NM_000631.5(NCF4):c.271+220C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 20, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001769617.2
Allele description [Variation Report for NM_000631.5(NCF4):c.271+220C>G]
NM_000631.5(NCF4):c.271+220C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Dec 24, 2023