NM_000257.4(MYH7):c.4806C>T (p.Asp1602=) AND Cardiovascular phenotype
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 8, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000618217.10
Allele description [Variation Report for NM_000257.4(MYH7):c.4806C>T (p.Asp1602=)]
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
Homo sapiens
Homo sapiensGenome
-
Genome Links for Protein (Select 1905437373) (1)
Genome
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Last Updated: Nov 10, 2024