NM_030578.4(B9D2):c.496C>T (p.Arg166Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 26, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000368498.4
Allele description [Variation Report for NM_030578.4(B9D2):c.496C>T (p.Arg166Cys)]
NM_030578.4(B9D2):c.496C>T (p.Arg166Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024