NM_001376852.1(TMEM181):c.1393C>T (p.Arg465Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004213231.1
Allele description [Variation Report for NM_001376852.1(TMEM181):c.1393C>T (p.Arg465Trp)]
NM_001376852.1(TMEM181):c.1393C>T (p.Arg465Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024