NM_025099.6(CTC1):c.2472C>T (p.Pro824=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 21, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001819834.4
Allele description [Variation Report for NM_025099.6(CTC1):c.2472C>T (p.Pro824=)]
NM_025099.6(CTC1):c.2472C>T (p.Pro824=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024