NM_144666.3(DNHD1):c.10006T>C (p.Tyr3336His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000585614.17
Allele description [Variation Report for NM_144666.3(DNHD1):c.10006T>C (p.Tyr3336His)]
NM_144666.3(DNHD1):c.10006T>C (p.Tyr3336His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024