NM_017772.4(TBC1D22B):c.1033C>G (p.Arg345Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004177593.1
Allele description [Variation Report for NM_017772.4(TBC1D22B):c.1033C>G (p.Arg345Gly)]
NM_017772.4(TBC1D22B):c.1033C>G (p.Arg345Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024