NM_003001.5(SDHC):c.61C>G (p.Gln21Glu) AND Hereditary pheochromocytoma-paraganglioma
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004000903.2
Allele description [Variation Report for NM_003001.5(SDHC):c.61C>G (p.Gln21Glu)]
NM_003001.5(SDHC):c.61C>G (p.Gln21Glu)
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: Jan 13, 2025