NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Apr 21, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000177655.13
Allele description [Variation Report for NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=)]
NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024