NM_000038.6(APC):c.7052C>G (p.Pro2351Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000563073.15
Allele description [Variation Report for NM_000038.6(APC):c.7052C>G (p.Pro2351Arg)]
NM_000038.6(APC):c.7052C>G (p.Pro2351Arg)
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
-
cytochrome b (mitochondrion) [Thraupis sayaca]
cytochrome b (mitochondrion) [Thraupis sayaca]gi|2317753558|gb|UYG47231.1|Protein
-
Mus musculus lectin, galactose binding, soluble 9 (Lgals9), transcript variant 2...
Mus musculus lectin, galactose binding, soluble 9 (Lgals9), transcript variant 2, mRNAgi|226531138|ref|NM_001159301.1|Nucleotide
-
cytochrome b, partial (mitochondrion) [Megastigmus spermotrophus nigrodorsatus]
cytochrome b, partial (mitochondrion) [Megastigmus spermotrophus nigrodorsatus]gi|60250701|gb|AAX14884.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 20, 2024