NM_017849.4(TMEM127):c.482A>G (p.His161Arg) AND Hereditary pheochromocytoma-paraganglioma
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001069257.8
Allele description [Variation Report for NM_017849.4(TMEM127):c.482A>G (p.His161Arg)]
NM_017849.4(TMEM127):c.482A>G (p.His161Arg)
Condition(s)
- Name:
- Hereditary pheochromocytoma-paraganglioma
- Synonyms:
- Hereditary Paraganglioma-Pheochromocytoma Syndromes; Hereditary Paragangliomas and Pheochromocytomas
- Identifiers:
- MONDO: MONDO:0017366; MedGen: C1708353
Assertion and evidence details
Last Updated: Jun 23, 2024