NM_152551.4(SNRNP48):c.329T>C (p.Leu110Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004267020.1
Allele description [Variation Report for NM_152551.4(SNRNP48):c.329T>C (p.Leu110Ser)]
NM_152551.4(SNRNP48):c.329T>C (p.Leu110Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024