NM_001017970.3(TMEM30B):c.446C>T (p.Pro149Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004169742.1
Allele description [Variation Report for NM_001017970.3(TMEM30B):c.446C>T (p.Pro149Leu)]
NM_001017970.3(TMEM30B):c.446C>T (p.Pro149Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024