NM_005359.6(SMAD4):c.679A>G (p.Ser227Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000777492.4
Allele description [Variation Report for NM_005359.6(SMAD4):c.679A>G (p.Ser227Gly)]
NM_005359.6(SMAD4):c.679A>G (p.Ser227Gly)
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
-
Mus musculus prion like protein doppel (Prnd), transcript variant 1, mRNA
Mus musculus prion like protein doppel (Prnd), transcript variant 1, mRNAgi|506326356|ref|NM_023043.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024