NM_152703.5(SAMD9L):c.4082T>C (p.Val1361Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002543693.2
Allele description [Variation Report for NM_152703.5(SAMD9L):c.4082T>C (p.Val1361Ala)]
NM_152703.5(SAMD9L):c.4082T>C (p.Val1361Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024