NM_002230.4(JUP):c.1854C>T (p.Ala618=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000422836.2
Allele description [Variation Report for NM_002230.4(JUP):c.1854C>T (p.Ala618=)]
NM_002230.4(JUP):c.1854C>T (p.Ala618=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024