NM_213720.3(CHCHD10):c.192C>T (p.Val64=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 10, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000963549.3
Allele description
NM_213720.3(CHCHD10):c.192C>T (p.Val64=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jan 7, 2023