NM_001278431.2(C1QTNF5):c.567C>T (p.Ala189=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001482327.7
Allele description [Variation Report for NM_001278431.2(C1QTNF5):c.567C>T (p.Ala189=)]
NM_001278431.2(C1QTNF5):c.567C>T (p.Ala189=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024