NM_000535.7(PMS2):c.1316C>T (p.Thr439Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001759565.2
Allele description [Variation Report for NM_000535.7(PMS2):c.1316C>T (p.Thr439Ile)]
NM_000535.7(PMS2):c.1316C>T (p.Thr439Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024