NM_000245.4(MET):c.2887+3G>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002440168.2
Allele description [Variation Report for NM_000245.4(MET):c.2887+3G>T]
NM_000245.4(MET):c.2887+3G>T
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
-
STEAP AND 1[s_discriminator] (0)
dbGaP
-
LOC103186370 [Callorhinchus milii]
LOC103186370 [Callorhinchus milii]Gene ID:103186370Gene
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Last Updated: May 1, 2024