NM_198252.3(GSN):c.1485C>T (p.Ile495=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002105644.5
Allele description [Variation Report for NM_198252.3(GSN):c.1485C>T (p.Ile495=)]
NM_198252.3(GSN):c.1485C>T (p.Ile495=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024