NM_000077.5(CDKN2A):c.458-15T>A AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000583808.3
Allele description [Variation Report for NM_000077.5(CDKN2A):c.458-15T>A]
NM_000077.5(CDKN2A):c.458-15T>A
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 premelanosome protein (PMEL), transcript variant 1, mRNA
Homo sapiens premelanosome protein (PMEL), transcript variant 1, mRNAgi|318037594|ref|NM_001200054.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 6, 2024