NM_022092.3(CHTF18):c.760T>C (p.Ser254Pro) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 30, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000898319.4
Allele description [Variation Report for NM_022092.3(CHTF18):c.760T>C (p.Ser254Pro)]
NM_022092.3(CHTF18):c.760T>C (p.Ser254Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024