NM_000257.4(MYH7):c.3158G>A (p.Arg1053Gln) AND not provided
- Germline classification:
- Pathogenic/Likely pathogenic (2 submissions)
- Last evaluated:
- Jun 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000158590.8
Allele description [Variation Report for NM_000257.4(MYH7):c.3158G>A (p.Arg1053Gln)]
NM_000257.4(MYH7):c.3158G>A (p.Arg1053Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024