NM_013243.4(SCG3):c.289T>C (p.Ser97Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004220697.1
Allele description [Variation Report for NM_013243.4(SCG3):c.289T>C (p.Ser97Pro)]
NM_013243.4(SCG3):c.289T>C (p.Ser97Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024