NM_175875.5(SIX5):c.1462C>T (p.Pro488Ser) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000608782.1
Allele description
NM_175875.5(SIX5):c.1462C>T (p.Pro488Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024