NM_175922.4(PRR18):c.530C>A (p.Pro177Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004507728.1
Allele description [Variation Report for NM_175922.4(PRR18):c.530C>A (p.Pro177Gln)]
NM_175922.4(PRR18):c.530C>A (p.Pro177Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024