NM_019892.6(INPP5E):c.1279+14T>C AND Joubert syndrome 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000343852.5
Allele description [Variation Report for NM_019892.6(INPP5E):c.1279+14T>C]
NM_019892.6(INPP5E):c.1279+14T>C
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024