NM_000504.4(F10):c.1347C>T (p.Tyr449=) AND Hereditary factor X deficiency disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001109101.4
Allele description [Variation Report for NM_000504.4(F10):c.1347C>T (p.Tyr449=)]
NM_000504.4(F10):c.1347C>T (p.Tyr449=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023