NM_001376861.1(ATP6V1G3):c.347C>G (p.Ala116Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004335413.1
Allele description [Variation Report for NM_001376861.1(ATP6V1G3):c.347C>G (p.Ala116Gly)]
NM_001376861.1(ATP6V1G3):c.347C>G (p.Ala116Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024