NM_001105569.3(MSGN1):c.11T>G (p.Leu4Arg) AND not specified
- Germline classification:
- Uncertain significance (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:
- RCV004297787.1
Allele description [Variation Report for NM_001105569.3(MSGN1):c.11T>G (p.Leu4Arg)]
NM_001105569.3(MSGN1):c.11T>G (p.Leu4Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024