NM_005732.4(RAD50):c.1269T>C (p.Thr423=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000219801.12
Allele description [Variation Report for NM_005732.4(RAD50):c.1269T>C (p.Thr423=)]
NM_005732.4(RAD50):c.1269T>C (p.Thr423=)
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 mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltran...
Homo sapiens mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase (MGAT3), transcript variant 1, mRNAgi|148539887|ref|NM_002409.4|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024