NM_000016.6(ACADM):c.199T>C (p.Tyr67His) AND not provided
- Germline classification:
- Pathogenic (5 submissions)
- Last evaluated:
- Sep 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000185668.32
Allele description [Variation Report for NM_000016.6(ACADM):c.199T>C (p.Tyr67His)]
NM_000016.6(ACADM):c.199T>C (p.Tyr67His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024