NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000766768.11
Allele description [Variation Report for NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro)]
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024