NM_001369623.2(PI4KB):c.1201G>A (p.Val401Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004154809.1
Allele description [Variation Report for NM_001369623.2(PI4KB):c.1201G>A (p.Val401Met)]
NM_001369623.2(PI4KB):c.1201G>A (p.Val401Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024