NM_018993.4(RIN2):c.1425C>A (p.Pro475=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000416056.27
Allele description [Variation Report for NM_018993.4(RIN2):c.1425C>A (p.Pro475=)]
NM_018993.4(RIN2):c.1425C>A (p.Pro475=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024