NM_001170880.2(GPR137):c.919A>G (p.Ser307Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004146902.1
Allele description [Variation Report for NM_001170880.2(GPR137):c.919A>G (p.Ser307Gly)]
NM_001170880.2(GPR137):c.919A>G (p.Ser307Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024