NM_000038.6(APC):c.5277A>G (p.Ala1759=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004522828.1
Allele description [Variation Report for NM_000038.6(APC):c.5277A>G (p.Ala1759=)]
NM_000038.6(APC):c.5277A>G (p.Ala1759=)
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
-
Kelch repeat-containing protein [Escherichia coli 'BL21-Gold(DE3)pLysS AG']
Kelch repeat-containing protein [Escherichia coli 'BL21-Gold(DE3)pLysS AG']gi|253326118|gnl|jgi|ECBD_3727|gb|A 20.1|Protein
-
Spinal Dysraphism and Myelomeningocele - StatPearls
Spinal Dysraphism and Myelomeningocele - StatPearls
-
chrna1 [Etheostoma spectabile]
chrna1 [Etheostoma spectabile]Gene ID:116705532Gene
-
GNPNAT1 [Mustela nigripes]
GNPNAT1 [Mustela nigripes]Gene ID:131999953Gene
-
ACADL [Crotalus tigris]
ACADL [Crotalus tigris]Gene ID:120312337Gene
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See more...Assertion and evidence details
Last Updated: Jul 23, 2024