NM_017841.4(SDHAF2):c.327T>G (p.Ile109Met) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002442711.2
Allele description [Variation Report for NM_017841.4(SDHAF2):c.327T>G (p.Ile109Met)]
NM_017841.4(SDHAF2):c.327T>G (p.Ile109Met)
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
-
Human sample from Homo sapiens
Human sample from Homo sapiensbiosample
-
CERS5 [Pan paniscus]
CERS5 [Pan paniscus]Gene ID:100980816Gene
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Last Updated: Sep 29, 2024