NM_001077418.3(TMEM231):c.490C>T (p.Pro164Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001938537.5
Allele description [Variation Report for NM_001077418.3(TMEM231):c.490C>T (p.Pro164Ser)]
NM_001077418.3(TMEM231):c.490C>T (p.Pro164Ser)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024