NM_052892.5(PKD1L2):c.5568G>A (p.Met1856Ile) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004130953.1
Allele description [Variation Report for NM_052892.5(PKD1L2):c.5568G>A (p.Met1856Ile)]
NM_052892.5(PKD1L2):c.5568G>A (p.Met1856Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024