NM_000183.3(HADHB):c.272C>T (p.Thr91Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 21, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001507553.5
Allele description [Variation Report for NM_000183.3(HADHB):c.272C>T (p.Thr91Ile)]
NM_000183.3(HADHB):c.272C>T (p.Thr91Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024