NM_152299.4(NCAPH2):c.946C>G (p.Pro316Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004098386.1
Allele description [Variation Report for NM_152299.4(NCAPH2):c.946C>G (p.Pro316Ala)]
NM_152299.4(NCAPH2):c.946C>G (p.Pro316Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024