NM_002185.5(IL7R):c.82+74C>G AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003487749.2
Allele description [Variation Report for NM_002185.5(IL7R):c.82+74C>G]
NM_002185.5(IL7R):c.82+74C>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024