NM_000128.4(F11):c.801A>G (p.Thr267=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001512065.7
Allele description [Variation Report for NM_000128.4(F11):c.801A>G (p.Thr267=)]
NM_000128.4(F11):c.801A>G (p.Thr267=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 30, 2024