NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002603405.2
Allele description [Variation Report for NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu)]
NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024