NM_006206.6(PDGFRA):c.1700_1701inv (p.Pro567Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002413470.3
Allele description [Variation Report for NM_006206.6(PDGFRA):c.1700_1701inv (p.Pro567Leu)]
NM_006206.6(PDGFRA):c.1700_1701inv (p.Pro567Leu)
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
-
Mus musculus BUD13 homolog (Bud13), mRNA
Mus musculus BUD13 homolog (Bud13), mRNAgi|118130241|ref|NM_146000.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024