NM_006412.4(AGPAT2):c.40CTG[5] (p.Leu17dup) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001651194.6
Allele description [Variation Report for NM_006412.4(AGPAT2):c.40CTG[5] (p.Leu17dup)]
NM_006412.4(AGPAT2):c.40CTG[5] (p.Leu17dup)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024