NM_001366145.2(TRPM3):c.3991G>T (p.Gly1331Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003404828.1
Allele description [Variation Report for NM_001366145.2(TRPM3):c.3991G>T (p.Gly1331Cys)]
NM_001366145.2(TRPM3):c.3991G>T (p.Gly1331Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 25, 2023