NM_000335.5(SCN5A):c.4076T>G (p.Phe1359Cys) AND Brugada syndrome
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000058639.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.4076T>G (p.Phe1359Cys)]
NM_000335.5(SCN5A):c.4076T>G (p.Phe1359Cys)
Condition(s)
- Name:
- Brugada syndrome
- Synonyms:
- Sudden unexpected nocturnal death syndrome; Sudden unexplained nocturnal death syndrome; Sudden Unexplained Death Syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015263; MedGen: C1142166; OMIM: PS601144
-
chemotaxis protein CheB [Fulvivirga ligni]
chemotaxis protein CheB [Fulvivirga ligni]gi|2174437936|gnl|PRJNA789060|LVD16 5|gb|UII19237.1|Protein
-
MAST4 microtubule associated serine/threonine kinase family member 4 [Bos taurus...
MAST4 microtubule associated serine/threonine kinase family member 4 [Bos taurus]Gene ID:529061Gene
-
OMIM Links for GEO Profiles (Select 81504422) (2)
OMIM
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Nov 5, 2022