NM_000330.4(RS1):c.399T>C (p.Ile133=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003723380.2
Allele description [Variation Report for NM_000330.4(RS1):c.399T>C (p.Ile133=)]
NM_000330.4(RS1):c.399T>C (p.Ile133=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 3, 2024