NM_024675.4(PALB2):c.3085_3092del (p.Thr1029fs) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jan 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000773460.4
Allele description [Variation Report for NM_024675.4(PALB2):c.3085_3092del (p.Thr1029fs)]
NM_024675.4(PALB2):c.3085_3092del (p.Thr1029fs)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
D003401 (1)
MeSH
-
Creatine
CreatineAn amino acid that occurs in vertebrate tissues and in urine. In muscle tissue, creatine generally occurs as phosphocreatine. Creatine is excreted as CREATININE in the urine....<br/>Year introduced: 1968MeSH
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023