NM_022455.5(NSD1):c.4378+26C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000250093.12
Allele description [Variation Report for NM_022455.5(NSD1):c.4378+26C>T]
NM_022455.5(NSD1):c.4378+26C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024