NM_004070.4(CLCNKA):c.868G>T (p.Gly290Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000517532.1
Allele description [Variation Report for NM_004070.4(CLCNKA):c.868G>T (p.Gly290Cys)]
NM_004070.4(CLCNKA):c.868G>T (p.Gly290Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022