NM_014141.6(CNTNAP2):c.862A>G (p.Ile288Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001751717.2
Allele description [Variation Report for NM_014141.6(CNTNAP2):c.862A>G (p.Ile288Val)]
NM_014141.6(CNTNAP2):c.862A>G (p.Ile288Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024