NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 5, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001810710.13
Allele description [Variation Report for NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp)]
NM_001145809.2(MYH14):c.5875C>T (p.Arg1959Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024