NM_002299.4(LCT):c.2714A>G (p.Asp905Gly) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000955965.8
Allele description [Variation Report for NM_002299.4(LCT):c.2714A>G (p.Asp905Gly)]
NM_002299.4(LCT):c.2714A>G (p.Asp905Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024