NM_000540.3(RYR1):c.14783T>A (p.Ile4928Asn) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003236147.1
Allele description [Variation Report for NM_000540.3(RYR1):c.14783T>A (p.Ile4928Asn)]
NM_000540.3(RYR1):c.14783T>A (p.Ile4928Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jun 24, 2023