NM_000132.4(F8):c.3864A>C (p.Ser1288=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243368.9
Allele description [Variation Report for NM_000132.4(F8):c.3864A>C (p.Ser1288=)]
NM_000132.4(F8):c.3864A>C (p.Ser1288=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024