NM_000257.4(MYH7):c.3853+7C>T 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:
- RCV000346163.13
Allele description [Variation Report for NM_000257.4(MYH7):c.3853+7C>T]
NM_000257.4(MYH7):c.3853+7C>T
Condition(s)
- Name:
- Left ventricular noncompaction cardiomyopathy
- Identifiers:
- MedGen: C4021133; Human Phenotype Ontology: HP:0011664
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hypothetical protein [Serratia phage CHI14]
hypothetical protein [Serratia phage CHI14]gi|1201093984|gb|ARW57663.1|Protein
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Homo sapiens chromosome 9 genomic contig HG2030_PATCH, GRC reference assembly FI...
Homo sapiens chromosome 9 genomic contig HG2030_PATCH, GRC reference assembly FIX PATCH for GRCh38gi|693592218|gnl|ASM:GCA_000005045. 2030_PATCH|gb|KN196479.1|Nucleotide
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EFNA4 [Pongo abelii]
EFNA4 [Pongo abelii]Gene ID:100449916Gene
-
ZNF726P1 zinc finger protein 726 pseudogene 1 [Homo sapiens]
ZNF726P1 zinc finger protein 726 pseudogene 1 [Homo sapiens]Gene ID:7618Gene
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Last Updated: Sep 16, 2024