NM_017841.4(SDHAF2):c.471T>C (p.Asp157=) AND Hereditary pheochromocytoma-paraganglioma
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003634275.1
Allele description [Variation Report for NM_017841.4(SDHAF2):c.471T>C (p.Asp157=)]
NM_017841.4(SDHAF2):c.471T>C (p.Asp157=)
Condition(s)
- Name:
- Hereditary pheochromocytoma-paraganglioma
- Synonyms:
- Hereditary Paraganglioma-Pheochromocytoma Syndromes; Hereditary Paragangliomas and Pheochromocytomas
- Identifiers:
- MONDO: MONDO:0017366; MedGen: C1708353
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024