NM_021625.4(TRPV4):c.2304G>C (p.Ser768=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000597518.3
Allele description
NM_021625.4(TRPV4):c.2304G>C (p.Ser768=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 10, 2021