NM_001146079.2(CLDN14):c.522G>A (p.Ser174=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 7, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001580485.3
Allele description [Variation Report for NM_001146079.2(CLDN14):c.522G>A (p.Ser174=)]
NM_001146079.2(CLDN14):c.522G>A (p.Ser174=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 9, 2023