NM_018192.4(P3H2):c.1557T>C (p.Tyr519=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001443785.5
Allele description [Variation Report for NM_018192.4(P3H2):c.1557T>C (p.Tyr519=)]
NM_018192.4(P3H2):c.1557T>C (p.Tyr519=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024