NM_000335.5(SCN5A):c.3944G>C (p.Arg1315Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001420834.1
Allele description [Variation Report for NM_000335.5(SCN5A):c.3944G>C (p.Arg1315Pro)]
NM_000335.5(SCN5A):c.3944G>C (p.Arg1315Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023