NM_171998.4(RAB39B):c.477T>C (p.Asn159=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000931813.3
Allele description [Variation Report for NM_171998.4(RAB39B):c.477T>C (p.Asn159=)]
NM_171998.4(RAB39B):c.477T>C (p.Asn159=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022