NM_000257.4(MYH7):c.2922+3A>G AND Hypertrophic cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001202232.4
Allele description [Variation Report for NM_000257.4(MYH7):c.2922+3A>G]
NM_000257.4(MYH7):c.2922+3A>G
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
-
Homo sapiens TALE homeobox protein Meis2e mRNA, complete cds
Homo sapiens TALE homeobox protein Meis2e mRNA, complete cdsgi|8925853|gb|AF179899.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024