NM_002775.5(HTRA1):c.337G>T (p.Ala113Ser) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jan 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000888759.8
Allele description [Variation Report for NM_002775.5(HTRA1):c.337G>T (p.Ala113Ser)]
NM_002775.5(HTRA1):c.337G>T (p.Ala113Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024