NM_016464.5(TMEM138):c.204T>C (p.Ala68=) AND Joubert syndrome 16
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002212378.6
Allele description [Variation Report for NM_016464.5(TMEM138):c.204T>C (p.Ala68=)]
NM_016464.5(TMEM138):c.204T>C (p.Ala68=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024