NM_001370259.2(MEN1):c.1634C>T (p.Pro545Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002397822.3
Allele description [Variation Report for NM_001370259.2(MEN1):c.1634C>T (p.Pro545Leu)]
NM_001370259.2(MEN1):c.1634C>T (p.Pro545Leu)
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 collagen type IV alpha 6 chain (COL4A6), transcript variant 4, mRNA
Homo sapiens collagen type IV alpha 6 chain (COL4A6), transcript variant 4, mRNAgi|1890315212|ref|NM_001287759.2|Nucleotide
-
Homo sapiens cDNA FLJ90425 fis, clone NT2RP3000444
Homo sapiens cDNA FLJ90425 fis, clone NT2RP3000444gi|22760655|dbj|AK074906.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024