NM_000179.3(MSH6):c.3698_3702dup (p.Leu1235fs) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000491792.3
Allele description [Variation Report for NM_000179.3(MSH6):c.3698_3702dup (p.Leu1235fs)]
NM_000179.3(MSH6):c.3698_3702dup (p.Leu1235fs)
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
-
ARL2BPP1 ARF like GTPase 2 binding protein pseudogene 1 [Homo sapiens]
ARL2BPP1 ARF like GTPase 2 binding protein pseudogene 1 [Homo sapiens]Gene ID:399666Gene
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024