NM_001387552.1(ADGRL3):c.1078C>G (p.Pro360Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004599436.1
Allele description [Variation Report for NM_001387552.1(ADGRL3):c.1078C>G (p.Pro360Ala)]
NM_001387552.1(ADGRL3):c.1078C>G (p.Pro360Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024