NM_001035.3(RYR2):c.12463T>A (p.Ser4155Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002282148.8
Allele description [Variation Report for NM_001035.3(RYR2):c.12463T>A (p.Ser4155Thr)]
NM_001035.3(RYR2):c.12463T>A (p.Ser4155Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024