NM_000038.6(APC):c.3413A>G (p.Asp1138Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002329286.9
Allele description [Variation Report for NM_000038.6(APC):c.3413A>G (p.Asp1138Gly)]
NM_000038.6(APC):c.3413A>G (p.Asp1138Gly)
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
-
MAN2A2 [Ovis aries]
MAN2A2 [Ovis aries]Gene ID:101106798Gene
-
Protein Interactions and Target Discovery in Huntington’s Disease - Neurobiology...
Protein Interactions and Target Discovery in Huntington’s Disease - Neurobiology of Huntington's Disease
-
LOC7498090 [Populus trichocarpa]
LOC7498090 [Populus trichocarpa]Gene ID:7498090Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024