NM_004813.4(PEX16):c.359+20A>G AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000252785.5
Allele description [Variation Report for NM_004813.4(PEX16):c.359+20A>G]
NM_004813.4(PEX16):c.359+20A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024