NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000194900.8
Allele description [Variation Report for NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=)]
NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024