NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000901084.6
Allele description [Variation Report for NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=)]
NM_001145809.2(MYH14):c.4617T>G (p.Arg1539=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024