NM_001077498.3(FAM222B):c.425G>A (p.Ser142Asn) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004173981.1
Allele description [Variation Report for NM_001077498.3(FAM222B):c.425G>A (p.Ser142Asn)]
NM_001077498.3(FAM222B):c.425G>A (p.Ser142Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024