NM_031908.6(C1QTNF2):c.496C>G (p.Pro166Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004159353.1
Allele description [Variation Report for NM_031908.6(C1QTNF2):c.496C>G (p.Pro166Ala)]
NM_031908.6(C1QTNF2):c.496C>G (p.Pro166Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
eggc.vipYsE (0)
BioProject
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Last Updated: May 19, 2024