NM_001943.5(DSG2):c.2340G>T (p.Ala780=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000608537.3
Allele description [Variation Report for NM_001943.5(DSG2):c.2340G>T (p.Ala780=)]
NM_001943.5(DSG2):c.2340G>T (p.Ala780=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024