NM_006514.4(SCN10A):c.4656G>A (p.Ala1552=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- May 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000604833.4
Allele description [Variation Report for NM_006514.4(SCN10A):c.4656G>A (p.Ala1552=)]
NM_006514.4(SCN10A):c.4656G>A (p.Ala1552=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024