NM_000535.7(PMS2):c.2062A>G (p.Ile688Val) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- May 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001800682.2
Allele description [Variation Report for NM_000535.7(PMS2):c.2062A>G (p.Ile688Val)]
NM_000535.7(PMS2):c.2062A>G (p.Ile688Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024