NM_000257.4(MYH7):c.4659C>T (p.His1553=) AND Left ventricular noncompaction cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000391904.12
Allele description [Variation Report for NM_000257.4(MYH7):c.4659C>T (p.His1553=)]
NM_000257.4(MYH7):c.4659C>T (p.His1553=)
Condition(s)
- Name:
- Left ventricular noncompaction cardiomyopathy
- Identifiers:
- MedGen: C4021133; Human Phenotype Ontology: HP:0011664
-
Autonomic neuropathy
Autonomic neuropathyMedGen
-
C0259749[conceptid] (1)
MedGen
-
Stmnl-ps1 stathmin like, pseudogene 1 [Rattus norvegicus]
Stmnl-ps1 stathmin like, pseudogene 1 [Rattus norvegicus]Gene ID:363652Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 16, 2024