NM_024422.6(DSC2):c.2112_2116del (p.Phe708fs) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Apr 10, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000627125.2
Allele description [Variation Report for NM_024422.6(DSC2):c.2112_2116del (p.Phe708fs)]
NM_024422.6(DSC2):c.2112_2116del (p.Phe708fs)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024