NM_024422.6(DSC2):c.1694T>G (p.Ile565Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001553573.1
Allele description [Variation Report for NM_024422.6(DSC2):c.1694T>G (p.Ile565Ser)]
NM_024422.6(DSC2):c.1694T>G (p.Ile565Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024