NM_002230.4(JUP):c.990C>T (p.Thr330=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 17, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000443059.1
Allele description [Variation Report for NM_002230.4(JUP):c.990C>T (p.Thr330=)]
NM_002230.4(JUP):c.990C>T (p.Thr330=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024