NM_000455.5(STK11):c.1233C>A (p.Pro411=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000575038.3
Allele description [Variation Report for NM_000455.5(STK11):c.1233C>A (p.Pro411=)]
NM_000455.5(STK11):c.1233C>A (p.Pro411=)
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
-
mitochondrial carnitine/acylcarnitine carrier protein-like [Penaeus monodon]
mitochondrial carnitine/acylcarnitine carrier protein-like [Penaeus monodon]gi|1935934546|ref|XP_037793567.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024