NM_001201380.3(CNTNAP3B):c.3811C>A (p.Gln1271Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004192537.1
Allele description [Variation Report for NM_001201380.3(CNTNAP3B):c.3811C>A (p.Gln1271Lys)]
NM_001201380.3(CNTNAP3B):c.3811C>A (p.Gln1271Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024