NM_005159.4(ACTC1):c.*422T>A AND Left ventricular noncompaction cardiomyopathy
- Germline classification:
- Uncertain significance (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:
- RCV000354798.14
Allele description [Variation Report for NM_005159.4(ACTC1):c.*422T>A]
NM_005159.4(ACTC1):c.*422T>A
Condition(s)
- Name:
- Left ventricular noncompaction cardiomyopathy
- Identifiers:
- MedGen: C4021133; Human Phenotype Ontology: HP:0011664
-
Homo sapiens proline rich 5 (salivary) (PROL5), mRNA
Homo sapiens proline rich 5 (salivary) (PROL5), mRNAgi|6912577|ref|NM_012390.1|Nucleotide
-
potassium channel subfamily K member 16 isoform 2 [Homo sapiens]
potassium channel subfamily K member 16 isoform 2 [Homo sapiens]gi|14149764|ref|NP_115491.1|Protein
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Last Updated: Oct 26, 2024