NM_001042492.3(NF1):c.2022C>T (p.Ser674=) AND not specified
- Germline classification:
- Benign (6 submissions)
- Last evaluated:
- May 3, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000218285.21
Allele description [Variation Report for NM_001042492.3(NF1):c.2022C>T (p.Ser674=)]
NM_001042492.3(NF1):c.2022C>T (p.Ser674=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024