NM_016169.4(SUFU):c.645C>T (p.Asn215=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000528157.10
Allele description [Variation Report for NM_016169.4(SUFU):c.645C>T (p.Asn215=)]
NM_016169.4(SUFU):c.645C>T (p.Asn215=)
Condition(s)
- Name:
- Gorlin syndrome
- Synonyms:
- Gorlin-Goltz Syndrome; Multiple Basal Cell Nevi, Odontogenic Keratocysts, And Skeletal Anomalies; Fifth Phacomatosis; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007187; MedGen: C0004779; Orphanet: 377; OMIM: PS109400
- Name:
- Medulloblastoma (MDB)
- Synonyms:
- Medulloblastoma, somatic; MEDULLOBLASTOMA PREDISPOSITION SYNDROME
- Identifiers:
- MONDO: MONDO:0007959; MeSH: D008527; MedGen: C0025149; Orphanet: 616; OMIM: 155255; Human Phenotype Ontology: HP:0002885
Assertion and evidence details
Last Updated: May 12, 2024