NM_001365951.3(KIF1B):c.*2032T>A AND Pheochromocytoma
- Germline classification:
- Uncertain significance (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:
- RCV000269858.5
Allele description [Variation Report for NM_001365951.3(KIF1B):c.*2032T>A]
NM_001365951.3(KIF1B):c.*2032T>A
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
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PUS10 pseudouridine synthase 10 [Homo sapiens]
PUS10 pseudouridine synthase 10 [Homo sapiens]Gene ID:150962Gene
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Gene Links for GEO Profiles (Select 30499917) (1)
Gene
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Homologene neighbors for GEO Profiles (Select 30488485) (0)
GEO Profiles
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Homologene neighbors for GEO Profiles (Select 30475573) (0)
GEO Profiles
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Last Updated: Dec 24, 2023