NM_000505.4(F12):c.922T>A (p.Ser308Thr) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003561523.2
Allele description [Variation Report for NM_000505.4(F12):c.922T>A (p.Ser308Thr)]
NM_000505.4(F12):c.922T>A (p.Ser308Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024