NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003137810.3
Allele description [Variation Report for NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln)]
NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024