NM_014855.3(AP5Z1):c.*880C>T AND Hereditary spastic paraplegia 48
- 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:
- RCV001158463.4
Allele description [Variation Report for NM_014855.3(AP5Z1):c.*880C>T]
NM_014855.3(AP5Z1):c.*880C>T
Condition(s)
-
PROP1-Related Combined Pituitary Hormone Deficiency - GeneReviews®
PROP1-Related Combined Pituitary Hormone Deficiency - GeneReviews®
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Last Updated: Oct 14, 2023