NM_020975.6(RET):c.718G>C (p.Val240Leu) AND Pheochromocytoma
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001103892.5
Allele description [Variation Report for NM_020975.6(RET):c.718G>C (p.Val240Leu)]
NM_020975.6(RET):c.718G>C (p.Val240Leu)
Condition(s)
- Name:
- Pheochromocytoma
- Synonyms:
- Chromaffinoma; Chromaffin paraganglioma; Chromaffin tumor; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008233; MedGen: C0031511; Orphanet: 29072; OMIM: 171300; Human Phenotype Ontology: HP:0002666
Assertion and evidence details
Last Updated: May 7, 2024