NM_001287.6(CLCN7):c.917G>T (p.Gly306Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000788792.2
Allele description [Variation Report for NM_001287.6(CLCN7):c.917G>T (p.Gly306Val)]
NM_001287.6(CLCN7):c.917G>T (p.Gly306Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024