NM_018112.3(TMEM38B):c.799G>A (p.Val267Ile) AND TMEM38B-related condition
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003940375.1
Allele description [Variation Report for NM_018112.3(TMEM38B):c.799G>A (p.Val267Ile)]
NM_018112.3(TMEM38B):c.799G>A (p.Val267Ile)
Condition(s)
- Name:
- TMEM38B-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 1, 2024