NM_000504.4(F10):c.1387G>C (p.Asp463His) AND Factor X deficiency
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001420419.3
Allele description [Variation Report for NM_000504.4(F10):c.1387G>C (p.Asp463His)]
NM_000504.4(F10):c.1387G>C (p.Asp463His)
Condition(s)
- Name:
- Factor X deficiency
- Synonyms:
- F10 DEFICIENCY
- Identifiers:
- MONDO: MONDO:0002247; MeSH: D005171; MedGen: C0015519
Assertion and evidence details
Last Updated: Aug 4, 2024