NM_001136018.4(EPHX1):c.1314G>A (p.Pro438=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000894531.3
Allele description [Variation Report for NM_001136018.4(EPHX1):c.1314G>A (p.Pro438=)]
NM_001136018.4(EPHX1):c.1314G>A (p.Pro438=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023