NM_001353179.2(OVCH1):c.1792A>G (p.Ile598Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004344036.1
Allele description [Variation Report for NM_001353179.2(OVCH1):c.1792A>G (p.Ile598Val)]
NM_001353179.2(OVCH1):c.1792A>G (p.Ile598Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024