NM_001009944.3(PKD1):c.3975C>T (p.Leu1325=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000244253.5
Allele description [Variation Report for NM_001009944.3(PKD1):c.3975C>T (p.Leu1325=)]
NM_001009944.3(PKD1):c.3975C>T (p.Leu1325=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024