NM_000360.4(TH):c.1368C>T (p.Ser456=) AND not provided
- Germline classification:
- Likely benign (4 submissions)
- Last evaluated:
- May 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001729518.19
Allele description [Variation Report for NM_000360.4(TH):c.1368C>T (p.Ser456=)]
NM_000360.4(TH):c.1368C>T (p.Ser456=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024