NM_004329.3(BMPR1A):c.396G>T (p.Gln132His) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001179443.3
Allele description [Variation Report for NM_004329.3(BMPR1A):c.396G>T (p.Gln132His)]
NM_004329.3(BMPR1A):c.396G>T (p.Gln132His)
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
-
inpp4aa [Anoplopoma fimbria]
inpp4aa [Anoplopoma fimbria]Gene ID:129104462Gene
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024