NM_001134232.2(TMEM106B):c.554C>G (p.Thr185Ser) AND Leukodystrophy, hypomyelinating, 16
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001838673.3
Allele description [Variation Report for NM_001134232.2(TMEM106B):c.554C>G (p.Thr185Ser)]
NM_001134232.2(TMEM106B):c.554C>G (p.Thr185Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024