NM_004329.3(BMPR1A):c.45G>C (p.Leu15Phe) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001526241.3
Allele description [Variation Report for NM_004329.3(BMPR1A):c.45G>C (p.Leu15Phe)]
NM_004329.3(BMPR1A):c.45G>C (p.Leu15Phe)
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
-
Homo sapiens early B-cell factor 1 (EBF1), transcript variant 3, mRNA
Homo sapiens early B-cell factor 1 (EBF1), transcript variant 3, mRNAgi|594140629|ref|NM_182708.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024