NM_172140.2(IFNL1):c.136G>C (p.Glu46Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004182998.1
Allele description [Variation Report for NM_172140.2(IFNL1):c.136G>C (p.Glu46Gln)]
NM_172140.2(IFNL1):c.136G>C (p.Glu46Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024