NM_012391.3(SPDEF):c.65C>T (p.Thr22Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004252397.1
Allele description [Variation Report for NM_012391.3(SPDEF):c.65C>T (p.Thr22Met)]
NM_012391.3(SPDEF):c.65C>T (p.Thr22Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024