NM_175875.5(SIX5):c.1023C>T (p.Gly341=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000907892.8
Allele description [Variation Report for NM_175875.5(SIX5):c.1023C>T (p.Gly341=)]
NM_175875.5(SIX5):c.1023C>T (p.Gly341=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024