NM_000313.4(PROS1):c.871T>C (p.Leu291=) AND Thrombophilia due to protein S deficiency, autosomal recessive
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001489356.6
Allele description [Variation Report for NM_000313.4(PROS1):c.871T>C (p.Leu291=)]
NM_000313.4(PROS1):c.871T>C (p.Leu291=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024