NM_052906.5(ELFN2):c.778C>T (p.Pro260Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004188062.1
Allele description [Variation Report for NM_052906.5(ELFN2):c.778C>T (p.Pro260Ser)]
NM_052906.5(ELFN2):c.778C>T (p.Pro260Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 8, 2024