NM_052909.5(PLEKHG4B):c.3107C>G (p.Pro1036Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004121055.1
Allele description [Variation Report for NM_052909.5(PLEKHG4B):c.3107C>G (p.Pro1036Arg)]
NM_052909.5(PLEKHG4B):c.3107C>G (p.Pro1036Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024