NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- 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:
- RCV000649975.8
Allele description [Variation Report for NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe)]
NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024