Annotation Detail
Information
- Associated Genes
- SCN5A
- Associated Variants
-
SCN5A p.Lys1493Arg (p.K1493R)
(
ENST00000333535.9,
ENST00000413689.6,
ENST00000414099.6,
ENST00000423572.7,
ENST00000449557.6,
ENST00000450102.6,
ENST00000455624.6 )
SCN5A p.Lys1493Arg (p.K1493R) ( ENST00000333535.9, ENST00000413689.6, ENST00000414099.6, ENST00000423572.7, ENST00000449557.6, ENST00000450102.6, ENST00000455624.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000335.5(SCN5A):c.4475A>G (p.Lys1492Arg) AND not provided
- ClinVar Allele ID
- 78791
- ClinVar RefSeq Alternation Syntax
- NM_001354701.2:c.4421A>G
- ClinVar RefSeq Alternation Syntax
- NM_198056.3:c.4478A>G
- ClinVar RefSeq Alternation Syntax
- NM_001099405.2:c.4424A>G
- ClinVar RefSeq Alternation Syntax
- NM_000335.5:c.4475A>G
- ClinVar RefSeq Alternation Syntax
- NM_001160161.2:c.4316A>G
- ClinVar RefSeq Alternation Syntax
- NM_001099404.2:c.4478A>G
- ClinVar RefSeq Alternation Syntax
- NM_001160160.2:c.4475A>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2024-01-14
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001508490
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs