NM_001807.6(CEL):c.472G>A (p.Val158Met) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003151896.1
Allele description [Variation Report for NM_001807.6(CEL):c.472G>A (p.Val158Met)]
NM_001807.6(CEL):c.472G>A (p.Val158Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 18, 2023