NM_001204424.2(RGS6):c.771A>G (p.Thr257=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002078664.5
Allele description [Variation Report for NM_001204424.2(RGS6):c.771A>G (p.Thr257=)]
NM_001204424.2(RGS6):c.771A>G (p.Thr257=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024