624.6 )
SCN5A p.Arg1826His (p.R1826H) ( ENST00000333535.9, ENST00000413689.6, ENST00000414099.6, ENST00000423572.7, ENST00000449557.6, ENST00000450102.6, ENST00000455624.6 ) - Associated Disease
- sudden infant death syndrome
- Source Database
- ClinVar
- Description
- NM_000335.5(SCN5A):c.5474G>A (p.Arg1825His) AND SUDDEN INFANT DEATH SYNDROME
- ClinVar Allele ID
- 24428
- ClinVar RefSeq Alternation Syntax
- NM_001099404.2:c.5477G>A
- ClinVar RefSeq Alternation Syntax
- NM_198056.3:c.5477G>A
- ClinVar RefSeq Alternation Syntax
- NM_000335.5:c.5474G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354701.2:c.5420G>A
- ClinVar RefSeq Alternation Syntax
- NM_001160161.2:c.5315G>A
- ClinVar RefSeq Alternation Syntax
- NM_001099405.2:c.5423G>A
- ClinVar RefSeq Alternation Syntax
- NM_001160160.2:c.5378G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2014-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000148848
- ClinVar Disease
- SUDDEN INFANT DEATH SYNDROME
- Observed Origin Sample
- germline
Drugs