NM_000038.6(APC):c.3111C>G (p.Asn1037Lys) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003177463.2
Allele description [Variation Report for NM_000038.6(APC):c.3111C>G (p.Asn1037Lys)]
NM_000038.6(APC):c.3111C>G (p.Asn1037Lys)
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 membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5) (M...
Homo sapiens membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5) (MPP5), mRNAgi|38570141|ref|NM_022474.2|Nucleotide
-
Plectobranchus evides voucher MFC202 cytochrome oxidase subunit 1 (COI) gene, pa...
Plectobranchus evides voucher MFC202 cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrialgi|294989252|gnl|uoguelph|MFC202-08 5P|gb|GU440464.1|Nucleotide
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Last Updated: May 1, 2024