NM_019616.4(F7):c.1094T>C (p.Met365Thr) AND Abnormality of coagulation
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Feb 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000852000.1
Allele description [Variation Report for NM_019616.4(F7):c.1094T>C (p.Met365Thr)]
NM_019616.4(F7):c.1094T>C (p.Met365Thr)
Condition(s)
- Name:
- Abnormality of coagulation
- Identifiers:
- MedGen: C1846821; Human Phenotype Ontology: HP:0001928
Assertion and evidence details
Last Updated: Apr 23, 2022