NM_006642.5(SDCCAG8):c.1501G>C (p.Asp501His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 21, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000193940.6
Allele description [Variation Report for NM_006642.5(SDCCAG8):c.1501G>C (p.Asp501His)]
NM_006642.5(SDCCAG8):c.1501G>C (p.Asp501His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 3, 2024