NM_015922.3(NSDHL):c.25A>G (p.Met9Val) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000146962.7
Allele description [Variation Report for NM_015922.3(NSDHL):c.25A>G (p.Met9Val)]
NM_015922.3(NSDHL):c.25A>G (p.Met9Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 5, 2024