NM_015160.3(PMPCA):c.634-10T>A AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004587989.1
Allele description [Variation Report for NM_015160.3(PMPCA):c.634-10T>A]
NM_015160.3(PMPCA):c.634-10T>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 23, 2024