NM_000130.5(F5):c.5621T>C (p.Met1874Thr) AND Abnormal bleeding
- Germline classification:
- Uncertain significance (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:
- RCV000851824.1
Allele description [Variation Report for NM_000130.5(F5):c.5621T>C (p.Met1874Thr)]
NM_000130.5(F5):c.5621T>C (p.Met1874Thr)
Condition(s)
- Name:
- Abnormal bleeding
- Identifiers:
- MedGen: C1458140; Human Phenotype Ontology: HP:0001892
Assertion and evidence details
Last Updated: Sep 29, 2024