NM_145807.4(NTN5):c.682T>C (p.Phe228Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004123101.1
Allele description [Variation Report for NM_145807.4(NTN5):c.682T>C (p.Phe228Leu)]
NM_145807.4(NTN5):c.682T>C (p.Phe228Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Patchy osteosclerosis
Patchy osteosclerosisMedGen
-
Leiomyosarcoma NCI Grade 2
Leiomyosarcoma NCI Grade 2MedGen
-
Axial osteosclerosis
Axial osteosclerosisMedGen
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Last Updated: Sep 8, 2024