NM_000534.5(PMS1):c.174G>T (p.Gly58=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000879374.4
Allele description [Variation Report for NM_000534.5(PMS1):c.174G>T (p.Gly58=)]
NM_000534.5(PMS1):c.174G>T (p.Gly58=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024