NM_152703.5(SAMD9L):c.652A>C (p.Ser218Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003866173.2
Allele description [Variation Report for NM_152703.5(SAMD9L):c.652A>C (p.Ser218Arg)]
NM_152703.5(SAMD9L):c.652A>C (p.Ser218Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024