NM_000222.3(KIT):c.1900C>G (p.Arg634Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003294000.3
Allele description [Variation Report for NM_000222.3(KIT):c.1900C>G (p.Arg634Gly)]
NM_000222.3(KIT):c.1900C>G (p.Arg634Gly)
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 fibroblast growth factor 14 (FGF14), mRNA
Homo sapiens fibroblast growth factor 14 (FGF14), mRNAgi|4758367|ref|NM_004115.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 12, 2024