NM_004304.5(ALK):c.3484C>T (p.Leu1162=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 6, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002457387.2
Allele description [Variation Report for NM_004304.5(ALK):c.3484C>T (p.Leu1162=)]
NM_004304.5(ALK):c.3484C>T (p.Leu1162=)
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 family with sequence similarity 120 member C (FAM120C), transcript ...
Homo sapiens family with sequence similarity 120 member C (FAM120C), transcript variant 2, mRNAgi|1676440371|ref|NM_198456.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024