NM_144773.4(PROKR2):c.1122C>A (p.Thr374=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 18, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000429503.1
Allele description [Variation Report for NM_144773.4(PROKR2):c.1122C>A (p.Thr374=)]
NM_144773.4(PROKR2):c.1122C>A (p.Thr374=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024