NM_015074.3(KIF1B):c.*5019T>C AND Pheochromocytoma
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000343588.5
Allele description [Variation Report for NM_015074.3(KIF1B):c.*5019T>C]
NM_015074.3(KIF1B):c.*5019T>C
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: Dec 24, 2023