NM_001289104.2(PRKCSH):c.935C>G (p.Thr312Arg) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003072685.2
Allele description [Variation Report for NM_001289104.2(PRKCSH):c.935C>G (p.Thr312Arg)]
NM_001289104.2(PRKCSH):c.935C>G (p.Thr312Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024